WO2022177744A1 - Procédés thérapeutiques agonistes doubles gip/glp1 - Google Patents
Procédés thérapeutiques agonistes doubles gip/glp1 Download PDFInfo
- Publication number
- WO2022177744A1 WO2022177744A1 PCT/US2022/014971 US2022014971W WO2022177744A1 WO 2022177744 A1 WO2022177744 A1 WO 2022177744A1 US 2022014971 W US2022014971 W US 2022014971W WO 2022177744 A1 WO2022177744 A1 WO 2022177744A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- ethoxy
- group
- glu
- amino
- acetyl
- Prior art date
Links
- 238000002560 therapeutic procedure Methods 0.000 title description 4
- 229940125542 dual agonist Drugs 0.000 title description 3
- 101100337060 Caenorhabditis elegans glp-1 gene Proteins 0.000 title 1
- 238000000034 method Methods 0.000 claims abstract description 164
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims abstract description 72
- 238000011282 treatment Methods 0.000 claims abstract description 62
- 206010020772 Hypertension Diseases 0.000 claims abstract description 56
- 108010023302 HDL Cholesterol Proteins 0.000 claims abstract description 49
- 150000003839 salts Chemical class 0.000 claims description 180
- -1 2-[2-(2-amino-ethoxy)- ethoxy]-acetyl Chemical group 0.000 claims description 149
- 150000001875 compounds Chemical class 0.000 claims description 121
- 239000000556 agonist Substances 0.000 claims description 111
- 239000003877 glucagon like peptide 1 receptor agonist Substances 0.000 claims description 106
- 229910052700 potassium Inorganic materials 0.000 claims description 60
- 150000004665 fatty acids Chemical class 0.000 claims description 59
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 58
- 229930195729 fatty acid Natural products 0.000 claims description 58
- 239000000194 fatty acid Substances 0.000 claims description 58
- 150000001413 amino acids Chemical class 0.000 claims description 52
- 230000004048 modification Effects 0.000 claims description 50
- 238000012986 modification Methods 0.000 claims description 50
- 230000003442 weekly effect Effects 0.000 claims description 45
- 229910052717 sulfur Inorganic materials 0.000 claims description 39
- 229910052739 hydrogen Inorganic materials 0.000 claims description 28
- 238000003556 assay Methods 0.000 claims description 27
- NOESYZHRGYRDHS-UHFFFAOYSA-N insulin Chemical compound N1C(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(NC(=O)CN)C(C)CC)CSSCC(C(NC(CO)C(=O)NC(CC(C)C)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CCC(N)=O)C(=O)NC(CC(C)C)C(=O)NC(CCC(O)=O)C(=O)NC(CC(N)=O)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CSSCC(NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2C=CC(O)=CC=2)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2NC=NC=2)NC(=O)C(CO)NC(=O)CNC2=O)C(=O)NCC(=O)NC(CCC(O)=O)C(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC(O)=CC=3)C(=O)NC(C(C)O)C(=O)N3C(CCC3)C(=O)NC(CCCCN)C(=O)NC(C)C(O)=O)C(=O)NC(CC(N)=O)C(O)=O)=O)NC(=O)C(C(C)CC)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C1CSSCC2NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(N)CC=1C=CC=CC=1)C(C)C)CC1=CN=CN1 NOESYZHRGYRDHS-UHFFFAOYSA-N 0.000 claims description 26
- XZWYZXLIPXDOLR-UHFFFAOYSA-N metformin Chemical compound CN(C)C(=N)NC(N)=N XZWYZXLIPXDOLR-UHFFFAOYSA-N 0.000 claims description 24
- 229960003105 metformin Drugs 0.000 claims description 24
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 22
- 229910052698 phosphorus Inorganic materials 0.000 claims description 22
- 206010020802 Hypertensive crisis Diseases 0.000 claims description 20
- OUYCCCASQSFEME-MRVPVSSYSA-N D-tyrosine Chemical compound OC(=O)[C@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-MRVPVSSYSA-N 0.000 claims description 19
- 229910052799 carbon Inorganic materials 0.000 claims description 19
- 108010086246 Glucagon-Like Peptide-1 Receptor Proteins 0.000 claims description 16
- NYHBQMYGNKIUIF-UUOKFMHZSA-N Guanosine Chemical compound C1=NC=2C(=O)NC(N)=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O NYHBQMYGNKIUIF-UUOKFMHZSA-N 0.000 claims description 16
- 108090001061 Insulin Proteins 0.000 claims description 13
- 102000004877 Insulin Human genes 0.000 claims description 13
- 229940125396 insulin Drugs 0.000 claims description 13
- 230000002526 effect on cardiovascular system Effects 0.000 claims description 11
- 210000004899 c-terminal region Anatomy 0.000 claims description 10
- 210000004027 cell Anatomy 0.000 claims description 10
- 238000000159 protein binding assay Methods 0.000 claims description 10
- 208000008589 Obesity Diseases 0.000 claims description 9
- 125000003277 amino group Chemical group 0.000 claims description 9
- 210000000170 cell membrane Anatomy 0.000 claims description 9
- 235000020824 obesity Nutrition 0.000 claims description 9
- MIKUYHXYGGJMLM-GIMIYPNGSA-N Crotonoside Natural products C1=NC2=C(N)NC(=O)N=C2N1[C@H]1O[C@@H](CO)[C@H](O)[C@@H]1O MIKUYHXYGGJMLM-GIMIYPNGSA-N 0.000 claims description 8
- NYHBQMYGNKIUIF-UHFFFAOYSA-N D-guanosine Natural products C1=2NC(N)=NC(=O)C=2N=CN1C1OC(CO)C(O)C1O NYHBQMYGNKIUIF-UHFFFAOYSA-N 0.000 claims description 8
- 229940123518 Sodium/glucose cotransporter 2 inhibitor Drugs 0.000 claims description 8
- 229940029575 guanosine Drugs 0.000 claims description 8
- 125000001424 substituent group Chemical group 0.000 claims description 8
- HNDVDQJCIGZPNO-RXMQYKEDSA-N D-histidine Chemical compound OC(=O)[C@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-RXMQYKEDSA-N 0.000 claims description 7
- 230000007115 recruitment Effects 0.000 claims description 7
- MTCFGRXMJLQNBG-UWTATZPHSA-N D-Serine Chemical compound OC[C@@H](N)C(O)=O MTCFGRXMJLQNBG-UWTATZPHSA-N 0.000 claims description 6
- 244000137850 Marrubium vulgare Species 0.000 claims description 6
- 230000008484 agonism Effects 0.000 claims description 6
- 230000036961 partial effect Effects 0.000 claims description 6
- YONJPLIBVIENNO-LAEOZQHASA-N (2s)-2-amino-5-[[(2r)-3-[(1s)-1-amino-1-carboxy-2-methylpropan-2-yl]sulfanyl-1-(carboxymethylamino)-1-oxopropan-2-yl]amino]-5-oxopentanoic acid Chemical compound OC(=O)[C@H](N)C(C)(C)SC[C@@H](C(=O)NCC(O)=O)NC(=O)CC[C@H](N)C(O)=O YONJPLIBVIENNO-LAEOZQHASA-N 0.000 claims description 5
- AGPKZVBTJJNPAG-RFZPGFLSSA-N D-Isoleucine Chemical compound CC[C@@H](C)[C@@H](N)C(O)=O AGPKZVBTJJNPAG-RFZPGFLSSA-N 0.000 claims description 5
- 125000003074 decanoyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C(*)=O 0.000 claims description 5
- 108700034543 penicillamine-glutathione mixed disulfide Proteins 0.000 claims description 5
- 125000004063 butyryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
- 102000003916 Arrestin Human genes 0.000 claims description 2
- 108090000328 Arrestin Proteins 0.000 claims description 2
- 102100032882 Glucagon-like peptide 1 receptor Human genes 0.000 claims 4
- 210000004978 chinese hamster ovary cell Anatomy 0.000 claims 3
- 240000007594 Oryza sativa Species 0.000 claims 1
- 101001032756 Rattus norvegicus Granzyme-like protein 1 Proteins 0.000 claims 1
- 230000003247 decreasing effect Effects 0.000 abstract description 2
- 102100039994 Gastric inhibitory polypeptide Human genes 0.000 description 183
- 108010004460 Gastric Inhibitory Polypeptide Proteins 0.000 description 182
- 108090000765 processed proteins & peptides Proteins 0.000 description 50
- 235000001014 amino acid Nutrition 0.000 description 49
- FUOOLUPWFVMBKG-UHFFFAOYSA-N 2-Aminoisobutyric acid Chemical compound CC(C)(N)C(O)=O FUOOLUPWFVMBKG-UHFFFAOYSA-N 0.000 description 37
- 125000005647 linker group Chemical group 0.000 description 33
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 29
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 18
- 125000000539 amino acid group Chemical group 0.000 description 16
- 239000003814 drug Substances 0.000 description 16
- 239000011347 resin Substances 0.000 description 15
- 229920005989 resin Polymers 0.000 description 15
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 14
- 102100040918 Pro-glucagon Human genes 0.000 description 14
- 230000027455 binding Effects 0.000 description 14
- 230000008878 coupling Effects 0.000 description 14
- 238000005859 coupling reaction Methods 0.000 description 14
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 14
- 238000010168 coupling process Methods 0.000 description 13
- 206010012601 diabetes mellitus Diseases 0.000 description 13
- 101710198884 GATA-type zinc finger protein 1 Proteins 0.000 description 12
- 102000007446 Glucagon-Like Peptide-1 Receptor Human genes 0.000 description 12
- DTHNMHAUYICORS-KTKZVXAJSA-N Glucagon-like peptide 1 Chemical compound C([C@@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](C)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCCN)C(=O)NCC(=O)N[C@@H](CCCNC(N)=N)C(N)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CO)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CC=1N=CNC=1)[C@@H](C)O)[C@@H](C)O)C(C)C)C1=CC=CC=C1 DTHNMHAUYICORS-KTKZVXAJSA-N 0.000 description 12
- 102000005962 receptors Human genes 0.000 description 12
- 108020003175 receptors Proteins 0.000 description 12
- 238000011161 development Methods 0.000 description 11
- 231100000673 dose–response relationship Toxicity 0.000 description 10
- 239000008188 pellet Substances 0.000 description 10
- 230000002829 reductive effect Effects 0.000 description 10
- 108091016366 Histone-lysine N-methyltransferase EHMT1 Proteins 0.000 description 9
- 230000002641 glycemic effect Effects 0.000 description 9
- 238000002360 preparation method Methods 0.000 description 9
- 102000004196 processed proteins & peptides Human genes 0.000 description 9
- 230000009467 reduction Effects 0.000 description 9
- 239000006228 supernatant Substances 0.000 description 9
- FYZPCMFQCNBYCY-WIWKJPBBSA-N Insulin degludec Chemical compound CC[C@H](C)[C@H](NC(=O)CN)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CSSC[C@@H]2NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CSSC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc3c[nH]cn3)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](NC(=O)[C@@H](N)Cc3ccccc3)C(C)C)C(=O)NCC(=O)N[C@@H](CO)C(=O)N[C@@H](Cc3c[nH]cn3)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc3ccc(O)cc3)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CSSC[C@H](NC(=O)[C@H](Cc3ccc(O)cc3)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](Cc3ccc(O)cc3)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC2=O)C(=O)N[C@@H](CC(N)=O)C(O)=O)C(=O)NCC(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)NCC(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](Cc2ccc(O)cc2)C(=O)N[C@@H]([C@@H](C)O)C(=O)N2CCC[C@H]2C(=O)N[C@@H](CCCCNC(=O)CC[C@H](NC(=O)CCCCCCCCCCCCCCC(O)=O)C(O)=O)C(O)=O)NC1=O)[C@@H](C)O)[C@@H](C)CC FYZPCMFQCNBYCY-WIWKJPBBSA-N 0.000 description 8
- 208000029078 coronary artery disease Diseases 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- 108010050259 insulin degludec Proteins 0.000 description 8
- 229960004225 insulin degludec Drugs 0.000 description 8
- 235000018977 lysine Nutrition 0.000 description 8
- 230000004044 response Effects 0.000 description 8
- 102100035043 Histone-lysine N-methyltransferase EHMT1 Human genes 0.000 description 7
- 101001015516 Homo sapiens Glucagon-like peptide 1 receptor Proteins 0.000 description 7
- 108091006269 SLC5A2 Proteins 0.000 description 7
- 102000058081 Sodium-Glucose Transporter 2 Human genes 0.000 description 7
- 108010046516 Wheat Germ Agglutinins Proteins 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Substances CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 7
- 230000036772 blood pressure Effects 0.000 description 7
- 239000000872 buffer Substances 0.000 description 7
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 7
- 239000005018 casein Substances 0.000 description 7
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 7
- 235000021240 caseins Nutrition 0.000 description 7
- 239000002131 composite material Substances 0.000 description 7
- 229940042399 direct acting antivirals protease inhibitors Drugs 0.000 description 7
- 239000000137 peptide hydrolase inhibitor Substances 0.000 description 7
- 238000002821 scintillation proximity assay Methods 0.000 description 7
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 6
- 108010057186 Insulin Glargine Proteins 0.000 description 6
- COCFEDIXXNGUNL-RFKWWTKHSA-N Insulin glargine Chemical compound C([C@@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@H]1CSSC[C@H]2C(=O)N[C@H](C(=O)N[C@@H](CO)C(=O)N[C@H](C(=O)N[C@H](C(N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC=3C=CC(O)=CC=3)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC=3C=CC(O)=CC=3)C(=O)N[C@@H](CSSC[C@H](NC(=O)[C@H](C(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC=3C=CC(O)=CC=3)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC=3NC=NC=3)NC(=O)[C@H](CO)NC(=O)CNC1=O)C(=O)NCC(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)NCC(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(=O)N[C@@H]([C@@H](C)O)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O)C(=O)NCC(O)=O)=O)CSSC[C@@H](C(N2)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C(C)C)NC(=O)[C@@H](NC(=O)CN)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](NC(=O)[C@@H](N)CC=1C=CC=CC=1)C(C)C)C1=CN=CN1 COCFEDIXXNGUNL-RFKWWTKHSA-N 0.000 description 6
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 6
- 239000011324 bead Substances 0.000 description 6
- 239000012148 binding buffer Substances 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 201000010099 disease Diseases 0.000 description 6
- 229960002869 insulin glargine Drugs 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 125000003088 (fluoren-9-ylmethoxy)carbonyl group Chemical group 0.000 description 5
- JKMHFZQWWAIEOD-UHFFFAOYSA-N 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid Chemical compound OCC[NH+]1CCN(CCS([O-])(=O)=O)CC1 JKMHFZQWWAIEOD-UHFFFAOYSA-N 0.000 description 5
- 108010063919 Glucagon Receptors Proteins 0.000 description 5
- 102100040890 Glucagon receptor Human genes 0.000 description 5
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 5
- 239000004472 Lysine Substances 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 238000002868 homogeneous time resolved fluorescence Methods 0.000 description 5
- 238000011534 incubation Methods 0.000 description 5
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 5
- 239000012528 membrane Substances 0.000 description 5
- 230000009871 nonspecific binding Effects 0.000 description 5
- 239000000902 placebo Substances 0.000 description 5
- 229940068196 placebo Drugs 0.000 description 5
- 125000006239 protecting group Chemical group 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 4
- 239000007995 HEPES buffer Substances 0.000 description 4
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 4
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 4
- 230000035487 diastolic blood pressure Effects 0.000 description 4
- 208000035475 disorder Diseases 0.000 description 4
- 229940079593 drug Drugs 0.000 description 4
- 239000011539 homogenization buffer Substances 0.000 description 4
- 239000003446 ligand Substances 0.000 description 4
- 125000003588 lysine group Chemical group [H]N([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(N([H])[H])C(*)=O 0.000 description 4
- 210000002966 serum Anatomy 0.000 description 4
- 238000004088 simulation Methods 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 230000035488 systolic blood pressure Effects 0.000 description 4
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
- BDNKZNFMNDZQMI-UHFFFAOYSA-N 1,3-diisopropylcarbodiimide Chemical compound CC(C)N=C=NC(C)C BDNKZNFMNDZQMI-UHFFFAOYSA-N 0.000 description 3
- 108010001478 Bacitracin Proteins 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
- 208000006011 Stroke Diseases 0.000 description 3
- KPFBUSLHFFWMAI-HYRPPVSQSA-N [(8r,9s,10r,13s,14s,17r)-17-acetyl-6-formyl-3-methoxy-10,13-dimethyl-1,2,7,8,9,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-17-yl] acetate Chemical compound C1C[C@@H]2[C@](CCC(OC)=C3)(C)C3=C(C=O)C[C@H]2[C@@H]2CC[C@](OC(C)=O)(C(C)=O)[C@]21C KPFBUSLHFFWMAI-HYRPPVSQSA-N 0.000 description 3
- 229960003071 bacitracin Drugs 0.000 description 3
- 229930184125 bacitracin Natural products 0.000 description 3
- CLKOFPXJLQSYAH-ABRJDSQDSA-N bacitracin A Chemical compound C1SC([C@@H](N)[C@@H](C)CC)=N[C@@H]1C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H]1C(=O)N[C@H](CCCN)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@H](CC=2C=CC=CC=2)C(=O)N[C@@H](CC=2N=CNC=2)C(=O)N[C@H](CC(O)=O)C(=O)N[C@@H](CC(N)=O)C(=O)NCCCC1 CLKOFPXJLQSYAH-ABRJDSQDSA-N 0.000 description 3
- 238000013262 cAMP assay Methods 0.000 description 3
- 235000005911 diet Nutrition 0.000 description 3
- 230000037213 diet Effects 0.000 description 3
- BGRWYRAHAFMIBJ-UHFFFAOYSA-N diisopropylcarbodiimide Natural products CC(C)NC(=O)NC(C)C BGRWYRAHAFMIBJ-UHFFFAOYSA-N 0.000 description 3
- 238000004128 high performance liquid chromatography Methods 0.000 description 3
- 102000056448 human GLP1R Human genes 0.000 description 3
- 238000000338 in vitro Methods 0.000 description 3
- 230000000977 initiatory effect Effects 0.000 description 3
- 150000002632 lipids Chemical class 0.000 description 3
- 150000002669 lysines Chemical class 0.000 description 3
- 239000006186 oral dosage form Substances 0.000 description 3
- 229920000136 polysorbate Polymers 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000002287 radioligand Substances 0.000 description 3
- 238000001525 receptor binding assay Methods 0.000 description 3
- 230000000638 stimulation Effects 0.000 description 3
- 208000024891 symptom Diseases 0.000 description 3
- 125000000297 undecanoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- YPTNAIDIXCOZAJ-LHEWISCISA-N (2s)-2-(9h-fluoren-9-ylmethoxycarbonylamino)-6-[[(4-methylphenyl)-diphenylmethyl]amino]hexanoic acid Chemical compound C1=CC(C)=CC=C1C(C=1C=CC=CC=1)(C=1C=CC=CC=1)NCCCC[C@@H](C(O)=O)NC(=O)OCC1C2=CC=CC=C2C2=CC=CC=C21 YPTNAIDIXCOZAJ-LHEWISCISA-N 0.000 description 2
- GOPWHXPXSPIIQZ-FQEVSTJZSA-N (4s)-4-(9h-fluoren-9-ylmethoxycarbonylamino)-5-[(2-methylpropan-2-yl)oxy]-5-oxopentanoic acid Chemical compound C1=CC=C2C(COC(=O)N[C@@H](CCC(O)=O)C(=O)OC(C)(C)C)C3=CC=CC=C3C2=C1 GOPWHXPXSPIIQZ-FQEVSTJZSA-N 0.000 description 2
- BYEAHWXPCBROCE-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropan-2-ol Chemical compound FC(F)(F)C(O)C(F)(F)F BYEAHWXPCBROCE-UHFFFAOYSA-N 0.000 description 2
- XQPYRJIMPDBGRW-UHFFFAOYSA-N 2-[2-[2-(9h-fluoren-9-ylmethoxycarbonylamino)ethoxy]ethoxy]acetic acid Chemical compound C1=CC=C2C(COC(=O)NCCOCCOCC(=O)O)C3=CC=CC=C3C2=C1 XQPYRJIMPDBGRW-UHFFFAOYSA-N 0.000 description 2
- MNBYXFWXRDWBOQ-UHFFFAOYSA-N 2-[2-[2-amino-3-(9H-fluoren-9-ylmethoxy)-3-oxopropoxy]ethoxy]acetic acid Chemical compound C(=O)(OCC1C2=CC=CC=C2C2=CC=CC=C12)C(COCCOCC(=O)O)N MNBYXFWXRDWBOQ-UHFFFAOYSA-N 0.000 description 2
- ARSWQPLPYROOBG-ZETCQYMHSA-N 2-methylleucine Chemical compound CC(C)C[C@](C)(N)C(O)=O ARSWQPLPYROOBG-ZETCQYMHSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 208000024172 Cardiovascular disease Diseases 0.000 description 2
- QNAYBMKLOCPYGJ-UWTATZPHSA-N D-alanine Chemical compound C[C@@H](N)C(O)=O QNAYBMKLOCPYGJ-UWTATZPHSA-N 0.000 description 2
- 108010024044 Glucagon-Like Peptide-2 Receptor Proteins 0.000 description 2
- 102100032879 Glucagon-like peptide 2 receptor Human genes 0.000 description 2
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
- 108010010234 HDL Lipoproteins Proteins 0.000 description 2
- 102000015779 HDL Lipoproteins Human genes 0.000 description 2
- 101100228914 Homo sapiens GIPR gene Proteins 0.000 description 2
- 108010028554 LDL Cholesterol Proteins 0.000 description 2
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 2
- 241000208125 Nicotiana Species 0.000 description 2
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 2
- 239000004809 Teflon Substances 0.000 description 2
- 229920006362 Teflon® Polymers 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- 230000004913 activation Effects 0.000 description 2
- 125000003275 alpha amino acid group Chemical group 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 238000009530 blood pressure measurement Methods 0.000 description 2
- 239000007853 buffer solution Substances 0.000 description 2
- 238000004364 calculation method Methods 0.000 description 2
- 239000006285 cell suspension Substances 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
- 238000003776 cleavage reaction Methods 0.000 description 2
- 230000034994 death Effects 0.000 description 2
- 238000010494 dissociation reaction Methods 0.000 description 2
- 230000005593 dissociations Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 238000004108 freeze drying Methods 0.000 description 2
- 230000002496 gastric effect Effects 0.000 description 2
- BRZYSWJRSDMWLG-CAXSIQPQSA-N geneticin Chemical compound O1C[C@@](O)(C)[C@H](NC)[C@@H](O)[C@H]1O[C@@H]1[C@@H](O)[C@H](O[C@@H]2[C@@H]([C@@H](O)[C@H](O)[C@@H](C(C)O)O2)N)[C@@H](N)C[C@H]1N BRZYSWJRSDMWLG-CAXSIQPQSA-N 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 229960004666 glucagon Drugs 0.000 description 2
- 239000008103 glucose Substances 0.000 description 2
- 239000004220 glutamic acid Substances 0.000 description 2
- 230000036541 health Effects 0.000 description 2
- 201000001421 hyperglycemia Diseases 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 230000003834 intracellular effect Effects 0.000 description 2
- 238000012417 linear regression Methods 0.000 description 2
- 229910001629 magnesium chloride Inorganic materials 0.000 description 2
- 239000004031 partial agonist Substances 0.000 description 2
- 102000014187 peptide receptors Human genes 0.000 description 2
- 108010011903 peptide receptors Proteins 0.000 description 2
- 238000010647 peptide synthesis reaction Methods 0.000 description 2
- 230000002085 persistent effect Effects 0.000 description 2
- 230000000144 pharmacologic effect Effects 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 238000011176 pooling 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
- 230000001105 regulatory effect Effects 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 238000004007 reversed phase HPLC Methods 0.000 description 2
- 238000009118 salvage therapy Methods 0.000 description 2
- 230000007017 scission Effects 0.000 description 2
- 238000012216 screening Methods 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 238000004448 titration Methods 0.000 description 2
- 238000011269 treatment regimen Methods 0.000 description 2
- ZGYICYBLPGRURT-UHFFFAOYSA-N tri(propan-2-yl)silicon Chemical compound CC(C)[Si](C(C)C)C(C)C ZGYICYBLPGRURT-UHFFFAOYSA-N 0.000 description 2
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 2
- 125000001493 tyrosinyl group Chemical group [H]OC1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])(N([H])[H])C(*)=O 0.000 description 2
- 230000037221 weight management Effects 0.000 description 2
- ZEQLLMOXFVKKCN-AWEZNQCLSA-N (2s)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-[4-[(2-methylpropan-2-yl)oxy]phenyl]propanoic acid Chemical compound CC(C)(C)OC(=O)N[C@H](C(O)=O)CC1=CC=C(OC(C)(C)C)C=C1 ZEQLLMOXFVKKCN-AWEZNQCLSA-N 0.000 description 1
- MXECDVKIKUSSNC-JTQLQIEISA-N (2s)-2-amino-3-(2-fluorophenyl)-2-methylpropanoic acid Chemical compound OC(=O)[C@](N)(C)CC1=CC=CC=C1F MXECDVKIKUSSNC-JTQLQIEISA-N 0.000 description 1
- FQFVANSXYKWQOT-ZETCQYMHSA-N (2s)-2-azaniumyl-3-pyridin-4-ylpropanoate Chemical compound OC(=O)[C@@H](N)CC1=CC=NC=C1 FQFVANSXYKWQOT-ZETCQYMHSA-N 0.000 description 1
- LWHHAVWYGIBIEU-LURJTMIESA-N (2s)-2-methylpyrrolidin-1-ium-2-carboxylate Chemical compound [O-]C(=O)[C@]1(C)CCC[NH2+]1 LWHHAVWYGIBIEU-LURJTMIESA-N 0.000 description 1
- CNBUSIJNWNXLQQ-NSHDSACASA-N (2s)-3-(4-hydroxyphenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid Chemical compound CC(C)(C)OC(=O)N[C@H](C(O)=O)CC1=CC=C(O)C=C1 CNBUSIJNWNXLQQ-NSHDSACASA-N 0.000 description 1
- NGJOFQZEYQGZMB-KTKZVXAJSA-N (4S)-5-[[2-[[(2S,3R)-1-[[(2S)-1-[[(2S,3R)-1-[[(2S)-1-[[(2S)-1-[[(2S)-1-[[(2S)-1-[[(2S)-1-[[(2S)-1-[[(2S)-1-[[(2S)-1-[[2-[[(2S)-5-amino-1-[[(2S)-1-[[(2S)-1-[[(2S)-6-amino-1-[[(2S)-1-[[(2S)-1-[[(2S,3S)-1-[[(2S)-1-[[(2S)-1-[[(2S)-1-[[(2S)-1-[[(2S)-6-amino-1-[[2-[[(1S)-4-carbamimidamido-1-carboxybutyl]amino]-2-oxoethyl]amino]-1-oxohexan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-3-(1H-indol-3-yl)-1-oxopropan-2-yl]amino]-1-oxopropan-2-yl]amino]-3-methyl-1-oxopentan-2-yl]amino]-1-oxo-3-phenylpropan-2-yl]amino]-4-carboxy-1-oxobutan-2-yl]amino]-1-oxohexan-2-yl]amino]-1-oxopropan-2-yl]amino]-1-oxopropan-2-yl]amino]-1,5-dioxopentan-2-yl]amino]-2-oxoethyl]amino]-4-carboxy-1-oxobutan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-3-(4-hydroxyphenyl)-1-oxopropan-2-yl]amino]-3-hydroxy-1-oxopropan-2-yl]amino]-3-hydroxy-1-oxopropan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]amino]-3-carboxy-1-oxopropan-2-yl]amino]-3-hydroxy-1-oxopropan-2-yl]amino]-3-hydroxy-1-oxobutan-2-yl]amino]-1-oxo-3-phenylpropan-2-yl]amino]-3-hydroxy-1-oxobutan-2-yl]amino]-2-oxoethyl]amino]-4-[[(2S)-2-[[(2S)-2-amino-3-(1H-imidazol-4-yl)propanoyl]amino]propanoyl]amino]-5-oxopentanoic acid Chemical compound C([C@@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](C)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCCN)C(=O)NCC(=O)N[C@@H](CCCNC(N)=N)C(O)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CO)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CC=1NC=NC=1)[C@@H](C)O)[C@@H](C)O)C(C)C)C1=CC=CC=C1 NGJOFQZEYQGZMB-KTKZVXAJSA-N 0.000 description 1
- ZTJJDVCSOPGGST-UHFFFAOYSA-N 10-[4-[(2-methylpropan-2-yl)oxycarbonyl]phenoxy]decanoic acid Chemical compound CC(C)(C)OC(=O)C1=CC=C(OCCCCCCCCCC(O)=O)C=C1 ZTJJDVCSOPGGST-UHFFFAOYSA-N 0.000 description 1
- CPUSCHYXEUZMSV-UHFFFAOYSA-N 2,6-diamino-2-methylhexanoic acid Chemical compound OC(=O)C(N)(C)CCCCN CPUSCHYXEUZMSV-UHFFFAOYSA-N 0.000 description 1
- KXSKAZFMTGADIV-UHFFFAOYSA-N 2-[3-(2-hydroxyethoxy)propoxy]ethanol Chemical compound OCCOCCCOCCO KXSKAZFMTGADIV-UHFFFAOYSA-N 0.000 description 1
- HXMVNCMPQGPRLN-UHFFFAOYSA-N 2-hydroxyputrescine Chemical compound NCCC(O)CN HXMVNCMPQGPRLN-UHFFFAOYSA-N 0.000 description 1
- CDUUKBXTEOFITR-BYPYZUCNSA-N 2-methyl-L-serine Chemical compound OC[C@@]([NH3+])(C)C([O-])=O CDUUKBXTEOFITR-BYPYZUCNSA-N 0.000 description 1
- APIXJSLKIYYUKG-UHFFFAOYSA-N 3 Isobutyl 1 methylxanthine Chemical compound O=C1N(C)C(=O)N(CC(C)C)C2=C1N=CN2 APIXJSLKIYYUKG-UHFFFAOYSA-N 0.000 description 1
- OGOMLUBUDYFIOG-UHFFFAOYSA-N 4-(4-iodophenyl)butanoic acid Chemical compound OC(=O)CCCC1=CC=C(I)C=C1 OGOMLUBUDYFIOG-UHFFFAOYSA-N 0.000 description 1
- MDPZCXXNCSUROL-UHFFFAOYSA-N 4-(4-tert-butylphenyl)butanoic acid Chemical compound CC(C)(C)C1=CC=C(CCCC(O)=O)C=C1 MDPZCXXNCSUROL-UHFFFAOYSA-N 0.000 description 1
- 201000001320 Atherosclerosis Diseases 0.000 description 1
- 210000002237 B-cell of pancreatic islet Anatomy 0.000 description 1
- 108091003079 Bovine Serum Albumin Proteins 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 241000699802 Cricetulus griseus Species 0.000 description 1
- 229930195711 D-Serine Natural products 0.000 description 1
- QNAYBMKLOCPYGJ-UHFFFAOYSA-N D-alpha-Ala Natural products CC([NH3+])C([O-])=O QNAYBMKLOCPYGJ-UHFFFAOYSA-N 0.000 description 1
- WHUUTDBJXJRKMK-GSVOUGTGSA-N D-glutamic acid Chemical compound OC(=O)[C@H](N)CCC(O)=O WHUUTDBJXJRKMK-GSVOUGTGSA-N 0.000 description 1
- 229930182847 D-glutamic acid Natural products 0.000 description 1
- 229930195721 D-histidine Natural products 0.000 description 1
- 229930195709 D-tyrosine Natural products 0.000 description 1
- 239000006144 Dulbecco’s modified Eagle's medium Substances 0.000 description 1
- HEMJJKBWTPKOJG-UHFFFAOYSA-N Gemfibrozil Chemical compound CC1=CC=C(C)C(OCCCC(C)(C)C(O)=O)=C1 HEMJJKBWTPKOJG-UHFFFAOYSA-N 0.000 description 1
- 102000051325 Glucagon Human genes 0.000 description 1
- 108060003199 Glucagon Proteins 0.000 description 1
- 101800004295 Glucagon-like peptide 1(7-36) Proteins 0.000 description 1
- 102000017011 Glycated Hemoglobin A Human genes 0.000 description 1
- 101000886868 Homo sapiens Gastric inhibitory polypeptide Proteins 0.000 description 1
- 101000604197 Homo sapiens Neuronatin Proteins 0.000 description 1
- 101000693243 Homo sapiens Paternally-expressed gene 3 protein Proteins 0.000 description 1
- GRRNUXAQVGOGFE-UHFFFAOYSA-N Hygromycin-B Natural products OC1C(NC)CC(N)C(O)C1OC1C2OC3(C(C(O)C(O)C(C(N)CO)O3)O)OC2C(O)C(CO)O1 GRRNUXAQVGOGFE-UHFFFAOYSA-N 0.000 description 1
- 208000035150 Hypercholesterolemia Diseases 0.000 description 1
- 206010022489 Insulin Resistance Diseases 0.000 description 1
- 229920001202 Inulin Polymers 0.000 description 1
- AHLPHDHHMVZTML-BYPYZUCNSA-N L-Ornithine Chemical compound NCCC[C@H](N)C(O)=O AHLPHDHHMVZTML-BYPYZUCNSA-N 0.000 description 1
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 description 1
- NHTGHBARYWONDQ-JTQLQIEISA-N L-α-methyl-Tyrosine Chemical compound OC(=O)[C@](N)(C)CC1=CC=C(O)C=C1 NHTGHBARYWONDQ-JTQLQIEISA-N 0.000 description 1
- ROHFNLRQFUQHCH-UHFFFAOYSA-N Leucine Natural products CC(C)CC(N)C(O)=O ROHFNLRQFUQHCH-UHFFFAOYSA-N 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 102100038816 Neuronatin Human genes 0.000 description 1
- AHLPHDHHMVZTML-UHFFFAOYSA-N Orn-delta-NH2 Natural products NCCCC(N)C(O)=O AHLPHDHHMVZTML-UHFFFAOYSA-N 0.000 description 1
- UTJLXEIPEHZYQJ-UHFFFAOYSA-N Ornithine Natural products OC(=O)C(C)CCCN UTJLXEIPEHZYQJ-UHFFFAOYSA-N 0.000 description 1
- 102100025757 Paternally-expressed gene 3 protein Human genes 0.000 description 1
- 229920001213 Polysorbate 20 Polymers 0.000 description 1
- 108010071390 Serum Albumin Proteins 0.000 description 1
- 102000007562 Serum Albumin Human genes 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- CDUUKBXTEOFITR-UHFFFAOYSA-N alpha-methylserine Natural products OCC([NH3+])(C)C([O-])=O CDUUKBXTEOFITR-UHFFFAOYSA-N 0.000 description 1
- 230000001174 ascending effect Effects 0.000 description 1
- 238000003149 assay kit Methods 0.000 description 1
- 210000000227 basophil cell of anterior lobe of hypophysis Anatomy 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 125000006367 bivalent amino carbonyl group Chemical group [H]N([*:1])C([*:2])=O 0.000 description 1
- 229940098773 bovine serum albumin Drugs 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 238000004422 calculation algorithm Methods 0.000 description 1
- 230000007211 cardiovascular event Effects 0.000 description 1
- 230000005779 cell damage Effects 0.000 description 1
- 208000037887 cell injury Diseases 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 239000002299 complementary DNA Substances 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 229940124301 concurrent medication Drugs 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 238000007405 data analysis Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000010511 deprotection reaction Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000003745 diagnosis Methods 0.000 description 1
- 235000013367 dietary fats Nutrition 0.000 description 1
- 238000002651 drug therapy Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000013613 expression plasmid Substances 0.000 description 1
- 238000013213 extrapolation Methods 0.000 description 1
- 125000005519 fluorenylmethyloxycarbonyl group Chemical group 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 238000002825 functional assay Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 108010036598 gastric inhibitory polypeptide receptor Proteins 0.000 description 1
- 229960003627 gemfibrozil Drugs 0.000 description 1
- MASNOZXLGMXCHN-ZLPAWPGGSA-N glucagon Chemical compound C([C@@H](C(=O)N[C@H](C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(O)=O)C(C)C)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)CC=1NC=NC=1)[C@@H](C)O)[C@@H](C)O)C1=CC=CC=C1 MASNOZXLGMXCHN-ZLPAWPGGSA-N 0.000 description 1
- 230000014101 glucose homeostasis Effects 0.000 description 1
- 108091005995 glycated hemoglobin Proteins 0.000 description 1
- 102000050325 human granulocyte inhibitory Human genes 0.000 description 1
- GRRNUXAQVGOGFE-NZSRVPFOSA-N hygromycin B Chemical compound O[C@@H]1[C@@H](NC)C[C@@H](N)[C@H](O)[C@H]1O[C@H]1[C@H]2O[C@@]3([C@@H]([C@@H](O)[C@@H](O)[C@@H](C(N)CO)O3)O)O[C@H]2[C@@H](O)[C@@H](CO)O1 GRRNUXAQVGOGFE-NZSRVPFOSA-N 0.000 description 1
- 229940097277 hygromycin b Drugs 0.000 description 1
- 238000000099 in vitro assay Methods 0.000 description 1
- MGXWVYUBJRZYPE-YUGYIWNOSA-N incretin Chemical class C([C@@H](C(=O)N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC=1NC=NC=1)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCCN)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC=1NC=NC=1)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCC(N)=O)C(O)=O)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CC=1C=CC(O)=CC=1)[C@@H](C)O)[C@@H](C)CC)C1=CC=C(O)C=C1 MGXWVYUBJRZYPE-YUGYIWNOSA-N 0.000 description 1
- 239000000859 incretin Substances 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 230000003914 insulin secretion Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- JYJIGFIDKWBXDU-MNNPPOADSA-N inulin Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)OC[C@]1(OC[C@]2(OC[C@]3(OC[C@]4(OC[C@]5(OC[C@]6(OC[C@]7(OC[C@]8(OC[C@]9(OC[C@]%10(OC[C@]%11(OC[C@]%12(OC[C@]%13(OC[C@]%14(OC[C@]%15(OC[C@]%16(OC[C@]%17(OC[C@]%18(OC[C@]%19(OC[C@]%20(OC[C@]%21(OC[C@]%22(OC[C@]%23(OC[C@]%24(OC[C@]%25(OC[C@]%26(OC[C@]%27(OC[C@]%28(OC[C@]%29(OC[C@]%30(OC[C@]%31(OC[C@]%32(OC[C@]%33(OC[C@]%34(OC[C@]%35(OC[C@]%36(O[C@@H]%37[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O%37)O)[C@H]([C@H](O)[C@@H](CO)O%36)O)[C@H]([C@H](O)[C@@H](CO)O%35)O)[C@H]([C@H](O)[C@@H](CO)O%34)O)[C@H]([C@H](O)[C@@H](CO)O%33)O)[C@H]([C@H](O)[C@@H](CO)O%32)O)[C@H]([C@H](O)[C@@H](CO)O%31)O)[C@H]([C@H](O)[C@@H](CO)O%30)O)[C@H]([C@H](O)[C@@H](CO)O%29)O)[C@H]([C@H](O)[C@@H](CO)O%28)O)[C@H]([C@H](O)[C@@H](CO)O%27)O)[C@H]([C@H](O)[C@@H](CO)O%26)O)[C@H]([C@H](O)[C@@H](CO)O%25)O)[C@H]([C@H](O)[C@@H](CO)O%24)O)[C@H]([C@H](O)[C@@H](CO)O%23)O)[C@H]([C@H](O)[C@@H](CO)O%22)O)[C@H]([C@H](O)[C@@H](CO)O%21)O)[C@H]([C@H](O)[C@@H](CO)O%20)O)[C@H]([C@H](O)[C@@H](CO)O%19)O)[C@H]([C@H](O)[C@@H](CO)O%18)O)[C@H]([C@H](O)[C@@H](CO)O%17)O)[C@H]([C@H](O)[C@@H](CO)O%16)O)[C@H]([C@H](O)[C@@H](CO)O%15)O)[C@H]([C@H](O)[C@@H](CO)O%14)O)[C@H]([C@H](O)[C@@H](CO)O%13)O)[C@H]([C@H](O)[C@@H](CO)O%12)O)[C@H]([C@H](O)[C@@H](CO)O%11)O)[C@H]([C@H](O)[C@@H](CO)O%10)O)[C@H]([C@H](O)[C@@H](CO)O9)O)[C@H]([C@H](O)[C@@H](CO)O8)O)[C@H]([C@H](O)[C@@H](CO)O7)O)[C@H]([C@H](O)[C@@H](CO)O6)O)[C@H]([C@H](O)[C@@H](CO)O5)O)[C@H]([C@H](O)[C@@H](CO)O4)O)[C@H]([C@H](O)[C@@H](CO)O3)O)[C@H]([C@H](O)[C@@H](CO)O2)O)[C@@H](O)[C@H](O)[C@@H](CO)O1 JYJIGFIDKWBXDU-MNNPPOADSA-N 0.000 description 1
- 229940029339 inulin Drugs 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 229940057428 lactoperoxidase Drugs 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004811 liquid chromatography Methods 0.000 description 1
- 239000012139 lysis buffer Substances 0.000 description 1
- 239000003550 marker Substances 0.000 description 1
- 238000004949 mass spectrometry Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002483 medication Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000010807 negative regulation of binding Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003538 oral antidiabetic agent Substances 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 229960003104 ornithine Drugs 0.000 description 1
- 210000001672 ovary Anatomy 0.000 description 1
- 230000001991 pathophysiological effect Effects 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 230000004141 reverse cholesterol transport Effects 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 230000009863 secondary prevention Effects 0.000 description 1
- 230000003248 secreting effect Effects 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- 239000007929 subcutaneous injection Substances 0.000 description 1
- 238000010254 subcutaneous injection Methods 0.000 description 1
- 230000002311 subsequent effect Effects 0.000 description 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical group C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
- NPDBDJFLKKQMCM-UHFFFAOYSA-N tert-butylglycine Chemical compound CC(C)(C)C(N)C(O)=O NPDBDJFLKKQMCM-UHFFFAOYSA-N 0.000 description 1
- HQHCYKULIHKCEB-UHFFFAOYSA-N tetradecanedioic acid Natural products OC(=O)CCCCCCCCCCCCC(O)=O HQHCYKULIHKCEB-UHFFFAOYSA-N 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/22—Hormones
- A61K38/26—Glucagons
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/22—Hormones
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
Definitions
- the present invention relates to the field of medicine.
- treatment methods for refractor ⁇ ' type 2 diabetes (T2D) in patients failing to reach recommended glucose targets with metformin and SGLT-2 treatment are provided.
- methods relating to increasing HDL-C levels in a patient in need thereof are provided.
- methods for lowering blood pressure in a patient in need thereof are provided.
- HbAlc Glycated hemoglobin
- ADA American Diabetes Association
- HbAlc Glycated hemoglobin
- ADA American Diabetes Association
- a patient with HbAlc less than or equal to 5.7% is considered normal glycemia.
- Patient treatment goals for HbAlc may vary by patient; however, persistently poorly controlled HbAlc contributes disproportionately to the development of complications associated with diabetes.
- Patients with type 2 diabetes often fail to achieve normal glycemia despite treatment using the ADA treatment paradigm.
- the ADA guidelines suggest a reasonable HbAlc treatment goal of less than or equal to 7% following current treatment options of diet, exercise, metformin, oral diabetes treatments, followed by basal insulin.
- Refractory type 2 diabetes is generally explained by an insulin secretory defect, or beta cell damage, becoming more and more profound with time, against a background of (relatively stable) insulin resistance. Patients living with type 2 diabetes for at least 8 years are more is likely to suffer from refractory type 2 diabetes. Therefore, there is a desire for a treatment method providing normal, or near normal glycemia, in a patient with refractory type 2 diabetes. There is a desire for a treatment method providing normal, or near normal glycemia, in a patient with refractory type 2 diabetes, wherein the patient has been treated for type 2 diabetes at least 8 years.
- High blood pressure is a risk factor for stroke, coronary heart disease (CHD), and other significant health threats.
- CHD coronary heart disease
- Many patients with type 2 diabetes and obesity experience high blood pressure; however, approved treatments for diabetes typically have little or no effect on controlling high blood pressure.
- treatment options There is a desire for treatment options to manage high blood pressure.
- Low serum levels of high-density lipoprotein cholesterol (HDL-C) is another known risk factor for coronary heart disease (CHD).
- CHD coronary heart disease
- Patients with type 2 diabetes often experience low serum levels of HDL-C; however, approved diabetes treatments generally fail to raise HDL-C.
- HDL-C is inversely and independently associated with the risk of developing CHD.
- a drug therapy to increase HDL-C levels.
- a treatment method to raise HDL-C in a patient with type 2 diabetes.
- the present invention provides methods for treating, preventing, or delaying high blood pressure, comprising administering a GIP/GLPl agonist or a pharmaceutically acceptable salt thereof.
- the present invention further provides methods for treating, preventing, or delaying high blood pressure in a patient diagnosed with type 2 diabetes, comprising administering a GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof.
- the present invention provides methods for treating, preventing, or delaying low HDL-C, comprising administering a GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof.
- the preset invention further provides methods for treating, preventing, or delaying HDL-C in a patient diagnosed with type 2 diabetes, comprising administering a GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof.
- the present invention provides methods for treating, preventing, or delaying refractory type 2 diabetes in a patient having type 2 diabetes for at least 8 years, comprising administering a GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof
- the present invention provides methods for treating refractory type 2 diabetes in a patient having type 2 diabetes for at least 8 years, comprising administering a GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof.
- the patient in need of treatment for refractory type 2 diabetes has an HbA1c of greater than 10%.
- the patient in need of treatment for refractory type 2 diabetes has an HbA1c of greater than 11%.
- the patient in need of treatment for refractory' type 2 diabetes has an HbAlc treatment goal of 5.7%. In an embodiment the patient in need of treatment for refractory type 2 diabetes has an HbAlc treatment goal of less than or equal to 5.7%. In an embodiment the patient in need of treatment for refractory type 2 diabetes has an HbA1c treatment goal of 6%.
- the patient in need of treatment for refractory type 2 diabetes has an HbA1c treatment goal of 7%.
- the present invention provides methods for treating refractory type 2 diabetes in a patient who is non-responsive to metformin, SGLT-2 or metformin plus an SGLT-2 inhibitor, comprising administering a GIP/GLP1 agonist, or a pharmaceutically acceptable salt thereof.
- an embodiment provides a method for treating, preventing, or delaying high blood pressure in a patient in need thereof, compri sing administering an effective amount of a GIP/GLPl agonist or a pharmaceutically acceptable salt thereof, to the patient once weekly.
- a further embodiment provides a method for treating high blood pressure in a patient diagnosed with type 2 diabetes, comprising administering an effective amount of a GIP/GLPl agonist or a pharmaceutically acceptable salt thereof, to the patient once weekly.
- the present invention provides a method of preventing or delaying high blood pressure in a patient, comprising administering a GIP/GLPl agonist in a therapeutically effective amount to the patient once weekly.
- the present invention provides a method of preventing or delaying high blood pressure in a patient diagnosed with type 2 diabetes, comprising administering a GIP/GLPl agonist in a therapeutically effective amount to the patient once weekly.
- the present invention provides use of a GIP/GLPl agonist for the preparation of a medicament for treating, preventing or delaying development of high blood pressure in a patient, wherein the medicament is administered once weekly.
- the present invention provides methods for treating, preventing or delaying high blood pressure, comprising administering an effective amount of a GIP/GLPl agonist, or a pharmaceutically acceptabl e salt thereof to a patient in need of such treatment.
- the patient in need of treatment for high blood pressure has type 2 diabetes and is non-obese.
- the patient in need of treatment for high blood pressure has type 2 diabetes and obesity. In an embodiment, the patient in need of treatment for high blood pressure has refractory type 2 diabetes.
- the patient in need of treatment for high blood pressure has type 2 diabetes for at least 8 years.
- an embodiment provides a method of treating, preventing or delaying development of hypertensive crisis in a patient with refractory type 2 diabetes, comprising administering an effective amount of a GIP/GLP1 agonist, or a pharmaceutically acceptable salt thereof, to the patient once weekly.
- the patient in need of treatment for hypertensive crisis has type 2 diabetes and is non-obese.
- the patient in need of treatment for hypertensive crisis has type 2 diabetes and obesity.
- the patient in need of treatment for hypertensive crisis has refractory type 2 diabetes.
- the patient in need of treatment for hypertensive crisis has type 2 diabetes for at least 8 years.
- an embodiment provides a method of treating, preventing or delaying development of low HDL-C in a patient, comprising administering an effective amount of a GIP/GLP1 agonist, or a pharmaceutically acceptable salt thereof, to the patient once weekly.
- the present invention provides a method of preventing or delaying hypertensive crisis in a patient, comprising administering an effective amount of a GIP/GLP1 agonist, or a pharmaceutically acceptable salt thereof, to the patient once weekly.
- the present invention provides a method of preventing or delaying low HDL-C in a patient, comprising administering an effective amount of a GIP/GLP1 agonist, or a pharmaceutically acceptable salt thereof, to the patient once weekly.
- the present invention provides a method of treating high blood pressure in a patient receiving clinical treatment for type 2 diabetes using oral anti diabetic agents for at least 1 year, 2 years, 3, year, 4 year or 5 years wherein the patient’s HbA1c is > 7%, comprising administering an effective amount of a GIP/GLP1 agonist, or a pharmaceutically acceptable salt thereof, to the patient once weekly.
- the present invention provides a method of improving glycemic control in a patient with type 2 diabetes mellitus and at risk for high blood pressure, comprising administering an effective amount of a GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, to the patient once weekly, wherein the method provides a reduction in the risk of the patient experiencing hypertensive crisis.
- the present invention provides a method of improving glycemic control in a patient with type 2 diabetes mellitus and at risk for high blood pressure, comprising administering an effective amount of a GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, to the patient once weekly for at least 30 weeks, wherein the method provides a reduction in the risk of the patient experiencing hypertensive crisis.
- the present invention provides a method of improving weight management in a patient with obesity and at risk for high blood pressure, comprising administering an effective amount of a GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, to the patient once weekly, wherein the method provides a reduction in the risk of the patient experiencing hypertensive crisis.
- the present invention provides a method for treating high blood pressure in patient, comprising administering an effective amount of a GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, to the patient once weekly, wherein the patient’s weight is within a normal weight range for the patient.
- the present invention provides a method of improving weight management in a patient with obesity and at risk for high blood pressure, comprising administering an effective amount of a GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, to the patient once weekly, wherein the method provides a reduction in the risk of the patient experiencing high blood pressure.
- a GIP/GLPl agonist for use in treating, preventing or delaying development of hypertensive crisis wherein the GIP/GLPl agonist is administered once weekly.
- a method provides a GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, for use in treating, preventing or delaying development of high blood pressure wherein the GIP/GLP1 agonist or pharmaceutically acceptable salt thereof is administered once weekly.
- an embodiment is the use of a GIP/GLP1 agonist, or a pharmaceutically acceptable salt thereof, for the preparation of a medicament for treating, preventing or delaying development of high blood pressure, wherein the medicament is administered once weekly.
- a GIP/GLP1 agonist for the preparation of a medicament for treating, preventing or delaying development of high blood pressure, wherein the medicament is administered once weekly.
- an embodiment is the use of a GIP/GLP1 agonist, or a pharmaceutically acceptable salt thereof, for the preparation of a medicament for treating, preventing or delaying development of hypertensive crisis, wherein the medicament is administered once weekly.
- a GIP/GLP1 agonist for the preparation of a medicament for treating, preventing or delaying development of hypertensive crisis, wherein the medicament is administered once weekly.
- the GIP/GLP1 agonist is described and claimed in W02020/023386 (Eli Lilly).
- hypertensive crisis means blood pressure is dangerously high and may threaten patient organs or life. Hypertensive crisis is typically blood pressure that is at least 180/120. High blood pressure is generally 130/80 systolic/diastolic pressure.
- refractory type 2 diabetes refers to a patient unable to achieve their HbA1c goal using oral standard of care medications, such as metformin.
- HbA1c goal means the desired average HbA1c level to be achieved by the patient, as determined by the patient’s clinical treatment plan, and as measured using clinically accepted methods.
- Current ADA guidelines suggest a reasonable HbA1c treatment goal of less than or equal to 7% following current treatment options of diet, exercise, metformin, oral diabetes treatments, followed by basal insulin.
- the HbA1c goal is 7% or less.
- the HbA1c goal is 5.7% or less.
- VA-HIT Veterans Administration HDL Intervention Trial
- treatment are meant to include slowing or attenuating the progression of a disease, condition or disorder. These terms also include alleviating, ameliorating, attenuating, eliminating, or reducing one or more symptoms of a disorder or condition, even if the disorder or condition is not actually eliminated and even if progression of the disorder or condition is not itself slowed or reversed.
- prevent prevent
- prevention prevention
- avoidance of the onset of a disease, condition, disorder or symptom are meant to include avoidance of the onset of a disease, condition, disorder or symptom.
- the terms “delay,” “delaying,” and the like are meant to include increasing the duration of time that occurs until onset of a disease, condition, disorder or symptom.
- the term “composite” refers to the first to occur of any of the outcomes.
- the term “increase HDL-C” means the measured HDL-C level increases from baseline. In an embodiment, increase HDL-C change is statistically significant increase. In an embodiment, increase HDL-C is greater than 2% increase from baseline. In an embodiment, increase HDL-C is greater than 5% increase from baseline. In an embodiment, increase HDL-C is greater than 7% increase from baseline. In an embodiment, increase HDL-C is greater than 10% increase from baseline.
- “Therapeutically effective amount” means the amount of GIP/GLP1 agonist, or a pharmaceutically acceptable salt thereof, for the methods and uses of the present invention, or pharmaceutical composition comprising a GIP/GLP agonist, or a pharmaceutically acceptable salt thereof, for the methods and uses of the present invention, that will elicit the biological or medical response of or desired therapeutic effect on the patient that is being sought by the researcher, medical doctor, or other clinician.
- An effective amount of GIP/GLP 1 agonist, or a pharmaceutically acceptable salt thereof may vary according to factors such as the disease state, age, sex, and weight of the individual, and the ability of GIP/GLP 1 agonist to elicit a desired response in the individual.
- an effective amount is also one in which any toxic or detrimental effect is outweighed by the therapeutically beneficial effects.
- the therapeutically effective amount of a GIP/GLP 1 agonist for use in the methods described herein is administered as an oral dosage form.
- the therapeutically effective amount of a GIP/GLP 1 agonist is administered once per day.
- the therapeutically effective amount of a GIP/GLP] agonist is administered twice per day.
- the therapeutically effective amount of a GIP/GLP 1 agonist is administered daily as an oral formulation.
- a method of improving glycemic control and increasing HDL- C, in a patient with type 2 diabetes mellitus comprising administering a GIP/GLP1 agonist, or a pharmaceutically acceptable salt thereof, in a therapeutically effective amount to the patient once weekly for at least 30 weeks.
- a GIP/GLP1 agonist, or a pharmaceutically acceptable salt thereof is administered for at least 40 weeks.
- a GIP/GLP1 agonist, or a pharmaceutically acceptable salt thereof is administered for at least 52 weeks.
- a method of treating, preventing or delaying development of high blood pressure in a patient comprising administering a GIP/GLP1 agonist, or a pharmaceutically acceptable salt thereof, in a therapeutically effective amount to the patient once weekly.
- the high blood pressure is selected from the group consisting of high blood pressure and hypertensive crisis.
- a method of preventing or delaying high blood pressure in a patient comprising administering a GIP/GLP1 agonist, or a pharmaceutically acceptable salt thereof, in a therapeutically effective amount to the patient once weekly.
- a method of preventing or delaying high blood pressure in a patient comprising administering a GIP/GLP1 agonist, or a pharmaceutically acceptable salt thereof, in a therapeutically effective amount to the patient in an oral dosage form.
- a method of improving glycemic control and treating, preventing or delaying high blood pressure in a patient in a patient diagnosed with type 2 diabetes mellitus comprising administering a GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, in a therapeutically effective amount to the patient once weekly.
- a method of improving glycemic control and treating, preventing or delaying high blood pressure in a patient in a patient diagnosed with type 2 diabetes mellitus comprising administering a GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, in a therapeutically effective amount to the patient in an oral dosage form.
- the method results in a reduction in the risk of the patient experiencing high blood pressure. In an embodiment, the method results in a reduction in the risk of the patient experiencing hypertensive crisis. In an embodiment, the method results in a reduction in the risk of the patient experiencing clinically low HDL-C.
- a method of improving glycemic control in a patient with type 2 diabetes mellitus comprising administering a GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, in a therapeutically effective amount to the patient once weekly, wherein the method results in a reduction in the risk of the patient experiencing high blood pressure.
- a method of any of the above embodiments wherein the once weekly administration of a GIP/GLP1 agonist continue for at least 40 weeks.
- the patient has one or more of: T2DM; high blood pressure; reduced HDL-C; and obesity.
- the patient has either: multiple cardiovascular risk factors without high blood pressure or clinically significant high blood pressure.
- the patient has either: multiple cardiovascular risk factors or HbA1c level above 11%.
- cardiovascular risk factors means risk for cardiovascular disease selected from the group consisting of: current tobacco use (any form of tobacco); use of at least 1 approved lipid modifying therapy to treat hypercholesterolemia or a documented untreated low-density lipoprotein cholesterol (LDL-C) >3.4 mmol/L (100 mg/dL) within the past 6 months; documented treated or untreated high-density lipoprotein cholesterol (HDL-C) ⁇ 1.0 mmol/L (40 mg/dL) for men and ⁇ 1.3 mmol/L (50 mg/dL) for women or triglycerides >2.3 mmol/L (150 mg/dL) within the past 6 months; use of at least 1 blood pressure medication to treat high blood pressure or untreated systolic blood pressure (SBP) >130mm Hg or diastolic blood pressure (DBP) >80 mmHg; measured waist circumference for a male 102 cm; for a female 88 cm.
- SBP high blood pressure or untreated systolic
- non-obese means a patient who is not obese by applicable standards.
- the non-obese patient has body mass index is less than 30 BMI.
- comorbid means that a patient is diagnosed with having 2 or more medical conditions.
- the patient’s risk of hypertensive crisis is reduced by at least about 14%. In an embodiment, the patient’s risk of hypertensive crisis is reduced by at least about 10%.
- the HDL-C levels are increased. In an embodiment, HDL-C levels are increased to a clinically desired level. In an embodiment, is a method of improving glycemic control and increasing HDL-C, in a patient with type 2 diabetes mellitus, comprising administering a GIP/GLP1 agonist, or a pharmaceutically acceptable salt thereof, in a therapeutically effective amount to the patient once weekly for at least 30 weeks.
- the risk of the occurrence of a composite of the following outcomes is reduced: hospitalization for high blood pressure or death.
- the risk of death or hospitalization for high blood pressure is reduced in a patient treated with an effective amount of a GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof.
- the risk of the occurrence of a composite of the following outcomes is reduced: high blood pressure and HbA1c above 5.7%. In an embodiment, the risk of the occurrence of a composite of the following outcomes is reduced: low HDL- C, high blood pressure, and HbA1c above 7%.
- the risk of the occurrence of a composite of the following outcomes is reduced: low HDL-C, high blood pressure and HbA1c above 5.7%.
- the risk of the occurrence of a composite of the following outcomes is reduced: low HDL-C, high blood pressure, and HbA1c above 6%.
- a method of reaching normal HbA1c glycemia in a patient with refractory type 2 diabetes comprising administering a GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, in a therapeutically effective amount to the patient once weekly.
- a GIP/GLPl agonist or a pharmaceutically acceptable salt thereof, is administered using a dose escalation protocol.
- the patient fails to achieve HbA1c ⁇ 7% using one or two oral diabetes agents for at least one year prior to treatment using a GIP/GLPl agonist, or pharmaceutically acceptable salt thereof.
- the patient fails to achieve HbA1c ⁇ 8% using one or two oral agents for at least one year prior to treatment using a GIP/GLPl agonist, or pharmaceutically acceptable salt thereof. In an embodiment, the patient fails to achieve HbA1c ⁇ 10% using one or two oral agents for at least one year prior to treatment using a GIP/GLP1 agonist, or pharmaceutically acceptable salt thereof.
- once weekly GIP/GLP1 agonist, or pharmaceutically acceptable salt thereof administration continues for at least 30 weeks. In an embodiment, once weekly GIP/GLPl agonist, or pharmaceutically acceptable salt thereof, administration continues for at least 40 weeks. In an embodiment, once weekly GIP/GLPl agonist, or pharmaceutically acceptable salt thereof, administration continues for at least 50 weeks. In an embodiment, once weekly GIP/GLPl agonist, or pharmaceutically acceptable salt thereof, administration continues for at least 2 years. In an embodiment, once weekly GIP/GLPl agonist, or pharmaceutically acceptable salt thereof, administration continues for at least 3 years. In an embodiment, once weekly GIP/GLPl agonist, or pharmaceutically acceptable salt thereof, administration continues for at least 5 years.
- the patient was diagnosed with type 2 diabetes at least 8 years prior to GIP/GLPl agonist, or pharmaceutically acceptable salt thereof, administration.
- the patient was diagnosed with type 2 diabetes at least 10 years prior to GIP/GLPl agonist, or pharmaceutically acceptable salt thereof, administration.
- the patient was diagnosed with type 2 diabetes at least 13 years prior to GIP/GLPl agonist, or pharmaceutically acceptable salt thereof, administration.
- the patient administered the GIP/GLPl agonist, or pharmaceutically acceptable salt thereof is at least 46 years old.
- the patient administered the GIP/GLPl agonist, or pharmaceutically acceptable salt thereof is at least 55 years old.
- the patient administered the GIP/GLPl agonist, or pharmaceutically acceptable salt thereof is at least 60 years old.
- the patient administered the GIP/GLPl agonist, or pharmaceutically acceptable salt thereof is also administered metformin and an SGLT2 oral agent.
- the patient administered the GIP/GLPl agonist, or pharmaceutically acceptable salt thereof is also administered an SGLT2 oral agent.
- the patient administered the GIP/GLP1 agonist, or pharmaceutically acceptable salt thereof is also administered metformin.
- the patient administered the GIP/GLP1 agonist, or pharmaceutically acceptable salt thereof is also administered a basal insulin.
- the patient administered the GIP/GLPl agonist, or pharmaceutically acceptable salt thereof is also administered metformin and a basal insulin.
- the patient administered the GIP/GLPl agonist, or pharmaceutically acceptable salt thereof is also administered an SGLT2 and a basal insulin.
- the patient administered the GIP/GLPl agonist, or pharmaceutically acceptable salt thereof is also administered metformin, an SGLT2, and a basal insulin.
- the basal insulin is insulin glargine.
- the basal insulin is insulin Degludec.
- the patient administered the GIP/GLPl agonist, or pharmaceutically acceptable salt thereof is also administered an SGLT2 oral pharmaceutical.
- the patient administered the GIP/GLPl agonist, or pharmaceutically acceptable salt thereof is also administered metformin, and 8GLT2 oral, and insulin Degludec.
- the patient administered the GIP/GLPl agonist, or pharmaceutically acceptable salt thereof is also administered metformin, and SGLT2 oral, and insulin Degludec.
- the patient administered the GIP/GLPl agonist, or pharmaceutically acceptable salt thereof is also administered metformin, an SGLT2 oral, and inulin glargine.
- the patient administered the GIP/GLPl agonist, or pharmaceutically acceptable salt thereof is also administered metformin and insulin glargine.
- the present invention provides a GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, for use in any of the above embodiments.
- the present invention provides use of a GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, in the preparation of a medicament for any of the above embodiments.
- the GIP/GLP l agonist is a compound of Formula I: R1X1X2X3GTX6TSDX10X11X12X13X14DX16X17AX19X20X21X22X23X24X25X26X27 X28X29X30X31 (SEQ ID NO:3) wherein:
- Ri is absent or an Ac modification of the N-terminal amino group
- Xi is selected from the group consisting of Y, H, D-Tyr, F, desH, and desY;
- X 2 is selected from the group consisting of Aib, aMeP, A, P, and D-Ala ; or Xi and X 2 combine to form desH- ///[NHCO]-Aib;
- X3 is selected from the group consisting of E, N, Aad, and cTA;
- X 6 is selected from the group consisting of F, aMeF, and aMeF(2F);
- X 10 is selected from the group consisting of A, L, H, 3Pal, 4Pal, V, Y, E, aMeF, aMeF(2F), I, aMeY, Q, D-His, D-Tyr, cTA, and K(2-[2-(2-amino-ethoxy)- ethoxy]-acetyl) 2 -(Y-Glu)-CO-(CH 2 )qC0 2 H;
- X 11 is selected from the group consisting of S, aMeS, and D-Ser;
- X 12 is selected from the group consisting of I, S, D-Ile, and K(2-[2-(2-amino- ethoxy)-ethoxy]-acetyl) 2 -(Y-Glu)-CO-(CH 2 )qC0 2 H;
- Xi 3 is selected from the group consisting of Me, Aib, L, aMeL, and K(2-[2-(2- amino-ethoxy)-ethoxy]-acetyl) 2 -(Y-Glu)-CO-(CH 2 )qC0 2 H;
- Xi 4 is selected from the group consisting of L and K, wherein K is conjugated to a C16-C22 fatty acid wherein said fatty acid is optionally conjugated to said K via a linker;
- Xi 6 is selected from the group consisting of K, E, Om, Dab, Dap, S, T, H, Aib, aMeK, R, and K(2-[2-(2-amino-ethoxy)-ethoxy]-acetyl) 2 -(Y-Glu)-CO-
- Xi 7 is selected from the group consisting of K, Q, I, and an amino acid conjugated to a C16-C22 fatty acid wherein said fatty acid is optionally conjugated to said amino acid via a linker;
- X 19 is selected from the group consisting of Q, A, and K(2-[2-(2-amino-ethoxy)- ethoxy]-acetyl) 2 -(y-Glu)-CO-(CH 2 )qC0 2 H;
- X20 is selected from the group consisting of Aib, Q, H, R, K, aMeK, and K(2-[2- (2-amino-ethoxy)-ethoxy]-acetyl) 2 -(y-Glu)-CO-(CH 2 )qC0 2 H;
- X21 is selected from the group consisting of H, Aad, D, Aib, T, A, E, I, and K(2- [2-(2-amino-ethoxy)-ethoxy]-acetyl) 2 -(y-Glu)-CO-(CH 2 )qC0 2 H;
- X22 is selected from the group consisting of F and aMeF;
- X23 is selected from the group consisting of I, L, A, G, F, H, E, V, and K(2-[2-(2- amino-ethoxy)-ethoxy]-acetyl) 2 -(y-Glu)-CO-(CH 2 )qC0 2 H;
- X24 is selected from the group consisting of S, Aad, D-Glu, E, Aib, H, V, A, Q, D, P, and K(2-[2-(2-amino-ethoxy)-ethoxy]-acetyl) 2 -(y-Glu)-CO-(CH 2 )qC0 2 H;
- X25 is selected from the group consisting of Y and aMeY;
- X26 is selected from the group consisting of L, aMeL, and K(2-[2-(2-amino- ethoxy)-ethoxy]-acetyl) 2 -(y-Glu)-CO-(CH 2 )qC0 2 H;
- X27 is selected from the group consisting of L, I, and K(2-[2-(2-amino-ethoxy)- ethoxy]-acetyl) 2 -(y-Glu)-CO-(CH 2 )qC0 2 H;
- X28 is selected from the group consisting of E, A, S, D-Glu, and K(2-[2-(2-amino- ethoxy)-ethoxy]-acetyl) 2 -(y-Glu)-CO-(CH 2 )qC0 2 H;
- X29 is selected from the group consisting of Aib, G, A, and K(2-[2-(2-amino- ethoxy)-ethoxy]-acetyl) 2 -(y-Glu)-CO-(CH 2 )qC0 2 H;
- X30 is selected from the group consisting of C, G, G-R2 and K(2-[2-(2-amino- ethoxy)-ethoxy]-acetyl) 2 -(y-Glu)-CO-(CH 2 )q-C0 2 H;
- X31 is absent or is selected from the group consisting of PX32X33X34-R2 (SEQ ID NO:4), PX32X33X34X35X36X37X38X39-R2 (SEQ ID NO:5) , PX32X33X34X35X36X37X38X39X40-R2 (SEQ ID NO:6) , K[(2-[2-(2-amino-ethoxy)- ethoxy]-acetyl) 2 -(Y-Glu)-CO-(CH 2 ) q -C0 2 H] X32X33X34-R2 (SEQ ID NO: 7) , K[(2-[2-amino-ethoxy)- ethoxy]-acetyl) 2 -(Y-Glu)-CO-(CH 2 ) q -C0 2 H] X32X33X34-R2 (SEQ ID NO: 7) , K[(2-[2-amino-ethoxy)- eth
- X32 is S or K[(2-[2-(2-amino-ethoxy)-ethoxy]-acetyl) 2 -(Y-Glu)-CO- (CH 2 ) q -C0 2 H];
- X33 is S or K[(2-[2-(2-amino-ethoxy)-ethoxy]-acetyl) 2 -(Y-Glu)-CO- (CH 2 ) q -C0 2 H];
- X34 is selected from the group consisting of G, C, and K[(2-[2-(2-amino- ethoxy)-ethoxy]-acetyl) 2 -(Y-Glu)-CO-(CH 2 )q-C0 2 H];
- X35 is A or K[(2-[2-(2-amino-ethoxy)-ethoxy]-acetyl) 2 -(Y-Glu)-CO- (CH 2 ) q -C0 2 H];
- X36 is P or K[(2-[2-(2-amino-ethoxy)-ethoxy]-acetyl) 2 -(Y-Glu)-CO- (CH 2 ) q -C0 2 H];
- X37 is P or K[(2-[2-(2-amino-ethoxy)-ethoxy]-acetyl) 2 -(Y-Glu)-CO- (CH 2 ) q -C0 2 H];
- X38 is P or K[(2-[2-(2-amino-ethoxy)-ethoxy]-acetyl) 2 -(Y-Glu)-CO- (CH 2 ) q -C0 2 H];
- X39 is selected from the group consisting of C, S, and K[(2-[2-(2-amino- ethoxy)-ethoxy]-acetyl) 2 -(Y-Glu)-CO-(CH 2 )q-C0 2 H];
- X40 is selected from the group consisting of C and K[(2-[2-(2-amino- ethoxy)-ethoxy]-acetyl) 2 -(Y-Glu)-CO-(CH 2 )q-C0 2 H]; q is selected from the group consisting of 14, 15, 16, 17, 18, 19, and 20; and R 2 is absent or a NH 2 modification of the C-terminal group; or a pharmaceutically acceptable salt thereof; wherein if X30 is G-R 2 , then X31 is absent; wherein no more than one of X10, Xi 2 , X13, X14, Xi6, X17, X19, X20, X21, X23, X24, X 26 , X 27 , X 28 , X 29 , X30, X31, X32, X33, X34, X35, X36, X37, X38, X39, and X40 may be
- the GIP/GLP1 agonist is a compound of Formula II, or pharmaceutically acceptable salt thereof, wherein:
- Xi7 is an amino acid conjugated to a C16-C22 fatty acid wherein said fatty acid is optionally conjugated to said amino acid via a linker; and X30 is selected from the group consisting of G-R2 and G; wherein if X 30 is G, then X 31 is selected from the group consisting of PX 32 X 33 X 34 - R 2 (SEQ ID NO: 4), wherein X 32 is S, X 33 is S and X 34 is G (SEQ ID NO: 15), and PX32X33X34X35X3 6 X37X3 8 X3 9 -R2 (SEQ ID NO: 5), wherein X32 is S, X33 is S, X 34 is G, X 35 is A, X 36 is P, X 37 is P, X 38 is P and X 39 is S (SEQ ID NO: 16) (hereafter a “Formula III” compound).
- a compound of Formula III or a pharmaceutically acceptable salt thereof, wherein the Xj ? amino acid is conjugated to the fatty acid via a linker (hereafter a “Formula Ilia” compound).
- the GIP/GLP1 agonist is a compound of Formula III and Ilia, or a pharmaceutically acceptable salt thereof, wherein:
- X10 is selected from the group consisting of A, L, H, 3 Pal, 4Pal, V, Y, E, aMeF, aMeF(2F), I, aMeY, Q, D-His, D-Tyr, and cTA;
- X12 is selected from the group consisting of I, S, and D-Ile;
- Xi 3 is selected from the group consisting of Me, Aib, L, and aMeL;
- Xi 4 is selected from the group consisting of L and K;
- Xi 6 is selected from the group consisting of K, E, Om, Dab, Dap, S, T, H, Aib, aMeK, and R;
- X 19 is selected from the group consisting of Q, and A;
- X20 is selected from the group consisting of Aib, Q, H, R, K, and aMeK;
- X21 is selected from the group consisting of H, Aad, D, Aib, T, A, E, and I;
- X 23 is selected from the group consisting of I, L, A, G, F, H, E, and V;
- X 24 is selected from the group consisting of S, Aad, D-Glu, E, Aib, H, V, A, Q, D, and P;
- X26 is selected from the group consisting of L, and aMeL;
- X 27 is selected from the group consisting of L, and I;
- X 28 is selected from the group consisting of E, A, S, and D-Glu;
- X 29 is selected from the group consisting of Aib, G, and A;
- X 30 is selected from the group consisting of G and G-R 2 ; wherein if X 30 is G; then X 31 is selected from the group consisting of PX 32 X 33 X 34 - R 2 (SEQ ID NO: 4), wherein X 32 is S, X 33 is S and X 34 is G (SEQ ID NO: 15) and PX32X33X34X35X3 6 X37X38X3 9 -R2 (SEQ ID NO:5), wherein X32 is S, X33 is S, X 34 is G, X 35 is A, X 36 is P, X 37 is P, X 38 is P and X 39 is S (SEQ ID NO: 16) (hereafter a “Formula Illb” compound).
- the GIP/GLP1 agonist is a compound of Formula III, or pharmaceutically acceptable salt thereof, wherein:
- Xi 7 is K conjugated to a C 16 -C 22 fatty acid wherein said fatty acid is optionally conjugated to said amino acid via a linker.
- the GIP/GLP1 agonist is a compound of Formula III, or pharmaceutically acceptable salt thereof, wherein:
- Xi Y
- X 2 is Aib
- X 3 is E
- X 10 is selected from the group consisting of A, L, H, 3Pal, 4Pal, V, and Y;
- X 11 is S
- Xi4 is L
- Xi 6 is selected from the group consisting of K, E, Om, Dab, and Dap;
- Xi 7 is K conjugated to a C 16 -C 22 fatty acid wherein said fatty acid is optionally conjugated to said amino acid via a linker;
- Xi9 is Q
- X20 is Aib
- X 21 is selected from the group consisting of H, Aad, D, Aib, T, A, and E;
- X22 is F
- X23 is I;
- X24 is selected from the group consisting of S, Aad, D-Glu, and E;
- X26 is L
- X 28 is selected from the group consisting of E and A.
- the GIP/GLP1 agonist is a compound of Formula III, or pharmaceutically acceptable salt thereof, wherein:
- Xi Y
- X2 is Aib
- X 3 is E
- X 6 is aMeF(2F);
- Xjo is selected from the group consisting of Y, 4-Pal, and V;
- Xu is S
- X 12 is I
- Xi 3 is selected from the group consisting of L, Aib, and aMeL;
- Xi4 is L
- Xi 6 is selected from the group consisting of E, K, and Om;
- Xu is K conjugated to a C 16 -C 22 fatty acid wherein said fatty acid is optionally conjugated to said amino acid via a linker,
- Xi9 is Q
- X20 is Aib
- X 21 is selected from the group consisting of E, A, and T;
- X22 is F
- X24 is D-Glu
- X 25 is selected from the group consisting of Y and ⁇ MeY;
- X26 is L
- X29 is G
- X30 is G
- X31 is PX32X33X34X35X36X37X38X39-R2 (SEQ ID NO:5), wherein X32 is S, X33 is S, X34 is G, X35 is A, X 36 is P, X37 is P, X 38 is P, X39 is S (SEQ ID NO: 16).
- the GIP/GLP1 agonist is a compound of Formula III, Ilia and Illb, or a pharmaceutically acceptable salt thereof, wherein X1 ⁇ 2 is Orn, XB is aMeL, and X 25 is Y.
- the GIP/GLP1 agonist is a compound of Formula III, Ilia and Illb, or a pharmaceutically acceptable salt thereof, wherein C 1 ⁇ 2 is E, Xn is aMeL, and X 25 is Y.
- the GIP/GLP1 agonist is a compound of Formula III, Ilia and Illb, or a pharmaceutically acceptable salt thereof, wherein X1 ⁇ 2 is E, XB is aMeL, X 10 is Y, and X 25 is aMeY.
- the GIP/GLPl agonist is a compound of Formula III, Ilia and Illb, or a pharmaceutically acceptable salt thereof, wherein C 1 ⁇ 2 is Orn, Xj 3 is aMeL, X 10 is 4Pal, and X 25 is Y.
- the GIP/GLPl agonist is a compound of Formula I selected from the group consisting of SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO: 13, and SEQ ID NO: 14, or a pharmaceutically acceptable salt thereof.
- the GIP/GLPl agonist is a compound of Formula I, or a pharmaceutically acceptable salt thereof, wherein Xi is selected from the group consisting of Y, F, and D-Tyr; Xr, is F; and X13 is selected from the group consisting of Aib, L, and aMeL.
- the GIP/GLPl agonist is a compound of Formula I, or a pharmaceutically acceptable salt thereof, wherein Riis absent; Xi is selected from the group consisting of Y, F, and D-Tyr; Xe is F; X 13 is selected from the group consisting of Aib, L, and aMeL; X 2 is Aib; X 3 is E; X 10 is Y; Xu is S; X 12 is I; X 14 is L; C 1 ⁇ 2 is selected from the group consisting of K, E, Orn, Dab, Dap, S, T, H, Aib, aMeK, and R; X 17 is an amino acid conjugated to a C 16 -C 22 fatty acid wherein said fatty acid is optionally conjugated to said amino acid via a linker; X 19 is Q; X 20 is selected from the group consisting of Aib, Q, H, and K; X 21 is selected from the group consisting of H,
- the GIP/GLP1 agonist is a compound of Formula I, or a pharmaceutically acceptable salt thereof, wherein Xi is selected from the group consisting of Y, F, and D-Tyr; Xr, is F; and X 13 is selected from the group consisting of Aib, L, and aMeL; X 28 is A; X 29 G; X 30 is G; X31 is PX 32 X33X34X35X36X37X38X39-R2 (SEQ ID NO:5); X 34 is G; and X 39 is S .
- the GIP/GLP1 agonist is a compound of Formula I, or a pharmaceutically acceptable salt thereof, wherein Xi is selected from the group consisting of Y and D-Tyr; and X 13 is aMeL.
- the GIP/GLP1 agonist is a compound of Formula I selected from the group consisting of SEQ ID NO:21, SEQ ID NO: 22, SEQ ID NO:23, SEQ ID NO:24, SEQ ID NQ:25, and SEQ ID NO:26, or a pharmaceutically acceptable salt thereof
- the GIP/GLP1 agonist is a compound of Formula VI X1X2EGTX6TSDX10X11X12X13LDX16X17AQX20X21X22IX24X25LIX28GX30 (SEQ ID NO:27) wherein
- Xi is selected from the group consisting of Y and RiY;
- Ri is an Ac modification of the N-terminal amino group
- X 6 is selected from the group consisting of ⁇ MeF and aMeF(2F);
- X 10 is selected from the group consisting of 4Pal, Y, aMeF, aMeF(2F), aMeL, aMeV, Ac4c, Ac5c, Ac6c, Bip, INal, 2Nal, OMeY, hTyr, Me, V, 4CPhe, ChG, ChA, Bzt, 2FA, 4TAA, 2TA, 3TA, and KZ 1 ;
- X 11 is selected from the group consisting of S, aMeS, Aib, G, Dap, Ac5c, and Tie;
- X 12 is selected from the group consisting of I and KZ 1 ;
- Xi 3 is selected from the group consisting of aMeL and aMeF;
- Xi 6 is Orn
- Xi 7 is selected from the group consisting of Q, I, and KZ 1 ;
- X 20 is selected from the group consisting of Aib, Orn, 4Pal, aMeF, Ac5c, and Ac6c;
- X 21 is selected from the group consisting of E, KZ 1 , G, Orn, and 4Pal;
- X 22 is selected from the group consisting of F, 2ClPhe, 3ClPhe, 2FPhe, 3FPhe, 3,5FPhe, INal, 2Nal, aMeF(2F), ChA, Bzt, and aMeF;
- X 24 is selected from the group consisting of D-Glu, E, G, and KZ 1 ;
- X 25 is selected from the group consisting of Y, aMeY, aMeF, and KZ 1 ;
- X 28 is selected from the group consisting of E, Orn, and KZ 1 ;
- X 30 is selected from the group consisting of G, Orn, KZ 1 , K(Z I )R 6 , OrnR 2 , and GR 2 ;
- R 2 is selected from the group consisting of X 31 , X 3i SSG(SEQ ID NO:28), X 31 SSG-R 3 (SEQ ID NO:29), X 31 SSGX 35 PPPX 39 (SEQ ID NO:30), X31SSGX35PPPX39R3 (SEQ ID NO:31), X31SSGX35PPPX39X40 (SEQ ID NO:32), X 31 SSGX 35 PPPX 39 X 40 R 3 (SEQ ID NO:33), and a modification of the c-terminal group wherein the modification is NEE;
- R 6 is selected from the group consisting of PSSG(SEQ ID NO:34), PSSG-R 3 (SEQ ID NO:35), PSSGX35PPPX39 (SEQ ID NO:36), PS SGX35PPPX39R3 (SEQ ID NO:37), PSSGX35PPPX39X40 (SEQ ID NO:38), P S S GX 35 PPPX39X40R3 (S
- X 31 is selected from the group consisting of P and KZ 1 ;
- X 35 is selected from the group consisting of A and Orn;
- X 39 is selected from the group consisting of S and Orn;
- X40 is KZ 1 ;
- R 3 is a modification of the C-terminal group, wherein the modification is NEE; wherein two, and only two, of X10, X12, X 17 , X21, X24, X25, X28, X30, X31, and X40 are KZ 1 or K(ZI)R 6 ;
- Zi is selected from the group consisting of R 5 and -R 4 R 5 ;
- R 4 is a linker; and R 5 is a fatty acid; or a pharmaceutically acceptable salt thereof.
- Xi is selected from the group consisting of Y and RiY;
- Ri is an Ac modification of the N-terminal amino group
- X 2 is Aib
- X 6 is selected from the group consisting of aMeF and aMeF(2F);
- X 10 is selected from the group consisting of 4Pal, Y, aMeF, aMeF(2F), aMeL, aMeV, Ac4c, Ac5c, Ac6c, Bip, INal, 2Nal, OMeY, hTyr, Nle, V, 4CPhe, ChG, ChA, Bzt, 2FA, 4TAA, 2TA, 3TA, and KZ 1 ;
- X 11 is selected from the group consisting of Ac5c, S, aMeS, Aib, G, Dap, and Tie;
- X 12 is selected from the group consisting of I and KZ 1 ;
- Xi 3 is selected from the group consisting of aMeL and aMeF;
- Xi6 is Orn;
- X 17 is selected from the group consisting of Q, I, and KZ 1 ;
- X 20 is selected from the group consisting of Aib, Orn, 4Pal, aMeF, Ac5c, and Ac6c;
- X 21 is selected from the group consisting of E, KZ 1 , G, Orn, and 4Pal;
- X 22 is selected from the group consisting of F, 2ClPhe, 3ClPhe, 2FPhe, 3FPhe, 3,5FPhe, INal, 2Nal, aMeF(2F), ChA, Bzt, and aMeF;
- X 24 is selected from the group consisting of D-Glu, E, G, and KZ 1 ;
- X 25 is selected from the group consisting of Y, aMeY, aMeF, and KZ 1 ;
- X 28 is selected from the group consisting of E, Orn, and KZ 1 ;
- X 30 is selected from the group consisting of G, Orn, KZ 1 , and GR 2 ;
- R 2 is selected from the group consisting of X 3i SSG(SEQ ID NO:28), X 31 SSG-R 3 (SEQ ID NO:29), X31SSGX35PPPX3 9 (SEQ ID NO:30), X 31 S SGX35PPPX39R3 (SEQ ID NO:31), X 31 S S GX 35 PPPX 39 X 40 (SEQ ID NO:32), X 31 SSGX 35 PPPX 39 X 40 R 3 (SEQ ID NO:33), and a modification of the c-terminal group wherein the modification is NEE;
- X 31 is selected from the group consisting of P and KZ 1 ;
- X 35 is selected from the group consisting of A and Orn;
- X 39 is selected from the group consisting of S and Orn;
- X40 is KZ 1 ;
- R 3 is a modification of the C-terminal group, wherein the modification is NFE; wherein two, and only two, of X1 0 , X12, X 17 , X21, X24, X25, X28, X30, X 31 , and X40 are KZ 1 ;
- Zi is selected from the group consisting of R 5 and -R 4 R 5 ; and R 4 is a linker;
- R 5 is a fatty acid; or a pharmaceutically acceptable salt thereof.
- the GIP/GLP1 agonist is a peptide of Formula VI, or a pharmaceutically acceptable salt thereof, wherein Zi is selected from the group consisting of
- the GIP/GLP1 agonist is a peptide of Formula I, or a pharmaceutically acceptable salt thereof, wherein Zi is selected from the group consisting of
- the GIP/GLP1 agonist is a peptide of Formula VI, or a pharmaceutically acceptable salt thereof, wherein Zi is selected from the group consisting of
- the GIP/GLP1 agonist is a compound of Formula VI, or a pharmaceutically acceptable salt thereof, wherein R5 is selected from the group consisting of
- the GIP/GLP1 agonist is a compound of Formula VI, or a pharmaceutically acceptable salt thereof, wherein R5 is selected from the group consisting of
- the GIP/GLP1 agonist is a compound of Formula VI, or a pharmaceutically acceptable salt thereof, wherein R4 is selected from the group consisting of
- the GIP/GLP1 agonist is a compound of Formula VI, or a pharmaceutically acceptable salt thereof, wherein R 4 is selected from the group consisting of
- the GIP/GLP1 agonist is a compound of Formula VI, or a pharmaceutically acceptable salt thereof, wherein X 17 and X 31 are each KZ 1 .
- the GIP/GLP1 agonist is a compound of Formula VI, or a pharmaceutically acceptable salt thereof, wherein Xn and X 24 are each KZ 1 .
- the GIP/GLP1 agonist is a compound of Formula VI, or a pharmaceutically acceptable salt thereof, wherein X17 and X 21 are each KZ 1 .
- the GIP/GLPl agonist is a compound of Formula VI, or a pharmaceutically acceptable salt thereof, wherein X 17 and X 28 are each KZ 1 .
- the GIP/GLPl agonist is a compound of Formula VI, or a pharmaceutically acceptable salt thereof, wherein X 17 and X 40 are each KZ 1 . In an embodiment, the GIP/GLPl agonist is a compound of Formula VI, or a pharmaceutically acceptable salt thereof, wherein X 21 and X 40 are each KZ 1 . In an embodiment, the GIP/GLPl agonist is a compound of Formula VI, or a pharmaceutically acceptable salt thereof, wherein X 21 and X 28 are each KZ 1 . In an embodiment, the GIP/GLPl agonist is a compound of Formula VI, or a pharmaceutically acceptable salt thereof, wherein X 24 and X 28 are each KZ 1 .
- the GIP/GLPl agonist is a compound of Formula VI, or a pharmaceutically acceptable salt thereof, wherein Xi is Y; Xe is aMeF(2F); X 10 is selected from the group consisting of 4Pal, Y, and KZ 1 ; X 17 is selected from the group consisting of S, aMeS, and Aib; X 12 is I; X 13 is aMeL; C 1 ⁇ 2 is Om; X 17 is selected from the group consisting of I and KZ 1 ; X 20 is Aib; X 21 is selected from the group consisting of KZ 1 and E; X 22 is selected from the group consisting of F and aMeF; X 24 is selected from the group consisting of D-Glu and KZ 1 ; X 25 is aMeY; X 28 is selected from the group consisting of E and KZ 1 ; X 30 is selected from the group consisting of G and GIG; R 2 is selected from the group consisting
- the GIP/GLPl agonist is a compound of Formula VI, or a pharmaceutically acceptable salt thereof, wherein the compound is selected from the group consisting of Y-Aib-EGT-aMeF(2F)-TSD-4Pal-SI-aMeL-LD-Orn-K((2-[2-(2-Amino-ethoxy)- ethoxy]-acetyl) 2 -(y-Glu)-CO-(CH 2 )i 2 -C0 2 H)AQ-Aib-EFI-(D-Glu)-aMeY- LIEGGK((2-[2-(2- Ami no-ethoxy )-ethoxy]-acetyl)2-(y-Glu)-CO-(CH2) i2- C0 2 H)SSGAPPPS-NH 2 (SEQ ID NO:41),
- the GIP/GLP1 agonist is a compond wherein the IQ linker is one to two amino acids selected from the group consisting of eK and y-Glu.
- the IG linker comprises from one to three (2-[2-(2-Amino-ethoxy)-ethoxy]- acetyl) moieties.
- the GIP/GLP1 agonist is a compound wherein the FG fatty acid moieties are conjugated to a lysine via an IG linker between the lysine and the IG fatty acid.
- the GIP/GLPl agonist is a compound of Formula VI, or a pharmaceutically acceptable salt thereof, wherein the IG linker comprises from zero to four amino acids; and from zero to three (2-[2-(2-Amino-ethoxy)-ethoxy]-acetyl) moieties.
- the GIP/GLPl agonist is a compound wherein the IG linker comprises from one to three amino acids each independently selected from the group consisting of eK and g-Glu.
- the GIP/GLP1 agonist is a compound of Formula VI, or a pharmaceutically acceptable salt thereof, wherein the R 4 linker comprises from one to two amino acids each independently selected from the group consisting of eK and g-Glu.
- the GIP/GLP1 agonist is a compound of Formula VI, or a pharmaceutically acceptable salt thereof, comprising two Zi fatty acid moieties wherein each R 5 fatty acid of the Zi moiety is conjugated to different lysines of the peptide via an R 4 linker wherein, the R 4 linker comprises from zero to two g-Glu amino acid residues.
- the GIP/GLP1 agonist is a compound of Formula VI, or a pharmaceutically acceptable salt thereof, comprising two Zi fatty acid moieties wherein each R 5 fatty acid of the Zi is conjugated to different lysines of the peptide via an R 4 linker wherein R 4 comprises from one to three amino acids and from one to three (2-[2-(2-Amino-ethoxy)-ethoxy]-acetyl) moieties.
- the GIP/GLPl agonist is a compound of Formula VI, or a pharmaceutically acceptable salt thereof, comprising two of the same Zi fatty acid moieties wherein the R 5 fatty acid of the Zi is each conjugated to a different lysine of the peptide via an R 4 linker wherein, R 4 comprises from one to three amino acids each independently selected from the group consisting of eK and x-Glu; and from one to three (2-[2-(2-Amino-ethoxy)-ethoxyj- acetyl) moieties attached to the amino acid.
- the GIP/GLPl agonist is a Formula VI compound, or a pharmaceutically acceptable salt thereof, comprising two of the same Zi fatty acid moieties wherein the R 5 fatty acid of the Zi is each conjugated to different lysines of the peptide via an R 4 linker wherein R 4 comprises up to three amino acids each independently selected from the group consisting of g-Glu and eK attached to one or two (2-[2-(2-Amino-ethoxy)-ethoxy]-acetyl) moieties.
- the GIP/GLPl agonist is a Formula VI compound, or a pharmaceutically acceptable salt thereof, comprising two of the same Zi fatty acid moieties wherein the R 5 fatty acid of the Zi is each conjugated via an R 4 linker, wherein the R 4 linker has the following formula:
- al is selected from the group consisting of 0, 1, and 2; a2 is selected from the group consisting of 0, 1, and 2; a3 is selected from the group consisting of 0, 1, 2, and 3; bl is 0 or 1; and b2 is 0 or 1.
- the GIP/GLPl agonist is a Formula VI compound, or a pharmaceutically acceptable salt thereof, comprising two of the same Zi fatty acid moieties wherein the R 5 fatty acid of the Zi is each conjugated via an R 4 linker wherein Zi is of the formula:
- a GIP/GLP1 agonist wherein al is 1, a2 is 0, a3 is 2, bl is 0, b2 is 1, and q is 12; and the structure is:
- the GIP/GLP1 agonist is a Formula VI compound, or a pharmaceutically acceptable salt thereof, comprising two of the same Zi fatty acid moieties wherein the R 5 fatty acid of the Zi is each conjugated via an R 4 linker, wherein the R 4 linker and R 5 fatty acid components have the following formula: group consisting of 7, 8, 10, 11, and 12.
- the GIP/GLP1 agonist is a Formula VI compound, or a pharmaceutically acceptable salt thereof, comprising two of the same Zi fatty acid moieties wherein the R 5 fatty acid of the Zi is each conjugated via an R 4 linker, wherein the R 5 fatty acid is selected from the group consisting of -(7-(4- carboxyphenoxy jheptanoyl ) and -(8-(4-carboxyphenoxy)octanoyl).
- the GIP/GLP1 agonist is a Formula VI compound, or a pharmaceutically acceptable salt thereof, comprising two of the same Zi fatty acid moieties each conjugated via an R 4 linker, wherein the R5 fatty acid is selected from the group consisting of -(10-(4- carboxyphenoxy)decanoyl), -(4-(4-iodophenyl)butanoyl), and -(4-(4-tert- butylphenyl)butanoyl).
- the GIP/GLP1 agonist is a Formula VI compound, or a pharmaceutically acceptable salt thereof, comprising two of the same Zi fatty acid moieties each conjugated via an R4 linker, wherein the R5 fatty acid is selected from the group consisting of -CO-(CH2)i4-CH3 , -CO-(CH2)i2-CH3, and -CO-(CH2)IO-CH3 .
- the GIP/GLP1 agonist is a Formula VI compound, or a pharmaceutically acceptable salt thereof, comprising two of the same Zi fatty acid moieties each conjugated via an R4 linker, wherein the R5 fatty acid is selected from the group consisting of -C0-(CH 2 )i 2 -C0 2 H and -CO-(CH 2 )10-CO 2 H.
- the GIP/GLPl agonist is a Formula VI compound, or a pharmaceutically acceptable salt thereof, comprising two of the same Zi fatty acid moieties each conjugated via an R4 linker, wherein the R5 fatty acid is selected from the group consisting of -CO-(CH2) IO - CH 3 and -CO-(CH 2 )i2-CH 3.
- the GIP/GLPl agonist is a compound wherein a R5 fatty acid is selected from the group consisting of -C0-(CH2)i2-C02H, -CO-(CH2) IO -C02H, -(10-(4- carboxyphenoxy jdecanoyl ), -(4-(4-iodophenyl)butanoyl), -(4-(4 -tert- butylphenyljbutanoyl), -CO-(CH 2 )i4-CH 3, -CO-(CH 2 )i2-CH 3 , -CO-(CH 2 )IO-CH 3, -(7-(4- carboxyphenoxy jheptanoyl ), and -(8-(4-carboxyphenoxy)octanoyl).
- a R5 fatty acid is selected from the group consisting of -C0-(CH2)i2-C02H, -CO-(CH2) IO -
- Certain GIP/GLPl agonist compounds are generally effective over a wide dosage range. For example, dosages for once weekly parenteral dosing may fall within the range of 0.05 mg to about 30 mg per person per week.
- GLP-1 is a 36 amino acid peptide, the major biologically active fragment of which is produced as a 30-amino acid, C-terminal amidated peptide (GLP-I7-36) (SEQ ID NO:2).
- GIP is a 42 amino acid peptide (SEQ ID NO: 1), which, like GLP-1, is also known as an incretin, and plays a physiological role in glucose homeostasis by stimulating insulin secretion from pancreatic beta cells in the presence of glucose.
- a GIP/GLPl agonist compounds have desirable GIP and GLP receptor activity wherein the GIP agonist potency is from 2.5 to 5 times the GLP1 receptor potency as measured by the casein cAMP assay described herein below, wherein the potency is normalized against native GIP and GLP on the day the assay is run.
- a GIP/GLPl agonist compounds have desirable GIP and GLP receptor activity wherein the GIP agonist potency is from 2.5 to 10 times the GLP1 receptor potency as measured by the casein cAMP assay, wherein the potency is normalized against native GIP and GLP on the day the assay is run.
- amino acid means both naturally occurring amino acids and unnatural amino acids.
- L leucine
- alpha-methyl substituted residues of natural amino acids e.g., a-methyl leucine, or aMeL and a-methyl lysine, or aMeK
- alpha amino isobutyric acid or “Aib,” “4Pal,” “Ora,” and the like.
- Ora means ornithine.
- 4Pa!” means 3-(4-Pyridyl)-L- alanine.
- aMeF(2F) means alpha-methyl 2-F -phenylalanine.
- aMeY means alpha methyl tyrosine, alpha methyl lysine, and alpha methyl leucine, respectively.
- each of “e” and “D-Glu” means D-glutamic acid.
- each of “D-His” and “h” means D-histidine.
- each of “D-Tyr” and “y” means D-tyrosine.
- each of “D-Ser” and “s” means D-serine.
- each of “D-Ala” and “a” means D-alanine.
- “aMeF(2F)” means alpha-methyl-F(2F) and alpha-methyl-Phe(2F).
- “aMeF” means alpha-methyl -F and alpha-methyl -Phe.
- aMeY means alpha-methyl -Tyr.
- aMeK means alpha-methyl-Lys.
- aMeL means alpha-methyl-Leu.
- aMeS means alpha- methyl-serine and alpha-methyl-Ser.
- ⁇ MeP means alpha-methyl- proline and alpha-methyl-Pro.
- desH means desHis.
- desY means desTyr.
- AEEA means (2-[2-(2-Amino-ethoxy)-ethoxy]-acetyl) ;
- AEEA2 means (2-[2-(2-Amino-ethoxy)-ethoxy]-acetyl)2;
- AEEA3 means (2-[2- (2-Amino-ethoxy)-ethoxy]-acetyl)3.
- Alkyl is 6-Aminohexanoyl-; “Aoc” is 8-Aminooctanoyl-;
- PEG3 is [3-(2-[2-(2-Amino-ethoxy)-ethoxy]-ethoxy)-propanoyl]-;
- PEG4 is (3-[2-(2- [2-(2-Amino-ethoxy)-ethoxy]-ethoxy)-ethoxy]-propanoyl)-;
- PEG5 is [3-(2-[2-(2-[2-(2-(2-(2- Amino-ethoxy)-ethoxy]-ethoxy)-ethoxy]-ethoxy)-propanoyl]-;
- PEG6 is (3-[2-(2- [2-(2-(2-(2-Amino-ethoxy)-ethoxy]-ethoxy]-ethoxy]-propanoyl)-.
- Tie is tert-Leucine.
- the terms “activity,” “activatejsj” “activat[ing]” and the like refers to the capacity of a compound, or a pharmaceutically acceptable salt thereof, to bind to and induce a response at the receptor(s), as measured using assays known in the art, such as the in vitro assays described below.
- the affinity of GIP/GLP1 agonist compounds, or pharmaceutically acceptable salts thereof, for each of the GIP and GLP-1 receptors may be measured using techniques known for measuring receptor binding levels in the art, including, for example those described in the examples below, and is commonly expressed as a Ki value.
- the activity of the GIP/GLP1 agonist compounds at each of the receptors may also be measured using techniques known in the art, including for example the in vitro activity assays described below, and is commonly expressed as an EC 50 value, which is the concentration of compound causing half-maximal simulation in a dose response curve
- the GIP/GLP1 agonist is a compound, or a pharmaceutically acceptable salt thereof, wherein the compound is a potent GIPR/GLP-IR dual agonist that is a partial agonist on the GLP-1R as demonstrated by a Cell Membrane Guanosine 5'- (gamma-thio) Triphosphate-[ 35 S] (GTPyS) Binding Assay, and a partial agonist on the GLP-1R as demonstarted by a P-arrestin-2 recruitment assay.
- the compound is a potent GIPR/GLP-IR dual agonist that is a partial agonist on the GLP-1R as demonstrated by a Cell Membrane Guanosine 5'- (gamma-thio) Triphosphate-[ 35 S] (GTPyS) Binding Assay, and a partial agonist on the GLP-1R as demonstarted by a P-arrestin-2 recruitment assay.
- the GIP/GLPl agonist is a compound, or pharmaceutically acceptable salt thereof, wherein the compound stimulates GLP-1R induced activation of Ga s in the GLP-1R HEK293 Cell Membrane Guanosine 5'-(gamma-thio) Triphosphate- [ 35 S] (GTPyS) Binding Assay.
- the GIP/GLP1 agonist is a compound showing partial agonism of 75% or less in the GLP-1R HEK293 Cell Membrane Guanosine 5'-(gamma-thio) Triphosphate- [ 35 S] (GTPyS) Binding Assay, and 35% or less in the GLP-CHO Cell b- Arrestin. Recruitment Assay.
- a GIP/GLP1 agonist means a compound showing 35% or less in the GLP-CHO Cell b-Arrestin.
- the term “effective amount” refers to the amount or dose of a compound of the present invention, or a pharmaceutically acceptable salt thereof, which, upon single or multiple dose administration to the patient, provides the desired effect in the patient under diagnosis or treatment.
- An effective amount can be determined by a person of skill in the art using known techniques and by observing results obtained under analogous circumstances.
- a number of factors are considered, including, but not limited to: the species of mammal: its size, age, and general health; the specific disease or disorder involved; the degree of or involvement or the severity of the disease or disorder; the response of the individual patient; the particular compound administered; the mode of administration; the bioavailability characteristics of the preparation administered; the dose regimen selected; the use of concomitant medication; and other relevant circumstances.
- EDT A means ethylenediaminetetraacetic acid.
- DMSO means dimethyl sulfoxide.
- CPM means counts per minute.
- IBMX 3-isobutyl-l-methylxanthine.
- LC/MS liquid chromatography/mass spectrometry.
- HTRF homogeneous time-resolved fluorescence.
- BSA bovine serum albumin.
- estimates refers to- efficacy and treatment- regimen - evaluated to determine the efficacy of a GIP/GLP1 agonist due to requirements by certain regulatory agencies.
- the efficacy estimand is used to evaluate results in people prior to their discontinuation of study drug or initiating rescue therapy for persistent severe hyperglycemia.
- present invention provides the following:
- Embodiment 1 A GIP/GLP1 agonist, or a pharmaceutically acceptable salt thereof, for use in the treatment of refractory type 2 diabetes in a patient, wherein the GIP/GLP1 agonist, or a pharmaceutically acceptable salt thereof, is administered once weekly.
- Embodiment 2 A GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, for use in the treatment of high blood pressure in a patient, wherein the GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, is administered once weekly.
- Embodiment 3 A GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, for use in raising HDL-C in a patient, wherein the GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, is administered once weekly.
- Embodiment 4. A GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, for use according to any one of embodiments 1 to 3, wherein the patient has type 2 diabetes for at least 8 years.
- Embodiment 5 A GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, for use according to any one of embodiments 1 to 4, wherein the patient HbA1c goal is less than 7%.
- Embodiment 6 A GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, for use according to any one of embodiments 1 to 5, wherein the patient HbA1c goal is equal to or less than 5.7%.
- Embodiment 7 A GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, for use according to any one of embodiments 1 to 6, wherein the patient HbA1c is greater than 10%.
- Embodiment 8 A GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, for use according to any one of embodiments 1 to 7, wherein the patient HbA1c is greater than 11%.
- Embodiment 9. A GIP/GLP1 agonist, or a pharmaceutically acceptable salt thereof, for use according to any one of embodiments 1 to 8, wherein the patient age is at least 46 years.
- Embodiment 10 A GIP/GLP1 agonist, or a pharmaceutically acceptable salt thereof, for use according to any one of embodiments 1 to 9, wherein the patient age is at least 60 years old.
- Embodiment 11 A GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, for use according to any one of embodiments 1 to 10, wherein the patient is taking an SGLT2 inhibitor.
- Embodiment 12 A GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, for use according to any one of embodiments 1 to 11, wherein the patient is taking metformin.
- Embodiment 13 A GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, for use according to any one of embodiments 1 to 12, wherein the patient is not administered a basal insulin.
- Embodiment 14 A GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, for use according to any one of embodiments 1 to 13, wherein the patient fails to reach their HbA1c goal while taking metformin and an SGLT2 inhibitor.
- Embodiment 15 A GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, for use according to any one of embodiments 1 to 14, wherein the GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, is administered for at least 40 weeks.
- Embodiment 16 A GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, for use according to any one of embodiments 1 to 15, wherein the GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, is administered for at least 50 weeks.
- Embodiment 17 A GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, for use according to any one of embodiments 1 to 16, wherein the GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, is administered for at least 2 years.
- Embodiment 18 A GIP/GLP1 agonist, or a pharmaceutically acceptable salt thereof, for use according to any one of embodiments 1 to 17, wherein the patient is non-ob ese.
- Embodiment 19 A GIP/GLP1 agonist, or a pharmaceutically acceptable salt thereof, for use according to any one of embodiments 1 to 18, wherein the patient has comorbid high blood pressure.
- Embodiment 20 A GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, for use according to any one of embodiments 1 to 19, wherein the patient has comorbid low HDL-C.
- Embodiment 21 A GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, for use according to any one of embodiments 1 to 17 or 19 to 20, wherein the patient has comorbid obesity.
- Embodiment 22 A GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, for use according to any one of embodiments 1 to 21, wherein the patient has at least two cardiovascular risk factors.
- Embodiment 23 A GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, for use according to any one of embodiments 1 to 21, wherein the patient has no cardiovascular risk factors.
- Embodiment 24 A GIP/GLPl agonist, or a pharmaceutically acceptable salt thereof, for use according to any one of embodiments 1 to 23, wherein the patient has type 2 diabetes for at least 10 years.
- Example 1 Clinical Trial using a GIP/GLPl Agonist
- the enrollment criteria set forth in Table 1 below, are designed to include participants who are similar to patients seen within a typical diabetes practice, and include some patient with type 2 diabetes that is refractory to oral treatment. Geriatric patients are included. Study continues for 52 weeks.
- the study is designed to consist of a screening visit followed by a single-blind 3- week placebo run-in period. Afterwards, patients are randomized to GIP/GLP1 agonist (dosed using an escalation dose protocol) or insulin degludec (standard titration protocol) and followed at approximately monthly intervals. Patients receiving insulin degludec follow standard insulin degludec titration protocol during the study. Study protocol includes blood pressure measurement at each visit and serum lipid profile at study initiation and at 52 weeks using standard clinical methods.
- the mean dose of insulin degludec at 52 weeks is about 48 units per day.
- a greater percent of patients randomized to GIP/GLP1 agonist achieve an HbA1c of less than 7 percent, the American Diabetes Association’s recommended target for people with diabetes, or less than 5.7 percent - the level seen in people without diabetes - than patients randomized to insulin degludec.
- Example 2 Clinical Trial using a GIP/GLP1 agonist
- the enrollment criteria set forth in Table 2 below, include patients considered refractory to type 2 diabetes oral treatment; however, oral diabetes treatment continues through the study. Study continues for 40 weeks.
- the study is designed to consist of a screening visit followed by a 3-week run-in period. Afterwards, patients begin a 40-week randomized, double-blind study with a GIP/GLP1 agonist or placebo, as add-on to their previous treatment with insulin glargine with or without metformin. Insulin glargine dose was titrated throughout the study using a validated treat-to-target algorithm’. Patients are followed at approximately weekly intervals, then approximately monthly. Study protocol includes blood pressure measurement at each visit and serum lipid profile at study initiation and at 40 weeks using standard clinical methods.
- the study shows doses of a GIP/GLPl agonist can be useful for HbA1c reduction and weight reduction from baseline compared to placebo as an add-on to titrated insulin glargine with or without metformin in adults with type 2 diabetes using the clinical trial dosing.
- Example 3 Clinical Trial using a GIP/GLPl agonist This study is a 4-week multiple ascending dose study investigating the safety and tolerability of the GIP/GLPl agonist of Example 7 administered as 4 once-weekly subcutaneous injections in patients with Type 2 Diabetes compared with placebo. Prespecified safety parameters to be studied include blood pressure.
- the study includes 4 cohorts for treatment with the GIP/GLPl agonist.
- Cohorts 1 and 2 receive 4 fixed doses of 0.3 mg or 1 mg, respectively.
- Cohorts 3 and 4 receive weekly doses in stepwise increments as shown in Table 3.
- Criteria are established to enroll patients whose glycemic control is not well controlled on diet and exercise or stable dose of metformin. Baseline demographics of patients enrolled are provided below in Table 4.
- Table 4 Baseline demographics.
- SEQ ID NO: 10 The structure of SEQ ID NO: 10 is depicted below using the standard single letter amino acid codes with the exception of residues Aib2, aMeF(2F)6, aMeL13, K17, Aib20, D-Glu24, and Ser39 where the structures of these amino acid residues have been expanded:
- the peptide backbone of Example 4 is synthesized using Fluorenylmetliyloxycarbonyl (Fmoc)/tert-ButyI (t-Bu) chemistry on a Symphony X peptide synthesizer (Gyros Protein Technologies. Arlington, AZ).
- the resin consists of 1% DVB cross-linked polystyrene (F moc-Rink-MBHA Low Loading resin, 100-200 mesh, EMD Millipore) at a substitution of 0.3-0.4 meq/g.
- Standard side-chain protecting groups were used. Fmoc-Lys(Mtt)-OH is used for the lysine at position 17 and Boc-Tyr(tBu) ⁇ OH) was used for the tyrosine at position 1. Fmoc groups are removed prior to each coupling step (2 x 7 minutes) using 20% piperidine in DMF. All standard amino acid couplings are performed for 1 hour to a primary amine and 3 hour to a secondary amine, using an equal molar ratio of Fmoc amino acid (0.3 mM), diisopropylcarbodiimide (0.9 mM) and Oxyma (0.9 mM), at a 9-fold molar excess over the theoretical peptide loading.
- the peptide resin is washed with DCM, and then thoroughly air-dried.
- the dry resin is treated with 10 raL of cleavage cocktail (trifluoroacetic acid: water: triisopropylsilane, 95:2.5:2.5 v/v) for 2 hours at room temperature.
- the resin is filtered off, washed twice each with 2 rnL of neat T ’ FA, and the combined filtrates are treated with 5-fold excess volume of cold diethyl ether (-20°C) to precipitate the crude peptide.
- the peptide/ether suspension is then centrifuged at 3500 rpm for 2 min to form a solid pellet, the supernatant is decanted, and the solid pellet is triturated with ether two additional times and dried in vacuo.
- the crude peptide is solubilized in 20% acetonitrile/20%Acetic acid/60%water and purified by RP- HPLC on a Luna 5 ⁇ m Phenyl-Hexyl preparative column (21 x 250 mm, Pbenomenex) with linear gradients of 100% acetonitrile and 0.1% TF A/water buffer system (30-50% acetonitrile in 60 min).
- the purity of peptide is assessed using analytical RP-HPLC and pooling criteria is >95%.
- the main pool purity of compound 1 is found to be 98.0%. Subsequent lyophilization of the final main product pool yielded the lyophilized peptide TFA sail.
- SEQ ID NO: 11 The structure of SEQ ID NO: 11 is depicted below using the standard single letter amino acid codes with the exception of residues Aib2, aMeF(2F)6, aMeL13, Ornl6, K17, Aib20 D-Glu24, and Ser39 where the structures of these amino acid residues have been expanded:
- the compound according to SEQ ID NO: 11 is prepared substantially as described by the procedures of Example 4.
- Example 6 is a compound represented by the following description:
- SEQ ID NO: 12 The structure of SEQ ID NO: 12 is depicted below using the standard single letter amino acid codes with the exception of residues Aib2, aMeF(2F)6, aMeL13, Ornl6, K17, Aib20, D-Glu24, and Ser39, where the stmctures of these amino acid residues have been expanded:
- the compound according to SEQ ID NO: 12 is prepared substantially as described by the procedures of Example 4.
- SEQ ID NO: 13 The structure of SEQ ID NO: 13 is depicted below using the standard single letter amino acid codes with the exception of residues Aib2, aMeF(2F)6, 4PallO, aMeL13, Oml6, K17, Aib20, D-Glu24 aMeY25, and Ser39, where the structures of these amino acid residues have been expanded:
- the compound according to SEQ ID NO: 13 is prepared substantially as described by the procedures of Example 4.
- the molecular weight is determined by LC- MS (obsd: M+3
- SEQ ID NO: 14 The structure of SEQ ID NO: 14 is depicted below using the standard single letter amino acid codes with the exception of residues Aib2, aMeF(2F)6, aMeL13, Oml 6, K17, Aib20, D-Glu24,aMeY25, and Ser39, where the structures of these amino acid residues have been expanded:
- SEQ ID N0:21 The structure of SEQ ID N0:21 is depicted below using the standard single letter amino acid codes with the exception of residues Aib2, K17, Aib20, and Ser39, where the structures of these amino acid residues have been expanded:
- the compound according to SEQ ID NO:21 is prepared substantially as described by the procedures of Example 4.
- SEQ ID NO:22 The structure of SEQ ID NO:22 is depicted below using the standard single letter amino acid codes with the exception of residues Aib2, aMeL13, K17, Aib20, and Ser39, where the structures of these amino acid residues have been expanded:
- the compound according to SEQ ID NO:22 is prepared substantially as described by the procedures of Example 4.
- SEQ ID NO:23 The structure of SEQ ID NO:23 is depicted below using the standard single letter amino acid codes with the exception of residues D-Tyrl, Aib2, aMeL13, K17, Aib20, and Ser39, where the structures of these amino acid residues have been expanded:
- the compound according to SEQ ID NO:23 is prepared substantially as described by the procedures of Example 4.
- SEQ ID NO:24 The structure of SEQ ID NO:24 is depicted below using the standard single letter amino acid codes with the exception of residues D-Tyrl, Aib2, aMeL13, Oml6, K17, Aib20, D-Glu24, and Ser39, where the structures of these amino acid residues have been expanded:
- the compound according to SEQ ID NO:24 is prepared substantially as described by the procedures of Example 4.
- SEQ ID NO:25 The structure of SEQ ID NO:25 is depicted below using the standard single letter amino acid codes with the exception of residues D-Tyrl, Aib2, aMeL13, K17, Aib20, aMeY25, and Ser39, where the structures of these amino acid residues have been expanded:
- the compound according to SEQ ID NO:25 is prepared substantially as described by the procedures of Example 4.
- the molecular weight is determined by LC- MS (obsd: M+3
- SEQ ID NO:26 The structure of SEQ ID NO:26 is depicted below using the standard single letter amino acid codes with the exception of residues D-Tyrl, Aib2, aMeL13, Oml6, K17, Aib20, aMeY25, and Ser39, where the structures of these amino acid residues have been expanded:
- the compound according to SEQ ID NO:26 is prepared substantially as described by the procedures of Example 4.
- SEQ ID NO:41 The structure of SEQ ID NO:41 is depicted below using the standard single letter amino acid codes with the exception of residues Aib2, aMeF(2F)6, 4PallO, aMeL13, Oml6, K17, Aib20, D-Glu24, aMeY25, K31 and Ser39, where the structures of these amino acid residues have been expanded:
- Example 15 The peptide backbone of Example 15 is synthesized using Fluorenylmethyloxycarbonyl (Fmoc)/tert-Butyl (t-Bu) chemistry on a Symphony multiplex peptide synthesizer (Gyros Protein Technologies. Arlington, A Z).
- the resin consists of 1% DVB cross-linked polystyrene (Fmoc-Rink-MBHA Low Loading resin, 100-200 mesh, EMD Millipore) at a substitution of 0.35 mmol/g. Standard side-chain protecting groups were used.
- Fmoc-Lys(Mtt)-OH is used for the lysine residues at positions 17 and 31, and Boc-Tyr(tBu)-OH was used for the tyrosine residue at position 1.
- Fmoc groups are removed prior to each coupling step (2 x 7 minutes) using 20% piperidine in DMF.
- the Mtt protecting groups on the lysine residues at positions 17 and 31 are selectively removed from the peptide resin using 30% hexafluoroisopropanol (Oakwood Chemicals) in DCM (3 x 1 hour treatments), and the resin is thoroughly washed with DCM and DMF.
- linker moieties Sub sequent attachment of the linker moieties is accomplished by stepwise coupling of 2-[2-(2-Fmoc-amino-ethoxy)-ethoxy]-acetic acid (Fmoc-AEEA-OH, ChemPep, Inc.) and Fmoc-glutamic acid a-t-butyl ester (Fmoc-Glu-OtBu, Ark Pharm, Inc.), following the procedures described above for standard coupling and deprotection reactions.
- Fmoc-AEEA-OH 2-[2-(2-Fmoc-amino-ethoxy)-ethoxy]-acetic acid
- Fmoc-Glu-OtBu Fmoc-Glu-OtBu
- the resin is filtered off, washed twice each with 2 mL of neat TFA, and the combined filtrates are treated with 5-fold excess volume of cold diethyl ether (-20°C) to precipitate the crude peptide.
- the peptide/ether suspension is then centrifuged at 3500 rpm for 2 min to form a solid pellet, the supernatant is decanted, and the solid pellet is triturated with ether two additional times and dried in vacuo.
- the crude peptide is solubilized in 20 mL of 20% acetonitrile/20%acetic acid/60%water and purified by RP- HPLC on a SymmetryPrep 7 ym C18 preparative column (19 x 300 mm, Waters) with linear gradients of 100% acetonitrile and 0.1% TF A/water buffer system (35-55% acetonitrile in 60 min).
- the purity of peptide is assessed using analytical RP-HPLC and pooling criteria is >95%.
- the main pool purity of Example 14 is found to be 96.0%.
- Subsequent lyophilization of the final main product pool yielded the lyophilized peptide TFA salt.
- SEQ ID NO: 17 The structure of SEQ ID NO: 17 is depicted below using the standard single letter amino acid codes with the exception of residues Aib2, aMeF(2F)6, 4PallO, aMeL13, Oml6, K17, Aib20, D-Glu24, aMeY25, K31 and Ser39, where the structures of these amino acid residues have been expanded:
- the compound according to SEQ ID NO: 17 is prepared substantially as described by the procedures of Example 15, except 4-(9-carboxy-nonyloxy)benzoic acid tert- butyl ester (WuXi AppTec, Shanghai, China) was used in the final coupling step.
- the compound according to SEQ ID NO: 18 is prepared substantially as described by the procedures of Example 15, except 4-(4-Iodophenyl)butyric acid (WuXi AppTec, Shanghai, China) was used in the final coupling step.
- SEQ ID NO: 19 The structure of SEQ ID NO: 19 is depicted below using the standard single letter amino acid codes with the exception of residues Aib2, aMeF(2F)6, 4PallO, aMeL13, Oml6, K17, Aib20, D-Glu24, aMeY25, K31 and Ser39, where the structures of these amino acid residues have been expanded:
- the compound according to SEQ ID NO: 19 is prepared substantially as described by the procedures of Example 15, except 4-(4-tert-Butylphenyl)butyric acid (WuXi AppTec, Shanghai, China) was used in the final coupling step.
- SEQ ID NO: 19 The structure of SEQ ID NO: 19 is depicted below using the standard single letter amino acid codes with the exception of residues Aib2, aMeF(2F)6, 4PallO, aMeL13, Oml6, K17, Aib20, D-Glu24, aMeY25, K31 and Ser39, where the structures of these amino acid residues have been expanded:
- the compound according to SEQ ID NO: 19 is prepared substantially as described by the procedures of Example 15, except Why acid (Sigma Aldrich) was used in the final coupling step.
- Glucagon (referred to as Gcg) is a Reference Standard prepared at Eli Lilly and Company.
- GLP-1, 7-36-NH 2 (referred to as GLP-1) is obtained from CPC Scientific (Sunnyvale, CA, 97.2% purity, 100 mM aliquots in 100% DMSO).
- GIP 1-42 (referred to as GIP) is prepared at Lilly Research Laboratories using peptide synthesis and HPLC chromatography as described above (>80% purity, 100 mM aliquots in 100% DMSO).
- [ 125 I]-radiolabeled Gcg, GLP-1, or GIP is prepared using [ 125 I]-lactoperoxidase and obtained from Perkin Elmer (Boston, MA).
- Stably transfected cell lines are prepared by subcloning receptor cDNA into a pcDNA3 expression plasmid and transfected into human embryonic kidney (HEK) 293 (hGcgR and hGLP-lR) or Chinese Hamster Ovary (CHO) (hGIPR) cells followed by selection with Geneticin (hGLP-lR and hGIPR) or hygromycin B (hGcgR).
- HEK human embryonic kidney
- hGcgR and hGLP-lR human embryonic kidney
- hGIPR Chinese Hamster Ovary cells
- Method 1 Frozen cell pellets are lysed on ice in hypotonic buffer containing 50 mM Tris HC1, pH 7.5, and Roche CompleteTM Protease Inhibitors with EDTA.
- the cell suspension is disrupted using a glass Potter-Elvehjem homogenizer fitted with a Teflon ® pestle for 25 strokes.
- the homogenate is centrifuged at 4°C at 1100 x g for 10 minutes.
- the supernatant is collected and stored on ice while the pellets are resuspended in homogenization buffer and rehomogenized as described above.
- the homogenate is centrifuged at 1100 x g for 10 minutes.
- the second supernatant is combined with the first supernatant and centrifuged at 35000 x g for 1 hour at 4°C.
- the resulting membrane pellet is resuspended in homogenization buffer containing protease inhibitors at approximately 1 to 3 mg/mL, quick frozen in liquid nitrogen and stored as aliquots in a - 80°C freezer until use.
- Method 2 Frozen cell pellets are lysed on ice in hypotonic buffer containing 50 mM Tris HC1, pH 7.5, 1 mM MgCl 2 , Roche CompleteTM EDTA-free Protease Inhibitors and 25 units/ml DNAse I (Invitrogen).
- the cell suspension is disrupted using a glass Potter-Elvehjem homogenizer fitted with a Teflon ® pestle for 20 to 25 strokes.
- the homogenate is centrifuged at 4°C at 1800 x g for 15 minutes. The supernatant is collected and stored on ice while the pellets are resuspended in homogenization buffer (without DNAse I) and rehomogenized as described above.
- the homogenate is centrifuged at 1800 x g for 15 minutes.
- the second supernatant is combined with the first supernatant and centrifuged an additional time at 1800 x g for 15 minutes.
- the overall supernatant is then centrifuged at 25000 x g for 30 minutes at 4°C.
- the resulting membrane pellet is resuspended in homogenization buffer (without DNAse I) containing protease inhibitors at approximately 1 to 3 mg/mL and stored as aliquots in a -80°C freezer until use.
- the equilibrium binding dissociation constants (K d ) for the various receptor/radioligand interactions are determined from homologous competition binding analysis instead of saturation binding due to high propanol content in the [ 125 I] stock material.
- the K d values determined for the receptor preparations were as follows: hGcgR (3.9 nM), hGLP-lR (1.2 nM) and hGIPR (0.14 nM). r 125 Il -Glucagon Binding
- the human Gcg receptor binding assays are performed using a Scintillation Proximity Assay (SPA) format with wheat germ agglutinin (WGA) beads (Perkin Elmer).
- the binding buffer contains 25 mM 4-(2-hydroxyethyl)-l-piperazineethanesulfonic acid (HEPES), pH 7.4, 2.5 mM CaCl 2 , 1 mM MgCl 2 , 0.1% (w/v) bacitracin (Research Products), 0.003% (w/v) Poly oxy ethyl enesorbitan monolaurate (TWEEN ® -20), and Roche CompleteTM Protease Inhibitors without EDTA.
- Peptides and Gcg are thawed and 3 -fold serially diluted in 100% DMSO (10 point concentration response curves).
- 5 pL serially diluted compound or DMSO is transferred into Coming ® 3632 clear bottom assay plates containing 45 pL assay binding buffer or unlabeled Gcg control (non-specific binding or NSB, at 1 pM final).
- 50 pL human GcgR membranes 1.5 pg/well
- 50 pL of WGA SPA beads 80 to 150 pg/well
- the binding buffer contains 25 mM HEPES, pH 7.4, 2.5 mM CaCE, 1 mM MgCE, 0.1% (w/v) bacitracin, 0.003% (w/v) TWEEN ® -20, and Roche CompleteTM Protease Inhibitors without EDTA.
- Peptides and GLP-1 are thawed and 3 -fold serially diluted in 100% DMSO (10 point concentration response curves).
- 5 ⁇ L serially diluted compound or DMSO is transferred into Corning ® 3632 clear bottom assay plates containing 45 pL assay binding buffer or unlabeled GLP-1 control (non-specific binding or NSB, at 0.25 pM final).
- the human GIP receptor binding assay is performed using an SPA format with WGA beads.
- the binding buffer contains 25 mM HEPES, pH 7.4, 2.5 mM CaCE, 1 mM MgCE, 0.1% (w/v) bacitracin, 0.003% (w/v) TWEEN ® -20, and Roche CompleteTM Protease Inhibitors without EDTA.
- Peptides and GIP are thawed and 3 fold serially diluted in 100% DMSO (10 point concentration response curves).
- 5 pL serially diluted compound or DMSO is transferred into Corning ® 3632 clear bottom assay plates containing 45 pL assay binding buffer or unlabeled GIP control (non-specific binding or NSB, at 0.25 pM final).
- Raw CPM data for concentration curves of peptides, Gcg, GLP-1, or GIP are converted to percent inhibition by subtracting nonspecific binding (binding in the presence of excess unlabeled Gcg, GLP-1, or GIP, respectively) from the individual CPM values and dividing by the total binding signal, also corrected by subtracting nonspecific binding.
- Data are analyzed using four-parameter (curve maximum, curve minimum, IC 50 , Hill slope) nonlinear regression routines (Genedata Screener, version 12.0.4, Genedata AG, Basal, Switzerland).
- Geometric Mean io(Arithmetic Mean of Log Ki Values)
- the Ki Ratio (Ki for native control peptide/Ki for test compound) at each receptor and each species is calculated.
- the Ki Ratio is a rapid indication of the apparent affinity of a peptide compared to the native control peptide.
- a Ki Ratio ⁇ 1 indicates that the test peptide has a lower affinity (higher Ki value) for the receptor than the native peptide, whereas a Ki Ratio >1 indicates that the test peptide has a higher affinity (lower Ki value) for the receptor than the native peptide.
- GLP-1R human GLP-1 receptor
- GIPR gastric inhibitory peptide receptor
- GcgR Glucagon receptor
- Pharmacological activity of the hGLPlR/GIPR peptides are determined in HEK293 cells stably expressing the human GLP-1 receptor (GLP-1R), gastric inhibitory peptide receptor (GIPR), or GLP-2 receptor (GLP-2R).
- Each receptor over expressing cell line (20 m ⁇ ) is treated with the test peptide in DMEM (Gibco Cat# 31053) supplemented with 0.1% Casein (Sigma Cat# C4765), 250 mM IBMX, IX GlutaMAXTM (Gibco Cat# 35050), and 20 mM HEPES (HyClone Cat# SH30237.01) in a 20 m ⁇ assay volume. After 60 minute incubation at room temperature, the resulting increase in intracellular cAMP is quantitatively determined using the CisBio cAMP Dynamic 2 HTRF Assay Kit (62AM4PEJ).
- the Lysis buffer containing cAMP-d2 conjugate (20 m ⁇ ) and the antibody anti-cAMP-Eu3+-Cryptate (20 m ⁇ ) are then added to determine the cAMP level.
- HTRF signal is detected with an Envision 2104 plate reader (PerkinElmer). Fluorescent emission at 620 nm and at 665 nm is measured and the ratio between 620 nm and at 665 nm is calculated and then are converted to nM cAMP per well using a cAMP standard curve.
- Dose response curves of compounds are plotted as the percentage of stimulation normalized to minimum (buffer only) and maximum (maximum concentration of each control ligand) values and analyzed using a four parameter non-liner regression fit with a variable slope (Genedata Screener 13).
- EC50 is the concentration of compound causing half-maximal simulation in a dose response curve.
- a relative EC50 value is derived by non-linear regression analysis using the percent maximal response vs. the concentration of peptide added, fitted to a four- parameter logistic equation.
- Example and comparator molecules are conducted to determine the intrinsic potency of Example and comparator molecules performed in the presence of casein (instead of serum albumin) as a nonspecific blocker, which does not interact with the fatty acid moieties of the analyzed molecules.
- Intracellular cAMP levels are determined by extrapolation using a standard curve. Dose response curves of compounds are plotted as the percentage of stimulation normalized to minimum (buffer only) and maximum (maximum concentration of each control ligand) values and analyzed using a four parameter non-linear regression fit with a variable slope (Genedata Screener 13). EC50 is the concentration of compound causing half-maximal simulation in a dose response curve. Each relative EC50 value for the Geometric mean calculation is determined from a curve fitting.
- Concentration response curves of compounds are plotted as the percentage of stimulation normalized to minimum (buffer only) and maximum (maximum concentration of each control ligand) values and analyzed using a four parameter nonliner regression fit with a variable slope (Genedata Screener 13).
- EC50 is the concentration of compound causing half-maximal simulation in a dose response curve.
- the EC50 summary statistics are computed as follows:
- GM 10 A (arithmetic mean of logio transformed EC50 values).
- the log transform accounts for the EC50 values falling on a multiplicative, rather than an arithmetic scale.
- test peptides are run plus the native ligands GIP and GLP-1, buffer only as baseline (minimum) and the highest concentration of the respective GIP and GLP-1 standard is used as maximum for calculations.
- the test peptide is tested in 8 runs of the assay.
- hGIP amide and hGLP-1 amide EC50 in Table 3 are illustrative of geometric mean values from a series of 18 assay values, and values will vary each day compared to the zero buffer. Accordingly, each Example will use the geometric mean of those values to normalize the Example assay runs.
- Example compounds stimulate cAMP from human GLP-1R and GIPR in the presence of 0.1% casein.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Diabetes (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Endocrinology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Zoology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Epidemiology (AREA)
- Immunology (AREA)
- Gastroenterology & Hepatology (AREA)
- Emergency Medicine (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
Abstract
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA3208873A CA3208873A1 (fr) | 2021-02-17 | 2022-02-02 | Procedes therapeutiques agonistes doubles gip/glp1 |
CN202280015672.2A CN117320740A (zh) | 2021-02-17 | 2022-02-02 | Gip/glp1双重激动剂治疗方法 |
EP22706153.8A EP4294423A1 (fr) | 2021-02-17 | 2022-02-02 | Procédés thérapeutiques agonistes doubles gip/glp1 |
JP2023549546A JP2024508745A (ja) | 2021-02-17 | 2022-02-02 | Gip/glp1デュアルアゴニスト治療方法 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US202163150408P | 2021-02-17 | 2021-02-17 | |
US63/150,408 | 2021-02-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2022177744A1 true WO2022177744A1 (fr) | 2022-08-25 |
Family
ID=80449178
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2022/014971 WO2022177744A1 (fr) | 2021-02-17 | 2022-02-02 | Procédés thérapeutiques agonistes doubles gip/glp1 |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP4294423A1 (fr) |
JP (1) | JP2024508745A (fr) |
CN (1) | CN117320740A (fr) |
CA (1) | CA3208873A1 (fr) |
WO (1) | WO2022177744A1 (fr) |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2016111971A1 (fr) * | 2015-01-09 | 2016-07-14 | Eli Lilly And Company | Composés co-agonistes de gip et de glp-1 |
WO2020023386A1 (fr) | 2018-07-23 | 2020-01-30 | Eli Lilly And Company | Composés co-agonistes de gip/glp1 |
WO2020023388A1 (fr) * | 2018-07-23 | 2020-01-30 | Eli Lilly And Company | Procédé d'utilisation d'un co-agoniste de gip/glp1 contre le diabète |
WO2020023382A1 (fr) * | 2018-07-23 | 2020-01-30 | Eli Lilly And Company | Procédés d'utilisation d'un co-agoniste de gip/glp1 pour une thérapie |
WO2021150673A1 (fr) * | 2020-01-23 | 2021-07-29 | Eli Lilly And Company | Composés co-agonistes de gip/glp1 |
-
2022
- 2022-02-02 WO PCT/US2022/014971 patent/WO2022177744A1/fr active Application Filing
- 2022-02-02 EP EP22706153.8A patent/EP4294423A1/fr active Pending
- 2022-02-02 JP JP2023549546A patent/JP2024508745A/ja active Pending
- 2022-02-02 CA CA3208873A patent/CA3208873A1/fr active Pending
- 2022-02-02 CN CN202280015672.2A patent/CN117320740A/zh active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2016111971A1 (fr) * | 2015-01-09 | 2016-07-14 | Eli Lilly And Company | Composés co-agonistes de gip et de glp-1 |
WO2020023386A1 (fr) | 2018-07-23 | 2020-01-30 | Eli Lilly And Company | Composés co-agonistes de gip/glp1 |
WO2020023388A1 (fr) * | 2018-07-23 | 2020-01-30 | Eli Lilly And Company | Procédé d'utilisation d'un co-agoniste de gip/glp1 contre le diabète |
WO2020023382A1 (fr) * | 2018-07-23 | 2020-01-30 | Eli Lilly And Company | Procédés d'utilisation d'un co-agoniste de gip/glp1 pour une thérapie |
WO2021150673A1 (fr) * | 2020-01-23 | 2021-07-29 | Eli Lilly And Company | Composés co-agonistes de gip/glp1 |
Non-Patent Citations (12)
Title |
---|
ANONYMOUS: "A quick guide to the SURPASS and SURMOUNT trials | diabetes.medicinematters.com", 26 October 2020 (2020-10-26), XP055918873, Retrieved from the Internet <URL:http://web.archive.org/web/20201026013317/https://diabetes.medicinematters.com/tirzepatide/type-2-diabetes/a-quick-guide-to-the-surpass-and-surmount-trials/18478154> [retrieved on 20220509] * |
ANONYMOUS: "History of Changes for Study: NCT03131687", 31 July 2019 (2019-07-31), XP055918703, Retrieved from the Internet <URL:https://clinicaltrials.gov/ct2/history/NCT03131687?V_18=View#StudyPageTop> [retrieved on 20220506] * |
ANONYMOUS: "History of Changes for Study: NCT03311724", 24 April 2019 (2019-04-24), XP055918724, Retrieved from the Internet <URL:https://clinicaltrials.gov/ct2/history/NCT03311724?V_9=View#StudyPageTop> [retrieved on 20220506] * |
ANONYMOUS: "History of Changes for Study: NCT04039503", 3 February 2021 (2021-02-03), XP055918558, Retrieved from the Internet <URL:https://clinicaltrials.gov/ct2/history/NCT04039503?V_25=View#StudyPageTop> [retrieved on 20220506] * |
ANONYMOUS: "History of Changes for Study: NCT04657003", 18 January 2021 (2021-01-18), XP055918887, Retrieved from the Internet <URL:https://www.clinicaltrials.gov/ct2/history/NCT04657003?V_4=View#StudyPageTop> [retrieved on 20220509] * |
ASSMANN G ET AL.: "High-density lipoprotein cholesterol as a predictor of coronary heart disease risk. The PROCAM experience and pathophysiological implications for reverse cholesterol transport", ATHEROSCLEROSIS, vol. 124, 1996, pages S 11 - S20 |
DAHL DOMINIK ET AL: "Effect of Subcutaneous Tirzepatide vs Placebo Added to Titrated Insulin Glargine on Glycemic Control in Patients With Type 2 Diabetes : The SURPASS-5 Randomized Clinical Trial", JAMA THE JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, vol. 327, no. 6, 8 February 2022 (2022-02-08), US, pages 534, XP055918557, ISSN: 0098-7484, Retrieved from the Internet <URL:http://dx.doi.org/10.1001/jama.2022.0078> DOI: 10.1001/jama.2022.0078 * |
FRIAS JUAN PABLO ET AL: "Efficacy and tolerability of tirzepatide, a dual glucose-dependent insulinotropic peptide and glucagon-like peptide-1 receptor agonist in patients with type 2 diabetes: A 12-week, randomized, double-blind, placebo-controlled study to evaluate different dose-escalation regimens", DIABETES, OBESITY AND METABOLISM, vol. 22, no. 6, 1 June 2020 (2020-06-01), GB, pages 938 - 946, XP055918875, ISSN: 1462-8902, Retrieved from the Internet <URL:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318331/pdf/DOM-22-938.pdf> DOI: 10.1111/dom.13979 * |
GORDON DJ ET AL.: "High-density lipoprotein cholesterol and cardiovascular disease: four prospective American studies", CIRCULATION, vol. 79, 1989, pages 8 - 15 |
JUAN PABLO FRIAS ET AL: "Efficacy and safety of LY3298176, a novel dual GIP and GLP-1 receptor agonist, in patients with type 2 diabetes: a randomised, placebo-controlled and active comparator-controlled phase 2 trial", THE LANCET, vol. 392, no. 10160, 4 October 2018 (2018-10-04), AMSTERDAM, NL, pages 2180 - 2193, XP055567738, ISSN: 0140-6736, DOI: 10.1016/S0140-6736(18)32260-8 * |
RUBINS HB ET AL.: "Gemfibrozil for the secondary prevention of coronary heart disease in men with low levels of high-density lipoprotein cholesterol. Veterans Affairs High-Density Lipoprotein Cholesterol Intervention Trial Study Group", N ENGL J MED, vol. 341, 1999, pages 410 - 8 |
WILSON JONATHAN M. ET AL: "The dual glucose-dependent insulinotropic peptide and glucagon-like peptide-1 receptor agonist, tirzepatide, improves lipoprotein biomarkers associated with insulin resistance and cardiovascular risk in patients with type 2 diabetes", DIABETES, OBESITY AND METABOLISM, vol. 22, no. 12, 15 September 2020 (2020-09-15), GB, pages 2451 - 2459, XP055918890, ISSN: 1462-8902, Retrieved from the Internet <URL:https://onlinelibrary.wiley.com/doi/full-xml/10.1111/dom.14174> DOI: 10.1111/dom.14174 * |
Also Published As
Publication number | Publication date |
---|---|
JP2024508745A (ja) | 2024-02-28 |
CA3208873A1 (fr) | 2022-08-25 |
CN117320740A (zh) | 2023-12-29 |
EP4294423A1 (fr) | 2023-12-27 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AU2019311000B2 (en) | GIP/GLP1 co-agonist compounds | |
US11897926B2 (en) | GIPR-agonist compounds | |
JP2019534248A (ja) | アミリン類似体 | |
JP2017501107A (ja) | アミリン類似体 | |
AU2021211451B2 (en) | GIP/GLP1 co-agonist compounds | |
WO2020023388A1 (fr) | Procédé d'utilisation d'un co-agoniste de gip/glp1 contre le diabète | |
US20120277151A1 (en) | Glp-1 pharmaceutical compositions | |
CA3220650A1 (fr) | Co-agonistes a action prolongee des recepteurs du glucagon et du glp-1 | |
WO2022177744A1 (fr) | Procédés thérapeutiques agonistes doubles gip/glp1 | |
US20120077746A1 (en) | Glp-1 analogues pharmaceutical compositions | |
US20100137204A1 (en) | Glp-1 pharmaceutical compositions | |
RU2779314C2 (ru) | Коагонисты рецепторов глюкагона и glp-1 длительного действия | |
US20070244034A1 (en) | GLP-1 pharmaceutical compositions | |
EA047589B1 (ru) | Двойные агонисты рецепторов амилина и кальцитонина и их применение |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 22706153 Country of ref document: EP Kind code of ref document: A1 |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2023549546 Country of ref document: JP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 202280015672.2 Country of ref document: CN Ref document number: 3208873 Country of ref document: CA |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2022706153 Country of ref document: EP |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
ENP | Entry into the national phase |
Ref document number: 2022706153 Country of ref document: EP Effective date: 20230918 |