OA20600A - [((1R,2S,5R)-2-Isopropyl-5-Methyl-Cyclohexanecarbonyl)-Amino]-Acetic acid Isopropyl ester for treatment of chronic cough. - Google Patents
[((1R,2S,5R)-2-Isopropyl-5-Methyl-Cyclohexanecarbonyl)-Amino]-Acetic acid Isopropyl ester for treatment of chronic cough. Download PDFInfo
- Publication number
- OA20600A OA20600A OA1202100537 OA20600A OA 20600 A OA20600 A OA 20600A OA 1202100537 OA1202100537 OA 1202100537 OA 20600 A OA20600 A OA 20600A
- Authority
- OA
- OAPI
- Prior art keywords
- cough
- treatment
- compound
- chronic cough
- rcc
- Prior art date
Links
- 206010011224 Cough Diseases 0.000 title claims abstract description 739
- -1 (1R,2S,5R)-2-Isopropyl-5-Methyl-Cyclohexanecarbonyl Chemical group 0.000 title abstract description 40
- 150000001875 compounds Chemical class 0.000 claims abstract description 281
- 230000035492 administration Effects 0.000 claims description 109
- 230000002354 daily Effects 0.000 claims description 45
- 206010043521 Throat irritation Diseases 0.000 claims description 34
- 230000000699 topical Effects 0.000 claims description 33
- 230000037396 body weight Effects 0.000 claims description 25
- 208000006673 Asthma Diseases 0.000 claims description 24
- 206010017885 Gastrooesophageal reflux disease Diseases 0.000 claims description 23
- 201000009794 idiopathic pulmonary fibrosis Diseases 0.000 claims description 22
- 230000001515 vagal Effects 0.000 claims description 18
- 206010029331 Neuropathy peripheral Diseases 0.000 claims description 17
- 230000011514 reflex Effects 0.000 claims description 16
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims description 15
- 206010006451 Bronchitis Diseases 0.000 claims description 13
- 201000009267 bronchiectasis Diseases 0.000 claims description 13
- 206010020751 Hypersensitivity Diseases 0.000 claims description 12
- 230000001953 sensory Effects 0.000 claims description 12
- 206010073508 Drug reaction with eosinophilia and systemic symptom Diseases 0.000 claims description 11
- 206010070488 Upper-airway cough syndrome Diseases 0.000 claims description 11
- 201000005794 allergic hypersensitivity disease Diseases 0.000 claims description 10
- 239000007921 spray Substances 0.000 claims description 9
- 230000009610 hypersensitivity Effects 0.000 claims description 8
- 206010070834 Sensitisation Diseases 0.000 claims description 7
- 239000003595 mist Substances 0.000 claims description 7
- 230000008313 sensitization Effects 0.000 claims description 7
- 230000001235 sensitizing Effects 0.000 claims description 7
- 206010064012 Central pain syndrome Diseases 0.000 claims description 6
- 206010061218 Inflammation Diseases 0.000 claims description 6
- 206010033775 Paraesthesia Diseases 0.000 claims description 6
- 230000001054 cortical Effects 0.000 claims description 6
- 230000004054 inflammatory process Effects 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 230000003959 neuroinflammation Effects 0.000 claims description 6
- 230000002739 subcortical Effects 0.000 claims description 6
- 241001602876 Nata Species 0.000 claims description 5
- 208000007920 Neurogenic Inflammation Diseases 0.000 claims description 5
- 201000001119 neuropathy Diseases 0.000 claims description 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 4
- 206010008415 Chediak-Higashi syndrome Diseases 0.000 claims 1
- 238000002560 therapeutic procedure Methods 0.000 abstract description 28
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract description 26
- 239000000203 mixture Substances 0.000 description 43
- NOOLISFMXDJSKH-KXUCPTDWSA-N (-)-(1R,3R,4S)-menthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@H]1O NOOLISFMXDJSKH-KXUCPTDWSA-N 0.000 description 42
- YKPUWZUDDOIDPM-SOFGYWHQSA-N Capsaicin Chemical compound COC1=CC(CNC(=O)CCCC\C=C\C(C)C)=CC=C1O YKPUWZUDDOIDPM-SOFGYWHQSA-N 0.000 description 39
- 229930003833 capsaicin Natural products 0.000 description 39
- 229960002504 capsaicin Drugs 0.000 description 39
- 235000017663 capsaicin Nutrition 0.000 description 39
- 229960004873 LEVOMENTHOL Drugs 0.000 description 37
- 230000000694 effects Effects 0.000 description 33
- 229940041616 Menthol Drugs 0.000 description 32
- 239000006191 orally-disintegrating tablet Substances 0.000 description 32
- 239000003814 drug Substances 0.000 description 31
- 210000003800 Pharynx Anatomy 0.000 description 30
- 239000000556 agonist Substances 0.000 description 30
- 230000004044 response Effects 0.000 description 29
- 239000003981 vehicle Substances 0.000 description 26
- JMMWKPVZQRWMSS-UHFFFAOYSA-N Isopropyl acetate Chemical compound CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 description 25
- 229940079593 drugs Drugs 0.000 description 24
- 239000003826 tablet Substances 0.000 description 23
- 241000700199 Cavia porcellus Species 0.000 description 20
- 238000001816 cooling Methods 0.000 description 18
- 230000002401 inhibitory effect Effects 0.000 description 18
- 210000000038 chest Anatomy 0.000 description 17
- 230000001684 chronic Effects 0.000 description 15
- 239000012071 phase Substances 0.000 description 15
- 230000003042 antagnostic Effects 0.000 description 14
- 239000000969 carrier Substances 0.000 description 14
- 239000003795 chemical substances by application Substances 0.000 description 13
- 210000001519 tissues Anatomy 0.000 description 13
- 238000000034 method Methods 0.000 description 12
- 239000003921 oil Substances 0.000 description 12
- 239000008194 pharmaceutical composition Substances 0.000 description 12
- 101700049319 INS Proteins 0.000 description 11
- 102100001147 TRPA1 Human genes 0.000 description 11
- 230000004913 activation Effects 0.000 description 11
- 231100000494 adverse effect Toxicity 0.000 description 11
- 230000000954 anitussive Effects 0.000 description 11
- 239000005557 antagonist Substances 0.000 description 11
- 231100000673 dose–response relationship Toxicity 0.000 description 11
- 239000007788 liquid Substances 0.000 description 11
- 239000000243 solution Substances 0.000 description 11
- 210000002700 Urine Anatomy 0.000 description 9
- 238000004166 bioassay Methods 0.000 description 9
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 9
- 238000009434 installation Methods 0.000 description 9
- 238000009597 pregnancy test Methods 0.000 description 9
- OROGSEYTTFOCAN-DNJOTXNNSA-N Codeine Chemical compound C([C@H]1[C@H](N(CC[C@@]112)C)C3)=C[C@H](O)[C@@H]1OC1=C2C3=CC=C1OC OROGSEYTTFOCAN-DNJOTXNNSA-N 0.000 description 8
- 102100010198 P2RX3 Human genes 0.000 description 8
- 101700006053 P2RX3 Proteins 0.000 description 8
- OYPRJOBELJOOCE-UHFFFAOYSA-N calcium Chemical group [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 8
- 229910052791 calcium Inorganic materials 0.000 description 8
- 239000011575 calcium Substances 0.000 description 8
- 239000003085 diluting agent Substances 0.000 description 8
- 230000001976 improved Effects 0.000 description 8
- 230000003522 irritant Effects 0.000 description 8
- 239000002085 irritant Substances 0.000 description 8
- 231100000021 irritant Toxicity 0.000 description 8
- 230000035807 sensation Effects 0.000 description 8
- 235000019615 sensations Nutrition 0.000 description 8
- 241000700198 Cavia Species 0.000 description 7
- 238000010171 animal model Methods 0.000 description 7
- 239000003434 antitussive agent Substances 0.000 description 7
- 230000003247 decreasing Effects 0.000 description 7
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 7
- 230000003364 opioid Effects 0.000 description 7
- 230000002085 persistent Effects 0.000 description 7
- 239000000843 powder Substances 0.000 description 7
- 230000014860 sensory perception of taste Effects 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 230000001270 agonistic Effects 0.000 description 6
- 239000006071 cream Substances 0.000 description 6
- 239000010432 diamond Substances 0.000 description 6
- 201000010099 disease Diseases 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 6
- 239000008164 mustard oil Substances 0.000 description 6
- 230000000275 pharmacokinetic Effects 0.000 description 6
- 229940068196 placebo Drugs 0.000 description 6
- 239000000902 placebo Substances 0.000 description 6
- 230000002685 pulmonary Effects 0.000 description 6
- 102000005962 receptors Human genes 0.000 description 6
- 108020003175 receptors Proteins 0.000 description 6
- 231100000486 side effect Toxicity 0.000 description 6
- 230000002269 spontaneous Effects 0.000 description 6
- 235000019640 taste Nutrition 0.000 description 6
- 230000035917 taste Effects 0.000 description 6
- 231100000730 tolerability Toxicity 0.000 description 6
- 230000035533 AUC Effects 0.000 description 5
- SKRDXYBATCVEMS-UHFFFAOYSA-N Isopropyl nitrite Chemical compound CC(C)ON=O SKRDXYBATCVEMS-UHFFFAOYSA-N 0.000 description 5
- 206010036790 Productive cough Diseases 0.000 description 5
- 239000003172 expectorant agent Substances 0.000 description 5
- 239000003925 fat Substances 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 239000007937 lozenge Substances 0.000 description 5
- 235000010603 pastilles Nutrition 0.000 description 5
- 230000002093 peripheral Effects 0.000 description 5
- 230000002829 reduced Effects 0.000 description 5
- 239000000600 sorbitol Substances 0.000 description 5
- 201000010874 syndrome Diseases 0.000 description 5
- 238000002562 urinalysis Methods 0.000 description 5
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 4
- FBPFZTCFMRRESA-KAZBKCHUSA-N D-Mannitol Natural products OC[C@@H](O)[C@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KAZBKCHUSA-N 0.000 description 4
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 4
- 102000004310 Ion Channels Human genes 0.000 description 4
- 108090000862 Ion Channels Proteins 0.000 description 4
- FBPFZTCFMRRESA-KVTDHHQDSA-N Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 4
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinylpyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 4
- 210000001331 Nose Anatomy 0.000 description 4
- 210000003491 Skin Anatomy 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 4
- 230000001070 adhesive Effects 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 4
- 229960004126 codeine Drugs 0.000 description 4
- 201000009910 diseases by infectious agent Diseases 0.000 description 4
- 239000002552 dosage form Substances 0.000 description 4
- 239000003995 emulsifying agent Substances 0.000 description 4
- 230000002708 enhancing Effects 0.000 description 4
- 239000000796 flavoring agent Substances 0.000 description 4
- 235000013305 food Nutrition 0.000 description 4
- 239000003112 inhibitor Substances 0.000 description 4
- 238000009533 lab test Methods 0.000 description 4
- 235000010355 mannitol Nutrition 0.000 description 4
- 239000000594 mannitol Substances 0.000 description 4
- 229960001855 mannitol Drugs 0.000 description 4
- 239000002324 mouth wash Substances 0.000 description 4
- 230000000510 mucolytic Effects 0.000 description 4
- 230000003533 narcotic Effects 0.000 description 4
- 230000000926 neurological Effects 0.000 description 4
- 230000035935 pregnancy Effects 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N propylene glycol Chemical group CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 229960002920 sorbitol Drugs 0.000 description 4
- 235000010356 sorbitol Nutrition 0.000 description 4
- 239000006188 syrup Substances 0.000 description 4
- 235000020357 syrup Nutrition 0.000 description 4
- 230000001225 therapeutic Effects 0.000 description 4
- 230000001052 transient Effects 0.000 description 4
- 230000000007 visual effect Effects 0.000 description 4
- AYXYPKUFHZROOJ-ZETCQYMHSA-N (3S)-3-(aminomethyl)-5-methylhexanoic acid Chemical compound CC(C)C[C@H](CN)CC(O)=O AYXYPKUFHZROOJ-ZETCQYMHSA-N 0.000 description 3
- HLWURFKMDLAKOD-UHFFFAOYSA-N 5-(2,4-diaminopyrimidin-5-yl)oxy-2-methoxy-4-propan-2-ylbenzenesulfonamide Chemical compound C1=C(S(N)(=O)=O)C(OC)=CC(C(C)C)=C1OC1=CN=C(N)N=C1N HLWURFKMDLAKOD-UHFFFAOYSA-N 0.000 description 3
- 108010082126 Alanine Transaminase Proteins 0.000 description 3
- 229960000836 Amitriptyline Drugs 0.000 description 3
- KRMDCWKBEZIMAB-UHFFFAOYSA-N Amitriptyline Chemical compound C1CC2=CC=CC=C2C(=CCCN(C)C)C2=CC=CC=C21 KRMDCWKBEZIMAB-UHFFFAOYSA-N 0.000 description 3
- 108010003415 Aspartate Aminotransferases Proteins 0.000 description 3
- 102000004625 Aspartate Aminotransferases Human genes 0.000 description 3
- MAFMQEKGGFWBAB-UHFFFAOYSA-N Benzonatate Chemical compound CCCCNC1=CC=C(C(=O)OCCOCCOCCOCCOCCOCCOCCOCCOCCOC)C=C1 MAFMQEKGGFWBAB-UHFFFAOYSA-N 0.000 description 3
- 108090000312 Calcium Channels Proteins 0.000 description 3
- 102000003922 Calcium Channels Human genes 0.000 description 3
- 229960001985 Dextromethorphan Drugs 0.000 description 3
- MKXZASYAUGDDCJ-SZMVWBNQSA-N Dextromethorphan Chemical compound C1CCC[C@H]2[C@@]3([H])N(C)CC[C@]21C1=CC(OC)=CC=C1C3 MKXZASYAUGDDCJ-SZMVWBNQSA-N 0.000 description 3
- 102100010966 GPT Human genes 0.000 description 3
- UGJMXCAKCUNAIE-UHFFFAOYSA-N Gabapen Chemical compound OC(=O)CC1(CN)CCCCC1 UGJMXCAKCUNAIE-UHFFFAOYSA-N 0.000 description 3
- 235000010643 Leucaena leucocephala Nutrition 0.000 description 3
- 240000007472 Leucaena leucocephala Species 0.000 description 3
- 210000000265 Leukocytes Anatomy 0.000 description 3
- 210000004072 Lung Anatomy 0.000 description 3
- BQJCRHHNABKAKU-KBQPJGBKSA-N Morphine Chemical compound O([C@H]1[C@H](C=C[C@H]23)O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O BQJCRHHNABKAKU-KBQPJGBKSA-N 0.000 description 3
- 210000000214 Mouth Anatomy 0.000 description 3
- 229940066491 Mucolytics Drugs 0.000 description 3
- 229940005483 OPIOID ANALGESICS Drugs 0.000 description 3
- 108060008568 TRPV4 Proteins 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000002775 capsule Substances 0.000 description 3
- 229950008597 drug INN Drugs 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 235000003599 food sweetener Nutrition 0.000 description 3
- 229960002870 gabapentin Drugs 0.000 description 3
- 229940121285 gefapixant Drugs 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- 230000002458 infectious Effects 0.000 description 3
- 239000002050 international nonproprietary name Substances 0.000 description 3
- 230000002045 lasting Effects 0.000 description 3
- 239000000314 lubricant Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 230000001404 mediated Effects 0.000 description 3
- 229960005181 morphine Drugs 0.000 description 3
- 229930014694 morphine Natural products 0.000 description 3
- 210000004877 mucosa Anatomy 0.000 description 3
- 230000000414 obstructive Effects 0.000 description 3
- 239000002674 ointment Substances 0.000 description 3
- 238000004806 packaging method and process Methods 0.000 description 3
- 239000011505 plaster Substances 0.000 description 3
- 229960001233 pregabalin Drugs 0.000 description 3
- 230000000069 prophylaxis Effects 0.000 description 3
- 239000002464 receptor antagonist Substances 0.000 description 3
- 230000035945 sensitivity Effects 0.000 description 3
- 230000001629 suppression Effects 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 239000003765 sweetening agent Substances 0.000 description 3
- 230000001960 triggered Effects 0.000 description 3
- 230000002618 waking Effects 0.000 description 3
- VUKAUDKDFVSVFT-UHFFFAOYSA-N 2-[6-[4,5-bis(2-hydroxypropoxy)-2-(2-hydroxypropoxymethyl)-6-methoxyoxan-3-yl]oxy-4,5-dimethoxy-2-(methoxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)-5-methoxyoxane-3,4-diol Chemical compound COC1C(OC)C(OC2C(C(O)C(OC)C(CO)O2)O)C(COC)OC1OC1C(COCC(C)O)OC(OC)C(OCC(C)O)C1OCC(C)O VUKAUDKDFVSVFT-UHFFFAOYSA-N 0.000 description 2
- 210000003626 Afferent Pathways Anatomy 0.000 description 2
- 241000416162 Astragalus gummifer Species 0.000 description 2
- 210000004369 Blood Anatomy 0.000 description 2
- 241000283690 Bos taurus Species 0.000 description 2
- 206010006458 Bronchitis chronic Diseases 0.000 description 2
- 241000282693 Cercopithecidae Species 0.000 description 2
- 208000007451 Chronic Bronchitis Diseases 0.000 description 2
- WQZGKKKJIJFFOK-GASJEMHNSA-N D-Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
- CZMRCDWAGMRECN-UGDNZRGBSA-N D-sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 2
- 210000000188 Diaphragm Anatomy 0.000 description 2
- 208000000059 Dyspnea Diseases 0.000 description 2
- 206010013975 Dyspnoeas Diseases 0.000 description 2
- 241000283073 Equus caballus Species 0.000 description 2
- 210000003743 Erythrocytes Anatomy 0.000 description 2
- 229940066493 Expectorants Drugs 0.000 description 2
- 241000282326 Felis catus Species 0.000 description 2
- 210000001035 Gastrointestinal Tract Anatomy 0.000 description 2
- 108010010803 Gelatin Proteins 0.000 description 2
- 210000004704 Glottis Anatomy 0.000 description 2
- 241000725303 Human immunodeficiency virus Species 0.000 description 2
- VQHSOMBJVWLPSR-WUJBLJFYSA-N Maltitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H]([C@H](O)CO)O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O VQHSOMBJVWLPSR-WUJBLJFYSA-N 0.000 description 2
- 229940100662 Nasal Drops Drugs 0.000 description 2
- 229940097496 Nasal Spray Drugs 0.000 description 2
- 241000658540 Ora Species 0.000 description 2
- 210000003300 Oropharynx Anatomy 0.000 description 2
- GPFAJKDEDBRFOS-FKQDBXSBSA-N Pholcodine Chemical compound O([C@@H]1[C@]23CCN([C@H](C4)[C@@H]3C=C[C@@H]1O)C)C1=C2C4=CC=C1OCCN1CCOCC1 GPFAJKDEDBRFOS-FKQDBXSBSA-N 0.000 description 2
- 229940069328 Povidone Drugs 0.000 description 2
- 210000003324 RBC Anatomy 0.000 description 2
- 241000700159 Rattus Species 0.000 description 2
- 206010038683 Respiratory disease Diseases 0.000 description 2
- 206010048908 Seasonal allergy Diseases 0.000 description 2
- 210000002265 Sensory Receptor Cells Anatomy 0.000 description 2
- 229940083542 Sodium Drugs 0.000 description 2
- 210000003802 Sputum Anatomy 0.000 description 2
- 210000002784 Stomach Anatomy 0.000 description 2
- CZMRCDWAGMRECN-GDQSFJPYSA-N Sucrose Natural products O([C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](CO)O1)[C@@]1(CO)[C@H](O)[C@@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-GDQSFJPYSA-N 0.000 description 2
- 102000003568 TRPV3 Human genes 0.000 description 2
- 108060008567 TRPV3 Proteins 0.000 description 2
- 102000003567 TRPV4 Human genes 0.000 description 2
- 229960003433 Thalidomide Drugs 0.000 description 2
- UEJJHQNACJXSKW-UHFFFAOYSA-N Thalidomide Chemical compound O=C1C2=CC=CC=C2C(=O)N1C1CCC(=O)NC1=O UEJJHQNACJXSKW-UHFFFAOYSA-N 0.000 description 2
- 210000003437 Trachea Anatomy 0.000 description 2
- 229940116362 Tragacanth Drugs 0.000 description 2
- 229920001615 Tragacanth Polymers 0.000 description 2
- 206010046306 Upper respiratory tract infection Diseases 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Substances CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- 230000001058 adult Effects 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 210000003484 anatomy Anatomy 0.000 description 2
- 230000001387 anti-histamine Effects 0.000 description 2
- 239000000739 antihistaminic agent Substances 0.000 description 2
- 230000002902 bimodal Effects 0.000 description 2
- 239000008280 blood Substances 0.000 description 2
- 235000021152 breakfast Nutrition 0.000 description 2
- RYYVLZVUVIJVGH-UHFFFAOYSA-N caffeine Chemical compound CN1C(=O)N(C)C(=O)C2=C1N=CN2C RYYVLZVUVIJVGH-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 210000004027 cells Anatomy 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 235000009508 confectionery Nutrition 0.000 description 2
- 239000002826 coolant Substances 0.000 description 2
- 230000002939 deleterious Effects 0.000 description 2
- 230000001419 dependent Effects 0.000 description 2
- 238000003745 diagnosis Methods 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000003937 drug carrier Substances 0.000 description 2
- 230000000534 elicitor Effects 0.000 description 2
- 239000003623 enhancer Substances 0.000 description 2
- 230000000763 evoked Effects 0.000 description 2
- 230000003419 expectorant Effects 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 235000019634 flavors Nutrition 0.000 description 2
- 238000000799 fluorescence microscopy Methods 0.000 description 2
- 235000013355 food flavoring agent Nutrition 0.000 description 2
- 230000037406 food intake Effects 0.000 description 2
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 229920000159 gelatin Polymers 0.000 description 2
- 239000008273 gelatin Substances 0.000 description 2
- 235000019322 gelatine Nutrition 0.000 description 2
- 235000011852 gelatine desserts Nutrition 0.000 description 2
- 239000008103 glucose Substances 0.000 description 2
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 2
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 2
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 2
- 210000002865 immune cell Anatomy 0.000 description 2
- 230000001939 inductive effect Effects 0.000 description 2
- 230000000977 initiatory Effects 0.000 description 2
- 238000009114 investigational therapy Methods 0.000 description 2
- 150000002632 lipids Chemical class 0.000 description 2
- 239000006210 lotion Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 239000004081 narcotic agent Substances 0.000 description 2
- 239000007923 nasal drop Substances 0.000 description 2
- 239000007922 nasal spray Substances 0.000 description 2
- 239000003883 ointment base Substances 0.000 description 2
- 239000006072 paste Substances 0.000 description 2
- 229960002808 pholcodine Drugs 0.000 description 2
- 239000006187 pill Substances 0.000 description 2
- 229920000191 poly(N-vinyl pyrrolidone) Polymers 0.000 description 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 2
- 230000003389 potentiating Effects 0.000 description 2
- 230000002335 preservative Effects 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 239000000651 prodrug Substances 0.000 description 2
- 229940002612 prodrugs Drugs 0.000 description 2
- 230000001681 protective Effects 0.000 description 2
- 235000018102 proteins Nutrition 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 230000001105 regulatory Effects 0.000 description 2
- 230000029058 respiratory gaseous exchange Effects 0.000 description 2
- 210000002345 respiratory system Anatomy 0.000 description 2
- 231100000247 serious adverse effect Toxicity 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 230000000638 stimulation Effects 0.000 description 2
- 239000005720 sucrose Substances 0.000 description 2
- 239000000196 tragacanth Substances 0.000 description 2
- 235000010487 tragacanth Nutrition 0.000 description 2
- 230000000294 tussive Effects 0.000 description 2
- 230000035899 viability Effects 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- WQZGKKKJIJFFOK-VFUOTHLCSA-N β-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 2
- BAQAVOSOZGMPRM-JVFSCRHWSA-N (2R,3R,4R,5R,6R)-2-[(2S,3R,4R,5R)-2,5-bis(chloromethyl)-3,4-dihydroxyoxolan-2-yl]oxy-5-chloro-6-(hydroxymethyl)oxane-3,4-diol Chemical compound O[C@@H]1[C@@H](O)[C@@H](Cl)[C@@H](CO)O[C@@H]1O[C@]1(CCl)[C@H](O)[C@@H](O)[C@H](CCl)O1 BAQAVOSOZGMPRM-JVFSCRHWSA-N 0.000 description 1
- IVBOUFAWPCPFTQ-SFYZADRCSA-N (3S)-3-azaniumyl-4-oxo-4-[[(2R)-1-oxo-1-[(2,2,4,4-tetramethylthietan-3-yl)amino]propan-2-yl]amino]butanoate Chemical compound OC(=O)C[C@H](N)C(=O)N[C@H](C)C(=O)NC1C(C)(C)SC1(C)C IVBOUFAWPCPFTQ-SFYZADRCSA-N 0.000 description 1
- PMATZTZNYRCHOR-CGLBZJNRSA-N (3S,6S,9S,12R,15S,18S,21S,24S,30S,33S)-30-ethyl-33-[(E,1R,2R)-1-hydroxy-2-methylhex-4-enyl]-1,4,7,10,12,15,19,25,28-nonamethyl-6,9,18,24-tetrakis(2-methylpropyl)-3,21-di(propan-2-yl)-1,4,7,10,13,16,19,22,25,28,31-undecazacyclotritriacontane-2,5,8,11,14,17 Chemical compound CC[C@@H]1NC(=O)[C@H]([C@H](O)[C@H](C)C\C=C\C)N(C)C(=O)[C@H](C(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](C(C)C)NC(=O)[C@H](CC(C)C)N(C)C(=O)CN(C)C1=O PMATZTZNYRCHOR-CGLBZJNRSA-N 0.000 description 1
- DDMOUSALMHHKOS-UHFFFAOYSA-N 1,2-dichloro-1,1,2,2-tetrafluoroethane Chemical compound FC(F)(Cl)C(F)(F)Cl DDMOUSALMHHKOS-UHFFFAOYSA-N 0.000 description 1
- WEEGYLXZBRQIMU-WAAGHKOSSA-N 1,8-cineol Chemical compound C1C[C@H]2CC[C@]1(C)OC2(C)C WEEGYLXZBRQIMU-WAAGHKOSSA-N 0.000 description 1
- WEEGYLXZBRQIMU-UHFFFAOYSA-N 1,8-cineole Natural products C1CC2CCC1(C)OC2(C)C WEEGYLXZBRQIMU-UHFFFAOYSA-N 0.000 description 1
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N 1-Tetradecanol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 1
- RTGDFNSFWBGLEC-SYZQJQIISA-N 2-(morpholin-4-yl)ethyl (4E)-6-(4-hydroxy-6-methoxy-7-methyl-3-oxo-1,3-dihydro-2-benzofuran-5-yl)-4-methylhex-4-enoate Chemical compound COC1=C(C)C=2COC(=O)C=2C(O)=C1C\C=C(/C)CCC(=O)OCCN1CCOCC1 RTGDFNSFWBGLEC-SYZQJQIISA-N 0.000 description 1
- SFAAOBGYWOUHLU-UHFFFAOYSA-N 2-ethylhexyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(CC)CCCC SFAAOBGYWOUHLU-UHFFFAOYSA-N 0.000 description 1
- HMFKFHLTUCJZJO-UHFFFAOYSA-N 2-{2-[3,4-bis(2-hydroxyethoxy)oxolan-2-yl]-2-(2-hydroxyethoxy)ethoxy}ethyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCOCC(OCCO)C1OCC(OCCO)C1OCCO HMFKFHLTUCJZJO-UHFFFAOYSA-N 0.000 description 1
- 102000035257 5-HT3 receptors Human genes 0.000 description 1
- 108091005518 5-HT3 receptors Proteins 0.000 description 1
- FINKDHKJINNQQW-UHFFFAOYSA-N 5-methyl-2-propan-2-ylcyclohexane-1-carboxamide Chemical compound CC(C)C1CCC(C)CC1C(N)=O FINKDHKJINNQQW-UHFFFAOYSA-N 0.000 description 1
- 239000005541 ACE inhibitor Substances 0.000 description 1
- 102100001249 ALB Human genes 0.000 description 1
- 101710027066 ALB Proteins 0.000 description 1
- 229960004784 ALLERGENS Drugs 0.000 description 1
- 210000001015 Abdomen Anatomy 0.000 description 1
- 210000003489 Abdominal Muscles Anatomy 0.000 description 1
- 210000003815 Abdominal Wall Anatomy 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- 229960001456 Adenosine Triphosphate Drugs 0.000 description 1
- ZKHQWZAMYRWXGA-KQYNXXCUSA-N Adenosine triphosphate Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O ZKHQWZAMYRWXGA-KQYNXXCUSA-N 0.000 description 1
- 206010067484 Adverse reaction Diseases 0.000 description 1
- 208000010470 Ageusia Diseases 0.000 description 1
- 239000004377 Alitame Substances 0.000 description 1
- 102000002260 Alkaline Phosphatase Human genes 0.000 description 1
- 108020004774 Alkaline Phosphatase Proteins 0.000 description 1
- 210000001367 Arteries Anatomy 0.000 description 1
- IAOZJIPTCAWIRG-QWRGUYRKSA-N Aspartame Chemical compound OC(=O)C[C@H](N)C(=O)N[C@H](C(=O)OC)CC1=CC=CC=C1 IAOZJIPTCAWIRG-QWRGUYRKSA-N 0.000 description 1
- 229960003438 Aspartame Drugs 0.000 description 1
- 108010011485 Aspartame Proteins 0.000 description 1
- 241000271566 Aves Species 0.000 description 1
- 229960002170 Azathioprine Drugs 0.000 description 1
- 206010004146 Basal cell carcinoma Diseases 0.000 description 1
- 210000003651 Basophils Anatomy 0.000 description 1
- 208000003373 Basosquamous Carcinoma Diseases 0.000 description 1
- 229960003789 Benzonatate Drugs 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- 230000036912 Bioavailability Effects 0.000 description 1
- 206010004938 Bipolar disease Diseases 0.000 description 1
- 210000001772 Blood Platelets Anatomy 0.000 description 1
- 210000004556 Brain Anatomy 0.000 description 1
- 210000000133 Brain Stem Anatomy 0.000 description 1
- 206010006334 Breathing abnormality Diseases 0.000 description 1
- 210000000621 Bronchi Anatomy 0.000 description 1
- 239000004358 Butane-1, 3-diol Substances 0.000 description 1
- DSSYKIVIOFKYAU-UHFFFAOYSA-N Camphor Chemical compound C1CC2(C)C(=O)CC1C2(C)C DSSYKIVIOFKYAU-UHFFFAOYSA-N 0.000 description 1
- 229960000846 Camphor Drugs 0.000 description 1
- 241000282465 Canis Species 0.000 description 1
- 235000008534 Capsicum annuum var annuum Nutrition 0.000 description 1
- 235000002568 Capsicum frutescens Nutrition 0.000 description 1
- 210000003169 Central Nervous System Anatomy 0.000 description 1
- 210000003467 Cheek Anatomy 0.000 description 1
- 206010008469 Chest discomfort Diseases 0.000 description 1
- 229940112822 Chewing Gum Drugs 0.000 description 1
- 241000723346 Cinnamomum camphora Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 240000007170 Cocos nucifera Species 0.000 description 1
- 229940064701 Corticosteroid nasal preparations for topical use Drugs 0.000 description 1
- 229960001334 Corticosteroids Drugs 0.000 description 1
- 241000699800 Cricetinae Species 0.000 description 1
- 229920002785 Croscarmellose sodium Polymers 0.000 description 1
- 229940119017 Cyclosporine Drugs 0.000 description 1
- 108010036949 Cyclosporine Proteins 0.000 description 1
- PXBRQCKWGAHEHS-UHFFFAOYSA-N Dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 1
- 239000004338 Dichlorodifluoromethane Substances 0.000 description 1
- 229940087091 Dichlorotetrafluoroethane Drugs 0.000 description 1
- 206010013911 Dysgeusia Diseases 0.000 description 1
- 239000001692 EU approved anti-caking agent Substances 0.000 description 1
- 239000004150 EU approved colour Substances 0.000 description 1
- 210000002049 Efferent Pathways Anatomy 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 210000003979 Eosinophils Anatomy 0.000 description 1
- QGFORSXNKQLDNO-UHFFFAOYSA-N Erdosteine Chemical compound OC(=O)CSCC(=O)NC1CCSC1=O QGFORSXNKQLDNO-UHFFFAOYSA-N 0.000 description 1
- 229940109501 Eucalyptol Drugs 0.000 description 1
- 241000289695 Eutheria Species 0.000 description 1
- 210000001508 Eye Anatomy 0.000 description 1
- 210000000744 Eyelids Anatomy 0.000 description 1
- 241000282324 Felis Species 0.000 description 1
- 102000003688 G-protein coupled receptors Human genes 0.000 description 1
- 108090000045 G-protein coupled receptors Proteins 0.000 description 1
- 102000027732 GABAA receptors Human genes 0.000 description 1
- 108091008003 GABAA receptors Proteins 0.000 description 1
- 210000001932 Glossopharyngeal Nerve Anatomy 0.000 description 1
- 229960002449 Glycine Drugs 0.000 description 1
- 102000011714 Glycine Receptors Human genes 0.000 description 1
- 108010076533 Glycine Receptors Proteins 0.000 description 1
- 241000282575 Gorilla Species 0.000 description 1
- 229960002146 Guaifenesin Drugs 0.000 description 1
- HSRJKNPTNIJEKV-UHFFFAOYSA-N Guaifenesin Chemical compound COC1=CC=CC=C1OCC(O)CO HSRJKNPTNIJEKV-UHFFFAOYSA-N 0.000 description 1
- JKMHFZQWWAIEOD-UHFFFAOYSA-N HEPES Chemical compound OCC[NH+]1CCN(CCS([O-])(=O)=O)CC1 JKMHFZQWWAIEOD-UHFFFAOYSA-N 0.000 description 1
- 239000007995 HEPES buffer Substances 0.000 description 1
- 229940030482 HORMONAL CONTRACEPTIVES FOR SYSTEMIC USE Drugs 0.000 description 1
- 230000036499 Half live Effects 0.000 description 1
- 210000003128 Head Anatomy 0.000 description 1
- 102000001554 Hemoglobins Human genes 0.000 description 1
- 108010054147 Hemoglobins Proteins 0.000 description 1
- 208000006454 Hepatitis Diseases 0.000 description 1
- GVGLGOZIDCSQPN-PVHGPHFFSA-N Heroin Chemical compound O([C@H]1[C@H](C=C[C@H]23)OC(C)=O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4OC(C)=O GVGLGOZIDCSQPN-PVHGPHFFSA-N 0.000 description 1
- 241000282412 Homo Species 0.000 description 1
- 241000282620 Hylobates sp. Species 0.000 description 1
- 206010020989 Hypogeusia Diseases 0.000 description 1
- 206010022114 Injury Diseases 0.000 description 1
- 235000002678 Ipomoea batatas Nutrition 0.000 description 1
- 240000003613 Ipomoea batatas Species 0.000 description 1
- SERLAGPUMNYUCK-DCUALPFSSA-N Isomalt Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O SERLAGPUMNYUCK-DCUALPFSSA-N 0.000 description 1
- AXISYYRBXTVTFY-UHFFFAOYSA-N Isopropyl myristate Chemical compound CCCCCCCCCCCCCC(=O)OC(C)C AXISYYRBXTVTFY-UHFFFAOYSA-N 0.000 description 1
- XUGNVMKQXJXZCD-UHFFFAOYSA-N Isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 description 1
- 102000004016 L-Type Calcium Channels Human genes 0.000 description 1
- 108090000420 L-Type Calcium Channels Proteins 0.000 description 1
- FBOZXECLQNJBKD-ZDUSSCGKSA-N L-methotrexate Chemical compound C=1N=C2N=C(N)N=C(N)C2=NC=1CN(C)C1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 FBOZXECLQNJBKD-ZDUSSCGKSA-N 0.000 description 1
- GUBGYTABKSRVRQ-UUNJERMWSA-N Lactose Natural products O([C@@H]1[C@H](O)[C@H](O)[C@H](O)O[C@@H]1CO)[C@H]1[C@@H](O)[C@@H](O)[C@H](O)[C@H](CO)O1 GUBGYTABKSRVRQ-UUNJERMWSA-N 0.000 description 1
- 241000283953 Lagomorpha Species 0.000 description 1
- 210000000867 Larynx Anatomy 0.000 description 1
- 102000004086 Ligand-Gated Ion Channels Human genes 0.000 description 1
- 108090000543 Ligand-Gated Ion Channels Proteins 0.000 description 1
- 206010024971 Lower respiratory tract infection Diseases 0.000 description 1
- 210000001165 Lymph Nodes Anatomy 0.000 description 1
- 210000004698 Lymphocytes Anatomy 0.000 description 1
- 241000289581 Macropus sp. Species 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 235000016247 Mentha requienii Nutrition 0.000 description 1
- 235000002899 Mentha suaveolens Nutrition 0.000 description 1
- LXCFILQKKLGQFO-UHFFFAOYSA-N Methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 1
- 229920000168 Microcrystalline cellulose Polymers 0.000 description 1
- 210000001616 Monocytes Anatomy 0.000 description 1
- 210000003097 Mucus Anatomy 0.000 description 1
- 241000282341 Mustela putorius furo Species 0.000 description 1
- 210000003739 Neck Anatomy 0.000 description 1
- 210000000118 Neural Pathways Anatomy 0.000 description 1
- 210000000440 Neutrophils Anatomy 0.000 description 1
- 102000019315 Nicotinic acetylcholine receptors Human genes 0.000 description 1
- 108050006807 Nicotinic acetylcholine receptors Proteins 0.000 description 1
- 210000000929 Nociceptors Anatomy 0.000 description 1
- 241000283973 Oryctolagus cuniculus Species 0.000 description 1
- 241000283898 Ovis Species 0.000 description 1
- 241000282577 Pan troglodytes Species 0.000 description 1
- 241001504519 Papio ursinus Species 0.000 description 1
- 241001420799 Phaselia Species 0.000 description 1
- 206010035664 Pneumonia Diseases 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229920001214 Polysorbate 60 Polymers 0.000 description 1
- 241000282405 Pongo abelii Species 0.000 description 1
- 241000288906 Primates Species 0.000 description 1
- QELSKZZBTMNZEB-UHFFFAOYSA-N Propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 1
- 102000014961 Protein Precursors Human genes 0.000 description 1
- 108010078762 Protein Precursors Proteins 0.000 description 1
- 229940077718 Proton pump inhibitors for peptic ulcer and GORD Drugs 0.000 description 1
- 208000003251 Pruritus Diseases 0.000 description 1
- 206010057190 Respiratory tract infection Diseases 0.000 description 1
- 241000283984 Rodentia Species 0.000 description 1
- GBFLZEXEOZUWRN-VKHMYHEASA-N S-carboxymethyl-L-cysteine Chemical compound OC(=O)[C@@H](N)CSCC(O)=O GBFLZEXEOZUWRN-VKHMYHEASA-N 0.000 description 1
- 210000003296 Saliva Anatomy 0.000 description 1
- 241001247145 Sebastes goodei Species 0.000 description 1
- 210000002966 Serum Anatomy 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 229940091252 Sodium supplements Drugs 0.000 description 1
- 229940075582 Sorbic Acid Drugs 0.000 description 1
- 239000004376 Sucralose Substances 0.000 description 1
- 206010042464 Suicide attempt Diseases 0.000 description 1
- 241000282898 Sus scrofa Species 0.000 description 1
- 102000012253 TRPA1 Cation Channel Human genes 0.000 description 1
- 108010036769 TRPA1 Cation Channel Proteins 0.000 description 1
- 102100009266 TRPV4 Human genes 0.000 description 1
- 229940034920 Tessalon Perles Drugs 0.000 description 1
- 210000000779 Thoracic Wall Anatomy 0.000 description 1
- 210000001685 Thyroid Gland Anatomy 0.000 description 1
- 238000008050 Total Bilirubin Reagent Methods 0.000 description 1
- 210000003901 Trigeminal Nerve Anatomy 0.000 description 1
- LEHOTFFKMJEONL-UHFFFAOYSA-N Trioxopurine Chemical compound N1C(=O)NC(=O)C2=C1NC(=O)N2 LEHOTFFKMJEONL-UHFFFAOYSA-N 0.000 description 1
- 101710042194 Trpgamma Proteins 0.000 description 1
- 210000003454 Tympanic Membrane Anatomy 0.000 description 1
- 229940116269 Uric Acid Drugs 0.000 description 1
- 210000001186 Vagus Nerve Anatomy 0.000 description 1
- 102000016913 Voltage-Gated Sodium Channels Human genes 0.000 description 1
- 108010053752 Voltage-Gated Sodium Channels Proteins 0.000 description 1
- 241000289674 Vombatidae Species 0.000 description 1
- 241001516311 Watermelon virus A Species 0.000 description 1
- 208000001877 Whooping Cough Diseases 0.000 description 1
- 238000001793 Wilcoxon signed-rank test Methods 0.000 description 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N Xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 229960002675 Xylitol Drugs 0.000 description 1
- 229940042530 Zonatuss Drugs 0.000 description 1
- NWGKJDSIEKMTRX-AAZCQSIUSA-N [(2R)-2-[(2R,3R,4S)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl] (Z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O NWGKJDSIEKMTRX-AAZCQSIUSA-N 0.000 description 1
- PNNCWTXUWKENPE-UHFFFAOYSA-N [N].NC(N)=O Chemical compound [N].NC(N)=O PNNCWTXUWKENPE-UHFFFAOYSA-N 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 230000001154 acute Effects 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 230000000240 adjuvant Effects 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 235000019666 ageusia Nutrition 0.000 description 1
- 229940050528 albumin Drugs 0.000 description 1
- 235000019409 alitame Nutrition 0.000 description 1
- 108010009985 alitame Proteins 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 230000002009 allergen Effects 0.000 description 1
- 230000003466 anti-cipated Effects 0.000 description 1
- 230000000111 anti-oxidant Effects 0.000 description 1
- 230000001754 anti-pyretic Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 239000002221 antipyretic Substances 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 235000010357 aspartame Nutrition 0.000 description 1
- 239000000605 aspartame Substances 0.000 description 1
- LMEKQMALGUDUQG-UHFFFAOYSA-N azathioprine Chemical compound CN1C=NC([N+]([O-])=O)=C1SC1=NC=NC2=C1NC=N2 LMEKQMALGUDUQG-UHFFFAOYSA-N 0.000 description 1
- 244000052616 bacterial pathogens Species 0.000 description 1
- 235000006682 bigleaf mint Nutrition 0.000 description 1
- BPYKTIZUTYGOLE-IFADSCNNSA-N bilirubin Chemical compound N1C(=O)C(C)=C(C=C)\C1=C\C1=C(C)C(CCC(O)=O)=C(CC2=C(C(C)=C(\C=C/3C(=C(C=C)C(=O)N\3)C)N2)CCC(O)=O)N1 BPYKTIZUTYGOLE-IFADSCNNSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000035514 bioavailability Effects 0.000 description 1
- 230000000903 blocking Effects 0.000 description 1
- 230000036772 blood pressure Effects 0.000 description 1
- UIIMBOGNXHQVGW-UHFFFAOYSA-M buffer Substances [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 1
- 235000019437 butane-1,3-diol Nutrition 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- PUPZLCDOIYMWBV-UHFFFAOYSA-N butylene glycol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
- 229960001948 caffeine Drugs 0.000 description 1
- FUFJGUQYACFECW-UHFFFAOYSA-L calcium hydrogenphosphate Chemical compound [Ca+2].OP([O-])([O-])=O FUFJGUQYACFECW-UHFFFAOYSA-L 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 229930007890 camphor Natural products 0.000 description 1
- 238000009924 canning Methods 0.000 description 1
- 229960004399 carbocisteine Drugs 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 230000000747 cardiac effect Effects 0.000 description 1
- 210000000748 cardiovascular system Anatomy 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 230000001413 cellular Effects 0.000 description 1
- 229940082500 cetostearyl alcohol Drugs 0.000 description 1
- 239000002561 chemical irritant Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 235000015218 chewing gum Nutrition 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 229960001265 ciclosporin Drugs 0.000 description 1
- 230000001886 ciliary Effects 0.000 description 1
- 229960005233 cineole Drugs 0.000 description 1
- 201000009230 common cold Diseases 0.000 description 1
- 239000007891 compressed tablet Substances 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000002591 computed tomography Methods 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 230000035597 cooling sensation Effects 0.000 description 1
- 200000000015 coronavirus disease 2019 Diseases 0.000 description 1
- 230000000875 corresponding Effects 0.000 description 1
- 239000003246 corticosteroid Substances 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000001767 crosslinked sodium carboxy methyl cellulose Substances 0.000 description 1
- 235000010947 crosslinked sodium carboxy methyl cellulose Nutrition 0.000 description 1
- 201000003883 cystic fibrosis Diseases 0.000 description 1
- 239000000850 decongestant Substances 0.000 description 1
- SASYSVUEVMOWPL-NXVVXOECSA-N decyl oleate Chemical compound CCCCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC SASYSVUEVMOWPL-NXVVXOECSA-N 0.000 description 1
- 230000003111 delayed Effects 0.000 description 1
- 230000002999 depolarising Effects 0.000 description 1
- 230000030810 detection of chemical stimulus involved in sensory perception of taste Effects 0.000 description 1
- 230000001627 detrimental Effects 0.000 description 1
- 229960002069 diamorphine Drugs 0.000 description 1
- 235000019700 dicalcium phosphate Nutrition 0.000 description 1
- 229940042935 dichlorodifluoromethane Drugs 0.000 description 1
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000007884 disintegrant Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000006196 drop Substances 0.000 description 1
- 238000001647 drug administration Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 235000019564 dysgeusia Nutrition 0.000 description 1
- 201000006549 dyspepsia Diseases 0.000 description 1
- 230000002500 effect on skin Effects 0.000 description 1
- 239000003974 emollient agent Substances 0.000 description 1
- 230000001804 emulsifying Effects 0.000 description 1
- 239000008387 emulsifying waxe Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 229960003262 erdosteine Drugs 0.000 description 1
- 230000005713 exacerbation Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000002349 favourable Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000003260 fluorescence intensity Methods 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000002496 gastric Effects 0.000 description 1
- 201000006860 gastroesophageal reflux disease Diseases 0.000 description 1
- 239000007903 gelatin capsule Substances 0.000 description 1
- 230000024924 glomerular filtration Effects 0.000 description 1
- 229940075507 glyceryl monostearate Drugs 0.000 description 1
- BEBCJVAWIBVWNZ-UHFFFAOYSA-N glycinamide Chemical compound NCC(N)=O BEBCJVAWIBVWNZ-UHFFFAOYSA-N 0.000 description 1
- DHMQDGOQFOQNFH-UHFFFAOYSA-N glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 1
- 235000013905 glycine and its sodium salt Nutrition 0.000 description 1
- 229940046528 grass pollen Drugs 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 230000003862 health status Effects 0.000 description 1
- 238000005534 hematocrit Methods 0.000 description 1
- 231100000283 hepatitis Toxicity 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 239000000938 histamine H1 antagonist Substances 0.000 description 1
- 238000002657 hormone replacement therapy Methods 0.000 description 1
- 239000008309 hydrophilic cream Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 235000019570 hypogeusia Nutrition 0.000 description 1
- 230000002519 immonomodulatory Effects 0.000 description 1
- 230000001506 immunosuppresive Effects 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 230000002757 inflammatory Effects 0.000 description 1
- 230000003434 inspiratory Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 229940074928 isopropyl myristate Drugs 0.000 description 1
- 229940075495 isopropyl palmitate Drugs 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 230000003907 kidney function Effects 0.000 description 1
- 239000000832 lactitol Substances 0.000 description 1
- 235000010448 lactitol Nutrition 0.000 description 1
- 229960003451 lactitol Drugs 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- GUBGYTABKSRVRQ-XLOQQCSPSA-N lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 239000010807 litter Substances 0.000 description 1
- 230000003908 liver function Effects 0.000 description 1
- 230000004199 lung function Effects 0.000 description 1
- 201000003895 major depressive disease Diseases 0.000 description 1
- 230000036210 malignancy Effects 0.000 description 1
- 239000000845 maltitol Substances 0.000 description 1
- 235000010449 maltitol Nutrition 0.000 description 1
- 229940035436 maltitol Drugs 0.000 description 1
- 241001515942 marmosets Species 0.000 description 1
- 230000000873 masking Effects 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 229960000485 methotrexate Drugs 0.000 description 1
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 1
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
- 229940016286 microcrystalline cellulose Drugs 0.000 description 1
- 239000008108 microcrystalline cellulose Substances 0.000 description 1
- 235000019813 microcrystalline cellulose Nutrition 0.000 description 1
- 235000006679 mint Nutrition 0.000 description 1
- 239000001788 mono and diglycerides of fatty acids Substances 0.000 description 1
- 150000002773 monoterpene derivatives Chemical class 0.000 description 1
- 229930003658 monoterpenes Natural products 0.000 description 1
- 230000003843 mucus production Effects 0.000 description 1
- 229960004866 mycophenolate mofetil Drugs 0.000 description 1
- 229940043348 myristyl alcohol Drugs 0.000 description 1
- 239000000133 nasal decongestant Substances 0.000 description 1
- 201000009240 nasopharyngitis Diseases 0.000 description 1
- 210000000653 nervous system Anatomy 0.000 description 1
- 230000036403 neuro physiology Effects 0.000 description 1
- 239000002858 neurotransmitter agent Substances 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-M nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 1
- 108091008022 nociceptors Proteins 0.000 description 1
- 230000000631 nonopiate Effects 0.000 description 1
- 229940006093 opthalmologic coloring agents Diagnostic Drugs 0.000 description 1
- 239000003539 oral contraceptive agent Substances 0.000 description 1
- 238000002638 palliative care Methods 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000008506 pathogenesis Effects 0.000 description 1
- 230000037361 pathway Effects 0.000 description 1
- 201000005702 pertussis Diseases 0.000 description 1
- 239000000546 pharmaceutic aid Substances 0.000 description 1
- 239000002587 phosphodiesterase IV inhibitor Substances 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 238000001126 phototherapy Methods 0.000 description 1
- 230000001830 phrenic Effects 0.000 description 1
- 230000035479 physiological effects, processes and functions Effects 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 230000001144 postural Effects 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- OZAIFHULBGXAKX-UHFFFAOYSA-N precursor Substances N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 1
- 238000009101 premedication Methods 0.000 description 1
- 239000000955 prescription drug Substances 0.000 description 1
- 230000002035 prolonged Effects 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 239000004405 propyl p-hydroxybenzoate Substances 0.000 description 1
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 238000000159 protein binding assay Methods 0.000 description 1
- 239000000612 proton pump inhibitor Substances 0.000 description 1
- 230000003482 proton pump inhibitor Effects 0.000 description 1
- 230000005180 public health Effects 0.000 description 1
- 238000000275 quality assurance Methods 0.000 description 1
- VBICKXHEKHSIBG-UHFFFAOYSA-N rac-1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000035812 respiration Effects 0.000 description 1
- 201000004193 respiratory failure Diseases 0.000 description 1
- 231100000279 safety data Toxicity 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 201000000980 schizophrenia Diseases 0.000 description 1
- 230000000697 serotonin reuptake Effects 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 201000009890 sinusitis Diseases 0.000 description 1
- 230000000391 smoking Effects 0.000 description 1
- 239000003195 sodium channel blocking agent Substances 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 239000008109 sodium starch glycolate Substances 0.000 description 1
- 229940079832 sodium starch glycolate Drugs 0.000 description 1
- 229920003109 sodium starch glycolate Polymers 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- WSWCOQWTEOXDQX-UHFFFAOYSA-N sorbic acid Chemical compound CC=CC=CC(O)=O WSWCOQWTEOXDQX-UHFFFAOYSA-N 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000002630 speech therapy Methods 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-M stearate Chemical compound CCCCCCCCCCCCCCCCCC([O-])=O QIQXTHQIDYTFRH-UHFFFAOYSA-M 0.000 description 1
- 235000019408 sucralose Nutrition 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000002459 sustained Effects 0.000 description 1
- 238000002636 symptomatic treatment Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 230000002123 temporal effect Effects 0.000 description 1
- 229940083878 topical for treatment of hemorrhoids and anal fissures Corticosteroids Drugs 0.000 description 1
- 239000012049 topical pharmaceutical composition Substances 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 230000001131 transforming Effects 0.000 description 1
- 102000038112 transient receptor (TC 1.A.4) family Human genes 0.000 description 1
- 108091007157 transient receptor (TC 1.A.4) family Proteins 0.000 description 1
- 229940046536 tree pollen allergenic extracts Drugs 0.000 description 1
- 239000003029 tricyclic antidepressant agent Substances 0.000 description 1
- OBHRVMZSZIDDEK-UHFFFAOYSA-N urobilinogen Chemical compound CCC1=C(C)C(=O)NC1CC1=C(C)C(CCC(O)=O)=C(CC2=C(C(C)=C(CC3C(=C(CC)C(=O)N3)C)N2)CCC(O)=O)N1 OBHRVMZSZIDDEK-UHFFFAOYSA-N 0.000 description 1
- 230000003612 virological Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 230000003442 weekly Effects 0.000 description 1
- 230000036642 wellbeing Effects 0.000 description 1
- 239000000811 xylitol Substances 0.000 description 1
- 235000010447 xylitol Nutrition 0.000 description 1
- 102000037289 κ-opioid receptors Human genes 0.000 description 1
- 108020001588 κ-opioid receptors Proteins 0.000 description 1
Abstract
The present invention pertains generally to the field of therapy. More specifically the present invention pertains to a certain compound, [((1 R,2S,5R)-2-isopropyl-5-5 methylcyclohexanecarbonyl)-amino]-acetic acid isopropyl ester (also referred to herein as "AX-8" or "Gly-O-iPr"), as described herein, for use in a method of treatment of the human or animal body by therapy, more specifically, for use in a method of treatment of chronic cough (CC), including, for example, refractory chronic cough (RCC) and idiopathic chronic cough (ICC), as described herein.
Description
[((1 R,2S.5R)-2-fSOPROPYL-5-METHYL-CYCLOHEXANECARBONYL)-AMINO]ACETIC ACID ISOPROPYL ESTER FOR TREATMENT OF CHRONIC COUGH
RELATED APPLICATION
This application îs related to United Kingdom (GB) patent application number 1908219.7 filed 10 June 2019, the contents of which are incorporated herein by reference in their entirety.
TECHNICAL FIELD
The présent invention pertains generally to the field of therapy. More specifically the présent invention pertains to a compound that is [((1 R,2S,5R)-2-isopropyl-5-methylcyclohexanecarbonyl)-amino]-acetic acid isopropyl ester (also referred to herein as “AX-8” or “Gly-O-iPr”), or a pharmaceutically acceptable sait, hydrate, or solvaté thereof, as described herein, for use in a method of treatment ofthe human or animal body by therapy, more specifically, for use in a method of treatment of chronic cough (CC), including, for example, refractory chronic cough (RCC) and idiopathic chronic cough (ICC), as described herein.
BACKGROUND
A number of publications are cited herein in order to more fulty describe and disclose the invention and the State of the art to which the invention pertains. Each of these publications is incorporated herein by reference in its entirety into the present disclosure, to the same extent as if each individual publication was specifically and individualîy indicated to be incorporated by reference.
Throughout this spécification, including the claims which follow, unless the context requires otherwise, the word “comprise, and variations such as “comprises” and “comprising,” will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps.
It must be noted that, as used in the spécification and the appended claims, the singular forms “a,” “an,” and “the” include plural referents unless the context clearly dictâtes otherwise. Thus, for example, reference to “a pharmaceutical carrier” includes mixtures of two or more such carriers, and the like.
Ranges are often expressed herein as from “about” one particular value, and/or to “about” another particular value. When such a range is expressed, another embodiment includes from the one particular value and/or to the other particular value. Similarly, when values are expressed as approximations, by the use of the antécédent “about,” it will be understood that the particular value forms another embodiment.
This disclosure includes information that may be useful in understanding the présent invention. It is not an admission that any of the information provided herein is prior art or relevant to the presently ctaimed invention, or that any publication specifically or implicîtly 10 referenced is prior art.
Couqh
A cough is a sudden and often repetitively occurring, protective reflex, which helps to 15 clear the large breathing passages from fluids, irritants, foreign particles, and microbes.
The cough reflex consists of three phases: an inhalation; a forced exhalation against a closed glottis; and a violent release of air from the lungs following opening of the glottis, usually accompanied by a distinctive sound.
Cough is a non-specific reaction to irritation anywhere from the pharynx to the lungs. The cough reflex is triggered by mechanical or inflammatory changes or irritants in the airways.
The Couqh Reflex
Cough occurs through the stimulation of a complex reflex arc (see, e.g., Polverino et al., 2012; Canning étal., 2014) constituted by:
• Sensory termîni expressing cough receptors: termini of sensory afferent fibres innervating extra-thoracic locations (e.g., nose, oropharynx, larynx, upper trachea), 30 intra-thoracic locations (e.g., lower trachea and large central bronchi), or other locations (e.g., tympanic membrane, diaphragm, oesophagus, stomach).
• Afferent pathway: sensory nerve fibres, mainly vagal (cranial nerve X) as well as tngeminal (cranial nerve V) and glossopharyngeal (cranial nerve IX).
• Central pathway (cough centre): a central coordinating/convergence région for coughing located in the brainstem (the core of the cough network is located in the ventrolateral région ofthe medulla).
• Efferent pathway: impulses from the cough centre travel via the vagus, phrenic, and spinal motor nerves to the diaphragm, abdominal wall, and muscles.
Prevaience of Couqh
Cough is one of the most common reasons for adults and children to visit their general practitioner. For example, at any one time, 20% of the United Kingdom (UK) population hâve a troublesome cough and sufferers consume 75 million doses of over-the-counter (OTC) antitussive médication annuaily (see, e.g., Birring et al., 2003). One study to grade cough severity found 7% of a general population had cough sufficient to interfère with activities of daily living on at least a weekly basis in the UK (see, e.g., Ford et al., 2006).
Classification of Cough
Cough can be divided into: (a) acute self-limiting cough, lasting less than three weeks; (b) subacute cough, lasting for an intermediate period of 3-8 weeks; and (c) chronic cough (CC), which lasts for a longer period (typically, more than 8 weeks in adults and more than 4 weeks in children).
Acute cough can also be classified according to its cause: infectious (caused by an infection) or non-infectious. Infectious causes of acute cough include: viral upper respiratory infections (the common cold), COVID-19 disease; sinus infections; acute bronchitis; pneumonia; and whooping cough. Non-infectious causes of acute cough include: exposure to Chemicals, exposure to irritants; and environmental allergies.
Chronic cough (CC) is common in clinical practice and is associated with decreased quality of life. It can persist for many months, and sometimes years, and is a troublesome and difficult-to-treat symptom.
Chronic Couqh (CC) as a Neuropathie Disorder
There is a widespread clinical récognition that CC reflects a neuropathie State whereby the basal protective cough reflex has been transformed to a level of heightened sensitivity such that cough is triggered by low-level stimuli not normally sufficient to cause cough (e.g., a change in ambient température, taking a deep breath, laughing, talking on the téléphoné, exposure to odours or aérosols, etc.', a concept termed allotussia) and by smaller amounts of known cough-inducing stimuli (e.g., capsaicin, citric acid, etc.', a concept termed hypertussîa) (see, e.g., Chung et al., 2013; Mazzone et al., 2018;
Gibson et al, 2015). In most CC patients, this hypersensitivity is also associated with abnormal sensations such persistent urge-to-cough and throat irritation, throat tickle, or throat itch (see, e.g., Song étal., 2017; Gibson et al, 2015). Both the motor (spontaneous cough) and sensory conséquences of this hypersensitivity are distressful for CC patients and should be addressed by treatment.
This concept is often referred as the cough hypersensîtivity syndrome (CHS) or cough reflex hypersensîtivity (CRH) (see, e.g., Chung, 2014; Birring, 2017; Song étal., 2017; Morice étal., 2011; Ryan étal., 2018; Mazzone et al., 2018). The conventîonal view is that an inflammation-induced disorder or injury ofthe nervous system (neuroinflammation) leads to CHS whereby neural pathways (in the airways and in the brain) hâve become affected by a heterogeneous range of factors including infection and physical and Chemical irritants (see, e.g., Mazzone et al., 2018; Chung et al., 2013).
By analogy with neuropathie pain (see, e.g., Chung étal., 2013), CHS can be due to: peripheral sensitization; central sensitization (cough centre); and/or cortical and subcortical maladaptive plasticity.
The term sensory neuropathie cough is now often recognized in cough guidelines. It has overlap with laryngeal paraesthesia and laryngeal hypersensîtivity syndrome (LHS) and cough hypersensîtivity (CHS) syndromes (see, e.g., Gibson et al., 2015; Ryan et al., 2018). The term laryngeal hypersensîtivity (LHS) is often used interchangeably with sensory neuropathie cough.
Types of Chronic Cough (CC)
Some patients hâve explained chronic cough, that is, chronic cough as a symptom of a diagnosed condition. Common causes of chronic cough are, for example, asthma, éosinophilie bronchitis, post-nasal drip syndrome (PNDS), gastro-oesophageal reflux dîsease (GORD), bronchiectasis chronic obstructive pulmonary dîsease (COPD), and idiopathic pulmonary fibrosis (IPF).
However, in many cases, despite extensive évaluation and trials of therapy, the chronic cough remains both unexplained and refractory to treatment in chronic coughers (up to 46% of patients seen in secondary care; see, e.g., Pavord et al., 2008; McGarvey, 2005).
Chronic cough that persiste despite assessment and treatment according to an accepted guideline is often referred to as refractory chronic cough (RCC) (sometimes also as chronic refractory cough), that is, chronic cough that is refractory to treatment of the associated condition. Chronic cough that has no identified cause is often referred to as unexplained or idiopathic chronic cough (ICC). Refractory chronic cough is sometimes also referred to as idiopathic chronic cough, for example, when the cause of the chronic cough is often no longer the original associated condition, but some other, as yet undetermined condition {e.g., a neurological condition) (see, e.g., Gibson et al., 2015; Ryan et ai., 2018).
For example, a patient suffering from chronic cough is diagnosed with asthma and treated for the asthma. Most of the asthma symptoms are improved; however, the chronic cough is not improved. The patient, who was initially considered to hâve explained chronic cough (due to asthma) is now diagnosed with refractory chronic cough (because it is refractory to the treatment of the associated condition, asthma) or idiopathic chronic cough (because, now, the associated condition causîng the persistent chronic cough is unknown, or not yet known).
Because patients with unexpiained chronic cough often receîve spécifie thérapies, such as inhaled corticosteroids or proton pump inhibitors, they can also be classified as having RCC.
Consequently, the terms refractory chronic cough (RCC), chronic refractory cough, unexplained chronic cough, and idiopathic chronic cough (ICC) are often used interchangeably (and sometimes înconsistently and/or incorrectly) in the literature and in clinical practice.
Treatment of Cough
In most cases, cough is treated by treating the underlying cause. However, in some cases (e.g., when the underlying cause cannot be identified, or cannot be readily or quickly treated), symptomatic treatment of cough is recommended.
Cough suppressants may be useful, particularly if sleep is dîsturbed. However, they may cause sputum rétention, and this may be harmful in patients with chronic bronchitis or bronchiectasis.
There are various drugs which may partially suppress cough, although the cough reflex is exceedîngiy dîfficuît to abolish. There is a lack of evidence for the efficacy of most antitussive drugs and many of them, especially narcotics, induce adverse side-effects. Moreover, abuse and overdose associated with narcotic cough suppressant is a major public health concern, especially in US. The British Thoracic Society guidelines State: “There are no effective treatments controlling the cough response per se with an acceptabletherapeutic ratio” (see, e.g., Morice étal., 2006).
Codeine (a narcotic drug) may be effective but can cause dependence.
Dextromethorphan (an opioid dérivative, non-narcotic) and pholcodine (also known as homocodeine) hâve fewer side-effects. Morphine or diamorphine at higher doses may be used for severe, distressing cough in palliative care.
Benzonatate (marketed under the names Tessalong, Tessalon Perles, and Zonatuss) is currently the only non-narcotic prescription drug for cough suppression.
Sedating antihistamines are used as the cough suppressant component of many compound cough préparations on sale to the public.
Mucolytics (e.g., carbocisteine or erdosteine) are prescribed to facilitate expectoration by reducing sputum viscosity. In some patients with COPD and a chronic productive cough, mucolytics can reduce exacerbations. Mucolytic therapy should be stopped if there is no benefit after a four-week trial. Steam inhalation with postural drainage is effective in bronchiectasis and in some cases of chronic bronchitis.
Demulcent cough préparations contain soothing substances such as syrup or glycerol and may be used to relieve a dry irritating cough. Préparations such as simple linctus hâve the advantage of being harmiess and inexpensive.
Expectorants are claimed to promote expulsion of bronchial sécrétions but there is no evidence that any drug can specifically facilitate expectoration.
Treatment of Chronic Cough
At présent, there is no dedicated treatment for chronic cough (CC), whether as a symptom of a diagnosed condition or a condition itself.
Among CC patients, those with RCC are the ones with the highest need. Only a few treatment options exist for patients with RCC (see, e.g., Gibson et al., 2015; Ryan et al., 2018). For that reason, pharmaceutical companies currently focus on RCC patients. Moreover, patients with RCC provide a useful model for studying antitussive agents for CC as cough frequency is high and stable over time making such clinical studies powerful for demonstrating treatment effects.
Centrally acting neuromodulators such as morphine (an opioid), amitriptyline (a tricyclic antidepressant and inhibitor of serotonin reuptake), gabapentin and pregabalin (two blockers of some voltage-gated calcium channels expressed in the central nervous system) may be useful for treatment of RCC (see, e.g., Gibson et ai., 2015; Ryan et al., 2018).
Speech therapy techniques hâve also shown benefit for treatment of RCC (see, e.g., Gibson et al., 2015; Ryan étal., 2018).
Patients and clinicians frequentty try over-the-counter (OTC) médications availabie for acute cough (such as dextromethorphan, codeine, and menthol), but with tittîe benefit.
Treatments recently or currently under development for RCC hâve new biological targets, 5 which were not previously targeted for acute cough, such as a7-nACh, P2X3, NK1,
TRPV1, TRPV4, and TRPA1 receptors (see, e.g., Ryan et al., 2018; Abdulqawi et al., 2015; Belvisi étal., 2017; Khalid étal., 2014; Smith et al., 2017a; Smith et al., 2017b; Smith étal., 2020; EudraCT Number 2013-002728-17).
Empirically, treatments for acute cough often hâve no effect for RCC, and vice versa.
Even if a treatment is known to be effective for acute cough, it cannot be predicted (with reasonably certainty) that it would also be effective for treating chronic cough. For exampie, two TRPV1 antagoniste (XEN-D0501 and SB-705498) inhibit acute cough induced by capsaicin (see, e.g., Belvisi étal., 2017; Khalid et ai., 2014), but do not reduce cough frequency in RCC patients. Conversely, MK-7264 (also known as AF-219 and Gefapixant), a P2X3 antagonist, is efficient in decreasing cough frequency in RCC patients but is not effective for acute cough induced by the tussive stimulus capsaicin (an irritant and agonist of TRPV1) in RCC patients or in healthy subjects (see,
e.g., Abdulqawi étal., 2015; Smith étal., 2016; Morice et al., 2017).
In the présent context, non-clinical studies hâve demonstrated that AX-8 inhibits cough induced by an irritant (i.e., capsaicin, a TRPV1 agonist). However, based on the current State of the art, the skilled person could not hâve predicted (with reasonably certainty) that AX-8 would also be effective for treating chronic cough (CC), let alone refractory chronic cough (RCC).
Animal Models for Cough
There are no perfect animal models ofthe human diseases associated with acute or chronic cough. Although existing models approximate these human conditions, the peculiarities of, for example, GORD, asthma, COPD, and various respiratory tract infections, are not reliably reproduced. Since coughing in humans during illness is spontaneous, it would be idéal to study animais that had developed spontaneous cough.
But this is essentially never donc, with coughing in animais typically studied in response to artificial delivery of a tussive stimulus (see, e.g., Canning et al., 2008).
For COPD, there is only one model in ferret with increased early morning spontaneous cough (but not chronic cough), and ail other models do not hâve spontaneous cough (see, e.g., Chow étal., 2017). Diverse animai models of enhanced cough hâve been developed, but none reproduce the features of RCC (see, e.g., Boiser, 2004; Xu et a!., 2016).
Furthermore, the physiology and pharmacology of spontaneous coughing and induced coughing is likeîy to be different. Consequently:
• The molecular mechanisms that cause and maintain CC are poorly understood, which explains the limited availability of antitussive médications for CC.
• Prospective drugs for the treatment of CC cannot be validated by using animal models.
• Resultsfrom currently available animal models (e.g., cough induced by tnhaled capsaicin or citric acid in guinea pig) cannot be translated to efficacy for CC.
Since the prédictive value of animal models for cough in chronic cough is so limited, the skilled person cannot predict (with reasonable certainty) that a particular treatment will, in fact, be useful for the treatment of chronic cough, let alone RCC. This situation is illustrated by the failure of proof-of-concept trials for the treatment of RCC, when studies in animal models had positive outcomes (see, e.g., Belvisi et al., 2017; Khalid et al., 2014; Smith et al., 2017c; Smith étal., 2020; Ludbrook et aL, 2019; Mukhopadhyay étal·, 2016; Bonvini étal.,. 2016; EudraCT number 2013-002728-17).
Therefore, until the current human clinical trial was completed (and found to be successful), and it had been demonstrated (via the clinical trial data) that AX-8 in fact is useful for the treatment of CC in RCC/ICC patients, that outcome could not hâve been predicted (with reasonable certainty).
Known Compound AX-8 I Gly-O-iPr
The compound, [((1 R,2S,5R)-2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester (also referred to herein as ‘AX-8” or “Gly-O-iPr”) was described in Wei et al., 2012. See, e.g., page 6 therein.
The use of the compound for the treatment of “cough” is also described therein. See, e.g., claim 53 at page 34 therein.
Study 4 (see page 14 therein) describes the treatment of a patient’s dry scratchy throat and cough that was associated with sensitization to cat litter box dust and aggravated by a seasonal allergy to grass pollen.
Study 5 (see pages 14-15 therein) describes treatment of a patient’s intense coughing fit that was triggered by eatîng a piece of fish that was heavily spiced with Chili peppers.
Study 6 (page 15 therein) describes treatment of cough in a patient with adult onset asthma aggravated by a seasonal allergy to tree pollen.
Coughing in the aforementioned studies was provoked by irritants and allergens.
Nowhere in Wei et ai, 2012 is there any teaching or suggestion ofthe treatment of chronic cough (CC), let alone refractory chronic cough (RCC) or idiopathic chronic cough (ICC).
SUMMARY OF THE INVENTION
One aspect ofthe invention pertains to a compound that is [((1R,2S,5R)-2-isopropyl-5methyl-cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester (also referred to herein as “AX-8” or “Gly-O-iPr”), or a pharmaceutically acceptable sait, hydrate, or solvaté thereof, as described herein, for use in a method of treatment ofthe human or animal body by therapy, more specifically, for use in a method of treatment of chronic cough (CC), including, for example, refractory chronic cough (RCC) and idiopathic chronic cough (ICC), and as described herein.
Another aspect ofthe présent invention pertains to use a compound that is [((1 R,2S,5R)2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester (also referred to herein as “AX-8” or “Gly-O-iPr”), or a pharmaceutically acceptable sait, hydrate, or solvaté thereof, as described herein, in the manufacture of a médicament for treatment, more specifically, for the treatment of chronic cough (CC), including, for example, refractory chronic cough (RCC) and idiopathic chronic cough (ICC), and as described herein.
Another aspect ofthe présent invention pertains to a method of treatment, more specifically, a method of treatment of chronic cough (CC), including, for example, refractory chronic cough (RCC) and idiopathic chronic cough (ICC), and as described herein, comprising administering to a patient in need of treatment a therapeutically effective amount of a compound that is [((1R,2S,5R)-2-isopropyl-5-methylcyclohexanecarbonyl)-amino]-acetic acid isopropyl ester (also referred to herein as “AX-8” or “Gly-O-iPr”), or a pharmaceutically acceptable sait, hydrate, or solvaté thereof, as described herein, preferably in the form of a pharmaceutical composition.
Another aspect ofthe présent invention pertains to a kit comprising (a) a compound that is [((1R,2S,5R)-2-isopropyl-5-methyl-cyctohexanecarbonyl)-amino]-acetic acid isopropyl ester (also referred to herein as “AX-8” or “Gly-O-iPr”), or a pharmaceutically acceptable sait, hydrate, or solvaté thereof, as described herein, preferably provided as a pharmaceutical composition and in a suitabîe container and/or with suitabîe packaging; and (b) instructions for its use, for example, written instructions on how to administer the compound for the treatment of chronic cough (CC), including, for example, refractory chronic cough (RCC) and idiopathic chronic cough (ICC), and as described herein.
As will be appreciated by one of skill in the art, features and preferred embodiments of one aspect of the invention will also pertain to other aspects of the invention.
BRIEF DESCRIPTION OF THE DRAWINGS
Figure 1 is a graph of médian cough frequency (coughs/hour) versus time after treatment (hours) for baseline (open Gircles) and treatment (filled circles).
Figure 2 is a graph showing mean awake cough frequency (coughs/hour) for the 12 individual patients, for both baseline and treatment.
Figure 3 is a graph showing mean asleep cough frequency (coughs/hour) for the 12 individual patients, for both baseline and treatment.
Figure 4 is a graph showing mean cough frequency (coughs/hour) for the 12 individual patients during the 24-hour period after treatment and the équivalent baseline period.
Figure 5 is a graph showing médian cough frequency (coughs/hour) for the 12 individual patients during the 8-hour period after treatment and the équivalent baseline period.
Figure 6 is a graph showing médian cough frequency (coughs/hour) for the 12 individual patients during the 4-hour period after treatment and the équivalent baseline period.
Figure 7 is a graph of médian cough severity (VAS) (mm) versus time after treatment (hours) for baseline (open downward triangles) and treatment (filled downward triangles).
Figure 8 is a graph of médian urge-to-cough (VAS) (mm) versus time after treatment (hours) for baseline (open diamonds) and treatment (filled diamonds).
Figure 9 is a graph of médian throat irritation (VAS) (mm) versus time after treatment (hours) for baseline (open squares) and treatment (filled squares).
Figure 10 is a graph of médian throat cooling (VAS) (mm) versus time after treatment (hours) (filled upward triangles).
Figure 11 is a composite graph showing, on the left, médian urge-to-cough (VAS) (mm) (filled diamonds), throat irritation (VAS) (mm) (filled squares), and throat cooling (VAS) (mm) (filled upward triangles) and on the right, médian cough frequency (coughs/hour) for baseline (open circles) and treatment (filled circles), versus time after treatment (hours).
Figure 12 is a graph representing the activation of human TRPM8 by AX-8, as obtained by FLIPR® assay. The dose response curve is represented as the calcium signal expressed in relative light units (calculated by the area under the curve - AUC, mean ± sem, n = 8) by the AX-8 concentration (μΜ, log scale). The half-maxîmal response concentration (ECso) for AX-8 was found to be 0.39 μΜ.
Figure 13 is a graph representing the activation of human TRPM8 by menthol, as obtained by FLIPR® assay. The dose response curve is represented as the calcium signal expressed in relative light units (calculated by the area under the curve - AUC, mean ± sem, n = 8) by the menthol concentration (μΜ, îog scale). The half-maximal response concentration (EC5o) for menthol was found to be 2.29 μΜ.
Figure 14 is a graph representing the comparative activation of human TRPA1 and human TRPV1 by AX-8 and their reference agonists. For hTRPAI, dose response curves for mustard oil (reference TRPA1 agonist) and AX-8 are represented as the percentage ofthe mustard oil maximal response (mean ± SD, n = 4) by the agonist concentration (μΜ, log scale). The data demonstrate that AX-8 has no significant agonistic activity on hTRPAI for concentrations < 100 μΜ. For hTRPVI, dose response curves for capsaicin (reference TRPV1 agonist) and AX-8 are represented as the percentage of the capsaicin maximal response (mean ± SD, n = 4) by the agonist concentration (μΜ, log scale). The data demonstrate that AX-8 has no agonistic activity on hTRPVI for concentrations i 100 μΜ.
Figure 15 is a bar graph representing the inhibition (%) ofthe capsaicin-induced response by AX-8 in guinea pig vagal nerve expiants versus the concentration (μΜ) of AX-8. Capsaicin-induced response in guinea pig vagal nerves is blocked in a dose-dependent manner by AX-8 (n = 3).
Figure 16 is a bar graph representing the inhibition (%) of the capsaicin-induced response by AX-8 (1 μΜ) in guinea pig vagal nerve expiants in the presence or absence ofthe sélective TRPM8 antagonist PF-05105679 (PF, 10 μΜ). Four different conditions of two consecutive 10-minute incubations were done as follows: Vehicle (0.1 % DMSO) / Vehicle, PF / Vehicle, Vehicle ! AX-8 and PF / AX-8 (n= 4). Inhibition of the response induced in guinea pig vagal nerve expiants by the irritant capsaicin was blocked by the sélective TRPM8 inhibitor PF-05105679, demonstrating that the effect of AX-8 is TRPM8-dependent.
Figure 17 is a bar graph representing the effect of AX-8 on capsaicin-induced cough in awake guinea pig. Vehicle did not significantly affect capsaicin-induced cough (Baseline (V) = 24.8 ± 2.1 coughs/10 min vs. vehicle = 21.4 ± 2.4 coughs/10 min) in guinea pigs. 75 pl_ of a 5 mg/mL AX-8 solution (i.e., 0.375 mg/animal) sprayed in the oropharyngeal 5 région inhibited capsaicin-induced cough ofthe guinea pig from 25.0 ± 2.0/10 min coughs (Baseline (T)) to 9.0 ± 2.0/10 min coughs (**p < 0.01 ). The number of animais is 10 per group (n = 10).
DETAILED DESCRIPTION OF THE INVENTION
Compound
The présent invention pertains to a compound that is [((1Rt2ST5R)-2-isopropyl-5-methylcyclohexanecarbonyl)-amîno]-acetic acid isopropyl ester (also referred to herein as “AX-8” or “Gly-O-iPr”, shown below), or a pharmaceutically acceptable sait, hydrate, or solvaté thereof, as described herein, for use in a method of treatment of the human or animal body by therapy, more specifically, for use in a method of treatment of chronic cough (CC), including, for example, refractory chronic cough (RCC) and idiopathic chronic cough (ICC), and as described herein.
Code Name | Chemical Name etc. | Chemical Structure |
“AX-8 “Gly-O-iPr” | [((1R,2S,5R)-2-isopropyl5-methyl-cyclohexanecarbonyl)amino]-acetic acid isopropyl ester Formula: C16H29NO3 Formula Weight: 283.41 | c. 0 r |
The compound is structurally related to (-)-menthol, and has the same chiral centres, in the same configuration, as those found in (-)-menthoL
Name | Chemical Name | Chemical Structure |
(-)-menthol | (1R,2S,5R)-2-isopropyî-5-methylcycîohexanol |
In structural terms, the compound may conveniently be described as the isopropyl ester of the glycine amide of the carboxylic acid corresponding to (-)-menthol.
It may also be conveniently described as a p-menthane carboxamide.
In one embodiment, the compound is [((1R,2S,5R)-2-isopropyl-5-methylcyclohexanecarbonyi)-amino]-acetîc acid isopropyl ester or a pharmaceutically acceptable sait, hydrate, or solvaté thereof.
In one embodiment, the compound is [((1R,2S,5R)-2-isopropyl-5-methylcyclohexanecarbonyl)-amino]-acetic acid isopropyl ester or a pharmaceutically acceptable sait thereof.
In one embodiment, the compound is [((1R,2S,5R)-2-isopropyl-5-methylcyclohexanecarbonyl)-amino]-acetic acid isopropyl ester.
Uses
The compound, [((1 R,2S,5R)-2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester (also referred to herein as “AX-8” or “Gly-O-iPr), as described herein, is useful, for example, in the treatment of chronic cough (CC), încluding, for example, refractory chronic cough (RCC) and idiopathic chronic cough (ICC), and as described herein.
Use in Methods of Therapy
One aspect ofthe invention pertains to compound that is [((1R,2S,5R)-2-isopropyl-5methyl-cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester (also referred to herein as “AX-8 or “Gly-O-iPr), or a pharmaceutically acceptable sait, hydrate, or solvaté thereof, as described herein, for use in a method of treatment of the human or animal body by therapy, more specifically, for use in a method of treatment of chronic cough (CC), încluding, for example, refractory chronic cough (RCC) and idiopathic chronic cough (ICC), and as described herein.
One aspect of the invention pertains to a compound that is [((1 R,2S,5R)-2-isopropyl-5methyl-cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester (also referred to herein as “AX-8 or Gly-O-iPr), or a pharmaceutically acceptable sait, hydrate, or solvaté thereof, as described herein, in combination with one or more (e.g., 1,2, 3, 4) additional therapeutic agents, as described herein, for use in a method of treatment ofthe human or animal body by therapy, more specifically, for use in a method of treatment of chronic cough (CC), încluding, for example, refractory chronic cough (RCC) and idiopathic chronic cough (ICC), and as described herein.
Use in the Manufacture of Médicaments
One aspect ofthe présent invention pertains to use of a compound that is [((1R,2S,5R)-2isopropyl-5-methyl-cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester (also referred to herein as “AX-8” or “Gly-O-iPr”), or a pharmaceutically acceptable sait, hydrate, or solvaté thereof, as described herein, in the manufacture of a médicament for treatment, more specifically, for the treatment of chronic cough (CC), încluding, for example, refractory chronic cough (RCC) and idiopathic chronic cough (ICC), and as described herein.
In one embodiment, the médicament comprises the compound.
One aspect of the présent invention pertains to use of a compound that is [((1 R,2S,5R)-2isopropyl-5-methyl-cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester (also referred to herein as “AX-8” or Gly-O-iPr”), or a pharmaceutically acceptable sait, hydrate, or solvaté thereof, as described herein, and one or more (e.g., 1, 2, 3, 4) additional therapeutic agents, as described herein, in the manufacture of a médicament for treatment, more specifically, for the treatment of chronic cough (CC), including, for example, refractory chronic cough (RCC) and idiopathic chronic cough (ICC), and as described herein.
In one embodiment, the médicament comprises the compound and the one or more (e.g., 1, 2, 3, 4) additional therapeutic agents.
Methods of Treatment
One aspect of the présent invention pertains to a method of treatment, more specifically, a method of treatment of chronic cough (CC), including, for example, refractory chronic cough (RCC) and idiopathic chronic cough (ICC), and as described herein, comprising administerîng to a patient in need of treatment a therapeutically effective amount of a compound that is [((1 R,2S,5R)-2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester (also referred to herein as “AX-8” or “Gly-O-iPr”), or a pharmaceutically acceptable sait, hydrate, or solvaté thereof, as described herein, preferably in the form of a pharmaceutical composition.
One aspect of the présent invention pertains to a method of treatment, more specifically, a method of treatment of chronic cough (CC), including, for exampîe, refractory chronic cough (RCC) and idiopathic chronic cough (ICC), and as described herein, comprising administerîng to a patient in need of treatment a therapeutically effective amount of a compound that is [((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester (also referred to herein as “AX-8” or Gly-O-iPr”), or a pharmaceutically acceptable sait, hydrate, or solvaté thereof, as described herein, preferably in the form of a pharmaceutical composition, and one or more (e.g., 1,2, 3, 4) additional therapeutic agents, as described herein, preferably in the form of a pharmaceutical composition.
Kits
Another aspect of the présent invention pertains to a kit comprising (a) a compound that is [((1 R,2S,5R)-2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester (also referred to herein as “AX-8” or “Gly-O-iPr), or a pharmaceutically acceptable sait, hydrate, or solvaté thereof, as described herein, preferably provided as a pharmaceutical composition and in a suitable container and/or with suitable packaging; and (b) instructions for its use, for example, written instructions on how to administerthe compound for the treatment of chronic cough (CC), including, for example, refractory chronic cough (RCC) and idiopathic chronic cough (ICC), and as described herein.
In one embodiment, the kit further comprises one or more (e.g., 1,2,3, 4) additional therapeutic agents, as described herein.
The written instructions may also include a list of spécifie indications for which the compound is a suitable treatment.
Chronic Cough
As used herein, the term “chronic cough (CC) refers to a cough lasting for more than about 8 weeks in adults, or for more than about 4 weeks in children.
Chronic cough is often considered to be a symptom of an associated condition.
In some cases, an associated condition that could cause chronic cough can be identified (i.e., explained chronic cough). Common causes of chronic cough are, for example, asthma, éosinophilie bronchitis, post-nasal drip syndrome (PNDS), gastro-oesophageal reflux disease (GORD), bronchiectasis chronic obstructive pulmonary disease (COPD), and idiopathic pulmonary fibrosis (IPF).
In other cases, an associated condition cannot be identified (i.e., unexplained or idiopathic chronic cough).
In some cases, the associated condition can be identified, and is treated, and chronic cough is improved following treatment ofthe associated condition.
In other cases, the associated condition that could cause chronic cough can be identified, and is treated, but chronic cough persists despite treatment ofthe associated condition. Here, the persistent chronic cough may be considered to be refractory chronic cough (i.e., refractory to treatment ofthe associated condition) or idiopathic chronic cough (i.e., the cause remains unexplained). This persistent chronic cough, whether described as idiopathic chronic cough or refractory chronic cough, can be considered to be a condition in its own rrght, rather than merely a symptom.
Therefore, a chronic cough-dedicated therapy can be used to improve the condition of chronic cough patients: with no identified associated condition (idiopathic chronic cough); with an identified associated condition causing the chronic cough but which cannot be treated; with an associated condition causing chronic cough which can be treated, but with a chronic cough refractory to treatment ofthe associated condition (refractory chronic cough).
In many cases, idiopathic / refractory chronic cough has a recognisable origin or history, for example, an earlier condition with chronic cough as a symptom which, despite treatment ofthe condition, gave rise to persistent chronic cough. This persistent chronic cough is usually independent of the earlier condition, and instead is often associated with neurological changes that arose concurrentiy with or subséquent to the earlier treatment.
For example, consider two patients with chronic cough as a symptom. Both are correctly diagnosed with asthma (the associated condition). Both are treated for their asthma (the associated condition). For both patients, most ofthe asthma symptoms are improved. However, for the first patient, chronic cough is improved, whereas for the second patient, it is not. This second patient, who was initially considered to hâve explained chronic cough (due to asthma) is now diagnosed with refractory chronic cough (because it is refractory to the treatment of the associated condition, asthma) or idiopathic chronic cough (because, now, the associated condition causing the persistent chronic cough is unknown, or not yet known).
In one embodiment, the treatment is treatment of chronic cough, !n one embodiment, the chronic cough is explained chronic cough.
In one embodiment, the chronic cough is chronic cough as a symptom of, associated with, or caused by: a diagnosed condition.
In one embodiment, the chronic cough is chronic cough as a symptom of, associated with, or caused by: a diagnosed cough-related condition.
In one embodiment, the chronic cough is chronic cough as a symptom of, associated with, or caused by: asthma, éosinophilie bronchitis, post-nasal drip syndrome (PNDS), gastro-oesophageal reflux disease (GORD), bronchiectasis chronic obstructive pulmonary disease (COPD), or idiopathic pulmonary fibrosis (IPF).
In one embodiment, the chronic cough is idiopathic chronic cough (ICC).
In one embodiment, the chronic cough is refractory chronic cough (RCC).
In one embodiment, the chronic cough is refractory chronic cough (RCC) that persists after assessment and treatment of a cough-related condition, e.g., according to an accepted guideline.
In one embodiment, the chronic cough is refractory chronic cough (RCC) that persists after assessment and treatment of: asthma, éosinophilie bronchitis, post-nasal drip syndrome (PNDS), gastro-oesophageal reflux dîsease (GORD), bronchiectasis chronic obstructive pulmonary dîsease (COPD), or idiopathic pulmonary fibrosis (IPF), e.g., according to an accepted guideline.
In one embodiment, the chronic cough (including, e.g., idiopathic chronic cough and refractory chronic cough) is a symptom of, associated with, or caused by: allotussia.
In one embodiment, the chronic cough (including, e.g., idiopathic chronic cough and refractory chronic cough) is a symptom of, associated with, or caused by: hypertussia.
In one embodiment, the chronic cough (including, e.g., idiopathic chronic cough and refractory chronic cough) is a symptom of, associated with, or caused by: cough hypersensîtivity syndrome (CHS).
In one embodiment, the chronic cough (including, e.g., idiopathic chronic cough and refractory chronic cough) is a symptom of, associated with, or caused by: cough hypersensîtivity reflex (CHR).
In one embodiment, the chronic cough (including, e.g., idiopathic chronic cough and refractory chronic cough) is a symptom of, associated with, or caused by: laryngeal paraesthesia.
In one embodiment, the chronic cough (including, e.g., idiopathic chronic cough and refractory chronic cough) is a symptom of, associated with, or caused by: laryngeal hypersensîtivity syndrome (LHS).
In one embodiment, the chronic cough (including, e.g., idiopathic chronic cough and refractory chronic cough) is sensory neuropathie cough.
In one embodiment, the chronic cough (including, e.g., idiopathic chronic cough and refractory chronic cough) is a symptom of, associated with, or caused by: peripheral sensitization; central sensitization (cough centre); and/or cortical and/or subcortical maladaptive plasticity.
In one embodiment, the chronic cough (including, e.g., idiopathic chronic cough and refractory chronic cough) is a symptom of, associated with, or caused by: vagal neuropathy.
In one embodiment, the chronic cough (including, e.g., idiopathic chronic cough and refractory chronic cough) is a symptom of, associated with, or caused by: airway inflammation.
In one embodiment, the chronic cough (including, e.g., idiopathic chronic cough and refractory chronic cough) is a symptom of, associated with, or caused by: neurogenic inflammation and/or neuroinflammation.
Treatment
The term “treatment,” as used herein in the context of treating a condition, pertains generally to treatment and therapy, whether of a human or an animal (e.g., in veterinary applications), in which some desired therapeutic effect is achieved, for example, the inhibition ofthe progress ofthe condition, and includes a réduction in the rate of progress, a hait in the rate of progress, alleviation of symptoms of the condition, amelioration of the condition, and cure ofthe condition. Treatment as a prophylactic measure (i.e., prophylaxis) is also included. For example, use with patients who hâve not yet developed the condition, but who are at risk of developing the condition, is encompassed by the term treatment.
For example, treatment of chronic cough (including, e.g., treatment of refractory chronic cough) includes the prophylaxis of cough, reducing the incidence of cough (e.g., urge-tocough), reducing the frequency of cough (e.g., cough frequency), reducing the severity of cough (e.g., cough severity), alleviating the symptoms of cough (e.g., reducing throat irritation), etc.
In one embodiment, the treatment is to reduce one or more or ail of: cough frequency, cough severity, urge-to-cough, and throat irritation.
In one embodiment, the treatment is to reduce cough frequency.
In one embodiment, the treatment is to reduce hourly cough frequency.
In one embodiment, the treatment is to reduce médian hourly cough frequency.
In one embodiment, the treatment is to reduce mean hourly cough frequency.
In one embodiment, the treatment is to reduce awake hourly cough frequency.
In one embodiment, the treatment is to reduce awake médian hourly cough frequency.
In one embodiment, the treatment is to reduce awake mean hourly cough frequency.
In one embodiment, the treatment is to reduce asleep hourly cough frequency.
In one embodiment, the treatment is to reduce asleep médian hourly cough frequency.
In one embodiment, the treatment is to reduce asleep mean hourly cough frequency.
In one embodiment, the treatment is to reduce cough severity.
In one embodiment, the treatment is to reduce urge-to-cough.
In one embodiment, the treatment is ta reduce throat irritation.
In one embodiment, the treatment reduces cough frequency.
în one embodiment, the treatment reduces hourly cough frequency.
In one embodiment, the treatment reduces médian hourly cough frequency.
In one embodiment, the treatment reduces mean hourly cough frequency.
In one embodiment, the treatment reduces awake hourfy cough frequency.
!n one embodiment, the treatment reduces awake médian hourly cough frequency.
In one embodiment, the treatment reduces awake mean hourly cough frequency.
In one embodiment, the treatment reduces asleep hourly cough frequency.
in one embodiment, the treatment reduces asleep médian hourly cough frequency.
In one embodiment, the treatment reduces asleep mean hourly cough frequency.
în one embodiment, the treatment reduces cough severity.
In one embodiment, the treatment reduces urge-to-cough.
In one embodiment, the treatment reduces throat irritation.
The term “iherapeutically-effective amount, as used herein, pertains to that amount of a compound, or a material, composition or dosage form comprising a compound, which is effective for producing some desired therapeutic effect, commensurate with a reasonable benefît/risk ratio, when administered in accordance with a desired treatment regimen.
Routes of Administration
The compound, [((1 R,2S,5R)-2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester (also referred to herein as “AX-8” or “Gly-O-iPr), as described herein, or pharmaceutical composition comprising the compound may be administered to a subject by any convenient route of administration, whether systemically/peripherally or topically (i.e., atthe site of desired action).
In one preferred embodiment, the route of administration is topical.
Routes of administration include: oral (e.g., by ingestion); oromucosal; buccal (e.g., between the gums and cheek); sublingual (e.g., under the tongue); transdermal (including, e.g., by a patch, plaster, etc.)·, transmucosal (including, e.g., by a patch, plaster, etc.)·, intranasal (e.g., by nasal spray, drops or from an atomiser or dry powder delivery device); pulmonary (e.g., by inhalation or insufflation therapy using, e.g., an aérosol, e.g., through the mouth or nose).
In one preferred embodiment, the route of administration is oral.
In one preferred embodiment, the route of administration is topical oral.
In one preferred embodiment, the route of administration is oromucosal.
In one preferred embodiment, the route of administration is topical oromucosal.
In one preferred embodiment, the route of administration is buccal.
In one preferred embodiment, the route of administration is topical buccal.
In one preferred embodiment, the route of administration is sublingual.
In one preferred embodiment, the route of administration is topical sublingual.
In one preferred embodiment, the route of administration is intranasal.
In one preferred embodiment, the route of administration is topical intranasal.
In one preferred embodiment, the route of administration is transmucosal.
In one preferred embodiment, the route of administration is topical transmucosal.
Dosage
It will be appreciated by one of skill in the art that an appropriate dosage of the compound, [((1 R,2S,5R)-2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester (also referred to herein as “AX-8” or “Gly-O-iPr”), as described herein, or composition comprising the compound, can vary from patient to patient. Determining the optimal dosage will generally involve the balancing ofthe level of therapeutic benefit against any risk or deleterious side effects. The selected dosage level will dépend on a variety of factors including the activity of the compound, the route of administration, the time of administration, the rate of excrétion of the compound, the duration of the treatment, other drugs, compounds, and/or materials used in combination, the severîty of the condition, and the species, sex, âge, weight, condition, general health, and prior medical history of the patient, The amount of compound and route of administration will ultimately be atthe discrétion ofthe physician, veterinarian, orclinician, aithough generally the dosage will be selected to achieve local concentrations at the site of action which achieve the desired effect without causing substantial harmful or deleterious sideeffects.
Administration can be effected in one dose, continuously or intermittently (e.g., in divided doses at appropriate intervals) throughout the course of treatment. Methods of determining the most effective means and dosage of administration are well known to those of skill in the art and will vary with the formulation used for therapy, the purpose of the therapy, the target cell(s) being treated, and the subject being treated. Single or multiple administrations can be carried out with the dose level and pattern being selected by the treating physician, veterinarian, or clinician.
In one embodiment, the dose is in the range of from about 1 pg to about 5 mg of the compound per kilogram body weight ofthe subject per day.
In one embodiment, the dose is in the range of from about 5 pg to about 2 mg ofthe compound per kilogram body weight ofthe subject per day.
In one embodiment, the dose is in the range of from about 15 pg to about 0.7 mg of the compound per kilogram body weight ofthe subject per day.
In one embodiment, the dose is in the range of from about 30 pg to about 0.4 mg of the compound per kilogram body weight of the subject per day.
In one embodiment, the dose is in the range offrom about 70 pg to about 0.3 mg ofthe compound per kilogram body weight of the subject per day.
Similarly, in one embodiment, the dose is in the range of from about 0.07 mg to about 350 mg ofthe compound per day.
In one embodiment, the dose is in the range of from about 0.35 mg to about 140 mg of the compound per day.
In one embodiment, the dose is in the range offrom about 1 mg to about 50 mg ofthe compound per day.
In one embodiment, the dose is in the range of from about 2 mg to about 30 mg of the 5 compound per day.
In one embodiment, the dose is in the range of from about 5 mg to about 20 mg ofthe compound per day.
Where the compound is a sait, an ester, an amide, a prodrug, or the like, the amount administered is calculated on the basis of the parent compound and so the actual weight to be used is increased proportionately.
Treatment Regimen
The compound, or pharmaceutical composition comprising the compound, may be administered according to any suitable treatment plan or regimen.
Mostly likely, administration will be performed by the patient, “on demand”, according to 20 the patient’s needs. For example, the patient may be directed to self-administer the compound, or pharmaceutical composition comprising the compound, upon anticipation of cough (e.g., as prophylaxis); immediately following the start of cough; after a period of prolonged cough; etc.
As described herein, a single administration of a 5 mg ODT was found to hâve an efficacy that lasted for up to about 8 hours, and so it may be anticipated that 2 to 4 administrations daily may be sufficient.
In one embodiment, the treatment regimen is 1 to 5 administrations daily 30 (i.e., administration one to five times daily).
In one embodiment, the treatment regimen is 1 to 4 administrations daily (i.e., administration one to four fîmes daily).
In one embodiment, the treatment regimen is 2 to 5 administrations daily (i.e., administration two to five times daily).
In one embodiment, the treatment regimen is 2 to 4 administrations daily (i.e., administration two to four times daily).
In one embodiment, the treatment regimen is 2 administrations daily (i.e., administration twice daily).
In one embodiment, the treatment regimen is 3 administrations daily (i.e., administration three times daily).
In one embodiment, the treatment regimen is 4 administrations daily (i.e., administration four times daily).
In one embodiment, the treatment regimen is pro re nata (PRN) (e.g., as needed, as the situation arises, etc.).
Formulations
While it is possible for the compound, [((1R,2S,5R)-2-isûpropy1-5-methylcyclohexanecarbonyl)-amino]-acetic acid isopropyî ester (also referred to herein as “AX-8” or “Gly-O-iPr”), as described herein, to be administered alone, it is préférable to présent it as a pharmaceutical formulation (e.g., composition, préparation, médicament) comprising the compound, as described herein, together with one or more other pharmaceutically acceptable ingrédients weil known to those skilled in the art, including pharmaceutically acceptable carriers, diluents, excipients, adjuvants, fillers, buffers, preservatives, anti-oxidants, lubricants, stabîlisers, solubilisers, surfactants (e.g., wetting agents), masking agents, colouring agents, flavouring agents, and sweetening agents. The formulation may further comprise other active agents, for example, other therapeutic or prophylactic agents.
Described herein are pharmaceutical compositions and methods of making a pharmaceutical composition comprising admixing the compound together with one or more other pharmaceutically acceptable ingrédients well known to those skilled in the art, e.g., carriers, diluents, excipients, etc. If formulated as discrète units (e.g., tablets, etc.), each unit contains a predetermined amount (dosage) of the compound.
The term “pharmaceuticaliy acceptable, as used herein, pertains to compounds, ingrédients, materials, compositions, dosage forms, etc., which are, within the scope of Sound medical judgment, suitable for use in contact with the tissues of the subject in question (e.g., human) without excessive toxicity, irritation, allergie response, or other problem or complication, commensurate with a reasonable benefit/risk ratio. Each carrier, diluent, excipient, etc. must also be “acceptable” in the sense of being compatible with the other ingrédients of the formulation.
Suitable carriers, diluents, excipients, etc. can be found in standard pharmaceutical texts, for example, Remingtoris Pharmaceutical Sciences, 18th édition, Mack Publishing Company, Easton, Pa., 1990; and Handbook of Pharmaceutical Excipients, 5th édition, 2005.
The formulations may be prepared by any methods well known in the art of pharmacy. Such methods include the step of bringing into association the compound with a carrier which constitutes one or more accessory ingrédients. In general, the formulations are prepared by uniformiy and intimately bringing into association the compound with carriers (e.g., liquid carriers, finely divided solid carrier, etc.), and then shaping the product, if necessary.
The formulation may be prepared to provide for rapid or slow release; immédiate, delayed, timed, or sustained release; or a combination thereof.
Formulations may suitably be in the form of liquids, solutions (e.g., aqueous, nonaqueous), suspensions (e.g., aqueous, non-aqueous), émulsions (e.g., oil-in~water, water-in-oil), élixirs, syrups, electuaries, mouthwashes, drops, tablets (including, e.g., coated tablets), granules, powders, lozenges, pastilles, capsules (including, e.g., hard and soft gelatin capsules), cachets, pilis, ampoules, boluses, tinctures, gels, pastes, ointments, creams, lotions, oils, foams, sprays, mists, or aérosols.
In one embodiment, the compound is formulated as a spray.
In one embodiment, the compound is formulated as a mist.
In one embodiment, the compound is formulated as an aerosol.
Formulations may suitably be provîded as a patch, adhesive plaster, bandage, dressing, or the like which is impregnated with one or more compounds and optionally one or more other pharmaceuticalty acceptable ingrédients, including, for example, pénétration, perméation, and absorption enhancers. Formulations may also suitably be provîded in the form of a depot or réservoir.
The compound may be dissolved in, suspended in, or admixed with one or more other pharmaceutically acceptable ingrédients.
Formulations suitable for oral administration (e.g., by ingestion) include liquids, solutions (e.g., aqueous, non-aqueous), suspensions (e.g., aqueous, non-aqueous), émulsions (e.g., oil-in-water, water-in-oil), elixirs, syrups, electuaries, tablets, granules, powders, capsules, cachets, pills, ampoules, and boluses.
In one embodiment, the compound is formulated as a tablet.
In one embodiment, the compound is formulated as an orally disintegrating tablet (ODT), also referred to as an orodispersible tablet, a mouth-dissolving tablet, a rapid-dissolving tablet, a fast-disintegrating tablet, or a fast-dissolving tablet. ODT’s, as contemplated herein, are pharmaceutical dosage forms that disintegrate in saliva within a few minutes of topical application on the surface of the tongue. Preferably, the disintegration time is long enough to permit the compound to cover the mucosa. Key advantages of the use of ODT’s to deliver the compound are the ease of administration (e.g., ora! administration) and delivery to the site of action (e.g., topical rather than system).
A typical ODT is composed predominantly of an inert vehicle, diluent, or carrier. The médicinal agent (i.e., AX-8) is interspersed within this carrier. The ODT will dissolve when placed on the dorsal surface of the tongue thereby releasing the médicinal agent so that it may corne in contact with the tissues ofthe lower oropharynx (LRO). A typical diluent, carrier, or vehicle may be a “polyhydric alcohol” construed as describing the following substances: xylitol, mannitol, sorbitol, maltitol, isomaltitol, maitotriitol, lactitol, and β-linked-glucopyranasido-sorbitol. Flavoring agents such as the sweeteners, aspartame, sucralose, or alitame, may be added to mask any fastes. Typically, the mix is granulated to a uniformly dispersed blend; dispersing agents, anti-caking agents, and/or lubricants may be added; and the mixture is then compressed to form the ODT. As an example, ODT used in the studied described herein contained Ludiflash® (Mannitol, Kollidon® CL-SF, Kollicoat® SR 30D), sorbitol, sïlica colloïdal anhydrous, and magnésium stéarate.
In one embodiment, the compound is formulated as an ODT containing from about 0.5 mg to about 50 mg of the compound.
In one embodiment, the compound is formulated as an ODT containing from about 1 to about 30 mg ofthe compound.
In one embodiment, the compound is formulated as an ODT containing from about 2 to about 20 mg ofthe compound.
In one embodiment, the compound is formulated as an ODT containing from about 2 to about 10 mg ofthe compound.
In one embodiment, the compound is formulated as an ODT containing about 5 mg ofthe compound.
In one embodiment, the compound is formulated as an ODT containing from about 50 mg to about 250 mg ofthe compound.
Where the compound is a sait, an ester, an amide, a prodrug, or the like, the amount administered is calculated on the basis of the parent compound and so the actual weight to be used is increased proportionately.
Formulations suitable for buccal administration include mouthwashes, lozenges, pastilles, as well as patches, adhesive plasters, depots, and réservoirs. Lozenges typically comprise the compound in a flavoured basis, usually sucrose and acacia or tragacanth. Pastilles typically comprise the compound in an inert matrix, such as gelatin and glycerin, or sucrose and acacia. Mouthwashes typically comprise the compound in a suitable liquid carrier.
Formulations suitable for sublingual administration include tablets, lozenges, pastilles, capsules, and pills.
Formulations suitable for oral transmucosal administration include liquids, solutions (e.g., aqueous, non-aqueous), suspensions (e.g., aqueous, non-aqueous), émulsions (e.g., oil-in-water, water-in-oil), mouthwashes, sprays, mists, lozenges, pastilles, as well as patches, adhesive plasters, depots, and réservoirs.
Formulations suitable for transdermal administration include gels, pastes, ointments, creams, lotions, and oils, as well as patches, adhesive plasters, bandages, dressings, depots, and réservoirs.
Tablets may be made by conventional means, e.g., compression or moulding, optionally with one or more accessory ingrédients. Compressed tablets may be prepared by compressing in a suitable machine the compound in a free-flowing form such as a powder or granules, optionally mixed with one or more binders (e.g., povidone, gelatin, acacia, sorbitoi, tragacanth, hydroxypropylmethyl cellulose); fillers or diluents (e.g., lactose, microcrystalline cellulose, calcium hydrogen phosphate); lubricants (e.g., magnésium stéarate, talc, silica); disintegrants (e.g., sodium starch glycolate, cross-linked povidone, cross-linked sodium carboxymethyl cellulose); surface-active or dispersing or wetting agents (e.g., sodium lauryl sulfate); preservatives (e.g., methyl p-hydroxybenzoate, propyl p-hydroxybenzoate, sorbic acid); flavours, flavour enhancing agents, and sweeteners. Moulded tablets may be made by moulding in a suitable machine a mixture ofthe powdered compound moistened with an inert liquid diluent. The tablets may optionally be coated or scored and may be formulated so as to provide slow or controlled release of the compound therein using, for example, hydroxypropylmethyl cellulose in varying proportions to provide the desired release profile. Tablets may optionally be provided with a coating, for example, to affect release, for example an entenc coating, to provide release in parts of the gut other than the stomach.
Ointments are typically prepared from the compound and a paraffinic or a water-miscible ointment base.
Creams are typically prepared from the compound and an oil-in-water cream base. If desired, the aqueous phase ofthe cream base may include, for example, at least about 30% w/w of a polyhydric alcohol, i.e., an alcohol having two or more hydroxyl groups such as propylene glycol, butane-1,3-diol, mannitol, sorbitol, glycerol and polyethylene glycol and mixtures thereof. The topical formulations may desirably include a compound which 10 enhances absorption or pénétration of the compound through the skin or other affected areas. Examples of such dermal pénétration enhancers include dimethylsulfoxide and related analogues.
Emulsions are typically prepared from the compound and an oily phase, which may 15 optîonally comprise merely an emulsifier (otherwise known as an emulgent), or it may comprise a mixture of at least one emuisifier with a fat or an oil or with both a fat and an oil. Preferably, a hydrophilic emulsifier is included together with a lipophilie emulsifier which acts as a stabiliser. It is also preferred to include both an oil and a fat. Together, the emulsifier(s) with or without stabiliser(s) make up the so-called emulsifying wax, and 20 the wax together with the oil and/or fat make up the so-called emulsifying ointment base which forms the oily dispersed phase ofthe cream formulations.
Suitable emulgents and émulsion stabilisera include Tween 60, Span 80, cetostearyl alcohol, myristyl alcohol, glyceryl monostearate and sodium iauryl sulfate. The choice of 25 suitable oils or fats for the formulation is based on achieving the desired cosmetic properties, since the solubility of the compound in most oils likely to be used in pharmaceutical émulsion formulations may be very low. Thus, the cream should preferably be a non-greasy, non-staining and washable product with suitable consistency to avoid leakage from tubes or other containers. Straight or branched chain, mono- or 30 dibasic alkyl estera such as di-isoadipate, isocetyl stéarate, propylene glycol diester of coconut fatty acids, isopropyl myristate, decyl oleate, isopropyl palmitate, butyl stéarate, 2-ethylhexyl palmitate or a blend of branched chain esters known as Crodamol CAP may be used, the last three being preferred esters. These may be used alone or in combination depending on the properties required. Alternatively, high melting point lipids 35 such as white soft paraffin and/or liquid paraffin or other minerai oils can be used.
Formulations suitable for intranasal administration, where the carrier is a liquid, include, for example, nasal spray, nasal drops, or by aérosol administration by nebuliser, include aqueous or oily solutions of the compound.
Formulations suitable for intranasal administration, where the carrier is a solid, include, for example, those presented as a coarse powder having a particîe size, for example, in the range of about 20 to about 500 microns which is administered in the manner in which snuff is taken, i.e., by rapid inhalation through the nasal passage from a container ofthe 5 powder held close up to the nose.
Formulations suitable for pulmonary administration (e.g., by inhalation or insufflation therapy) include those presented as an aérosol spray from a pressurised pack, with the use of a suitable propellant, such as dichlorodifluoromethane, tnchlorofluoromethane, 10 dichloro-tetrafluoroethane, carbon dioxide, or other suitable gases.
In one embodiment, the compound is formulated as an aérosol spray.
Combination Thérapies
The term “treatment” includes combination treatments and thérapies, in which two or more treatments or thérapies are combined, for example, sequentially or simultaneousty. For example, the compound, [((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexanecarbonyl)amino]-acetic acid isopropyl ester (also referred to herein as “AX-8” or “Gly-O-iFT”), as 20 described herein, may also be used in combination thérapies, e.g., in conjunction with other agents, for example, one or more antitussive agents, expectorants, mucolytics, decongestants, nasal decongestants, first génération antihistamines, antihistamines, opioid analgésies, non-opiate analgésies, antipyretics, etc., and combinations thereof.
The particular combination would be at the discrétion of the physician who would select dosages using his common general knowledge and dosing regimens known to a skilled practitioner.
The agents (i.e., the compound, plus one or more other agents) may be administered 30 simultaneousiy or sequentially, and may be administered in individually varying dose schedules and via different routes. For example, when administered sequentially, the agents can be administered at closely spaced intervals (e.g., over a period of 5-10 minutes) or at longer intervals (e.g., 1,2, 3, 4 or more hours apart, or even longer periods apart where required), the précisé dosage regimen being commensurate with the 35 properties of the therapeutic agent(s).
The agents (i.e., the compound, plus one or more other agents) may be formulated together in a single dosage form, or alternatively, the individual agents may be formulated separately and presented together in the form of a kit, optionally with instructions for their 40 use.
The Subiect/Patient
The subject/patient may be a mammal, a placental mammal, a marsupial {e.g., kangaroo, wombat), a rodent {e.g., a guinea pig, a hamster, a rat, a mouse), murine {e.g., a mouse), a lagomorph {e.g., a rabbit), avian {e.g., a bird), canine {e.g., a dog), feline {e.g., a cat), equine {e.g., a horse), porcine {e.g., a pig), ovine {e.g., a sheep), bovine {e.g., a cow), a primate, simian {e.g., a monkey or ape), a monkey {e.g., marmoset, baboon), an ape (e.g., gorilla, chimpanzee, orangutan, gibbon), or a human.
In one preferred embodiment, the subject/patient is a human.
Compounds Configured for Use in Treatment of Chronic Couah
Also described herein is a compound comprising:
[((1 R,2S,5R)-2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]-acetîc acid isopropyl ester, or a pharmaceutically acceptable sait, hydrate, or solvaté thereof configured for use in treatment of chronic cough.
In one embodiment, the [((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]acetic acid isopropyl ester, or the pharmaceutically acceptable sait, hydrate, or solvaté thereof is configured for use in treatment of explained chronic cough.
In one embodiment, the [((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]acetic acid isopropyl ester, or the pharmaceutically acceptable sait, hydrate, or solvaté thereof is configured for use in treatment of the chronic cough as a symptom of, associated with, or caused by a diagnosed condition.
In one embodiment, the [((1 R,2S,5R)-2-isopropyl-5-methyl-cyclohexanecarbony!)-amino]acetic acid isopropyl ester, or the pharmaceutically acceptable sait, hydrate, or solvaté thereof is configured for use in treatment ofthe chronic cough as a symptom of, associated with, or caused by a diagnosed cough-related condition.
In one embodiment, the [((1R,2S,5R)-2-isopropy!-5-methyl-cyc!ohexanecarbonyl)-amîno]acetic acid isopropyl ester, or the pharmaceutically acceptable sait, hydrate, or solvaté thereof is configured for use in treatment of the chronic cough as a symptom of, associated with, or caused by asthma, éosinophilie bronchitis, post-nasal drip syndrome (PNDS), gastro-oesophageal reflux disease (GORD), bronchiectasis chronic obstructive pulmonary disease (COPD), or idiopathic pulmonary fibrosis (IPF).
In one embodiment, the [((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]acetic acid isopropyl ester, or the pharmaceutically acceptable sait, hydrate, or solvaté thereof is configured for use in treatment of idiopathic chronic cough (ICC).
In one embodiment, the [((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]acetic acid isopropyl ester, or the pharmaceutically acceptable sait, hydrate, or solvaté thereof is configured for use in treatment of refractory chronic cough (RCC).
In one embodiment, the [((1 R,2S,5R)-2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]acetic acid isopropyl ester, or the pharmaceutically acceptable sait, hydrate, or solvaté thereof is configured for use in treatment of refractory chronic cough (RCC) that persists after assessment and treatment of a cough-related condition.
In one embodiment, the [((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]acetic acid isopropyl ester, or the pharmaceutically acceptable sait, hydrate, or solvaté thereof is configured for use in treatment of refractory chronic cough (RCC) that persists after assessment and treatment of: asthma, éosinophilie bronchitis, post-nasal drip syndrome (PNDS), gastro-oesophageal reflux disease (GORD), bronchiectasis chronic obstructive pulmonary disease (COPD), or idiopathic pulmonary fibrosis (IPF).
In one embodiment, the [((1R,2S,5R)-2-isopropyl-5-methyî-cyclohexanecarbonyl)-amino]acetic acid isopropyl ester, or the pharmaceutically acceptable sait, hydrate, or solvaté thereof is configured for use in treatment of the chronic cough being a symptom of, associated with, or caused by allotussia.
!n one embodiment, the [((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]acetic acid isopropyl ester, or the pharmaceutically acceptable sait, hydrate, or solvaté thereof is configured for use in treatment of the chronic cough being a symptom of, associated with, or caused by hypertussia.
In one embodiment, the [((1 R,2S,5R)-2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]acetic acid isopropyl ester, or the pharmaceutically acceptable sait, hydrate, or solvaté thereof is configured for use in treatment of the chronic cough being a symptom of, associated with, or caused by cough hypersensitivity syndrome (CHS).
In one embodiment, the [((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexanecarbonyl)-aminoJacetic acid isopropyl ester, or the pharmaceutically acceptable sait, hydrate, or solvaté thereof is configured for use in treatment of the chronic cough is a symptom of, associated with, or caused by cough hypersensitivity reflex (CHR).
In one embodiment, the [((1R,2S,5R)-2-isopropyf-5-methyl·cyclohexanecaΓbonyl)-amino]acetic acid isopropyl ester, or the pharmaceutically acceptable sait, hydrate, or solvaté thereof is configured for use in treatment of the chronic cough being a symptom of, associated with, or caused by laryngeal paraesthesia.
In one embodiment, the [((1 RΊ2S,5R)-2-iΞopropyl·5-methyl-cyclohexanecarbonyl)-amino]acetic acid isopropyl ester, or the pharmaceutically acceptable sait, hydrate, or solvaté thereof is configured for use in treatment of the chronic cough being a symptom of, associated with, or caused by laryngeal hypersensitivity syndrome (LHS).
In one embodiment, the [((1R,2S,5R)-2-isopropyl-5-methyl·cyclohexanecarbonyl)-amino]acetic acid isopropyl ester, or the pharmaceutically acceptable sait, hydrate, or solvaté thereof is configured for use in treatment of the chronic cough being sensory neuropathie cough.
In one embodiment, the [((1R,2S,5R)-2-isopropyl-5~methyl-cyclohexanecarbonyl)-amino]acetic acid isopropyl ester, or the pharmaceutically acceptable sait, hydrate, or solvaté thereof is configured for use in treatment of the chronic cough being a symptom of, associated with, or caused by peripheral sensitization; central sensitization (cough centre); and/or cortical and/or subcortical maladaptive plasticity.
In one embodiment, the [((1 R,2S,5R)-2-isopropyl-5-methyl·cyclohexanecarbonyl)-amino]acetic acid isopropyl ester, or the pharmaceutically acceptable sait, hydrate, or solvaté thereof is configured for use in treatment of the chronic cough being a symptom of, associated with, or caused by vagal neuropathy.
In one embodiment, the [((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]acetic acid isopropyl ester, or the pharmaceutically acceptable sait, hydrate, or solvaté thereof is configured for use in treatment of the chronic cough being a symptom of, associated with, or caused by airway inflammation.
In one embodiment, the [((1R,2S,5R)-2-isopropyl-5-methy!-cyclohexanecarbonyl)-amino]acetic acid isopropyl ester, or the pharmaceutically acceptable sait, hydrate, or solvaté thereof is configured for use in treatment of the chronic cough being a symptom of, associated with, or caused by neurogenic inflammation and/or neuroinflammation.
In one embodiment, the wherein the [((1R,2S,5R)-2-isopropyl-5-methylcyclohexanecarbonyl)-amino]-acetic acid isopropyl ester, or the pharmaceuticaily acceptable sait, hydrate, or solvaté thereof is configured for use in treatment to: reduce cough frequency;
reduce hourly cough frequency;
reduce médian hourly cough frequency;
reduce mean hourly cough frequency;
reduce awake hourly cough frequency;
reduce awake médian houriy cough frequency;
reduce awake mean hourly cough frequency;
reduce asleep hourly cough frequency;
reduce asleep médian hourly cough frequency;
reduce asleep mean houriy cough frequency;
reduce cough severity;
reduce urge-to-cough; and/or reduce throat irritation.
In one embodiment, the [((1R,2S,5R)-2-isopropyb5-methyi-cyclohexanecarbonyl)-amino]acetic acid isopropyl ester, or the pharmaceutically acceptable sait, hydrate, or solvaté thereof is configured for:
topical oral administration ofthe compound;
topical oromucosal administration of the compound;
topical buccal administration ofthe compound;
topical sublingual administration ofthe compound;
topical intranasai administration ofthe compound; or topical transmucosal administration of the compound.
In one embodiment, the [((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]acetic acid isopropyl ester, or the pharmaceutically acceptable sait, hydrate, or solvaté thereof is configured for:
a dose in the range of from about 1 pg to about 5 mg ofthe compound per kilogram body weight per day;
a dose in the range of from about 5 pg to about 2 mg ofthe compound per kilogram body weight per day;
a dose in the range of from about 15 pg to about 0.7 mg of the compound per kilogram body weight per day;
a dose in the range of from about 30 pg to about 0.4 mg of the compound per kilogram body weight per day; or a dose in the range of from about 70 pg to about 0.3 mg ofthe compound per kilogram body weight per day.
In one embodiment, the [((1R,2S,5R)-2-isopropyF5-methyl-cyclohexanecarbonyl)-amino]acetic acid isopropyl ester, or the pharmaceuticaily acceptable sait, hydrate, or solvaté thereof is configured for:
a dose in the range of from about 0.07 mg to about 350 mg ofthe compound per day;
a dose in the range of from about 0.35 mg to about 140 mg of the compound per day;
a dose in the range offrom about 1 mg to about 50 mg ofthe compound per day;
a dose in the range offrom about 2 mg to about 30 mg ofthe compound per day; or a dose in the range of from about 5 mg to about 20 mg ofthe compound per day.
In one embodiment, the [((1 R,2S,5R)-2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]acetic acid isopropyl ester, or the pharmaceuticaily acceptable sait, hydrate, or solvaté thereof is configured for:
a treatment regimen of 1 to 5 administrations daily;
a treatment regimen of 1 to 4 administrations daily;
a treatment regimen of 2 to 5 administrations daily;
a treatment regimen of 2 to 4 administrations daily;
a treatment regimen of 2 administrations daily;
a treatment regimen of 3 administrations daily; or a treatment regimen of 4 administrations daily.
In one embodiment, the [((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]acetic acid isopropyl ester, or the pharmaceuticaily acceptable sait, hydrate, or solvaté thereof is configured for a pro re nata (PRN) treatment regimen.
In one embodiment, the [((1R,2S,5R)-2-isopropy!-5-methy!-cyclohexanecarbony1)-amino]acetic acid isopropyl ester, or the pharmaceuticaily acceptable sait, hydrate, or solvaté thereof is configured as:
a tablet;
an orally disintegrating tablet (ODT);
a spray;
a mist; or an aérosol.
Methods of Manufacturmq a Médicament
Also described herein is a method of manufacturing a médicament, the method comprising:
preparing a médicament for the treatment of chronic cough having a compound that is [((1R,2S,5R)-2-isopropyl-5-methyi-cyclohexanecarbonyl)~amino]-acetic acid isopropyl ester, or a pharmaceutically acceptable sait, hydrate, or solvaté thereof.
In one embodiment, the preparing the médicament having the compound comprises preparing the médicament having the compound for the treatment of explained chronic cough.
In one embodiment, the preparing the médicament having the compound comprises preparing the médicament having the compound for the treatment of the chronic cough as a symptom of, associated with, or caused by a diagnosed condition.
In one embodiment, the preparing the médicament having the compound comprises preparing the médicament having the compound for the treatment of the chronic cough as a symptom of, associated with, or caused by a diagnosed cough-related condition.
In one embodiment, the preparing the médicament having the compound comprises preparing the médicament having the compound for the treatment of the chronic cough as a symptom of, associated with, or caused by asthma, éosinophilie bronchitis, post-nasal drip syndrome (PNDS), gastro-oesophageal reflux disease (GORD), bronchiectasis chronic obstructive pulmonary disease (COPD), or idiopathic pulmonary fibrosis (IPF).
In one embodiment, the preparing the médicament having the compound comprises preparing the médicament having the compound for the treatment of idiopathic chronic cough (ICC).
In one embodiment, the preparing the médicament having the compound comprises preparing the médicament having the compound for the treatment of refractory chronic cough (RCC).
In one embodiment, the preparing the médicament having the compound comprises preparing the médicament having the compound for the treatment of refractory chronic cough (RCC) that persists after assessment and treatment of a cough-related condition.
In one embodiment, the preparmg the médicament having the compound comprises preparing the médicament having the compound for the treatment of refractory chronic cough (RCC) that persists after assessment and treatment of: asthma, éosinophilie bronchîtis, post-nasal drip syndrome (PNDS), gastro-oesophageal reflux disease (GORD), bronchiectasis chronic obstructive pulmonary disease (COPD), or idiopathic pulmonary fibrosis (IPF).
In one embodiment, the preparing the médicament having the compound comprises preparing the médicament having the compound for the treatment of the chronic cough being a symptom of, associated with, or caused by allotussia.
In one embodiment, the preparing the médicament having the compound comprises preparing the médicament having the compound for the treatment of the chronic cough being a symptom of, associated with, or caused by hypertussia.
In one embodiment, the preparing the médicament having the compound comprises preparing the médicament having the compound for the treatment of the chronic cough being a symptom of, associated with, or caused by cough hypersensitivity syndrome (CHS).
In one embodiment, the preparing the médicament having the compound comprises preparing the médicament having the compound for the treatment of the chronic cough is a symptom of, associated with, or caused by cough hypersensitivity reflex (CHR).
In one embodiment, the preparing the médicament having the compound comprises preparing the médicament having the compound for the treatment of the chronic cough being a symptom of, associated with, or caused by laryngeal paraesthesia.
In one embodiment, the preparing the médicament having the compound comprises preparing the médicament having the compound for the treatment of the chronic cough being a symptom of, associated with, or caused by laryngeal hypersensitivity syndrome (LHS).
In one embodiment, the preparing the médicament having the compound comprises preparing the médicament having the compound for the treatment of the chronic cough being sensory neuropathie cough.
In one embodiment, the preparing the médicament having the compound comprises preparing the médicament having the compound for the treatment of the chronic cough being a symptom of, associated with, or caused by peripheral sensitization; central sensitization (cough centre); and/or cortical and/or subcortical maiadaptive plasticity.
In one embodiment, the preparing the médicament having the compound comprises preparing the médicament having the compound for the treatment of the chronic cough being a symptom of, associated with, or caused by vagal neuropathy.
In one embodiment, the preparing the médicament having the compound comprises preparing the médicament having the compound for the treatment of the chronic cough being a symptom of, associated with, or caused by airway inflammation.
In one embodiment, the preparing the médicament having the compound comprises preparing the médicament having the compound for the treatment of the chronic cough being a symptom of, associated with, or caused by neurogenic inflammation and/or neuroinflammation.
In one embodiment, the preparing the médicament having the compound comprises preparing the médicament having the compound to: reduce cough frequency;
reduce hourly cough frequency;
reduce médian hourly cough frequency;
reduce mean hourly cough frequency;
reduce awake hourly cough frequency;
reduce awake médian hourly cough frequency;
reduce awake mean hourly cough frequency;
reduce asleep hourly cough frequency;
reduce asleep médian hourly cough frequency;
reduce asleep mean hourly cough frequency;
reduce cough severity;
reduce urge-to-cough; and/or reduce throat irritation.
In one embodiment, the preparing the médicament having the compound comprises preparing the médicament for:
topical oral administration ofthe compound;
topical oromucosal administration ofthe compound;
topical buccal administration ofthe compound;
topical sublingual administration ofthe compound;
topical intranasal administration ofthe compound; or topical transmucosal administration of the compound.
In one embodiment, the preparing the médicament having the compound comprises preparing the médicament having the compound as:
a dose in the range of from about 1 pg to about 5 mg ofthe compound per kilogram body weight per day;
a dose in the range of from about 5 pg to about 2 mg of the compound per kilogram body weight per day;
a dose in the range of from about 15 pg to about 0.7 mg of the compound per kilogram body weight per day;
a dose in the range of from about 30 pg to about 0.4 mg of the compound per kilogram body weight per day; or a dose in the range of from about 70 pg to about 0.3 mg of the compound per kilogram body weight per day.
In one embodiment, the preparing the médicament having the compound comprises preparing the médicament having the compound as:
a dose in the range of from about 0.07 mg to about 350 mg of the compound per day;
a dose in the range of from about 0.35 mg to about 140 mg of the compound per day;
a dose in the range of from about 1 mg to about 50 mg of the compound per day;
a dose in the range of from about 2 mg to about 30 mg of the compound per day; or a dose in the range of from about 5 mg to about 20 mg of the compound per day.
In one embodiment, the preparing the médicament having the compound comprises preparing the médicament having the compound as:
a treatment regimen of 1 to 5 administrations daily;
a treatment regimen of 1 to 4 administrations daily;
a treatment regimen of 2 to 5 administrations daily;
a treatment regimen of 2 to 4 administrations daily;
a treatment regimen of 2 administrations daily;
a treatment regimen of 3 administrations daily; or a treatment regimen of 4 administrations daily.
In one embodiment, the preparing the médicament having the compound comprises preparing the médicament having the compound as a pro re nata (PRN) treatment regimen.
In one embodiment, the preparing the médicament having the compound comprises preparing the médicament having the compound as:
a tablet;
an orally disintegrating tablet (ODT);
a spray;
a mist; or an aérosol.
Methods of Treatment of Chronic Cough
Also described herein is a method of treatment of chronic cough in a patient, the method comprising:
administering to the patient in need of treatment of chronic cough a therapeutically effective amount of a compound that is [((1R,2S,5R)-2-isopropyl-5-methylcyclohexanecarbonyl)-amino]-acetic acid isopropyl ester, or a pharmaceutically acceptable sait, hydrate, or solvaté thereof.
In one embodiment, the administering step comprises administering the compound to a patient in need of treatment of explained chronic cough.
In one embodiment, the administering step comprises administering the compound to a patient in need of treatment of the chronic cough as a symptom of, associated with, or caused by a diagnosed condition.
In one embodiment, the administering step comprises administering the compound to a patient in need of treatment of the chronic cough as a symptom of, associated with, or caused by a diagnosed cough-related condition.
In one embodiment, the administering step comprises administering the compound to a patient in need of treatment of the chronic cough as a symptom of, associated with, or caused by asthma, éosinophilie bronchitis, post-nasal drip syndrome (PNDS), gastrooesophageal reflux disease (GORD), bronchiectasis chronic obstructive pulmonary disease (COPD), or idiopathic pulmonary fibrosis (IPF).
In one embodiment, the administering step comprises administering the compound to a patient in need of treatment of idiopathic chronic cough (ICC).
In one embodiment, the administering step comprises administering the compound to a patient in need of treatment of refractory chronic cough (RCC).
In one embodiment, the administering step comprises administering the compound to a patient in need of treatment of refractory chronic cough (RCC) that persists after assessment and treatment of a cough-related condition.
In one embodiment, the administering step comprises administering the compound to a patient in need of treatment of refractory chronic cough (RCC) that persists after assessment and treatment of: asthma, éosinophilie bronchitis, post-nasal drip syndrome (PNDS), gastro-oesophageal reflux disease (GORD), bronchiectasis chronic obstructive pulmonary disease (COPD), or idiopathic pulmonary fibrosis (IPF).
In one embodiment, the administering step comprises administering the compound to a patient in need of treatment ofthe chronic cough being a symptom of, associated with, or caused by allotussia.
In one embodiment, the administering step comprises administering the compound to a patient in need of treatment of the chronic cough being a symptom of, associated with, or caused by hypertussia.
In one embodiment, the administering step comprises administering the compound to a patient in need of treatment of the chronic cough being a symptom of, associated with, or caused by cough hypersensitivity syndrome (CHS).
In one embodiment, the administering step comprises administering the compound to a patient in need of treatment ofthe chronic cough being a symptom of, associated with, or caused by cough hypersensitivity reflex (CHR).
In one embodiment, the administering step comprises administering the compound to a patient in need of treatment ofthe chronic cough being a symptom of, associated with, or caused by laryngeal paraesthesia.
In one embodiment, the administering step comprises administering the compound to a patient in need of treatment of the chronic cough being a symptom of, associated with, or caused by laryngeal hypersensitivity syndrome (LHS),
In one embodiment, the administering step comprises administering the compound to a patient in need of treatment ofthe chronic cough being sensory neuropathie cough.
In one embodiment, the administering step comprises administering the compound to a patient in need of treatment of the chronic cough being a symptom of, associated with, or caused by peripheral sensitization; central sensitization (cough centre); and/or cortical and/or subcortical maladaptive plasticity.
In one embodiment, the administering step comprises administering the compound to a patient in need of treatment of the chronic cough being a symptom of, associated with, or caused by vagal neuropathy.
In one embodiment, the administering step comprises administering the compound to a patient in need of treatment of the chronic cough being a symptom of, associated with, or caused by airway inflammation.
In one embodiment, the administering step comprises administering the compound to a patient in need of treatment of the chronic cough being a symptom of, associated with, or caused by neurogenic inflammation and/or neuroinflammation.
In one embodiment, the administering step comprises admmistenng the compound to a patient to:
reduce cough frequency;
reduce hourly cough frequency;
reduce médian hourly cough frequency;
reduce mean hourly cough frequency;
reduce awake hourly cough frequency;
reduce awake médian hourly cough frequency;
reduce awake mean hourly cough frequency;
reduce asleep hourly cough frequency;
reduce asleep médian hourly cough frequency;
reduce asleep mean hourly cough frequency;
reduce cough severity;
reduce urge-to-cough; and/or reduce throat irritation.
In one embodiment, the administering step comprises administering the compound to a patient in need of treatment via:
topical ora! administration of the compound;
topîcal oromucosal administration of the compound;
topical buccal administration ofthe compound;
topical sublingual administration ofthe compound;
topical intranasal administration ofthe compound; or topical transmucosal administration of the compound.
In one embodiment, the administering step comprises administering the compound to a patient in need of treatment as:
a dose in the range offrom about 1 pg to about 5 mg ofthe compound per kilogram body weight per day;
a dose in the range of from about 5 pg to about 2 mg of the compound per kilogram body weight per day;
a dose in the range of from about 15 pg to about 0.7 mg of the compound per kilogram body weight per day;
a dose in the range offrom about 30 pg to about 0.4 mg ofthe compound per kilogram body weight per day; or a dose in the range of from about 70 pg to about 0.3 mg of the compound per kilogram body weight per day.
In one embodiment, the administering step comprises administenng the compound to a patient in need of treatment as:
a dose in the range of from about 0.07 mg to about 350 mg of the compound per day;
a dose in the range of from about 0.35 mg to about 140 mg ofthe compound per day;
a dose in the range of from about 1 mg to about 50 mg ofthe compound per day;
a dose in the range of from about 2 mg to about 30 mg ofthe compound per day; or a dose in the range of from about 5 mg to about 20 mg of the compound per day.
In one embodiment, the administering step comprises administering the compound to a patient in need of treatment as:
a treatment regimen of 1 to 5 administrations daily;
a treatment regimen of 1 to 4 administrations daily;
a treatment regimen of 2 to 5 administrations daily;
a treatment regimen of 2 to 4 administrations daily;
a treatment regimen of 2 administrations daily;
a treatment regimen of 3 administrations daily; or a treatment regimen of 4 administrations daily.
In one embodiment, the administering step comprises administering the compound to a patient in need of treatment as a pro re nata (PRN) treatment regimen.
In one embodiment, the administering step comprises administering the compound to a patient in need of treatment as:
a tablet;
an orally disintegrating tablet (ODT);
a spray;
a mist; or an aérosol.
CLINICAL TRIAL 1
A first clinica! trial for the use of the compound, [((1R,2S,5R)-2-isopropyl-5-methylcyclohexanecarbonyl)-amino]-acetic acid isopropyl ester (also referred to herein as L'AX-8 or “Gly-O-iPr”), for the treatment of RCC was started, but was prematurely ended.
Basic details of the trial are set out in the following table.
Currently, some details may be seen online at;
https://www.clinicaltrialsregister.eu/ctr-search/triaK2016-004803-30/GB
Table 1 First Clinical Trial | |
EudraCT number | 2016-004803-30 |
National Competent Authority | UK-MHRA |
Date on which this record was first entered in the EudraCT database | 2017-01-19 |
Full title of the trial | A multi-centre, randomised, placebo and active-controlled, double-blind, cross-over, phase lia proof-of-concept trial to investigate the efficacy and safety of AX-8 Tablets 5 mg in patients with chronic refractory cough and associated upper airway symptoms |
INN - Proposed INN | Recommended International Nonproprietary Name (rINN): [(1 R,2S,5R)-5-Methyl-2-isopropyl cyclohexane carbonyl]aminoacetic acid isopropylester |
Medical condition(s) being investigated | Chronic refractory cough and associated upper airway symptoms |
Main objective of the trial | The primary research question is to study the efficacy of AX-8 Tablets 5 mg in suppressing cough in patients with chronic refractory cough and associated upper airway symptoms when compared to 5 mg menthol (active comparator) and placebo. As assessed by measuring the changes from baseline in cough frequency over 8 hours (4 hours after intake of 1 st dose and 4 hours after intake of 2nd dose) for AX-8, menthol and placebo. |
CLINICAL TRIAL 2
A second ciinical trial (open-label Phase Ha) forthe use ofthe compound, [((1R,2S,5R)-2isopropyl-5-methyl-cyclohexanecarbonyl)-amino]-acetic acid îsopropyl ester (also referred to herein as “AX-8” or “Gly-O-iPr”), for the treatment of RCC has just been completed.
Basic details ofthe trial are set out in the following table.
Currently, some details may be seen online at:
https://www.clinicaltrialsregister.eu/ctr-search/trial/2017-003108-27/GB
Table 2 Second Clinicai Trial | |
EudraCT number | 2017-003108-27 |
National Competent Authority | UK-MHRA |
Date on which this record was first entered in the EudraCT database | 2017-08-31 |
Full title ofthe trial | A pilot study ofthe efficacy, safety, and tolerability of AX-8 for the treatment of refractory chronic cough |
Other descriptive name | Gly-O-iPr, [((1R,2S,5R)-2-isopropyl-5-methylcyclohexanecarbonyl)-amino]-acetic acid isopropyl ester |
Pharmaceutical form | Orodispersible tablet |
Route of administration | Oromucosal use |
Strength | 5 mg |
Medical condition(s) being investigated | Refractory Chronic Cough (RCC). |
Main objective of the trial | To assess the effectiveness of AX-8 for the treatment of RCC and associated upper airway symptoms after one dose of treatment in reducing awake cough frequency compared to baseline, for the purpose of planning a future randomised controlled trial. |
Upon completion ofthe second ciinical trial (described in detail below), the compound was found to hâve unexpected antitussive properties in patients with RCC, decreasing awake hourly cough frequency, throat irritation, urge-to-cough, and cough severity. No 15 compound-related adverse effects were observed.
As demonstrated in the clinical trial, a 5 mg dose ofthe compound improves cough m RCC patients by decreasing cough frequency and also Visual analog scale (VAS) scores for ail of the coughing characteristics assessed (i.e., cough severity, urge to cough, throat irritation).
This is unexpected because MK-7264 (also known as AF-219 and Gefapixant), the more advanced RCC drug currently under development (Phase 3 clinical trials started March 2018) is efficient in reducing cough frequency but poorly effective in improving the VAS scores in RCC patients (see, e.g., Abdulqawi et al., 2015; Smith étal., 2017a;
Smith et al., 2017b; Smith étal., 2020). Cough severity was improved significantly only for doses of 50 mg and 1200 mg per day with respectively adverse events related to taste (i.e., dysgeusia, hypogeusia, or ageusia) in 81% and 100% of patients. Urge-to-cough was shown to be improved significantly only with the 1200 mg per day dose. Phase 3 clinical trials (NCT03449134 and NCT03449147, still ongoing in June 2020) are studying 15 mg and 45 mg doses of MK-7264.
AX-8 is the only compound which has been shown to decrease throat irritation in RCC patients.
Study Objectives
AX-8 bioavailability and safety hâve been previously addressed in a Phase 1 study in healthy human subjects. However, until now, AX-8 has not been studied in patients with chronic cough (CC). This study was a pilot study of the efficacy, safety, and tolerability of AX-8 for the treatment of Refractory chronic cough (RCC).
The primary objective of the study was to assess the effectiveness of AX-8 (the study drug) for the treatment of RCC and associated upper airway symptoms after one dose of treatment (an orally disintegrating tablet (ODT) having 5 mg AX-8, administered orally and dissolved on the tongue) in reducing awake cough frequency compared to baseline, for the purpose of planning a future randomized controiled trial.
A secondary objective ofthe study wasto evaluate the duration of effectiveness of AX-8 after 1 dose of treatment in reducing hourly objective cough frequency over a 24-hour monitoring period.
An additional secondary objective of the study was to evaluate the effectiveness of AX-8 in: (a) reducing the cough severity measured by a Visual Analog Scaie (VAS); (b) reducing the throat irritation and the urge-to-cough (VAS); (c) inducing a sensation of throat cooling (VAS).
An additional secondary objective of the study was to assess the safety and tolerability of AX-8 treatment in patients with RCC.
An exploratory objective (added to the study after initiation) was to evaluate the pharmacokinetic (RK) profile of AX-8.
Ethics, Approvai and Location
The study protocol încluding ail relevant documents were reviewed and approved by the appropriate independent ethics committees. The study was performed in accordance with the current version of the déclaration of Helsinki (52nd WMA General Assembly, Edinburgh, Scotland, October 2000). The study was conducted în agreement with the International Conférence on Harmonisation (ICH) guîdelines on Good Clinical Practice (GCP). The study was performed in compliance with the requirements of the Medicines and Healthcare products Regulatory Agency (MHRA). AH patients provided written informed consent (ICF) to participate in the study prior to being screened. The study was conducted at NI HR Manchester Clinical Research Facility (CRF), Manchester University NHS Foundation Trust (MFT), Southmoor Rd, Wythenshawe, Manchester M23 9LT, UK.
Study Timing
The study consisted of five periods, for a total study period of approximately 4 weeks:
Table 3 Visit Summary | ||
Period | Visit | Visit Schedule |
Screening | Visit 1 (“Screening Visit) | Day -14 to -1 |
Baseline | Visit 2 (“Baseline Visit”) | Day 0 |
Treatment | Visit 3 (“Treatment Visit”) | Day 1 |
Visit 4 (“Follow-Up Visit”) | Day 2 | |
End of Study | Visit 5 (End of Study Visit”) | Day 7 to 14 |
During the screening period, subjects underwent eligibillty évaluation and were enrofled.
At Day 0 (Visit 2; Baseline Visit), eligible subjects had cough monitoring conducted over 24 hours and urge-to-cough (UTC), cough severity, and throat irritation were assessed separately using VAS over 4 hours in the clinic and followed up with a patient diary at home.
Subjects were required to fast overnight (at least 8 hours) before the Day 0 visit. A breakfast was provided in the unit at least 30 minutes before subjects hâve the Cough
Monitor installed. No food was permitted for 4 hours after the Cough Monitor was înstalled. Liquids were permitted until the time the Cough Monitor was installed and not permitted (including water) until 2 hours after the Cough Monitor was installed; after 2 hours, water only in a reasonable amount was permitted. After 4 hours, no food or liquid restrictions applied.
At Day 1 (Visit 3; Treatment Visit), eligible subjects received one 5 mg AX-8 ODT. Cough monitoring was conducted over 24 hours and different VAS for UTC, Cough Severity, Throat Irritation, Throat Cooling, and Taste Perception were assessed using VAS over 4 hours in the clinic after dosing and followed up with a patient diary at home.
Subjects were required to fast overnight (at least 8 hours) before the Day 1 visit. A breakfast was provided in the unit at least 30 minutes before subjects received the dose of AX-8. No food was permitted for 4 hours after dose administration. Liquids were permitted until the time of dose administration and not permitted until 2 hours after dosing (including water); after 2 hours, water only in a reasonable amount were permitted. After 4 hours, no food or liquid restrictions applied.
The primary efticacy endpoint was assessed after one day of treatment.
At Day 2 (Visit 4; Follow-Up Visit), the Cough Monitor was removed, and the patient diary returned.
Between 7-14 days after Day 1 (Visit 5; End of Study Visit), an end of study visit was performed.
Subjects who withdrew from the study after receiving the study drug and prier to completing the End of Study Visit were asked to complété an Early Withdrawal Visit (EWV), whereby the same procedures as for the End of Study Visit were performed.
Enrolment
Adult subjects with a history of RCC and associated upper airway symptoms (i.e., throat irritation/tickling associated with coughing épisodes) were enrolled in the study.
Inclusion Criteria:
Subjects had to meet the following criteria to be enrolled into the study:
• Females and males between 18 and 80 years of âge inclusive.
• Hâve a diagnosis of RCC or unexplained cough for at least one year (see Brîtish Thoracic Society (BTS) guidelines) and associated upper airway symptoms (throat or laryngeal irritation, tickling, dryness or discomfort) of at least 8-week duration. Regular pattern of cough with expected daily épisodes of cough that occur throughout the day, as ascertained by medical history.
• Chest radiograph or thorax computed tomography scan within the last 5 years not demonstrating any abnormality considered to be significantly contributing to the chronic cough in the opinion of the Principal Investigator and Medical Monitor.
• At the Screening Visit, hâve a score of a 40mm on the Cough Severity VAS.
• At the Baseline Visit, hâve a score of a 40mm on the Cough Severity VAS.
♦ AH female subjects who are of childbearing potential must practice highly effective contraception (i.e., pregnancy prévention method with a failure rate of < 1% per year) from the time of the initial Screening visit until 4 weeks after last dose of study drug.
• At the Baseline Visit, hâve a body mass index (BMI) < 33kg/m2.
• Be willing and able to comply with ail aspects of the protocol.
• Provided written informed consent.
Exclusion Criteria:
Subjects who met any of the following criteria were not eligible for participation in the study:
• Prior treatment with AX-8.
• Hypersensitivity or intolérance to AX-8 or other TRPM8 agonists (e.g., menthol, menthol-like compounds), or any of the excipients of AX-8 ODT.
• Current smoker or individuels who hâve given up smoking within the past 12 months or ex-smoker with > 20 pack-years.
• Forced expiratory volume in one second (FEV1) / forced vital capacity (FVC) < 60%.
• History of upper or lower respiratory tract infection or recent significant change in pulmonary status within 4 weeks of the Baseline Visit.
• History of cystic fibrosis.
• History of opioid use within 1 week of the Baseline Visit if used for the treatment of RCC. Opioids, if required for other indications are permitted providing that subject is receiving a stable dose for at least 1 week prior to the Baseline Visit and are still experiencing a troublesome cough. Subjects must remain on a stable dose for the duration of the study until the Follow-Up Visit.
• Requiring concomitant therapy with prohibited médications.
• Treatment with biologie thérapies within 8 weeks or 5 half-lives prior to the Baseline Visit, whichever is longer.
• Treatment with any investigational therapy within 4 weeks prior to the Baseline Visit.
• Clinîcally significant abnormality of hepatic function defined as total bihrubm, alanine aminotransferase (ALT) or aspartate aminotransferase (AST) > 2x the upper limit of normal (ULN) during screening, • Clinîcally significant abnormality of renal function, defined as estimated glomerular filtration rate (eGFR) < 60 ml/min.
• Positive test for any drug-of-abuse (unless this can be explained by the subject’s médication).
• History of malignancy within 5 years prior to the Baseline Visit, with the exception of completely treated and ηοπ-metastatic basal cell carcinoma or squamous cell carcinoma ofthe skin.
• History of a major psychiatrie condition (including major depressive disorder, bipolar disorder, or schizophrenia), suicidai idéation, or suicide attempt, • Known active hepatitis infection.
• Known history of human immunodeficiency virus (HIV) infection.
• Presence of any medical condition or disability that, in the investigator’s opinion, could interfère with the assessment of safety or efficacy in this trial or compromise the safety ofthe subject, including clinîcally significant ECG abnormalities during the Screening Visit, the Baseline Visit, or Treatment Visit.
• Currently pregnant or breastfeeding female subject, or male subject with a pregnant or breastfeeding partner.
• Females of childbearing potential who are unable or unwilling to practice highly effective contraception (pregnancy prévention).
Patients were free to withdraw from the study at any time without giving a reason. The învestigator could also withdraw patients from the trial if they deemed it appropriate for safety or ethlcal reasons or if it was considered to be to be detrimental to the well-being of the patient. The study protocol specified that subjects had to be discontinued from study if the following events occurred between recruitment and drug administrations:
• A female subject becomes pregnant.
• A subject décidés to discontinue the study, or a subject décidés to withdraw consent from the study, • Any medical condition that may jeopardize the subject’s safety if the study drug is administered, in the investigator’s opinion.
• Discontinuation is deemed to be in the best interest of the subject, in the investigator’s opinion.
Ultimately, no patient withdrew from the study, and consequentiy, no EWV were performed.
A total of 16 patients were screened. A total of 12 patients received the treatment and completed the study. Efficacy and safety data were analysed for the 12 patients. A sample size of 10-15 patients was considered sufficient to estimate the antitussive effect of a single dose of therapy, in ternis of magnitude and duration, as compared with the baseline measurement.
Treatment
Subjects took a single orally disintegrating tablet (ODT) with 5 mg AX-8 in the morning on the first day of the treatment period (Day 1). This Investigational Medical Product (IMP) was let to dissolve on the tongue. Patients were observed for 5 minutes to ensure that the tablet was dissolved on the tongue and not swaîlowed.
The ODT was administered on Day 1 (Visit 3; Treatment Visit) after the cough monitor from Day 0 (Visit 2, Baseline Visit) had been removed and before 10 am (because patients with RCC primarily cough during the daytime).
The AX-8 ODTs also contaîn Ludiflash® (Mannitol, Kollidon® CL-SF, Kollicoat® SR 30D), sorbitol, silica coltoidal anhydrous, and magnésium stearate. The IMP batch was number 17081402 (expiry date November 2018). The ODTs were kept in the original packaging (i.e., HDPE bottle with polypropylene twist-off cap contained 50 tablets) until administration. The ODT’s were stored in a secure, temperature-controlled (not above 30°C), controlled access location at the study site.
The 5 mg AX-8 dose was selected for this study based on the favourable safety and tolerability profile of AX-8 at the 5 mg ODT dose level, as demonstrated in the Phase 1 study in healthy volunteers. In that study, AX-8 was well tolerated in the 12 subjects exposed to a single dose of AX-8 and there were no remarkable adverse events (AEs).
AH study treatment was administered by the study investigator or designated member of staff. To ensure drug accountability, the investigator or designated deputy maintained accurate records of the dates and amounts of drug received, to whom it was dispensed and accounts of any supplies which were accidentally or deliberateiy destroyed; these details were recorded on a drug accountability form. Ail unused clinical supplies and the drug accountability forms were returned at the end of the study.
Prior and Concomitant Therapv
Concomitant therapies included any thérapies (including over-the-counter (OTC) médications) used by a subject from initiation of treatment through the follow-up period. A record of ail médications used was maintained for each subject throughout the study. Reported information included a description ofthe type of drug, treatment period, dosing regimen, the route of administration, and drug indication.
Subjects using oral contraceptives, hormone-replacement therapy, or other maintenance thérapies that were not excluded thérapies could continue their use during the study. A record of ail concomitant thérapies was maintained for each subject.
The following thérapies and products were excluded within the last 6 hours prior to and during ail visit days:
• Consumption of cough sweets, over the counter cough syrups, chewing gum, caffeine, Chili or products containing mint and/or menthol within the last 6 hours prior to and during visit days.
The following thérapies were excluded from 1 week prior to the Baseline Visit (Day 0, Visit 2) until the end of the Follow-Up Visit (Day 2, Visit 4):
• Opioids (including codeine and morphine). Opioids (including codeine), if required for other indications, were permitted provided that subjects were receiving a stable dose for at least one week prior to the Baseline Visit (Day 0) and still experiencing a troublesome cough. Subjects had to remain on a stable dose for the duration of the treatment period.
The following cough therapies were excluded from 2 weeks prior to the Baseline Visit (Day 0, Visit 2) until the End of Study Visit (Visit 5):
• Dextromethorphan;
• Guaifenesin.
The following therapies were excluded from 2 weeks prior to the Baseline Visit (Day 0, Visit 2) until the End of Study Visit (Visit 5):
• Pregabalin, gabapentin, thalidomide, or amitriptyline for the treatment of cough. Pregabalin, gabapentin, thalidomide, or amitriptyline if required for other indications, were permitted if subjects were receiving a stable dose and still experiencing a troublesome cough. Subjects had to remain on a stable dose for the duration of the treatment period.
The following therapies were excluded from 4 weeks prior to the Baseline Visit (Day 0, Visit 2) until the End of Study Visit (Visit 5):
• Systemic immunosuppressive/immunomodulatory therapies (including but not limîted to PDE4 inhibitors, cyclosporine, mycophenolate-mofetil, methotrexate, azathioprine, or phototherapy);
• Any investigational therapy.
The following thérapies were excluded from 8 weeks prior to the Baseline Visit (Day 0, Visit 2) until the End of Study Visit (Visit 5):
• Biologie thérapies;
• Investigational biologie thérapies.
The following therapy was excluded from 12 weeks prior to the Baseline Visit (Day 0, Visit 2) until the End of Study Visit (Visit 5):
• Treatment with an ACE-inhibitor.
Subjects were asked to take appropriate measures to minimize exposure to UV-radiation (e.g., sunlight, tanning booths) from the Treatment Visit (Day 1, Visit 3) through to the End of Study Visit (Visit 5).
Assessment of Efficacy
Objective Cough Frequency:
Objective cough frequency was measured as 24-hour sound recordings using a custombuilt digital recording device (VitaloJAK, Vitalograph, Ltd).
VitaioJAK™ is a semi-automated 24-hour ambulatory cough monitoring System (Vitalograph; Buckinghamshire, England) operating in a manner which completely replicates routine practice. The 24-hour recordings are compressed using custom designed compression software, using an algorithm. The VitaloJAK™ is a reliable, robust and efficient tool for the objective measurement of cough frequency. Importantly it reduces 24-hour recordings by up to 98% whilst preserving close to 100% of recorded cough sounds. It is worn like a Holter monitor, with a single sensor affixed to the patients chest wall. An optional second channel via a conventional microphone (worn, for example, on the patients shirt) allows quality assurance with human intervention. The device itself is attached on the trousers, skirt, etc.
Cough Severity;
Cough Severity was scored on a 100 mm Visual Analog Scale (VAS) at the specified time points. The patient was asked to indicate their assessment by marking (e.g., with a pen) a position along a 100 mm line between two extremes, e.g., “no cough” and “worst cough”.
Urge-to-Cough (UTC):
Urge-to-cough was scored on a 100 mm VAS at the specified time points.
Throat Irritation:
Throat irritation was scored on a 100 mm VAS at the specified time points.
Throat Cooling:
Throat cooling was scored on a 100 mm VAS at the specified time points.
Global Rating of Change Scale (GRCS):
The GRCS was used by subjects to assess their overall status for the specified periods (the 4-hour period following dose; and the 24-hour period following dose). It consisted of a 14-point scale ranging from ‘a very great deal better’ to ‘a very great deal worse’.
Taste Questionnaire:
A simple taste observation (qualitative) was completed. Freshness, basic tastes (i.e., sweet, sour, bitter, and salty), and palatabilîty were scored on 100 mm VAS’s at the specified time points.
Assessment of Safety
Safety assessments consisted of monitoring and recording protocol-defîned adverse events (AEs) and serious adverse events (SAEs); vital signs; physical examinations; clinical laboratory assessments; electrocardiograms (ECGs); and other protocol-specified tests that were deemed critical to the safety évaluation of the study drug.
Vital signs included measurements of heart rate, sitting blood pressure, respiration rate, and température. Vital signs were assessed at the specified time points and at unscheduled study visits when clinically indicated. The subjects’ height and weight were also measured.
Physical examinations were performed at the specified time points and at unscheduled study visits when clinically indicated, covering major body Systems (assessment ofthe ears, eyes, nose and throat, head, neck, thyroid, neurological System, respiratory system, cardiovascular system, lymph nodes, abdomen, skin, muscuioskeletal, neurological).
Samples for hematology, chemistry, urinalysis, and sérum pregnancy testing (when necessary) were collected at the specified time points and at unscheduled study visits when clinically indicated and analysed at a local laboratory unless otherwise specified.
Laboratory assessments inciuded the following:
• Hematology: haematocrit, hemoglobin, red blood cell count, red blood cell indices, platelets, white blood cell count, white blood cell differential (neutrophils, lymphocytes, monocytes, basophils, eosinophils).
• Chemistry: sodium, potassium, chloride, bicarbonate, glucose, blood urea nitrogen, créatinine, eGFR, calcium, phosphorus, magnésium, albumin, ALT, AST, alkaline phosphatase, total bilirubin, LDH, uric acid, total protein, lipid panel.
• Pregnancy testing: ail females of childbearing potential had a local urine pregnancy test performed. Positive or equivocal urine pregnancy test results were confirmed by a sérum pregnancy test analysed at a local laboratory. A sérum pregnancy test was done at in the Screening Visit (Visit 1 ).
• Urinalysis: pH, spécifie gravity, bilirubin, glucose, ketones, leukocytes, nitrite, blood, protein, urobilinogen, microscopie analysis.
A standard 12-lead ECG was performed at the specified time points and at unscheduled study visits when clinically indicated.
Lung function tests (FEV1, FVC and FEV1/FVC ratio) was assessed using a spirometer:
• Forced expiratory volume in one second (FEV1) isthe amount of air exhaled within one second using the spirometer.
• Forced vital capacity (FVC) is the total amount of air that can be exhaled in one breath.
• FEV1 divided by FVC (FEV1/FVC) this is the proportion ofthe total that can be exhaled in one second.
Schedule of Activities and Assessments
Informed consent was obtained prior to any protocol-mandated procedures, including the stopping of any excluded thérapies.
Screening Visit (Visit 1):
Screening assessments were conducted over a 14-day period prior to the Baseline Visit. The Screening Period could hâve been extended beyond 14 days if any additional follow-up on findings from any of the Screening assessments was required.
The following screening procedures were performed (not specified by the order below):
• Inclusion/exclusion criteria review.
• Demographics and Medical history (including chronic cough history, history of any médications within 30 days prior to Screening Visit and chronic cough treatments within 1 year prior to Screening Visit).
• Physical examination.
• Vital signs (including height and weight).
• 12-Lead ECG.
• Spirometry.
• Chest radiograph or CT Thorax (if not done within the past 5 years).
• Laboratory tests:
• Sérum pregnancy test for females of childbearing potential.
« Hematology.
• Chemistry.
• Urinalysis.
• Urine drug screen.
• Cough severity VAS assessment.
• Urge-to-cough VAS assessment.
• Throat irritation VAS assessment.
• Schedule Baseline Visit.
Baseline Visit (Visit 2; Day 0):
At the Baseline visit, the following procedures and assessments were performed (not specified by the order below):
• Inclusion/exclusion criteria review.
• Update medical history.
• Record ail concomitant médication use.
• Vital signs.
• 12-Lead ECG.
• Laboratory tests:
• Urine pregnancy test for females of childbearing potential.
• Urine drug screen.
• Provide subject with VAS diary and instruct them to complété VAS assessments at +5 and +6 hours at home (see below).
• Attach and activate the Baseline Visit cough monitor (preferably before 10 am).
» Cough severity VAS assessment:
Prior to cough monitor installation:
- 30 minutes.
After cough monitor installation:
+ 1, +2, +3, +4, +5, +6 hours.
• Urge-to-cough VAS assessment:
Prior to cough monitor installation: - 30 minutes.
After cough monitor installation:
+ 1, +2, +3, +4, +5, +6 hours.
• Throat irritancy VAS assessment:
Prior to cough monitor installation: - 30 minutes.
After cough monitor installation: +1, +2, +3, +4, +5, +6 hours.
• Schedule Treatment Visit.
The VAS assessments at +5 and +6 hours were completed at home by the patient using a VAS diary. VAS assessments at ail other time points were completed in the unit. A time window of +1- 5 minutes was permitted at ali VAS time points.
Treatment Visit (Visit 3; Day 1):
At least 24 hours after the Baseline Visit cough monitor has been attached on Day 0, and preferably before 10 am, the following activities were performed by ciinic staff (not specified by the order below):
• Remove the Baseline Visit cough monitor.
• Update medical history.
• Record ail concomitant médication use.
• Inclusion/exclusion criteria review.
• If ail inclusion and exclusion criteria were met, enrol patient into study.
• Vital signs: before dose and 4 hours after dose.
• 12-lead ECG (before dose).
• Laboratory tests:
• Urine drugs-of-abuse testing.
• Pharmacokinetic (PK) sampletaken.
• Provide subject with VAS diary and instruct them to complété VAS assessments at +5 and +6 hours at home (see below).
• Before dosing, attach and activate Treatment Visit cough monitor.
• Administerthe dose ofthe study drug (preferably before 10 am).
• Cough severity VAS assessment:
Prior to dose:
- 30 minutes.
After dose:
+1, +2, +3, +4, +5, +6 hours.
• Urge-to-cough VAS assessment:
Prior to dose:
- 30 minutes.
After dose:
+1, +2, +3, +4, +5, +6 hours.
• Throat irrita ncy VAS assessment:
Prior to dose:
- 30 minutes.
After dose:
+ 1, +2, +3, +4, +5, +6 hours.
• Throat cooling VAS assessment:
Prior to dose:
- 30 minutes.
After dose:
+1, +2, +3, +4, +5, +6 hours.
• GRCS assessment at 4 hours after dose.
• Schedule Follow-Up Visit.
• Once the Investigator confirmed it was safe to do so, the subject could leave the unit after the assessments 4 hours after dose were complété.
The VAS assessments at +5 and +6 hours were completed at home by the patient using a VAS diary, VAS assessments at ail other time points were completed in the unit. A time window of +/- 5 minutes was permitted at ail VAS time points.
Foilow-Up Visit (Visit 4; Day 2):
At least 24 hours after the Treatment Visit cough monitor has been attached (on Day 1), the following activities were performed by clinic staff (not specified by the order below):
• Remove the Treatment Visit cough monitor.
• Collect and review the VAS diary for completeness.
• Overall impression of the treatment day (24 hours) with:
• Cough severity VAS assessment.
• Urge-to-cough VAS assessment.
• Throat irritancy VAS assessment.
• Throat cooling VAS assessment.
• GRCS assessment.
• Record ail adverse events.
• Record ail concomitant médication use.
• Schedule End of Study visit.
End of Study Visit (Visit 5):
The following procedures and évaluations were performed at the clinic between Day 7 and 14. At this visit, the following procedures and assessments were performed by clinic staff (not specified by the order below):
• Cough severity VAS assessment.
• Urge-to-cough VAS assessment.
• Throat irritancy VAS assessment.
• GRCS assessment.
• Vital signs.
• Weight.
• Physical examination.
• 12-lead ECG.
• Laboratory tests:
• Hematology.
• Chemistry.
• Urinalysis.
• Urine pregnancy test for females of childbearing potential.
• Record ail adverse events.
• Record ail concomitant médication use.
The following table summarises the timing of the various procedures and évaluations.
Table 4 Schedule of Procedures and Evaluations | |||||
Study Period | Screening | Baseline | T reatment | End of Study | |
Study Visit | Visit 1 Screening Visit | Visit 2 Baseline Visit | Visit 3 T reatment Visit | Visit 4 Follow-up Visit | Visit 5 End of Study Visit |
Study Schedule | Day -14 to Day -1 a·b | Day 0 n | Day 1 0 | Day 2 | Day 7-14 |
Study Procedure | - | - | * | - | - |
Written Informed Consent a | Xa | ||||
Inclusion/Exclusion Criteria | X | X | X | ||
Demographics; Medical & Médication History | X | X | |||
Chest Radiograph or CT Thoraxe | Xe | ||||
Physical Examination | X | X |
Table 4 Schedule of Procedures and Evaluations | |||||
Study Period | Screening | Baseline | Treatment | End of Study | |
Study Visit | Visit 1 Screening Visit | Visit 2 Baseline Visit | Visit 3 T reatment Visit | Visit 4 Follow-up Visit | Visit 5 End of Study Visit |
Vital Signs | X | X | Xl | X | |
Height & Weight | X | xf | |||
ECG (12-lead) | X | X | X' | X | |
Spirometry | X | ||||
Ciinical Laboratory Sampling | X | X | |||
Urinalysis | X | X | |||
Urine Drug Screen | X | X | X | ||
Serum Pregnancy Test | X | ||||
Urine Pregnancy Test | X | X | |||
PK Sample | xk | ||||
Attach Cough Monitor | xd | XC,d | |||
Remove cough monitor | Xe | X | |||
Adverse Event Monitoring | X | X | X | ||
Concomitant Médications | X | X | X | X | X |
Cough Severity VAS Assessment | X | xh | xh | XJ | X |
Urge-to-Cough VAS Assessment | X | X h | X h | XJ | X |
Throat Irritation VAS Assessment | X | xh | X h | XJ | X |
Throat Cooling VAS Assessment | X ’ | Xj | |||
Study Drug Administration | Xe | ||||
Issue VAS diary for subjects to take home | X | ||||
Collect and review VAS diary | X | ||||
GRCS Assessment | X | X | X | ||
Taste Questionnaire | xm | I xi |
Notes:
a | Multiple clinic visits could be required to complété ail screening assessments. |
b | The Screening Period could hâve been extended beyond 14 days if any additional follow-up on findings from any of the Screening assessments was required. |
c | Single dose of study drug (an orally disintegrating tablet (ODT) having 5 mg AX-8, administered orally and dissolved on the tongue) administered on Day 1 after the Baseline Visit cough monitor had been removed and preferably before 10 am. The Treatment Visit cough monitor was attached and started before dosing. _ |
d | Cough monitor was attached, preferably before 10 am, and worn for 24 hours during each assessment. ___ |
e f | If not done within the past 5 years.____.__ Weight only. _____ |
g | Informed consent had to be obtained prior to any protocol-mandated procedures, including stopping of any excluded thérapies. |
h | Performed at the following time points: • On Day 0: prior to cough monitor installation: -30 minutes; after cough monitor installation: +1, +2, +3, +4, +5, +6 hours. • On Day 1: prior to dosing: -30 minutes; after doing: +1, +2, +3, +4, +5, +6 hours. • The VAS assessments at +5 and +6 hours were completed at home by the patient using a VAS diary. VAS assessments at ail other time points were completed in the unit. A time window of +/- 5 minutes was permitted at ail VAS time points. ____ |
i | Performed at the following time points: • On Day 1: prior to dosing: -30 minutes; after doing: +1, +2, +3, +4, +5, +6 hours. • The VAS assessments at +5 and +6 hours were completed at home by the patient using a VAS diary. VAS assessments at ail other time points were completed in the unit. A time window of +/- 5 minutes was permitted at ail VAS time points. |
j | VAS orTaste Questionnaire for last 24 hours, overall impression ofthe treatment day. |
k | A pharmacokinetic (PK) sample was taken any time before dosing on Day 1, and then after dosing: +15 minutes, +30 minutes, +45 minutes, +1 hour, +1.25 hours, +1.50 hours, +1.75 hours, +2 hours, +2.5 hours, +3 hours, +3.5 hours, and +4 hours. |
1 | 12-Lead ECG and vital sign assessments were performed any time before dose and 4 hours after dose. |
m | Taste Questionnaire was completed 15 minutes before dosing, after dosing: +3 to 10 minutes, +2 hours. |
n | Day 0: (Baseline Visit) Patient stayed for a minimum of 4 h at the clinic after installation of cough monitor, in total 4-5 hours. |
0 | Day 1 : (Treatment Visit) Patient stayed for a minimum of 4 hours after dosing at the clinic, in total 5-6 hours. |
Endpoints
The primary efficacy endpoint was the change from baseline in awake objective cough 5 frequency over 24 hours after 1 dose of treatment.
The key secondary efficacy endpoints were:
• Change from Baseline in houriy objective cough frequency over a 24-hour monitoring period.
· Proportion of subjects with > 30% réduction in 24-hour cough frequency per hour.
• Proportion of subjects with £ 30% réduction in awake cough frequency per hour.
• Change from Baseline in cough severity VAS.
• Change from Baseline in urge-to-cough VAS.
• Change from Baseline throat irritation.
· Throat cooling VAS.
• Global Rating of Change Scale (GRCS).
Efficacy Variables
The 24-hour cough frequency (coughs per hour) for a specified visit was caîculated as:
24-hour cough frequency = (total number of cough events during the monitoring period (24-hour interval)) l 24.
The awake cough frequency (coughs per hour) is defined as below:
Awake cough frequency = (total number of cough events during the monitoring period (24-hour interval) while the subject was awake) / (total duration (in hours) during the monitoring period (24-hour interval) that the subject was awake).
Awake duration (hours) was defined as the time between waking up and sleeping during the 24-hour monitoring period.
The cough data contams ail cough events that occurred during that 24-hour monitoring period as well as the information about asleep time” and “awake time. Any session with duration of recording < 4 hours was considered as missing.
In general, each 24-hour session was composed of an awake monitoring period and an asleep monitoring period. If a subject did not wake up before the end of the recording session, it was assumed that the subject slept for the rest of the session. The session will then hâve missing awake time, and the rest of session will be considered under the asleep monitoring period. For any session with both asleep time and awake time missing, the entire 24-hour session was considered under the awake monitoring period, unless the session had early termination of recording.
On each collection day, the cough count, the actual cough monitoring duration (in hours), and the coughs per hour were derived for the total 24-hour period, the awake period, and the asleep period, respectively.
The percent change in awake coughs per hour is defined as below:
Percent change in awake cough frequency = [ (Change from baseline in awake cough frequency * 100) / (Baseline awake cough frequency) ].
The proportion of participants with > 30% of réduction from baseline in awake cough frequency is the number of participants with £ -30% change in awake cough frequency divided by the total number of participants with available data.
Where the géométrie mean (95% confidence interval (Cl)) of 24-hour cough frequency was presented, any observation of zéro cough per hour was replaced by a cough rate of 0.1/hourforthe calculation ofthe géométrie mean.
Patient Participation
Sixteen patients were screened between 12 December 2017 and 16 May 2018 and 11 patients completed end of study visits between 08 January 2018 and 11 June 2018.
Patient participation is summarised in the following tables.
Table 5A Individual Patient Visits | ||||||
Subject # | Screening Visit (Visit 1) | Baseline Visit (Visit 2) | Treatment Visit (Visit 3) | |||
Date (mm/dd/yyyy) | Status | Date (mm/dd/yyyy) | Status | Date (mm/dd/yyyy) | Status | |
1 | 12/12/2017 | drop-out | n.a. | n.a. | n.a. | n.a. |
2 | 12/18/2017 | accepted | 12/20/2017 | done | 12/21/2017 | done |
3 | 12/21/2017 | accepted | 01/03/2018 | done | 01/04/2018 | done |
4 | 01/02/2018 | accepted | 01/08/2018 | done | 01/09/2018 | done |
5 | 01/03/2018 | accepted | 01/15/2018 | done | 01/16/2018 | done |
6 | 01/08/2018 | accepted | 01/16/2018 | done | 01/17/2018 | done |
7 | 01/08/2018 | accepted | 01/17/2018 | done | 01/18/2018 | done |
8 | 01/15/2018 | drop-out | n.a. | n.a. | n.a. | n.a. |
9 | 01/22/2018 | accepted | 01/30/2018 | done | 01/31/2018 | done |
10 | 02/28/2018 | accepted | 03/07/2018 | done | 03/08/2018 | done |
11 | 03/13/2018 | accepted | 03/19/2018 | done | 03/20/2018 | done |
12 | 03/19/2018 | drop-out | n.a. | n.a. | n.a. | n.a. |
13 | 04/30/2018 | accepted | 05/08/2018 | done | 05/09/2018 | done |
14 | 05/01/2018 | accepted | 05/09/2018 | done | 05/10/2018 | done |
15 | 05/09/2018 | drop-out | n.a. | n.a. | n.a. | n.a. |
16 | 05/16/2018 | accepted | 05/29/2018 | done | 5/30/2018 | done |
Table 5B Individual Patient Visits | |||||
Subject # | Fûllow-Up Visit (Visit 4) | End of Study Visit (Visit 5) | Comments | ||
Date (mm/dd/yyyy) | Status | Date (mm/dd/yyyy) | Status | ||
1 | n.a. | n.a. | n.a. | n.a. | Screen fa il |
2 | 12/22/2017 | done | 01/04/2018 | done | |
3 | 01/05/2018 | done | 01/12/2018 | done | |
4 | 01/10/2018 | done | 01/22/2018 | done | |
5 | 01/17/2018 | n.a. | 01/24/2018 | done | Did not attend |
6 | 01/18/2018 | done | 01/24/2018 | done | |
7 | 01/19/2018 | done | 01/29/2018 | n.a. | |
8 | n.a. | n.a. | n.a. | n.a. | Screen fa il |
9 | 02/01/2018 | done | 02/08/2018 | done | |
10 | 03/09/2018 | done | 03/16/2018 | done | |
11 | 03/21/2018 | done | 03/28/2018 | done | |
12 | n.a. | n.a. | n.a. | n.a. | Screen fa il |
13 | 05/10/2018 | done | 05/16/2018 | done | |
14 | 05/11/2018 | done | 05/23/2018 | done | |
15 | n.a. | n.a. | n.a. | n.a. | Screen fa il |
16 | 05/31/2018 | done | 06/11/2018 | done |
Patient Demographics
The demographics ofthe 12 patients are summarised in the following table.
Table 6 Patient Demographics | ||
Gender | n | 12 |
Male | 3 | |
Female | 9 | |
Age (years) | n | 12 |
Mean | 63.9 | |
Min | 50 | |
Max | 78 | |
Ethnicity | n | 12 |
White | 12 | |
Height (m) | n | 12 |
Mean | 1.63 | |
Min | 1.50 | |
Max | 1.84 | |
Weight (kg) | n | 12 |
Mean | 67.5 | |
Min | 42.2 | |
Max | 108.0 | |
BMI (kg/m2) | n | 12 |
Mean | 25.0 | |
Min | 18.8 | |
Max | 32.3 | |
FEV1 % predicted | n | 12 |
Mean | 97.5 | |
Min | 69.0 | |
Max | 133.0 | |
FVC % predicted | n | 12 |
Mean | 111.6 | |
Min | 79.0 | |
Max | 152.0 | |
Duration Chronic Cough (years) | n | 8 (*) |
Médian | 12.5 | |
Min | 2.6 | |
Max | 40 |
(*) No data available for 4 of the 12 patients.
Results - Cough Frequency
The raw hourly cough count data relative to dosing time was plotted for the full analysis set and inspected as an initial step.
Figure 1 is a graph of médian cough frequency (coughs/hour) versus time after treatment (hours) for baseline (open circles) and treatment (filled circles).
The data suggest that treatment with a single dose of 5 mg AX-8 resulted in improvement in the hourly cough frequency as compared to baseline over a period of approximately 8 hours.
Summary cough frequency data for each of the five time Windows (24 hours; awake;
asieep; 8 hours; 4 hours) are shown in the following table.
Table 7 Cough Frequency Data for Various Time Windows | ||||
Time Window | Variable | Baseline (coughs/hour) | T reatment (coughs/hour) | Change |
24 hours | n | 12 | 12 | |
Médian | 48.1 | 44.3 | - 7.90 % | |
Min | 10.7 | 1.6 | ||
Max | 83.8 | 185.7 | ||
Awake | n | 12 | 12 | |
Médian | 64.1 | 54.8 | - 14.5 % | |
Min | 15.2 | 2.4 | ||
Max | 107.0 | 232.8 | ||
Asieep | n | 12 | 12 | |
Médian | 7.1 | 3.7 | -47.9% | |
Min | 0.6 | 0.0 | ||
Max | 49.5 | 92.8 | ||
8 hours | n | 12 | 12 | |
Médian | 75.5 | 45.4 | - 39.9 % | |
Min | 13.3 | 1.2 | ||
Max | 107.1 | 203.5 | ||
4 hours | n | 12 | 12 | |
Médian | 71.0 | 53.4 | - 24.8 % | |
Min | 13.5 | 0.5 | ||
Max | 123.3 | 202.0 |
For awake and asleep cough frequencies, baseline and treatment data were compared using Wilcoxon signed rank test due to the skewed nature of the data. The data are summarised in the following table.
Table 8 Cough Frequency (Coughs/Hour) for Awake and Asleep Time Windows (Wilcoxon sîgned-ranktest) | |||
Awake | Baseline | n | 12 |
Médian (IQR) | 64.1 (27.4-94.4) | ||
T reatment | n | 12 | |
Médian (IQR) | 54.8 (16.4-79.5) | ||
p-value | 0.034 | ||
Asleep | Baseline | n | 12 |
Médian (IQR) | 7.1 (1.6-19.8) | ||
T reatment | n | 12 | |
Médian (IQR) | 3.7 (0.6-17.5) | ||
p-value | 0.272 |
IQR = Interquartile Range.
These data suggest a significant réduction in cough frequency during waking hours (from 64.1 to 54.8; 14.5% réduction). During sleep, cough frequency is much lower and more variable and therefore although the cough rate is numerically reduced (from 7.1 to 3.7;
48% réduction), the différence may not be statistically significant for the sampie size (12 patients) used.
For 24 hour-, 8 hour-, and 4 hour-cough frequencies, baseline and treatment data were compared using General Estimating Equations (GEE) models. Prior to analysis, these 15 cough count data were natural log (Ln) transformed in order to normalise the distribution of the data. As some individual hourly cough counts were zero, 0.1 was added to ail values prior to transformation. The data are summarised in the following table.
Table 9
Cough Frequency (Coughs/Hour) for 24, 8, and 4 Hour Time Windows (General Estimating Equations (GEE) models)
24 hours | Baseline | n | 12 |
Ln Mean (5E) | 2.87 (0.19) | ||
T reatment | n | 12 | |
Ln Mean (SE) | 2.70 (0.33) | ||
Treatment ratio | -0.166 | ||
95% Cl | -0.53 to 0.20 | ||
Percentage Change* | -15.3% | ||
p-vaîue | 0.368 | ||
8 hours | Baseline | n | 12 |
Ln Mean (SE) | 3.72 (0.22) | ||
Treatment | n | 1224 | |
Ln Mean (SE) | 3.26 (0.39) | ||
Treatment ratio (95% Cl) | -0.461 (-0.88 to -0.04) | ||
Percentage Change* | -36.9% | ||
p-va lue | 0.033 | ||
4 hours | Baseline | n | 12 |
Ln Mean (SE) | 3.92 (0.19) | ||
T reatment | n | 12 | |
Ln Mean (SE) | 3.38 (0.39) | ||
Treatment ratio (95% Cl) | -0.54 (-1.08 to -0.01) | ||
Percentage Change* | -42.0% | ||
p-value | 0.047 |
SE = Standard Error. Cl = Confidence Interval.
These data suggest that hourly cough frequency was significantly improved for treatment as compared to baseline over both the 4-hour period and the 8-hour period. It appears 5 that the effect may diminish after 8 hours, and so, when analysed over the full 24-hour recording period, cough frequency is not significantly reduced.
Data for individual subjects for each of the five time Windows (awake; asleep; 24 hours;
hours; 4 hours) are shown in Figures 2-6.
Figure 2 is a graph showing mean awake cough frequency (coughs/hour) for the individual patients, for both baseline and treatment.
Figure 3 is a graph showing mean asleep cough frequency (coughs/hour) for the 15 12 individual patients, for both baseline and treatment.
Figure 4 is a graph showing mean cough frequency (coughs/hour) for the 12 individual patients during the 24-hour period after treatment and the équivalent baseline period.
(It was subsequently determined that the values reported in Figure 2, Figure 3, and
Figure 4 are “mean values and not “médian” values as onginalîy reported.)
Figure 5 is a graph showing médian cough frequency (coughs/hour) for the 12 individual patients during the 8-hour period after treatment and the équivalent baseline period.
Figure 6 is a graph showing médian cough frequency (coughs/hour) for the 12 individual patients during the 4-hour period after treatment and the équivalent baseline period.
The data demonstrate that:
• 4/12 subjects (33.3%) experienced a > 30% réduction in awake cough frequency per hour.
• 4/12 subjects (33.3%) experienced a > 30% réduction in 24-hour cough frequency per hour.
• 5/12 subjects (41.7%) experienced a £ 30% réduction in 4-hour cough frequency per hour.
• 7/12 subjects (58.3%) experienced a > 30% réduction in 8-hour cough frequency per hour.
Results - Cough Severity and Associated Sensations
At various time points, patients were asked to report cough severity, throat irritation, urge-to-cough, and throat cooling using 100 mm Visual Analog Scales (VASs).
Data for the Screening Visit and End of Study Visit as well as data for the Follow-Up visit (assessment ofthe overall > 24-hour period after dosing) are shown in the following table.
Table 10
Cough Severity and Associated Sensations
Screening (Visit 1) | Follow-Up (Visit 4): >24-hour period after treatment | End of Study (Visit 5) | ||
Cough Severity | n | 12 | 11 | 11 |
Médian (a) | 61.5 (62.5) (b) | 47.0 | 64.0 | |
Min | 46 | 6.0 | 24.0 | |
Max | 86 | 96.0 | 87.0 | |
Throat Irritation | n | 12 | 11 | 11 |
Médian (a) | 55.0 (48.7) (b) | 9.0 | 47.0 | |
Min | 0 | 1.0 | 0.0 | |
Max | 91 | 97.0 | 87.0 | |
Urge-to-Cough | n | 12 | 11 | 11 |
Médian (a) | 51.5(51.4) (b) | 46.0 | 57.0 | |
Min | 1 | 3.0 | 38.0 | |
Max | 92 | 95.0 | 85.0 |
(a) It was subsequently determined that these values are “médian values and not “mean” values as originally reported.
(b) It was subsequently determined that the originally reported values (shown in brackets) were incorrectly calculated.
The data show that cough severity decreased substantially following treatment (from 61.5 at Screening, to 47.0 at Follow-Up, and then returning to 64.0 at End of Study). Similarly, the data show that throat irritation decreased substantially following treatment (from 55.0 at Screening, to 9.0 at Foliow-Up, and then returning to 47.0 at End of Study). Finally, the 10 data show that urge-to-cough also decreased following treatment (from 51.5 at
Screening, to 46.0 at Follow-Up, and then returning to 57.0 at End of Study).
Data for cough severity, throat irritation, urge-to-cough, and throat cooling, both immediately before treatment and hourly for the six hours following treatment, are shown 15 in Figures 7-10. (Throat cooling was assessed half-hourly for the first 3 hours following treatment.)
Figure 7 is a graph of médian cough severity (VAS) (mm) versus time after treatment (hours) for baseline (open downward triangles) and treatment (filled downward triangles).
Figure 8 is a graph of médian urge-to-cough (VAS) (mm) versus time after treatment (hours) for baseline (open diamonds) and treatment (filled diamonds).
Figure 9 is a graph of médian throat irritation (VAS) (mm) versus time aner treatment (hours) for baseline (open squares) and treatment (filled squares).
Figure 10 is a graph of médian throat cooling (VAS) (mm) versus time after treatment (hours) (filled upward triangles).
The cough severity data indicates that patients perceived a réduction from the first hour that persisted for the 6 hours of monitoring (see Figure 7). The urge-to-cough data also indicates an improvement from the first hour that persisted for the 6 hours of monitoring, with an apparent maximum at about 3 hours (see Figure 8). The throat irritation data also indicates an improvement from the first hour that persisted for the 6 hours of monitoring; however, the baseline is lower on the treatment compared with the baseline day (see Figure 9). The throat cooling data show an increase only at 30 minutes, and a barely perceptible différence by 1 hour and thereafter (see Figure 10).
Figure 11 is a composite graph showing, on the left, médian urge-to-cough (VAS) (mm) (filled diamonds), throat irritation (VAS) (mm) (filled squares), and throat cooling (VAS) (mm) (filled upward triangles) and on the right, médian cough frequency (coughs/hour) for baseline (open circles) and treatment (filled circles), versus time after treatment (hours).
When the data for throat irritation, urge-to-cough, and throat cooling are overlaid with the data for cough frequency (baseline and treatment) (see Figure 11), the temporal relationships between sensations and possible antitussive effect may be assessed. The data suggest that the throat cooling sensation preceded (and had resolved before) the subséquent improvements in throat irritation and urge-to-cough. This suggests that the main mechanism of action is not one of counter-irritation. This also suggests that the observed effects (e.g., reduced coughing frequency) are not solely due to a placebo effect, because the patients will hâve experienced the immédiate effects (i.e., throat cooling) subsiding. The data also suggest that improvements in throat irritation and urgeto-cough may be precursors for improvements in cough frequency.
Results - Global Ratinq of Change Scales (GRCS)
The Global Rating of Change Scale (GRCS) assessment data obtained 4 hours after treatment and 24 hours after treatment are summarized in the following table.
Table 11 Global Rating of Change Scale (GRCS) | |||
4 hours after treatment | 24 hours after treatment | ||
Cough Frequency | n | 12 | 11* |
better | 4 (33.3%) | 4 (36.4%) | |
about the same | 7 (58.3%) | 6 (54.5%) | |
worse | 1 (8.3%) | 1 (9.1%) | |
Cough Severity | n | 12 | 11* |
better | 5 (41.7%) | 4 (36.4%) | |
about the same | 6 (50%) | 6 (54.5%) | |
worse | 1 (8.3%) | 1 (9.1%) |
*0ne patient provided GRCS at 4 hours but not 24 hours.
Efficacv Conclusions
Based on the data, the following conclusions may be reached:
• AX-8 significantly reduced cough frequency during waking hours in refractory chronic cough (RCC) patients compared with baseline (no therapy) in this uncontrolled pilot study.
• The effect appears to be most marked over 4-8 hours.
· The effect was accompanied by réduction in patient-reported cough severity.
• The effect was also accompanied by réduction in patient-reported throat irritation and urge-to-cough, both of which are sensations associated with coughing in patients with refractory chronic cough.
• Throat cooling was experienced only transiently and appeared to précédé improvements in cough frequency, cough severity, and sensations associated with cough.
ADDITIONAL STUDIES: MODE-OF-ACTION
The mode-of-action by which the compound, [((1 R,2S,5R)-2-isopropyl-5-methylcyclohexanecarbonyl)-amino]-acetic acid isopropyl ester (also referred to herein as “AX-8” or “Gly-O-iPr”), acts in the treatment of chronic cough (CC) (including, for example, refractory chronic cough (RCC) and idiopathic chronic cough (ICC)) is not yet completely understood, in part because the mechanism of CC (including, e.g., RCC, ICC) is still poorly understood.
The compound is an agonist ofthe transient receptor potential melastatin 8 (TRPM8) cation ion channel, also referred to as cold and menthol receptor 1 (CMR1).
However, evidence suggests that the unique combination of several properties of the compound (e.g., topical mode of action; high potency; high selectivity over TRPM8; high efficacy on spécifie target tissues, e.g., on non-keratinized stratified epithelia - NKSE), as compared to other TRPM8 agonists and known antitussive drugs, gives rises to its unexpected efficacy for treatment of CC (including, e.g., RCC, ICC).
Menthol is the archétypal agonist ofthe TRPM8 ion channel. Menthol has been used in antitussive over-the-counter (OTC) treatments for décades. The efficacy of menthol is recognized in acute cough, even though several studies could not demonstrate a significant antitussive effect (see, e.g., Kenia et al., 2008; Haidl et al., 2001). Menthol has never been shown to improve chronic coughing in CC patients; instead, it has been shown to improve evoked cough (see, e.g., Millqvist étal., 2013). Moreover, menthol can induce adverse reactions such as airway irritation, dyspnea, increased mucus production with simuitaneously reduced ciliary activity leading to mucus stagnation, chest tightness, and potentially respiratory failure, mainly in children, when inhaîed; and acid reflux and heartburn when taken orally (see, e.g., Gavliakova étal., 2013).
Menthol’s antitussive effect (see, e.g., Maher étal., 2014) and some of its side effects may be due to its activity on targets other than TRPM8. Dozens of publications hâve demonstrated that menthol can significantly influence the functional characteristics of a number of different kinds of channels and receptors, including TRP channels (TRPA1, TRPV1, TRPV3, see, e.g., Takaishi et al., 2016), other ligand-gated channels (e.g., GABAa, Glycine, nACh, and 5-HT3 receptors), G-protein coupled receptors (e.g., kappa-opioid receptors; see, e.g., Galeotti et al., 2002) and voltage-gated channels (e.g., voltage-gated sodium and calcium channels) (for review see Oz étal., 2017).
Camphor and eucalyptol, each ofwhich is also an agonist ofthe TRPM8 ion channel, are also used in cold and cough over-the-counter (OTC) treatments. Like menthol, they are poorly sélective and suffer from potential adverse effects (see, e.g., Gavliakova et al., 2013).
AX-8 potency was assessed using Fluorescence Imaging Plate Reader (FLIPR®) assays (study performed by ChanTest/Charles River). The in vitro effects were evaluated on cloned human TRPM8 channels expressed in CHO cells using a Fluo-8 calcium kit and a Fluorescence Imaging Plate Reader (FLIPRTETRA™) instrument. Changes is fluorescence intensity, reflecting the calcium flux through hTRPM8, were measured and the area under the signais (area under the curve, AUC) calculated and expressed in relative light units. Changes induced by the vehicle (HEPES-buffered physiological saline solution, HB-PS) were subtracted. The half-maximal response concentrations (ECSo) were calculated, demonstrating that AX-8 is almost 6 times more potent than menthol, as a TRPM8 agonist (respectively, ECso = 0.39 μΜ and 2.29 μΜ, n = 8; see Figure 12 and Figure 13).
Similarly, selectivity against hTRPAI (expressed in CHO) and hTRPVI (expressed in HEK-293) was assessed using FLIPR® calcium assay (at 100 pM, i.e., 10-fold more than the concentration for maximal response; see Figure 12). Indeed, menthol has been shown to hâve a bimodal activity on TRPA1 (see, e.g., Karashima et al., 2007) and to inhibit TRPV1 (see, e.g., Takaishi et al., 2016), two thermo-sensitive ion channels related to TRPM8 and expressed in nociceptors (sensory neurons responding to harmful stimuli). For the agonist effect assessment, the effect of AX-8 was evaluated in the absence of the positive control agonist. The maximal signal elicited in the presence of the respective agonist (300 μΜ mustard oil forTRPAI; 3 μΜ capsaicin for TRPV1) was setto 100% activation and the signal in the presence of the vehicle control (HB-PS) was set to 0% activation. For the antagonist effect assessment, the channels were activated with the respective positive control agonist (100 pM mustard oil for TRPA1; 0.1 μΜ capsaicin for TRPV1). The effects of AX-8 to inhibit the signal was examined after agonist stimulation and compared to the respective positive control antagonist (3 μΜ ruthénium red). For each channel, the signal elicited in the presence ofthe respective positive control agonist was set to 100 (0% inhibition) and the signal in the presence of the respective positive control antagonist was set to 0 (100% inhibition). The assay demonstrated that AX-8 is sélective on TRPM8 channels, with no agonistic or antagonistic interactions with TRPV1 and TRPA1 channels being observed (see Figure 14 for the agonistic effect).
Figure 12 is a graph representing the activation of human TRPM8 by AX-8, as obtained by FLIPR® assay. The dose response curve is represented as the calcium signal expressed in relative light units (calculated by the area under the curve - AUC, mean ± sem, n = 8) by the AX-8 concentration (μΜ, log scale). The half-maximal response concentration (ECso) for AX-8 was found to be 0.39 μΜ.
Figure 13 is a graph representing the activation of human TRPM8 by menthol, as obtained by FLIPR® assay. The dose response curve is represented as the calcium signal expressed in relative light units (calculated by the area under the curve - AUC, mean ± sem, n = 8) by the menthol concentration (μΜ, log scale). The half-maximal response concentration (ECso) for menthol was found to be 2.29 μΜ.
Figure 14 is a graph representing the comparative activation of human TRPA1 and human TRPV1 by AX-8 and their reference agonists. For hTRPAI, dose response curves for mustard oil (reference TRPA1 agonist) and AX-8 are represented as the percentage of the mustard oil maximal response (mean ± SD, n = 4) by the agonist concentration (μΜ, log scale). The data demonstrate that AX-8 has no significant agonistic activity on hTRPAI for concentrations < 100 μΜ. For hTRPVI, dose response curves for capsaicin (reference TRPV1 agonist) and AX-8 are represented as the percentage of the capsaicin maximal response (mean ± SD, n = 4) by the agonist concentration (μΜ, log scale). The data demonstrate that AX-8 has no agonistic activity on hTRPVI for concentrations <100 μΜ.
In addition, an off-target pharmacology study (SafetyScreen87 assay by Eurofins Pharma Discovery Services) has been performed. This assay package consists of 87 primary molecular targets including 13 enzyme and 74 binding assays, representing potential safety issues. No significant responses were observed with 100 μΜ AX-8, confirming the high selectivity of AX-8 in its effective range of concentration.
The vagal nerve is the main afferent pathway of the cough reflex loop. Therefore, the ability - and dependence on TRPM8 - of AX-8 to inhibit the capsaicin-induced depolarîzation on isolated guinea pig vagal nerves was assessed. The tissue was assayed using an O2/CO2 gassed, grease-gap recording System as previously described (see, e.g., Birrell et al., 2009). Briefly, after the tissue has stabilised, it was exposed to a challenge (capsaicin, 1 μΜ, TRPV1 agonist for 2 minutes), then washed. This was then repeated to confirm the basal response. After washing, the tissue was incubated with vehicle or AX-8 (10 nM-1 mM) for 10 minutes. Following this, the tissue was re-challenged with capsaicin (in the presence of vehicle or AX-8). After a wash phase, the tissue was stimulated with capsaicin to demonstrate tissue viability and recovery of the response.
Where the TRPM8 antagonist PF-05105679 (PF, 10 μΜ) was used, following the two reproducible responses to capsaicin, the nerve was incubated with the TRPM8 antagonist or vehicle (0.1 % DMSO) for 10 minutes, prior to incubation with AX-8 or vehicle for minutes. The nerve was then restimulated with capsaicin m the presence of PF / Vehicle and AX-8 / Vehicle and the percentage of inhibition ofthe original response calculated. Following a wash period, the nerve was then restimulated with capsaicin to détermine viability. The level of depolarization was recorded at each phase. The data were recorded as actual depolarisation leveis and as a percentage inhibition (caused by the vehicle or test compound) of the mean of the initial, control recordings.
This study demonstrated that AX-8 inhîbits up to 80 % of the capsaicin-induced response in guinea pig vagal nerve expiants, in a dose-dependent manner (see Figure 15, n = 3, i.e., tissue from 3 different guinea pigs). This inhibition was suppressed by preapplication of the TRPM8 antagonist PF-05105679, confirming that the effect of AX-8 is mediated by a sélective activation of TRPM8 (see Figure 16, n = 4). By comparison, menthol inhibits capsaicin-induced response in guinea pig vagal nerve expiants in a TRPM8-independent way (see, e.g., Maher et al., 2014).
Figure 15 is a bar graph representing the inhibition (%) ofthe capsaicin-induced response by AX-8 in guinea pig vagal nerve expiants versus the concentration (μΜ) of AX-8. Capsaicin-induced response in guinea pig vagal nerves is blocked in a dose-dependent manner by AX-8 (n = 3).
Figure 16 is a bar graph representing the inhibition (%) of the capsaicin-induced response by AX-8 (1 μΜ) in guinea pig vagal nerve expiants in the presence or absence of the sélective TRPM8 antagonist PF-05105679 (PF, 10 pM). Four different conditions of two consecutive 10-minute incubations were done as follows: Vehicle (0.1 % DMSO) / Vehicle, PF / Vehicle, Vehicle / AX-8 and PF / AX-8 (n= 4). Inhibition ofthe response induced in guinea pig vagal nerve expiants by the irritant capsaicin was blocked by the sélective TRPM8 inhibitor PF-05105679, demonstrating that the effect of AX-8 is TRPM8-dependent.
AX-8’s antitussive effect was evaluated in a standardized guinea pig model of cough (see, e.g., Brozmanova et al., 2012; Dong étal., 2016). Guinea pigs were placed in a plethysmography chamber and exposed for 10 minutes to nebulized capsaicin solution (0.1 mM) to induce cough. The cough frequency was detected as a transient change in airflow in the chamber and the signal recorded via a pressure transducer and computer. Additionally, the audio-amplified count was also recorded electronically. Coughs were counted for the 10-minute exposure period. The experiment was visually monitored by the investigator. A 5 mg/mL AX-8 solution was prepared by dissolving AX-8 in absolute éthanol at 200 mg/mL and then diluting in a solution of 4 mg/mL of sweet potato powder in saline (i.e., vehicle).
The baseline frequency of coughing in response to exposure to capsaîcin mist was recorded for the control (vehicle only) and treated (AX-8) group of animais (n = 10 animais per group). Seven days later, animais were anesthetized with diethyl ether and a small animal laryngoscope was used to place the tip of a micro sprayer syringe in the oral cavity. Vehicle or AX-8 was administered into the oropharyngeal région at 75 pL per animal (n = 10 animais per group). This corresponds to a dose of 0.375 mg per animal. Ten minutes after administration, the guinea pigs were exposed to the capsaicin mist and the number of coughs recorded.
AX-8 solution inhibited significantly capsaicin-induced cough (p < 0.01, see Figure 17).
Figure 17 is a bar graph representing the effect of AX-8 on capsaicin-induced cough in awake guinea pig. Vehicle did not significantly affect capsaicin-induced cough (Baseline (V) = 24.8 ± 2.1 coughs/10 min vs. vehicle = 21.4 ± 2.4 coughs/10 min) in guinea pigs. 75 pL of a 5 mg/mL AX-8 solution (i.e., 0.375 mg/animal) sprayed in the oropharyngeal région inhibited capsaicin-induced cough ofthe guinea pig from 25.0 ± 2.0/10 min coughs (Baseline (T)) to 9.0 ± 2.0/10 min coughs (**p < 0.01). The number of animais is 10 per group (n = 10).
Similarly, the putative site of action of the investigational medical product (I MP) containing AX-8 to treat CC (including, e.g., RCC, ICC) is on the upper respiratory and digestive tracts: the surface ofthe oropharyngeal mucosa - at the back ofthe buccal cavity - and the oesophagus. Therefore, the expected mode of action of AX-8 as antitussive is through the activation of TRPM8-expressing sensory nerve endings in this région. The lining mucosa of oral cavity and oesophagus are typical examples of non-keratinized stratified squamous epithelia (NKSE). AX-8 is a potent, long acting, and selectively cooling agent for non-keratinized épithélial tissues (and permeable keratinized tissues such as eyelid skin) as compared to keratinized épithélial tissues, and as compared to other related cooling agents (e.g., Gly-OEt also known as WS-5, see, e.g., Wei étal., 2012). These unique properties not only differentiate AX-8 from other TRPM8 agonists, but most likely also act synergistically to give rise to the unexpected efficacy of AX-8 as an effective antitussive for use in the treatment of CC (including, e.g., RCC, ICC).
REFERENCES
A number of publications are cited herein in orderto more fully describe and disclose the invention and the State of the art to which the invention pertains. Full citations for these publications are provîded below.
Each of these publications is incorporated herein by reference in its entirety into the présent disclosure, to the same extent as if each individual publication was specifically and individually indicated to be incorporated by reference.
Abdulqawi et al., 2015, “P2X3 receptor antagonist (AF-219) in refractory chronic cough: a randomised, double-blind, placebo-controlled phase 2 study”, The Lancet, Vol. 385, pp. 1198-1205.
Baylie et al., 2010, “Inhibition ofthe cardiac L-type calcium channel current by the TRPM8 agonist, (-)-menthol”, J. Physiol. Pharmacol. Off. J. Pol. Physiol. Soc., Vol. 61, pp. 543-550.
Belvisi et al, 2017, “XEN-D0501, a Novel Transient Receptor Potential Vanilloid 1 Antagonist, Does Not Reduce Cough in Patients with Refractory Cough”, Am. J. Respir. Crit. Care Med., Vol. 196, pp. 1255-1263.
Birrell et al., 2009, “TRPA1 Agonists Evoke Coughing in Guinea Pig and Human Volunteers”, Am J Respir Crit Care Med., Vol. 180, pp 1042-1047.
Birring et al., 2003, Development of a symptom spécifie health status measure for patients with chronic cough: Leicester Cough Questionnaire (LCQ), Thorax. Vol. 58, pp. 339-343.
Birring, 2017, “The search for the hypersensîtivity in chronic cough”, Eur. Respir. J., Vol. 49, Article 1700082.
Boiser, 2004, Experimental models and mechanisms of enhanced coughing, Pulm. Pharmacol. Ther., Vol. 17, pp. 383-388.
Bonvini et al„ 2016, “Transient receptor potential cation channel, subfamily V, member4 and airway sensory afferent activation: Rôle of adenosine triphosphate”, J Allergy Clin Immunol-, Vol. 138(1), pp. 249-261.
Brozmanova étal., 2012, “Comparison of TRPA1-versus TRPV1-mediated cough in guinea pigs, Eur J Pharmacol., Vol. 689, pp 211-218.
Canning et al., 2014, “Anatomy and neurophysiology of cough: CHEST Guideline and Expert Panel report”, Chest. Vol. 146, pp. 1633-1648.
Chow et al., 2017, “Animal Models of Chronic Obstructive Pulmonary Dîsease” in COPD - An Update in Pathogenesis and Ciinical Management (editor: McCarthy) £DOI: 10.5772/intechopen.70262).
Chung et al., 2013, “Chronic cough as a neuropathie disorder”, Lancet Respir. Med.. Vol.
1, pp. 414-422.
Chung, 2014, “Approach to chronic cough: the neuropathie basis for cough hypersensitivity syndrome”, J. Thorac. Dis., Vol. 6, pp. S699-S707.
Dong et al., 2016, “A TRPM8 Agonist Ax-8 Inhibits Capsaicin-lnduced Cough in Guinea Pig, Chest, Vol. 149, pp. A545-A545.
EudraCT Number 2013-002728-17, “A Phase 2a, Mufti-Centre, Randomised, DoubleBlind, Parallel Group, Placebo-Controlled Study to Evaluate Efficacy, Safety and Tolerability of Inhaled GRC 17536, Administered for 4 Weeks, in Patients with Refractory Chronic Cough”, https://www.clinicaltrialsregister.eu/ctrsearch/trial/2013-002728-17/GB.
Ford et al., 2006, “Cough in the community: a cross sectional survey and the relationship to gastrointestinal symptoms”, Thorax, Vol. 61, pp. 975-979.
Galeotti et al., 2002, “Menthol: a natural analgésie compound”, Neurosci. Lett., Vol. 322, pp. 145-148.
Gavliakova et al., 2013, “Analysis of pathomechanisms involved in side effects of menthol treatment in respiratory diseases”, Open J. Mol. Integr. PhysioL, Vol. 03, pp. 2126.
Gibson et al., 2015, “Management of chronic refractory cough”, BMJ, 2015, Vol. 351, Article h5590.
Haidl et al., 2001, “Does the inhalation of a 1% L-menthol solution in the premedication of fiberoptic bronchoscopy affect coughing and the sensation of dyspnea?”, Pneumol. Stuttg. Ger., Vol. 55, pp. 115-119,
Karashima et al., 2007, “Bimodal Action of Menthol on the Transient Receptor Potential Channel TRPA1”, J. Neurosci., Vol. 27, pp. 9874-9884.
Kenia et al., 2008, “Does inhaling menthol affect nasal patency or cough?’’, Pediatr. Pulmonol., Vol. 43, pp. 532-537.
Khalid et al., 2014, Transient receptor potential vanilloid 1 (TRPV1) antagonism in patients with refractory chronic cough: a double-blind randomized controlled trial, J. Aliergy Clin. Immunol., Vol. 134, No. 2, pp. 56-62.
Ludbrook et al., 2019, “S27 A placebo-controlled, double-blind, randomised, crossover study to assess the efficacy, safety and tolerability of TRPV4 inhibitor GSK2798745 in participants with chronic cough, Thorax. Vol. 74 (Suppl 2), pp. A18-A18.
Maher et al., 2014, “P6 Menthol Has Bénéficiai Effects In The Airways Through A Trpm8independent Mechanism”, Thorax. Vol. 69, pp. A79-A80.
Mazzone étal., 2018, “The heterogeneity of chronic cough: a case for endotypes of cough hypersensitivity”, Lancet Respir Med., Vol. 6(8), pp 636-646.
McGarvey, 2005, “Idiopathic chronic cough: a real disease or a failure of diagnosis?”, Cough Lond. Engl., Vol. 1, p. 9.
Meianaphy et al., 2016, “Effects of menthol on rat tail artery mediated by TRPM8 and voltage-gated calcium channels”, Am. J. PhysioL Heart Cire, PhysioL Vol. 311, No. 6, pp. 1416-1430.
Millqvist étal., 2013, “Inhalation of menthol reduces capsaicin cough sensitivity and influences inspiratory flows in chronic cough, Respir. Med., Vol. 107, pp, 433438.
Morice et al., 2006, “Recommendations for the management of cough in adults”, Thorax, Vol. 61 (Suppl 1), pp. i1-i24.
Morice et al., 2011, “Hypersensitivity Syndrome: A Distinct Clinical Entity, Lung, Vol. 189, pp. 73-79.
Morice et al., 2017, “The Effect of MK-7264, a P2X3 antagonist, on Cough Reflex Sensitivity in a Randomized Crossover Trial of Healthy and Chronic Cough Subjects, Eur. Respir. J., Vol. 50, OA2931.
Mukhopadhyay étal., 2016, “Blocking TRPA1 in Respiratory Disorders: Does It Hold a Promise?”, Pharmaceuticals (Basel), Vol. 9(4), Article 70.
Oz et al., 2017, “Cellular and Molecular Targets of Menthol Actions, Front. Pharmacol., Vol. 8, Article 472.
Pavord et al., 2008, “Management of chronic cough”, The Lancet, Vol. 371, pp. 13751384.
Polverino et al., 2012, “Anatomy and neuro-pathophysiology of the cough reflex arc, Multidiscip. Respir. Med.. Vol. 7, p. 5.
Ryan et al., 2018, “An update and systematic review on drug thérapies for the treatment of refractory chronic cough”, Expert Opin. Pharmacother., Vol. 19, pp. 687-711.
Smith et al., 2020, “Gefapixant, a P2X3 receptor antagonist, for the treatment of refractory or unexplained chronic cough: a randomised, double-blind, controlled, parallelgroup, phase 2b trial”. Lancet Respir. Med., DOl: 10.1016/32213-2600(19)304710.
Smith et al., 2016, “S27 The effect of P2X3 antagonism (AF-219) on expérimentally evoked cough in healthy volunteers and chronic cough patients”, Thorax, Vol. 71, pp. A17-A17.
Smith et al., 2017a, “Inhibition of P2X3 by MK-7264 reduces 24-hour cough frequency in a randomized, controlled, Phase 2b clinical trial, Eur. Respir. J., Vol. 50, OA2932.
Smith et al., 2017b, “MK-7264, a P2X3 Receptor Antagonist, Reduces Cough Frequency in Patients with Refractory Chronic Cough: Results from a Randomized, Controlled, Phase 2b Clinical Trial”, Am. J. Respir. Crit. Care Med., Vol. 195, pp. A7608-A7608,
Smith et al., 2017c, “Effects of a nove! sodium channel blocker, GSK2339345, in patients with refractory chronic cough”, Int, J. Clin. Pharmacol. Ther., Vol 55, pp. 712-719.
Song et al., 2017, “Cough Hypersensitivity Syndrome: A Few More Steps Forward”, Allergy Asthma Immunol. Res., Vol. 9, pp. 394-402.
Takaishi étal., 2016, “Reciprocal effects of capsaicin and menthol on thermosensation through regulated activities of TRPV1 and TRPM8”, J. PhysioL Sci., Vol. 22, No. 2, pp. 143-155.
Vogt-Eisele étal., 2007, “Monoterpenoid agonists of TRPV3”, Br. J. Pharmacol., Vol, 151, pp. 530-540.
Wei et al., 2012, “[((1R,2S,5R)-2-lsopropyl-5-methyl-cyclohexanecarbonyl-amino]-acetic acid isopropyl ester and related compounds and their use in therapy”, United
States patent publication number US 2012/0251461 A1, published 04 October
2012.
Wei et al., 2012, “[((1R,2S,5R)-2-lsopropyl-5-methyl-cyclohexanecarbonyl-amino]-acetic acid isopropyl ester and related compounds and their use in therapy”, international patent (PCT) publication number WO 2012/076831 A1, published 14 June 2012.
Xu et al., 2016, “Establishment of chronic cough model in guinea pigs by citric acid inhalation, Chest, Vol. 149, pp. A543-A543.
Claims (14)
1. A compound that is [((1 R,2S,5R)-2-isopropyl-5-methyl-cyclohexanecarbonyl)amino]-acetic acid isopropyl ester, or a pharmaceutically acceptable sait, hydrate, or solvaté thereof, for use in a method of treatment of refractory chronic cough (RCC) or idiopathic chronic cough (ICC).
2. Use of a compound that is [((1 R,2S,5R)-24sopropyl-5-methyicyclohexanecarbonyl)-amino]-acetic acid isopropyl ester, or a pharmaceutically acceptable sait, hydrate, or solvaté thereof, in the manufacture of a médicament for the treatment of refractory chronic cough (RCC) or idiopathic chronic cough (ICC).
3. A compound according to claim 1, or use according to claim 2, wherein: the chronic cough is idiopathic chronic cough (ICC).
4. A compound according to claim 1, or use according to claim 2 wherein: the chronic cough is refractory chronic cough (RCC).
5. A compound according to claim 1, or use according to claim 2, wherein: the chronic cough is refractory chronic cough (RCC) that persists after assessment and treatment of a cough-related condition.
6. A compound according to claim 1, or use according to claim 2, wherein: the chronic cough is refractory chronic cough (RCC) that persists after assessment and treatment of: asthma, éosinophilie bronchitis, post-nasal drip syndrome (PNDS), gastro-oesophageal reflux disease (GORD), bronchiectasis chronic obstructive pulmonary disease (COPD), or idiopathic pulmonary fibrosis (IPF).
7. A compound according to any one of ciaims 1 and 3 to 6, or use according to any one of ciaims 2 to 6, wherein:
the refractory chronic cough (RCC) or idiopathic chronic cough (ICC) is associated with allotussia; or wherein:
the refractory chronic cough (RCC) or idiopathic chronic cough (ICC) is associated with hypertussia; or wherein:
the refractory chronic cough (RCC) or idiopathic chronic cough (ICC) is associated with cough hypersensitivity syndrome (CHS; or wherein:
the refractory chronic cough (RCC) or idiopathic chronic cough (ICC) is associated with cough hypersensitivity reflex (CHR; or wherein:
the refractory chronic cough (RCC) or idiopathic chronic cough (ICC) is associated with iaryngeal paraesthesia; or wherein:
the refractory chronic cough (RCC) or idiopathic chronic cough (tCC) is associated with laryngeaî hypersensitivity syndrome (LHS; or wherein:
the refractory chronic cough (RCC) or idiopathic chronic cough (ICC) is sensory neuropathie cough; or wherein:
the refractory chronic cough (RCC) or idiopathic chronic cough is associated with peripherai sensitization; central sensitization (cough centre); and/or cortical and/or subcortical maladaptive plasticity; or wherein:
the refractory chronic cough (RCC) or idiopathic chronic cough is associated with vagal neuropathy; or wherein:
the refractory chronic cough (RCC) or idiopathic chronic cough is associated with airway inflammation; or wherein:
the refractory chronic cough (RCC) or idiopathic chronic cough is associated with neurogenic inflammation and/or neuroinflammation.
8. A compound according to any one of claims 1 and 3 to 7, or use according to any one of claims 2 to 7, wherein:
the treatment is to reduce cough frequency;
the treatment is to reduce hourly cough frequency;
the treatment is to reduce médian hourly cough frequency;
the treatment is to reduce mean hourly cough frequency;
the treatment is to reduce awake hourly cough frequency;
the treatment is to reduce awake médian hourly cough frequency;
the treatment is to reduce awake mean hourly cough frequency;
the treatment is to reduce asleep hourly cough frequency;
the treatment is to reduce asleep médian hourfy cough frequency;
the treatment is to reduce asleep mean hourly cough frequency;
the treatment is to reduce cough severity;
the treatment is to reduce urge-to-cough; and/or the treatment is to reduce throat irritation.
9. A compound according to any one of claims 1 and 3 to 8, or use according to any one of claims 2 to 8, wherein:
the treatment is by topical oral administration of the compound;
the treatment is by topical oromucosal administration of the compound;
the treatment is by topical buccal administration of the compound;
the treatment is by topical sublingual administration of the compound;
the treatment is by topical intranasal administration of the compound; or the treatment is by topical transmucosal administration of the compound.
10. A compound according to any one of claims 1 and 3 to 19, or use according to any one of claims 2 to 19, wherein:
the treatment is with a dose in the range of from about 1 pg to about 5 mg of the compound per kilogram body weight of the subject per day;
the treatment is with a dose in the range of from about 5 pg to about 2 mg of the compound per kilogram body weight of the subject per day;
the treatment is with a dose in the range of from about 15 pg to about 0.7 mg ofthe compound per kilogram body weight of the subject per day;
the treatment is with a dose in the range of from about 30 pg to about 0.4 mg of the compound per kilogram body weight of the subject per day; or the treatment is with a dose in the range of from about 70 pg to about 0.3 mg of the compound per kilogram body weight of the subject per day.
11. A compound according to any one of claims 1 and 3 to 9, or use according to any one of claims 2 to 9, wherein:
the treatment is with a dose in the range of from about 0.07 mg to about 350 mg of the compound per day;
the treatment is with a dose in the range of from about 0.35 mg to about 140 mg ofthe compound perday;
the treatment is with a dose in the range of from about 1 mg to about 50 mg of the compound per day;
the treatment is with a dose in the range of from about 2 mg to about 30 mg ofthe compound per day; or the treatment is with a dose in the range of from about 5 mg to about 20 mg ofthe compound per day.
12. A compound according to any one of claims 1 and 3 to 11, or use according to any one of claims 2 to 111, wherein:
the treatment is by a treatment regimen of 1 to 5 administrations daily;
the treatment is by a treatment regimen of 1 to 4 administrations daily;
the treatment is by a treatment regimen of 2 to 5 administrations daily;
the treatment is by a treatment regimen of 2 to 4 administrations daily;
the treatment is by a treatment regimen of 2 administrations daily;
the treatment is by a treatment regimen of 3 administrations daily; or the treatment is by a treatment regimen of 4 administrations daily.
13. A compound according to any one of claims 1 and 3 to 12, or use according to any one of claims 2 to 12, wherein:
the treatment is by a pro æ nata (PRN) treatment regimen.
14. A compound according to any one of claims 1 and 3 to 13, or use according to any one of claims 2 to 13, wherein:
the compound is formulated as a tabiet;
the compound is formulated as an orally disintegrating tabiet (ODT);
5 the compound is formulated as a spray;
the compound is formulated as a mist; or the compound is formulated as an aérosol.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1908219.7 | 2019-06-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
OA20600A true OA20600A (en) | 2022-11-29 |
Family
ID=
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US10940110B2 (en) | Method and system for the treatment of chronic COPD with nebulized anticholinergic administrations | |
JP2021073232A (en) | Treatment of respiratory diseases | |
US20090215734A1 (en) | Method and system for the treatment of chronic obstructive pulmonary disease with nebulized anticholinergic administrations | |
CA3035528A1 (en) | Cromolyn compositions for treatment of chronic cough due to idiopathic pulmonary fibrosis | |
US20150111852A1 (en) | 1-Di(sec-butyl)-phosphinoyl-pentane (dapa-2-5) as a topical agent... | |
US20100292325A1 (en) | P-menthawe-3-carboxylic acid esters to treat airways diseases | |
CA3143094C (en) | [((1r,2s,5r)-2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester for treatment of chronic cough | |
OA20600A (en) | [((1R,2S,5R)-2-Isopropyl-5-Methyl-Cyclohexanecarbonyl)-Amino]-Acetic acid Isopropyl ester for treatment of chronic cough. | |
US11406649B2 (en) | Treatment of upper aerodigestive tract disorders and cough | |
TW200922600A (en) | DHEAS inhalation compositions | |
JP6527305B2 (en) | Use of beta-adrenergic inverse agonists for smoking cessation | |
EP2649046B1 (en) | [((1r,2s,5r)-2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester and related compounds and their use in therapy | |
TW201021792A (en) | Arformoterol and tiotropium compositions and methods for use | |
US8476317B2 (en) | N-alkylcarbonyl-amino acid ester compounds and their use for cough and pharyngitis | |
US20200261477A1 (en) | Treatment of airway disorders and cough | |
JP2016027032A (en) | Therapeutic agent for chronic obstructive pulmonary disease |