AU2018347804A1 - Methods of treating prostate cancer by administering abiraterone acetate plus prednisone with androgen deprivation therapy - Google Patents
Methods of treating prostate cancer by administering abiraterone acetate plus prednisone with androgen deprivation therapy Download PDFInfo
- Publication number
- AU2018347804A1 AU2018347804A1 AU2018347804A AU2018347804A AU2018347804A1 AU 2018347804 A1 AU2018347804 A1 AU 2018347804A1 AU 2018347804 A AU2018347804 A AU 2018347804A AU 2018347804 A AU2018347804 A AU 2018347804A AU 2018347804 A1 AU2018347804 A1 AU 2018347804A1
- Authority
- AU
- Australia
- Prior art keywords
- drug product
- patients
- prednisone
- zytiga
- prostate cancer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 229960004103 abiraterone acetate Drugs 0.000 title claims abstract description 115
- UVIQSJCZCSLXRZ-UBUQANBQSA-N abiraterone acetate Chemical compound C([C@@H]1[C@]2(C)CC[C@@H]3[C@@]4(C)CC[C@@H](CC4=CC[C@H]31)OC(=O)C)C=C2C1=CC=CN=C1 UVIQSJCZCSLXRZ-UBUQANBQSA-N 0.000 title claims abstract description 113
- 229960004618 prednisone Drugs 0.000 title claims abstract description 112
- XOFYZVNMUHMLCC-ZPOLXVRWSA-N prednisone Chemical compound O=C1C=C[C@]2(C)[C@H]3C(=O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 XOFYZVNMUHMLCC-ZPOLXVRWSA-N 0.000 title claims abstract description 102
- 206010060862 Prostate cancer Diseases 0.000 title claims abstract description 77
- 208000000236 Prostatic Neoplasms Diseases 0.000 title claims abstract description 76
- 238000009167 androgen deprivation therapy Methods 0.000 title claims abstract description 55
- 238000000034 method Methods 0.000 title claims abstract description 54
- GZOSMCIZMLWJML-VJLLXTKPSA-N abiraterone Chemical compound C([C@H]1[C@H]2[C@@H]([C@]3(CC[C@H](O)CC3=CC2)C)CC[C@@]11C)C=C1C1=CC=CN=C1 GZOSMCIZMLWJML-VJLLXTKPSA-N 0.000 claims description 265
- 238000011282 treatment Methods 0.000 claims description 106
- 230000004083 survival effect Effects 0.000 claims description 72
- 229960000853 abiraterone Drugs 0.000 claims description 64
- 206010061289 metastatic neoplasm Diseases 0.000 claims description 63
- 239000000825 pharmaceutical preparation Substances 0.000 claims description 61
- 229940126534 drug product Drugs 0.000 claims description 60
- 230000001394 metastastic effect Effects 0.000 claims description 59
- 239000003814 drug Substances 0.000 claims description 38
- 229940079593 drug Drugs 0.000 claims description 35
- 208000002193 Pain Diseases 0.000 claims description 22
- 238000011474 orchiectomy Methods 0.000 claims description 14
- 238000002648 combination therapy Methods 0.000 claims description 11
- 239000002547 new drug Substances 0.000 claims description 10
- 230000000153 supplemental effect Effects 0.000 claims description 9
- 229960003911 histrelin acetate Drugs 0.000 claims description 5
- BKEMVGVBBDMHKL-VYFXDUNUSA-N histrelin acetate Chemical compound CC(O)=O.CC(O)=O.CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CO)NC(=O)[C@H](CC=1C2=CC=CC=C2NC=1)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@H]1NC(=O)CC1)CC(N=C1)=CN1CC1=CC=CC=C1 BKEMVGVBBDMHKL-VYFXDUNUSA-N 0.000 claims description 5
- 108010069236 Goserelin Proteins 0.000 claims description 4
- 108010000817 Leuprolide Proteins 0.000 claims description 4
- 108010050144 Triptorelin Pamoate Proteins 0.000 claims description 4
- GFIJNRVAKGFPGQ-LIJARHBVSA-N leuprolide Chemical compound CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](CC=1C2=CC=CC=C2NC=1)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@H]1NC(=O)CC1)CC1=CC=C(O)C=C1 GFIJNRVAKGFPGQ-LIJARHBVSA-N 0.000 claims description 4
- 229960004338 leuprorelin Drugs 0.000 claims description 4
- 229960004824 triptorelin Drugs 0.000 claims description 4
- VXKHXGOKWPXYNA-PGBVPBMZSA-N triptorelin Chemical compound C([C@@H](C(=O)N[C@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N1[C@@H](CCC1)C(=O)NCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@H](CC=1C2=CC=CC=C2NC=1)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@H]1NC(=O)CC1)C1=CC=C(O)C=C1 VXKHXGOKWPXYNA-PGBVPBMZSA-N 0.000 claims description 4
- 238000002679 ablation Methods 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 2
- 229960003690 goserelin acetate Drugs 0.000 claims description 2
- 230000003054 hormonal effect Effects 0.000 claims description 2
- BLCLNMBMMGCOAS-UHFFFAOYSA-N n-[1-[[1-[[1-[[1-[[1-[[1-[[1-[2-[(carbamoylamino)carbamoyl]pyrrolidin-1-yl]-5-(diaminomethylideneamino)-1-oxopentan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-3-[(2-methylpropan-2-yl)oxy]-1-oxopropan-2-yl]amino]-3-(4-hydroxyphenyl)-1-oxopropan-2-yl]amin Chemical compound C1CCC(C(=O)NNC(N)=O)N1C(=O)C(CCCN=C(N)N)NC(=O)C(CC(C)C)NC(=O)C(COC(C)(C)C)NC(=O)C(NC(=O)C(CO)NC(=O)C(CC=1C2=CC=CC=C2NC=1)NC(=O)C(CC=1NC=NC=1)NC(=O)C1NC(=O)CC1)CC1=CC=C(O)C=C1 BLCLNMBMMGCOAS-UHFFFAOYSA-N 0.000 claims description 2
- 229940051084 zytiga Drugs 0.000 description 218
- 239000000902 placebo Substances 0.000 description 89
- 229940068196 placebo Drugs 0.000 description 58
- 238000004458 analytical method Methods 0.000 description 46
- 239000003826 tablet Substances 0.000 description 45
- 231100000517 death Toxicity 0.000 description 42
- 230000034994 death Effects 0.000 description 42
- 230000000694 effects Effects 0.000 description 31
- 208000019423 liver disease Diseases 0.000 description 29
- 208000019025 Hypokalemia Diseases 0.000 description 26
- 208000024896 potassium deficiency disease Diseases 0.000 description 26
- 206010020772 Hypertension Diseases 0.000 description 24
- 230000002411 adverse Effects 0.000 description 24
- 206010067484 Adverse reaction Diseases 0.000 description 20
- 102000007066 Prostate-Specific Antigen Human genes 0.000 description 19
- 108010072866 Prostate-Specific Antigen Proteins 0.000 description 19
- 230000006838 adverse reaction Effects 0.000 description 19
- 241000700159 Rattus Species 0.000 description 18
- 206010019851 Hepatotoxicity Diseases 0.000 description 17
- 231100000304 hepatotoxicity Toxicity 0.000 description 17
- 230000007686 hepatotoxicity Effects 0.000 description 17
- 229940102542 prednisone 5 mg Drugs 0.000 description 17
- MUMGGOZAMZWBJJ-DYKIIFRCSA-N Testostosterone Chemical compound O=C1CC[C@]2(C)[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CCC2=C1 MUMGGOZAMZWBJJ-DYKIIFRCSA-N 0.000 description 16
- 238000002560 therapeutic procedure Methods 0.000 description 16
- 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 14
- 206010028980 Neoplasm Diseases 0.000 description 14
- 239000000556 agonist Substances 0.000 description 14
- 230000003908 liver function Effects 0.000 description 14
- 235000012054 meals Nutrition 0.000 description 14
- 208000017515 adrenocortical insufficiency Diseases 0.000 description 13
- 239000003098 androgen Substances 0.000 description 13
- 229940126601 medicinal product Drugs 0.000 description 13
- 239000000758 substrate Substances 0.000 description 13
- 208000000130 Cytochrome P-450 CYP3A Inducers Diseases 0.000 description 12
- 206010016807 Fluid retention Diseases 0.000 description 12
- 101000904173 Homo sapiens Progonadoliberin-1 Proteins 0.000 description 12
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 12
- 102100024028 Progonadoliberin-1 Human genes 0.000 description 12
- 101000996723 Sus scrofa Gonadotropin-releasing hormone receptor Proteins 0.000 description 12
- 230000005856 abnormality Effects 0.000 description 12
- 239000007941 film coated tablet Substances 0.000 description 12
- XLXSAKCOAKORKW-UHFFFAOYSA-N gonadorelin Chemical compound C1CCC(C(=O)NCC(N)=O)N1C(=O)C(CCCN=C(N)N)NC(=O)C(CC(C)C)NC(=O)CNC(=O)C(NC(=O)C(CO)NC(=O)C(CC=1C2=CC=CC=C2NC=1)NC(=O)C(CC=1NC=NC=1)NC(=O)C1NC(=O)CC1)CC1=CC=C(O)C=C1 XLXSAKCOAKORKW-UHFFFAOYSA-N 0.000 description 12
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 12
- 206010061818 Disease progression Diseases 0.000 description 11
- 206010019280 Heart failures Diseases 0.000 description 11
- ZDZOTLJHXYCWBA-VCVYQWHSSA-N N-debenzoyl-N-(tert-butoxycarbonyl)-10-deacetyltaxol Chemical compound O([C@H]1[C@H]2[C@@](C([C@H](O)C3=C(C)[C@@H](OC(=O)[C@H](O)[C@@H](NC(=O)OC(C)(C)C)C=4C=CC=CC=4)C[C@]1(O)C3(C)C)=O)(C)[C@@H](O)C[C@H]1OC[C@]12OC(=O)C)C(=O)C1=CC=CC=C1 ZDZOTLJHXYCWBA-VCVYQWHSSA-N 0.000 description 11
- 238000008050 Total Bilirubin Reagent Methods 0.000 description 11
- 230000008901 benefit Effects 0.000 description 11
- 238000002512 chemotherapy Methods 0.000 description 11
- 230000005750 disease progression Effects 0.000 description 11
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 11
- 229960003668 docetaxel Drugs 0.000 description 11
- XLXSAKCOAKORKW-AQJXLSMYSA-N gonadorelin Chemical compound C([C@@H](C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N1[C@@H](CCC1)C(=O)NCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@H](CC=1C2=CC=CC=C2NC=1)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@H]1NC(=O)CC1)C1=CC=C(O)C=C1 XLXSAKCOAKORKW-AQJXLSMYSA-N 0.000 description 11
- 230000003902 lesion Effects 0.000 description 11
- 230000009885 systemic effect Effects 0.000 description 11
- 108010001237 Cytochrome P-450 CYP2D6 Proteins 0.000 description 10
- 206010013710 Drug interaction Diseases 0.000 description 10
- 238000011393 cytotoxic chemotherapy Methods 0.000 description 10
- 230000009467 reduction Effects 0.000 description 10
- 230000004044 response Effects 0.000 description 10
- 210000002966 serum Anatomy 0.000 description 10
- 102100021704 Cytochrome P450 2D6 Human genes 0.000 description 9
- 206010030113 Oedema Diseases 0.000 description 9
- 230000002280 anti-androgenic effect Effects 0.000 description 9
- 201000010099 disease Diseases 0.000 description 9
- 235000013305 food Nutrition 0.000 description 9
- 230000004048 modification Effects 0.000 description 9
- 238000012986 modification Methods 0.000 description 9
- 230000001850 reproductive effect Effects 0.000 description 9
- 239000000579 Gonadotropin-Releasing Hormone Substances 0.000 description 8
- 241001465754 Metazoa Species 0.000 description 8
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 8
- 238000007469 bone scintigraphy Methods 0.000 description 8
- 201000011510 cancer Diseases 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 8
- 230000000977 initiatory effect Effects 0.000 description 8
- HYAFETHFCAUJAY-UHFFFAOYSA-N pioglitazone Chemical compound N1=CC(CC)=CC=C1CCOC(C=C1)=CC=C1CC1C(=O)NC(=O)S1 HYAFETHFCAUJAY-UHFFFAOYSA-N 0.000 description 8
- 230000002829 reductive effect Effects 0.000 description 8
- 208000024891 symptom Diseases 0.000 description 8
- 229960003604 testosterone Drugs 0.000 description 8
- 206010011224 Cough Diseases 0.000 description 7
- 108010081668 Cytochrome P-450 CYP3A Proteins 0.000 description 7
- 206010060800 Hot flush Diseases 0.000 description 7
- 206010027476 Metastases Diseases 0.000 description 7
- 102000001854 Steroid 17-alpha-Hydroxylase Human genes 0.000 description 7
- 108010015330 Steroid 17-alpha-Hydroxylase Proteins 0.000 description 7
- 239000000051 antiandrogen Substances 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 7
- 238000002591 computed tomography Methods 0.000 description 7
- 230000007423 decrease Effects 0.000 description 7
- 230000003247 decreasing effect Effects 0.000 description 7
- 238000000338 in vitro Methods 0.000 description 7
- 239000003112 inhibitor Substances 0.000 description 7
- 239000002395 mineralocorticoid Substances 0.000 description 7
- 210000000056 organ Anatomy 0.000 description 7
- 230000035935 pregnancy Effects 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- WSVLPVUVIUVCRA-KPKNDVKVSA-N Alpha-lactose monohydrate Chemical compound O.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 WSVLPVUVIUVCRA-KPKNDVKVSA-N 0.000 description 6
- 229920002785 Croscarmellose sodium Polymers 0.000 description 6
- 108010000561 Cytochrome P-450 CYP2C8 Proteins 0.000 description 6
- 102100029359 Cytochrome P450 2C8 Human genes 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 6
- 101000857870 Squalus acanthias Gonadoliberin Proteins 0.000 description 6
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 6
- 238000011260 co-administration Methods 0.000 description 6
- 229940075614 colloidal silicon dioxide Drugs 0.000 description 6
- 229960001681 croscarmellose sodium Drugs 0.000 description 6
- 235000010947 crosslinked sodium carboxy methyl cellulose Nutrition 0.000 description 6
- 230000006378 damage Effects 0.000 description 6
- 239000002552 dosage form Substances 0.000 description 6
- 230000035558 fertility Effects 0.000 description 6
- 229940035638 gonadotropin-releasing hormone Drugs 0.000 description 6
- 229940088597 hormone Drugs 0.000 description 6
- 239000005556 hormone Substances 0.000 description 6
- 229960001021 lactose monohydrate Drugs 0.000 description 6
- 238000001325 log-rank test Methods 0.000 description 6
- 235000019359 magnesium stearate Nutrition 0.000 description 6
- 229940057948 magnesium stearate Drugs 0.000 description 6
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 6
- 210000002784 stomach Anatomy 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 230000009278 visceral effect Effects 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 208000006820 Arthralgia Diseases 0.000 description 5
- 206010061728 Bone lesion Diseases 0.000 description 5
- 241000282693 Cercopithecidae Species 0.000 description 5
- 102100039205 Cytochrome P450 3A4 Human genes 0.000 description 5
- 206010012735 Diarrhoea Diseases 0.000 description 5
- 102000004190 Enzymes Human genes 0.000 description 5
- 108090000790 Enzymes Proteins 0.000 description 5
- 206010019233 Headaches Diseases 0.000 description 5
- 206010028813 Nausea Diseases 0.000 description 5
- 206010057190 Respiratory tract infections Diseases 0.000 description 5
- 206010046306 Upper respiratory tract infection Diseases 0.000 description 5
- 239000008186 active pharmaceutical agent Substances 0.000 description 5
- 206010003119 arrhythmia Diseases 0.000 description 5
- 230000006793 arrhythmia Effects 0.000 description 5
- 230000002146 bilateral effect Effects 0.000 description 5
- 210000004369 blood Anatomy 0.000 description 5
- 239000008280 blood Substances 0.000 description 5
- 238000009534 blood test Methods 0.000 description 5
- 210000000988 bone and bone Anatomy 0.000 description 5
- 238000009826 distribution Methods 0.000 description 5
- 231100000869 headache Toxicity 0.000 description 5
- 201000001421 hyperglycemia Diseases 0.000 description 5
- 230000001976 improved effect Effects 0.000 description 5
- 230000006872 improvement Effects 0.000 description 5
- 208000015181 infectious disease Diseases 0.000 description 5
- 230000005764 inhibitory process Effects 0.000 description 5
- 238000002372 labelling Methods 0.000 description 5
- 210000004185 liver Anatomy 0.000 description 5
- 238000002595 magnetic resonance imaging Methods 0.000 description 5
- 230000010534 mechanism of action Effects 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 238000012544 monitoring process Methods 0.000 description 5
- 230000008693 nausea Effects 0.000 description 5
- 210000002307 prostate Anatomy 0.000 description 5
- 238000001356 surgical procedure Methods 0.000 description 5
- 230000001988 toxicity Effects 0.000 description 5
- 231100000419 toxicity Toxicity 0.000 description 5
- 231100000027 toxicology Toxicity 0.000 description 5
- 206010023232 Joint swelling Diseases 0.000 description 4
- MKXZASYAUGDDCJ-SZMVWBNQSA-N LSM-2525 Chemical compound C1CCC[C@H]2[C@@]3([H])N(C)CC[C@]21C1=CC(OC)=CC=C1C3 MKXZASYAUGDDCJ-SZMVWBNQSA-N 0.000 description 4
- 206010025327 Lymphopenia Diseases 0.000 description 4
- 206010027457 Metastases to liver Diseases 0.000 description 4
- 229920000168 Microcrystalline cellulose Polymers 0.000 description 4
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 4
- 206010030124 Oedema peripheral Diseases 0.000 description 4
- 239000002202 Polyethylene glycol Substances 0.000 description 4
- 239000004372 Polyvinyl alcohol Substances 0.000 description 4
- 206010062237 Renal impairment Diseases 0.000 description 4
- 208000032327 Respiratory, thoracic and mediastinal disease Diseases 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 4
- 206010047700 Vomiting Diseases 0.000 description 4
- 239000004480 active ingredient Substances 0.000 description 4
- 230000001919 adrenal effect Effects 0.000 description 4
- 208000007502 anemia Diseases 0.000 description 4
- 238000013475 authorization Methods 0.000 description 4
- 230000008406 drug-drug interaction Effects 0.000 description 4
- 230000001605 fetal effect Effects 0.000 description 4
- 230000002440 hepatic effect Effects 0.000 description 4
- 238000002513 implantation Methods 0.000 description 4
- 238000001727 in vivo Methods 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 238000007449 liver function test Methods 0.000 description 4
- 231100001023 lymphopenia Toxicity 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 208000010658 metastatic prostate carcinoma Diseases 0.000 description 4
- 229940016286 microcrystalline cellulose Drugs 0.000 description 4
- 235000019813 microcrystalline cellulose Nutrition 0.000 description 4
- 239000008108 microcrystalline cellulose Substances 0.000 description 4
- 238000011275 oncology therapy Methods 0.000 description 4
- 229960005095 pioglitazone Drugs 0.000 description 4
- 229920001223 polyethylene glycol Polymers 0.000 description 4
- 229920002451 polyvinyl alcohol Polymers 0.000 description 4
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 4
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 4
- 229940069328 povidone Drugs 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- 229910021653 sulphate ion Inorganic materials 0.000 description 4
- 239000000454 talc Substances 0.000 description 4
- 229910052623 talc Inorganic materials 0.000 description 4
- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 4
- 239000004408 titanium dioxide Substances 0.000 description 4
- 231100000402 unacceptable toxicity Toxicity 0.000 description 4
- 230000008673 vomiting Effects 0.000 description 4
- XMAYWYJOQHXEEK-OZXSUGGESA-N (2R,4S)-ketoconazole Chemical compound C1CN(C(=O)C)CCN1C(C=C1)=CC=C1OC[C@@H]1O[C@@](CN2C=NC=C2)(C=2C(=CC(Cl)=CC=2)Cl)OC1 XMAYWYJOQHXEEK-OZXSUGGESA-N 0.000 description 3
- 102100033350 ATP-dependent translocase ABCB1 Human genes 0.000 description 3
- 102100036475 Alanine aminotransferase 1 Human genes 0.000 description 3
- 108010082126 Alanine transaminase Proteins 0.000 description 3
- 108010003415 Aspartate Aminotransferases Proteins 0.000 description 3
- 102000004625 Aspartate Aminotransferases Human genes 0.000 description 3
- 208000020446 Cardiac disease Diseases 0.000 description 3
- 241000282412 Homo Species 0.000 description 3
- 208000029027 Musculoskeletal and connective tissue disease Diseases 0.000 description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- 208000032023 Signs and Symptoms Diseases 0.000 description 3
- 206010041549 Spinal cord compression Diseases 0.000 description 3
- 230000002159 abnormal effect Effects 0.000 description 3
- 102000001307 androgen receptors Human genes 0.000 description 3
- 108010080146 androgen receptors Proteins 0.000 description 3
- 229940030486 androgens Drugs 0.000 description 3
- HJBWBFZLDZWPHF-UHFFFAOYSA-N apalutamide Chemical compound C1=C(F)C(C(=O)NC)=CC=C1N1C2(CCC2)C(=O)N(C=2C=C(C(C#N)=NC=2)C(F)(F)F)C1=S HJBWBFZLDZWPHF-UHFFFAOYSA-N 0.000 description 3
- 229950007511 apalutamide Drugs 0.000 description 3
- 238000003556 assay Methods 0.000 description 3
- 210000004027 cell Anatomy 0.000 description 3
- 208000020832 chronic kidney disease Diseases 0.000 description 3
- 230000009850 completed effect Effects 0.000 description 3
- 238000009223 counseling Methods 0.000 description 3
- 229960001985 dextromethorphan Drugs 0.000 description 3
- 238000003745 diagnosis Methods 0.000 description 3
- 201000000523 end stage renal failure Diseases 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 210000003754 fetus Anatomy 0.000 description 3
- 208000019622 heart disease Diseases 0.000 description 3
- 229920001903 high density polyethylene Polymers 0.000 description 3
- 239000004700 high-density polyethylene Substances 0.000 description 3
- 208000006575 hypertriglyceridemia Diseases 0.000 description 3
- 230000003993 interaction Effects 0.000 description 3
- 229960004125 ketoconazole Drugs 0.000 description 3
- 230000009401 metastasis Effects 0.000 description 3
- 231100000350 mutagenesis Toxicity 0.000 description 3
- 238000002703 mutagenesis Methods 0.000 description 3
- 208000010125 myocardial infarction Diseases 0.000 description 3
- 229940127240 opiate Drugs 0.000 description 3
- 239000006186 oral dosage form Substances 0.000 description 3
- 230000001575 pathological effect Effects 0.000 description 3
- 230000000144 pharmacologic effect Effects 0.000 description 3
- 239000011591 potassium Substances 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 238000001959 radiotherapy Methods 0.000 description 3
- 238000012552 review Methods 0.000 description 3
- JQXXHWHPUNPDRT-WLSIYKJHSA-N rifampicin Chemical compound O([C@](C1=O)(C)O/C=C/[C@@H]([C@H]([C@@H](OC(C)=O)[C@H](C)[C@H](O)[C@H](C)[C@@H](O)[C@@H](C)\C=C\C=C(C)/C(=O)NC=2C(O)=C3C([O-])=C4C)C)OC)C4=C1C3=C(O)C=2\C=N\N1CC[NH+](C)CC1 JQXXHWHPUNPDRT-WLSIYKJHSA-N 0.000 description 3
- 229960001225 rifampicin Drugs 0.000 description 3
- 210000001550 testis Anatomy 0.000 description 3
- 231100001274 therapeutic index Toxicity 0.000 description 3
- 208000019553 vascular disease Diseases 0.000 description 3
- GUBGYTABKSRVRQ-UHFFFAOYSA-N 2-(hydroxymethyl)-6-[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol Chemical compound OCC1OC(OC2C(O)C(O)C(O)OC2CO)C(O)C(O)C1O GUBGYTABKSRVRQ-UHFFFAOYSA-N 0.000 description 2
- 208000007788 Acute Liver Failure Diseases 0.000 description 2
- 206010000804 Acute hepatic failure Diseases 0.000 description 2
- 206010001367 Adrenal insufficiency Diseases 0.000 description 2
- 108020004774 Alkaline Phosphatase Proteins 0.000 description 2
- 102000002260 Alkaline Phosphatase Human genes 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 206010003658 Atrial Fibrillation Diseases 0.000 description 2
- 206010006002 Bone pain Diseases 0.000 description 2
- 208000005623 Carcinogenesis Diseases 0.000 description 2
- 206010007559 Cardiac failure congestive Diseases 0.000 description 2
- 206010007617 Cardio-respiratory arrest Diseases 0.000 description 2
- 208000024172 Cardiovascular disease Diseases 0.000 description 2
- 208000002177 Cataract Diseases 0.000 description 2
- 206010008479 Chest Pain Diseases 0.000 description 2
- 108010074922 Cytochrome P-450 CYP1A2 Proteins 0.000 description 2
- 102100026533 Cytochrome P450 1A2 Human genes 0.000 description 2
- 108090000371 Esterases Proteins 0.000 description 2
- 206010017076 Fracture Diseases 0.000 description 2
- 108700012941 GNRH1 Proteins 0.000 description 2
- 208000018522 Gastrointestinal disease Diseases 0.000 description 2
- 206010018092 Generalised oedema Diseases 0.000 description 2
- BLCLNMBMMGCOAS-URPVMXJPSA-N Goserelin Chemical compound C([C@@H](C(=O)N[C@H](COC(C)(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1[C@@H](CCC1)C(=O)NNC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@H](CC=1C2=CC=CC=C2NC=1)NC(=O)[C@H](CC=1NC=NC=1)NC(=O)[C@H]1NC(=O)CC1)C1=CC=C(O)C=C1 BLCLNMBMMGCOAS-URPVMXJPSA-N 0.000 description 2
- 101000585365 Homo sapiens Sulfotransferase 2A1 Proteins 0.000 description 2
- 208000035150 Hypercholesterolemia Diseases 0.000 description 2
- 208000032911 Injury, poisoning and procedural complications Diseases 0.000 description 2
- 206010023230 Joint stiffness Diseases 0.000 description 2
- 208000001940 Massive Hepatic Necrosis Diseases 0.000 description 2
- 206010053156 Musculoskeletal discomfort Diseases 0.000 description 2
- 150000001204 N-oxides Chemical class 0.000 description 2
- 206010035664 Pneumonia Diseases 0.000 description 2
- RJKFOVLPORLFTN-LEKSSAKUSA-N Progesterone Chemical compound C1CC2=CC(=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H](C(=O)C)[C@@]1(C)CC2 RJKFOVLPORLFTN-LEKSSAKUSA-N 0.000 description 2
- 208000033475 Renal and urinary disease Diseases 0.000 description 2
- 208000005250 Spontaneous Fractures Diseases 0.000 description 2
- 102100029867 Sulfotransferase 2A1 Human genes 0.000 description 2
- 108090000340 Transaminases Proteins 0.000 description 2
- 102000003929 Transaminases Human genes 0.000 description 2
- 230000006978 adaptation Effects 0.000 description 2
- 210000004100 adrenal gland Anatomy 0.000 description 2
- AEMFNILZOJDQLW-QAGGRKNESA-N androst-4-ene-3,17-dione Chemical compound O=C1CC[C@]2(C)[C@H]3CC[C@](C)(C(CC4)=O)[C@@H]4[C@@H]3CCC2=C1 AEMFNILZOJDQLW-QAGGRKNESA-N 0.000 description 2
- 229960005471 androstenedione Drugs 0.000 description 2
- AEMFNILZOJDQLW-UHFFFAOYSA-N androstenedione Natural products O=C1CCC2(C)C3CCC(C)(C(CC4)=O)C4C3CCC2=C1 AEMFNILZOJDQLW-UHFFFAOYSA-N 0.000 description 2
- 206010003246 arthritis Diseases 0.000 description 2
- 230000036772 blood pressure Effects 0.000 description 2
- 208000006218 bradycardia Diseases 0.000 description 2
- 230000036952 cancer formation Effects 0.000 description 2
- 230000000711 cancerogenic effect Effects 0.000 description 2
- 231100000504 carcinogenesis Toxicity 0.000 description 2
- 231100000315 carcinogenic Toxicity 0.000 description 2
- NCEXYHBECQHGNR-UHFFFAOYSA-N chembl421 Chemical compound C1=C(O)C(C(=O)O)=CC(N=NC=2C=CC(=CC=2)S(=O)(=O)NC=2N=CC=CC=2)=C1 NCEXYHBECQHGNR-UHFFFAOYSA-N 0.000 description 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- 230000001684 chronic effect Effects 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000003246 corticosteroid Substances 0.000 description 2
- 229960001334 corticosteroids Drugs 0.000 description 2
- FMGSKLZLMKYGDP-USOAJAOKSA-N dehydroepiandrosterone Chemical compound C1[C@@H](O)CC[C@]2(C)[C@H]3CC[C@](C)(C(CC4)=O)[C@@H]4[C@@H]3CC=C21 FMGSKLZLMKYGDP-USOAJAOKSA-N 0.000 description 2
- 231100000415 developmental toxicity Toxicity 0.000 description 2
- 230000007673 developmental toxicity Effects 0.000 description 2
- 238000000502 dialysis Methods 0.000 description 2
- 208000035475 disorder Diseases 0.000 description 2
- 208000002173 dizziness Diseases 0.000 description 2
- 201000006549 dyspepsia Diseases 0.000 description 2
- 208000028208 end stage renal disease Diseases 0.000 description 2
- 229960004671 enzalutamide Drugs 0.000 description 2
- WXCXUHSOUPDCQV-UHFFFAOYSA-N enzalutamide Chemical compound C1=C(F)C(C(=O)NC)=CC=C1N1C(C)(C)C(=O)N(C=2C=C(C(C#N)=CC=2)C(F)(F)F)C1=S WXCXUHSOUPDCQV-UHFFFAOYSA-N 0.000 description 2
- 230000007717 exclusion Effects 0.000 description 2
- 235000020937 fasting conditions Nutrition 0.000 description 2
- 206010016256 fatigue Diseases 0.000 description 2
- 210000003608 fece Anatomy 0.000 description 2
- SZVJSHCCFOBDDC-UHFFFAOYSA-N ferrosoferric oxide Chemical compound O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 2
- 231100000502 fertility decrease Toxicity 0.000 description 2
- 239000007888 film coating Substances 0.000 description 2
- 238000009501 film coating Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 229960002913 goserelin Drugs 0.000 description 2
- 235000020256 human milk Nutrition 0.000 description 2
- 210000004251 human milk Anatomy 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
- 229960003943 hypromellose Drugs 0.000 description 2
- 238000003384 imaging method Methods 0.000 description 2
- 239000005414 inactive ingredient Substances 0.000 description 2
- 208000000509 infertility Diseases 0.000 description 2
- 230000036512 infertility Effects 0.000 description 2
- 231100000535 infertility Toxicity 0.000 description 2
- 230000003907 kidney function Effects 0.000 description 2
- 230000006651 lactation Effects 0.000 description 2
- 235000004213 low-fat Nutrition 0.000 description 2
- 230000013011 mating Effects 0.000 description 2
- 239000002207 metabolite Substances 0.000 description 2
- 208000031225 myocardial ischemia Diseases 0.000 description 2
- 229940005483 opioid analgesics Drugs 0.000 description 2
- 238000011375 palliative radiation therapy Methods 0.000 description 2
- 239000008194 pharmaceutical composition Substances 0.000 description 2
- 230000001817 pituitary effect Effects 0.000 description 2
- 238000010837 poor prognosis Methods 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
- 230000005855 radiation Effects 0.000 description 2
- 210000004994 reproductive system Anatomy 0.000 description 2
- 208000020029 respiratory tract infectious disease Diseases 0.000 description 2
- 230000002441 reversible effect Effects 0.000 description 2
- 231100000279 safety data Toxicity 0.000 description 2
- 231100000847 severe hepatotoxicity Toxicity 0.000 description 2
- 210000004872 soft tissue Anatomy 0.000 description 2
- 230000008961 swelling Effects 0.000 description 2
- 229960000278 theophylline Drugs 0.000 description 2
- 210000001519 tissue Anatomy 0.000 description 2
- 231100000041 toxicology testing Toxicity 0.000 description 2
- 208000019206 urinary tract infection Diseases 0.000 description 2
- 210000002700 urine Anatomy 0.000 description 2
- 208000037911 visceral disease Diseases 0.000 description 2
- SGEUQNHSMHUUKU-UHFFFAOYSA-N (10,13-dimethyl-2,3,4,7,8,9,11,12,14,15-decahydro-1h-cyclopenta[a]phenanthren-3-yl) acetate Chemical compound C12CCC3(C)C=CCC3C2CC=C2C1(C)CCC(OC(=O)C)C2 SGEUQNHSMHUUKU-UHFFFAOYSA-N 0.000 description 1
- 208000003200 Adenoma Diseases 0.000 description 1
- 102000009027 Albumins Human genes 0.000 description 1
- 229940123407 Androgen receptor antagonist Drugs 0.000 description 1
- 206010002383 Angina Pectoris Diseases 0.000 description 1
- 206010002388 Angina unstable Diseases 0.000 description 1
- 206010003495 Aspermia Diseases 0.000 description 1
- 206010003662 Atrial flutter Diseases 0.000 description 1
- 206010003673 Atrioventricular block complete Diseases 0.000 description 1
- 206010003694 Atrophy Diseases 0.000 description 1
- 208000008035 Back Pain Diseases 0.000 description 1
- 102000004506 Blood Proteins Human genes 0.000 description 1
- 108010017384 Blood Proteins Proteins 0.000 description 1
- 206010049765 Bradyarrhythmia Diseases 0.000 description 1
- 101150022946 CYP3 gene Proteins 0.000 description 1
- 206010058019 Cancer Pain Diseases 0.000 description 1
- 201000009030 Carcinoma Diseases 0.000 description 1
- 208000006029 Cardiomegaly Diseases 0.000 description 1
- 208000031229 Cardiomyopathies Diseases 0.000 description 1
- 108010078791 Carrier Proteins Proteins 0.000 description 1
- 206010008469 Chest discomfort Diseases 0.000 description 1
- 208000014526 Conduction disease Diseases 0.000 description 1
- 206010010774 Constipation Diseases 0.000 description 1
- 208000034656 Contusions Diseases 0.000 description 1
- 229940124766 Cyp17 inhibitor Drugs 0.000 description 1
- 108010026925 Cytochrome P-450 CYP2C19 Proteins 0.000 description 1
- 108010000543 Cytochrome P-450 CYP2C9 Proteins 0.000 description 1
- 102100029363 Cytochrome P450 2C19 Human genes 0.000 description 1
- 102100029358 Cytochrome P450 2C9 Human genes 0.000 description 1
- 102000018832 Cytochromes Human genes 0.000 description 1
- 108010052832 Cytochromes Proteins 0.000 description 1
- FMGSKLZLMKYGDP-UHFFFAOYSA-N Dehydroepiandrosterone Natural products C1C(O)CCC2(C)C3CCC(C)(C(CC4)=O)C4C3CC=C21 FMGSKLZLMKYGDP-UHFFFAOYSA-N 0.000 description 1
- 206010012559 Developmental delay Diseases 0.000 description 1
- 239000012848 Dextrorphan Substances 0.000 description 1
- 101100137368 Dictyostelium discoideum cypD gene Proteins 0.000 description 1
- 208000000059 Dyspnea Diseases 0.000 description 1
- 206010013975 Dyspnoeas Diseases 0.000 description 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 1
- 208000010201 Exanthema Diseases 0.000 description 1
- 229940124602 FDA-approved drug Drugs 0.000 description 1
- 206010049438 General physical health deterioration Diseases 0.000 description 1
- 206010018735 Groin pain Diseases 0.000 description 1
- 206010019663 Hepatic failure Diseases 0.000 description 1
- 238000010163 Hochberg test Methods 0.000 description 1
- 208000029422 Hypernatremia Diseases 0.000 description 1
- 208000029663 Hypophosphatemia Diseases 0.000 description 1
- 206010064919 Hypospermia Diseases 0.000 description 1
- 206010022998 Irritability Diseases 0.000 description 1
- 206010049694 Left Ventricular Dysfunction Diseases 0.000 description 1
- 201000004462 Leydig Cell Tumor Diseases 0.000 description 1
- 102000004317 Lyases Human genes 0.000 description 1
- 108090000856 Lyases Proteins 0.000 description 1
- 108010047230 Member 1 Subfamily B ATP Binding Cassette Transporter Proteins 0.000 description 1
- 208000036642 Metabolism and nutrition disease Diseases 0.000 description 1
- 102000008109 Mixed Function Oxygenases Human genes 0.000 description 1
- 108010074633 Mixed Function Oxygenases Proteins 0.000 description 1
- 208000007101 Muscle Cramp Diseases 0.000 description 1
- 208000010428 Muscle Weakness Diseases 0.000 description 1
- 208000021642 Muscular disease Diseases 0.000 description 1
- 206010028372 Muscular weakness Diseases 0.000 description 1
- 206010028391 Musculoskeletal Pain Diseases 0.000 description 1
- 206010052904 Musculoskeletal stiffness Diseases 0.000 description 1
- 208000000112 Myalgia Diseases 0.000 description 1
- 201000009623 Myopathy Diseases 0.000 description 1
- 208000012902 Nervous system disease Diseases 0.000 description 1
- 231100000264 OECD 451 Carcinogenicity Study Toxicity 0.000 description 1
- 102000012404 Orosomucoid Human genes 0.000 description 1
- 108010061952 Orosomucoid Proteins 0.000 description 1
- 101150009380 PPIF gene Proteins 0.000 description 1
- 206010034156 Pathological fracture Diseases 0.000 description 1
- 102100034943 Peptidyl-prolyl cis-trans isomerase F, mitochondrial Human genes 0.000 description 1
- CXOFVDLJLONNDW-UHFFFAOYSA-N Phenytoin Chemical compound N1C(=O)NC(=O)C1(C=1C=CC=CC=1)C1=CC=CC=C1 CXOFVDLJLONNDW-UHFFFAOYSA-N 0.000 description 1
- 208000014993 Pituitary disease Diseases 0.000 description 1
- 206010036018 Pollakiuria Diseases 0.000 description 1
- ORNBQBCIOKFOEO-YQUGOWONSA-N Pregnenolone Natural products O=C(C)[C@@H]1[C@@]2(C)[C@H]([C@H]3[C@@H]([C@]4(C)C(=CC3)C[C@@H](O)CC4)CC2)CC1 ORNBQBCIOKFOEO-YQUGOWONSA-N 0.000 description 1
- 206010036790 Productive cough Diseases 0.000 description 1
- 206010037660 Pyrexia Diseases 0.000 description 1
- 206010039020 Rhabdomyolysis Diseases 0.000 description 1
- 108091006731 SLCO1B1 Proteins 0.000 description 1
- 101100222691 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CPR3 gene Proteins 0.000 description 1
- 101100276454 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYC7 gene Proteins 0.000 description 1
- 108010071390 Serum Albumin Proteins 0.000 description 1
- 208000019498 Skin and subcutaneous tissue disease Diseases 0.000 description 1
- 208000013738 Sleep Initiation and Maintenance disease Diseases 0.000 description 1
- 208000005392 Spasm Diseases 0.000 description 1
- 206010042434 Sudden death Diseases 0.000 description 1
- 208000003734 Supraventricular Tachycardia Diseases 0.000 description 1
- 208000001871 Tachycardia Diseases 0.000 description 1
- KLBQZWRITKRQQV-UHFFFAOYSA-N Thioridazine Chemical compound C12=CC(SC)=CC=C2SC2=CC=CC=C2N1CCC1CCCCN1C KLBQZWRITKRQQV-UHFFFAOYSA-N 0.000 description 1
- 206010045169 Tumour flare Diseases 0.000 description 1
- 206010070488 Upper-airway cough syndrome Diseases 0.000 description 1
- 206010047281 Ventricular arrhythmia Diseases 0.000 description 1
- ZWBTYMGEBZUQTK-PVLSIAFMSA-N [(7S,9E,11S,12R,13S,14R,15R,16R,17S,18S,19E,21Z)-2,15,17,32-tetrahydroxy-11-methoxy-3,7,12,14,16,18,22-heptamethyl-1'-(2-methylpropyl)-6,23-dioxospiro[8,33-dioxa-24,27,29-triazapentacyclo[23.6.1.14,7.05,31.026,30]tritriaconta-1(32),2,4,9,19,21,24,26,30-nonaene-28,4'-piperidine]-13-yl] acetate Chemical compound CO[C@H]1\C=C\O[C@@]2(C)Oc3c(C2=O)c2c4NC5(CCN(CC(C)C)CC5)N=c4c(=NC(=O)\C(C)=C/C=C/[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C)c(O)c2c(O)c3C ZWBTYMGEBZUQTK-PVLSIAFMSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 231100000836 acute liver failure Toxicity 0.000 description 1
- 208000025368 adrenal gland disease Diseases 0.000 description 1
- -1 advanced patient age Chemical compound 0.000 description 1
- 208000026935 allergic disease Diseases 0.000 description 1
- 239000003936 androgen receptor antagonist Substances 0.000 description 1
- 239000005557 antagonist Substances 0.000 description 1
- 229940030495 antiandrogen sex hormone and modulator of the genital system Drugs 0.000 description 1
- 239000002246 antineoplastic agent Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 206010003668 atrial tachycardia Diseases 0.000 description 1
- 230000037444 atrophy Effects 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 230000036471 bradycardia Effects 0.000 description 1
- BMQGVNUXMIRLCK-OAGWZNDDSA-N cabazitaxel Chemical compound O([C@H]1[C@@H]2[C@]3(OC(C)=O)CO[C@@H]3C[C@@H]([C@]2(C(=O)[C@H](OC)C2=C(C)[C@@H](OC(=O)[C@H](O)[C@@H](NC(=O)OC(C)(C)C)C=3C=CC=CC=3)C[C@]1(O)C2(C)C)C)OC)C(=O)C1=CC=CC=C1 BMQGVNUXMIRLCK-OAGWZNDDSA-N 0.000 description 1
- 229960001573 cabazitaxel Drugs 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- FFGPTBGBLSHEPO-UHFFFAOYSA-N carbamazepine Chemical compound C1=CC2=CC=CC=C2N(C(=O)N)C2=CC=CC=C21 FFGPTBGBLSHEPO-UHFFFAOYSA-N 0.000 description 1
- 229960000623 carbamazepine Drugs 0.000 description 1
- 230000000747 cardiac effect Effects 0.000 description 1
- 206010007625 cardiogenic shock Diseases 0.000 description 1
- 230000001364 causal effect Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000009104 chemotherapy regimen Methods 0.000 description 1
- 238000000546 chi-square test Methods 0.000 description 1
- 231100000505 clastogenic Toxicity 0.000 description 1
- 230000003541 clastogenic effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000001010 compromised effect Effects 0.000 description 1
- 238000012790 confirmation Methods 0.000 description 1
- 230000009519 contusion Effects 0.000 description 1
- 210000004246 corpus luteum Anatomy 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 230000001186 cumulative effect Effects 0.000 description 1
- 230000002559 cytogenic effect Effects 0.000 description 1
- 229940127089 cytotoxic agent Drugs 0.000 description 1
- 231100001066 decreased fetal body weight Toxicity 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 229940071320 dextromethorphan 30 mg Drugs 0.000 description 1
- JAQUASYNZVUNQP-PVAVHDDUSA-N dextrorphan Chemical compound C1C2=CC=C(O)C=C2[C@@]23CCN(C)[C@@H]1[C@H]2CCCC3 JAQUASYNZVUNQP-PVAVHDDUSA-N 0.000 description 1
- 229950006878 dextrorphan Drugs 0.000 description 1
- 230000004069 differentiation Effects 0.000 description 1
- 208000010643 digestive system disease Diseases 0.000 description 1
- 230000010339 dilation Effects 0.000 description 1
- 231100000673 dose–response relationship Toxicity 0.000 description 1
- 230000002526 effect on cardiovascular system Effects 0.000 description 1
- 210000002257 embryonic structure Anatomy 0.000 description 1
- 210000003743 erythrocyte Anatomy 0.000 description 1
- 201000005884 exanthem Diseases 0.000 description 1
- 230000029142 excretion Effects 0.000 description 1
- 235000020650 eye health related herbal supplements Nutrition 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 210000004996 female reproductive system Anatomy 0.000 description 1
- 231100001048 fetal toxicity Toxicity 0.000 description 1
- 230000027950 fever generation Effects 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 239000003168 generic drug Substances 0.000 description 1
- 230000002710 gonadal effect Effects 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 238000001631 haemodialysis Methods 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 230000007407 health benefit Effects 0.000 description 1
- 208000006750 hematuria Diseases 0.000 description 1
- 230000000322 hemodialysis Effects 0.000 description 1
- 208000027700 hepatic dysfunction Diseases 0.000 description 1
- 208000024557 hepatobiliary disease Diseases 0.000 description 1
- 238000001794 hormone therapy Methods 0.000 description 1
- 206010020718 hyperplasia Diseases 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 206010022437 insomnia Diseases 0.000 description 1
- 210000002570 interstitial cell Anatomy 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 230000002147 killing effect Effects 0.000 description 1
- 231100000225 lethality Toxicity 0.000 description 1
- 150000002634 lipophilic molecules Chemical class 0.000 description 1
- 208000007903 liver failure Diseases 0.000 description 1
- 231100000835 liver failure Toxicity 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 210000001165 lymph node Anatomy 0.000 description 1
- 208000010949 lymph node disease Diseases 0.000 description 1
- 210000004698 lymphocyte Anatomy 0.000 description 1
- 210000004995 male reproductive system Anatomy 0.000 description 1
- 230000036210 malignancy Effects 0.000 description 1
- 210000005075 mammary gland Anatomy 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 231100001052 maternal toxicity Toxicity 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000001404 mediated effect Effects 0.000 description 1
- 238000002483 medication Methods 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 210000001589 microsome Anatomy 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 231100000219 mutagenic Toxicity 0.000 description 1
- 230000003505 mutagenic effect Effects 0.000 description 1
- 201000009240 nasopharyngitis Diseases 0.000 description 1
- 238000009099 neoadjuvant therapy Methods 0.000 description 1
- 230000000955 neuroendocrine Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 206010029446 nocturia Diseases 0.000 description 1
- 235000020925 non fasting Nutrition 0.000 description 1
- 239000000820 nonprescription drug Substances 0.000 description 1
- HGASFNYMVGEKTF-UHFFFAOYSA-N octan-1-ol;hydrate Chemical compound O.CCCCCCCCO HGASFNYMVGEKTF-UHFFFAOYSA-N 0.000 description 1
- 230000005305 organ development Effects 0.000 description 1
- 230000027758 ovulation cycle Effects 0.000 description 1
- 239000004031 partial agonist Substances 0.000 description 1
- 238000005192 partition Methods 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 229940127557 pharmaceutical product Drugs 0.000 description 1
- 238000001050 pharmacotherapy Methods 0.000 description 1
- DDBREPKUVSBGFI-UHFFFAOYSA-N phenobarbital Chemical compound C=1C=CC=CC=1C1(CC)C(=O)NC(=O)NC1=O DDBREPKUVSBGFI-UHFFFAOYSA-N 0.000 description 1
- 229960002695 phenobarbital Drugs 0.000 description 1
- 229960002036 phenytoin Drugs 0.000 description 1
- 230000036470 plasma concentration Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 229960002847 prasterone Drugs 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 229960000249 pregnenolone Drugs 0.000 description 1
- ORNBQBCIOKFOEO-QGVNFLHTSA-N pregnenolone Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H](C(=O)C)[C@@]1(C)CC2 ORNBQBCIOKFOEO-QGVNFLHTSA-N 0.000 description 1
- 229940126532 prescription medicine Drugs 0.000 description 1
- 229940002612 prodrug Drugs 0.000 description 1
- 239000000651 prodrug Substances 0.000 description 1
- 229960003387 progesterone Drugs 0.000 description 1
- 239000000186 progesterone Substances 0.000 description 1
- 238000004393 prognosis Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000000069 prophylactic effect Effects 0.000 description 1
- 238000011321 prophylaxis Methods 0.000 description 1
- 238000011471 prostatectomy Methods 0.000 description 1
- 208000020016 psychiatric disease Diseases 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 238000007409 radiographic assessment Methods 0.000 description 1
- HCWPIIXVSYCSAN-OIOBTWANSA-N radium-223 Chemical compound [223Ra] HCWPIIXVSYCSAN-OIOBTWANSA-N 0.000 description 1
- 229960005562 radium-223 Drugs 0.000 description 1
- 206010037844 rash Diseases 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000011268 retreatment Methods 0.000 description 1
- 229960000885 rifabutin Drugs 0.000 description 1
- 229960002599 rifapentine Drugs 0.000 description 1
- WDZCUPBHRAEYDL-GZAUEHORSA-N rifapentine Chemical compound O([C@](C1=O)(C)O/C=C/[C@@H]([C@H]([C@@H](OC(C)=O)[C@H](C)[C@H](O)[C@H](C)[C@@H](O)[C@@H](C)\C=C\C=C(C)/C(=O)NC=2C(O)=C3C(O)=C4C)C)OC)C4=C1C3=C(O)C=2\C=N\N(CC1)CCN1C1CCCC1 WDZCUPBHRAEYDL-GZAUEHORSA-N 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 230000011664 signaling Effects 0.000 description 1
- 231100000161 signs of toxicity Toxicity 0.000 description 1
- 208000017520 skin disease Diseases 0.000 description 1
- 208000000649 small cell carcinoma Diseases 0.000 description 1
- 229940124547 specific antidotes Drugs 0.000 description 1
- 230000019100 sperm motility Effects 0.000 description 1
- 229960002256 spironolactone Drugs 0.000 description 1
- LXMSZDCAJNLERA-ZHYRCANASA-N spironolactone Chemical compound C([C@@H]1[C@]2(C)CC[C@@H]3[C@@]4(C)CCC(=O)C=C4C[C@H]([C@@H]13)SC(=O)C)C[C@@]21CCC(=O)O1 LXMSZDCAJNLERA-ZHYRCANASA-N 0.000 description 1
- 238000007619 statistical method Methods 0.000 description 1
- 150000003431 steroids Chemical class 0.000 description 1
- 238000013517 stratification Methods 0.000 description 1
- 230000003319 supportive effect Effects 0.000 description 1
- 238000009121 systemic therapy Methods 0.000 description 1
- 230000006794 tachycardia Effects 0.000 description 1
- 230000002381 testicular Effects 0.000 description 1
- 229960002784 thioridazine Drugs 0.000 description 1
- 201000002931 third-degree atrioventricular block Diseases 0.000 description 1
- 230000009261 transgenic effect Effects 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 230000004614 tumor growth Effects 0.000 description 1
- 230000004222 uncontrolled growth Effects 0.000 description 1
- 210000000626 ureter Anatomy 0.000 description 1
- 208000022934 urinary frequency Diseases 0.000 description 1
- 230000036318 urination frequency Effects 0.000 description 1
- 230000002861 ventricular Effects 0.000 description 1
- 206010047302 ventricular tachycardia Diseases 0.000 description 1
- 210000001835 viscera Anatomy 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000019195 vitamin supplement Nutrition 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/58—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids containing heterocyclic rings, e.g. danazol, stanozolol, pancuronium or digitogenin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4406—Non condensed pyridines; Hydrogenated derivatives thereof only substituted in position 3, e.g. zimeldine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/57—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone
- A61K31/573—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone substituted in position 21, e.g. cortisone, dexamethasone, prednisone or aldosterone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
- G16H10/00—ICT specially adapted for the handling or processing of patient-related medical or healthcare data
- G16H10/60—ICT specially adapted for the handling or processing of patient-related medical or healthcare data for patient-specific data, e.g. for electronic patient records
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
Landscapes
- Health & Medical Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Medical Informatics (AREA)
- Primary Health Care (AREA)
- Steroid Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201762570781P | 2017-10-11 | 2017-10-11 | |
| US62/570,781 | 2017-10-11 | ||
| PCT/US2018/017438 WO2019074536A1 (en) | 2017-10-11 | 2018-02-08 | METHODS OF TREATING PROSTATE CANCER BY ADMINISTERING ABIRATERONE ACETATE AND PREDNISONE WITH ANDROGENIC SEPARATION THERAPY |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AU2018347804A1 true AU2018347804A1 (en) | 2020-04-16 |
Family
ID=61283312
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2018347804A Abandoned AU2018347804A1 (en) | 2017-10-11 | 2018-02-08 | Methods of treating prostate cancer by administering abiraterone acetate plus prednisone with androgen deprivation therapy |
Country Status (16)
| Country | Link |
|---|---|
| US (2) | US20190105332A1 (enExample) |
| EP (1) | EP3694604A1 (enExample) |
| JP (1) | JP2020536903A (enExample) |
| KR (1) | KR20200068689A (enExample) |
| CN (1) | CN111542373A (enExample) |
| AU (1) | AU2018347804A1 (enExample) |
| BR (1) | BR112020007090A2 (enExample) |
| CA (1) | CA3077678A1 (enExample) |
| EA (1) | EA202090916A1 (enExample) |
| IL (1) | IL273826A (enExample) |
| JO (1) | JOP20200072A1 (enExample) |
| MA (1) | MA50341A (enExample) |
| MX (1) | MX2020003830A (enExample) |
| PH (1) | PH12020550151A1 (enExample) |
| UA (1) | UA124865C2 (enExample) |
| WO (1) | WO2019074536A1 (enExample) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2018023017A1 (en) | 2016-07-29 | 2018-02-01 | Janssen Pharmaceutica Nv | Methods of treating prostate cancer |
| EP4438126A3 (en) | 2017-10-16 | 2025-01-01 | Aragon Pharmaceuticals, Inc. | Anti-androgens for the treatment of non-metastatic castration-resistant prostate cancer |
| WO2021224471A1 (en) * | 2020-05-08 | 2021-11-11 | Janssen Pharmaceutica Nv | Pharmaceutical formulations of abiraterone acetate and niraparib |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102898495B (zh) * | 2012-11-12 | 2014-11-26 | 浙江神洲药业有限公司 | 醋酸阿比特龙酯的制备方法 |
-
2018
- 2018-02-08 KR KR1020207012842A patent/KR20200068689A/ko not_active Ceased
- 2018-02-08 US US15/891,974 patent/US20190105332A1/en not_active Abandoned
- 2018-02-08 MX MX2020003830A patent/MX2020003830A/es unknown
- 2018-02-08 JO JOP/2020/0072A patent/JOP20200072A1/ar unknown
- 2018-02-08 EA EA202090916A patent/EA202090916A1/ru unknown
- 2018-02-08 UA UAA202002743A patent/UA124865C2/uk unknown
- 2018-02-08 CN CN201880079993.2A patent/CN111542373A/zh active Pending
- 2018-02-08 AU AU2018347804A patent/AU2018347804A1/en not_active Abandoned
- 2018-02-08 EP EP18707472.9A patent/EP3694604A1/en not_active Withdrawn
- 2018-02-08 CA CA3077678A patent/CA3077678A1/en active Pending
- 2018-02-08 MA MA050341A patent/MA50341A/fr unknown
- 2018-02-08 WO PCT/US2018/017438 patent/WO2019074536A1/en not_active Ceased
- 2018-02-08 JP JP2020520290A patent/JP2020536903A/ja active Pending
- 2018-02-08 BR BR112020007090-4A patent/BR112020007090A2/pt not_active IP Right Cessation
-
2019
- 2019-11-05 US US16/674,323 patent/US20200069704A1/en not_active Abandoned
-
2020
- 2020-03-26 PH PH12020550151A patent/PH12020550151A1/en unknown
- 2020-04-06 IL IL273826A patent/IL273826A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| KR20200068689A (ko) | 2020-06-15 |
| EA202090916A1 (ru) | 2020-12-11 |
| BR112020007090A2 (pt) | 2020-09-24 |
| UA124865C2 (uk) | 2021-12-01 |
| MX2020003830A (es) | 2020-11-06 |
| JOP20200072A1 (ar) | 2020-04-29 |
| IL273826A (en) | 2020-05-31 |
| PH12020550151A1 (en) | 2021-02-08 |
| WO2019074536A1 (en) | 2019-04-18 |
| MA50341A (fr) | 2020-08-19 |
| CN111542373A (zh) | 2020-08-14 |
| JP2020536903A (ja) | 2020-12-17 |
| US20190105332A1 (en) | 2019-04-11 |
| CA3077678A1 (en) | 2019-04-18 |
| US20200069704A1 (en) | 2020-03-05 |
| EP3694604A1 (en) | 2020-08-19 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP7201694B2 (ja) | 非転移性去勢抵抗性前立腺癌の治療のための抗アンドロゲン剤 | |
| EP3442531A1 (en) | Method of treating renal cell carcinoma using n-(4-(6,7-dimethoxyquinolin-4-yloxy) phenyl)-n'-(4-fluoropheny)cyclopropane-1,1-dicarboxamide, (2s)-hydroxybutanedioate | |
| US20200069704A1 (en) | Methods Of Treating Prostate Cancer | |
| JP2024510612A (ja) | ソトラシブ投与レジメン | |
| US20190262330A1 (en) | Method of Treating Hepatocellular Carcinoma Using N-(4-(6,7-dimethoxyquinolin-4-yloxy)phenyl)-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide, (2S)-hydroxybutanedioate | |
| JP2023504436A (ja) | 乳がんの治療のための併用療法 | |
| KR20210153038A (ko) | 전이성 거세-민감성 전립선암의 치료를 위한 항안드로겐 | |
| TW202302084A (zh) | 以安森司坦和帕博西尼治療乳癌 | |
| KR20240083178A (ko) | Kras g12c 돌연변이를 포함하는 암의 치료를 위한 소토라십 및 egfr 항체 | |
| US20250177414A1 (en) | Combination therapies for treatment of breast cancer | |
| WO2025027138A9 (en) | Combination of niraparib and abiraterone for use in the treatment of metastatic castration-resistant prostate cancer | |
| CN117580572A (zh) | 用安森司坦和帕博西尼治疗乳腺癌 | |
| HK40116445A (en) | Anti-androgens for the treatment of non-metastatic castration-resistant prostate cancer | |
| WO2023209555A1 (en) | Approved drug products and methods for treating prostate cancer | |
| JP2025506402A (ja) | 転移性去勢抵抗性前立腺癌及びhrr変化を有する患者における臨床アウトカムを改善するためのニラパリブ及び酢酸アビラテロン+プレドニゾン | |
| WO2020144647A1 (en) | Pharmaceutical composition comprising apalutamide dispersed in apple sauce | |
| TO | PREVENT RECURRENCE1, 2 | |
| WO2014193589A1 (en) | Cancer treatment method |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MK1 | Application lapsed section 142(2)(a) - no request for examination in relevant period |