JP2019535731A5 - - Google Patents
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- JP2019535731A5 JP2019535731A5 JP2019527170A JP2019527170A JP2019535731A5 JP 2019535731 A5 JP2019535731 A5 JP 2019535731A5 JP 2019527170 A JP2019527170 A JP 2019527170A JP 2019527170 A JP2019527170 A JP 2019527170A JP 2019535731 A5 JP2019535731 A5 JP 2019535731A5
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- JP
- Japan
- Prior art keywords
- cancer
- group
- adc
- antibody
- antigen
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 239000000611 antibody drug conjugate Substances 0.000 claims 20
- 108091008116 antibody drug conjugates Proteins 0.000 claims 20
- 239000000203 mixture Substances 0.000 claims 15
- 108090001123 antibodies Proteins 0.000 claims 14
- 102000004965 antibodies Human genes 0.000 claims 14
- 239000000427 antigen Substances 0.000 claims 14
- 108091007172 antigens Proteins 0.000 claims 14
- 102000038129 antigens Human genes 0.000 claims 14
- 201000011510 cancer Diseases 0.000 claims 14
- 108010047041 Complementarity Determining Regions Proteins 0.000 claims 12
- 125000003275 alpha amino acid group Chemical group 0.000 claims 12
- 239000003814 drug Substances 0.000 claims 8
- 125000005647 linker group Chemical group 0.000 claims 8
- 239000008194 pharmaceutical composition Substances 0.000 claims 6
- 125000002947 alkylene group Chemical group 0.000 claims 5
- 238000000034 method Methods 0.000 claims 5
- -1 polymethacrylicamide Polymers 0.000 claims 5
- STQGQHZAVUOBTE-VGBVRHCVSA-N DAUNOMYCIN Chemical compound O([C@H]1C[C@@](O)(CC=2C(O)=C3C(=O)C=4C=CC=C(C=4C(=O)C3=C(O)C=21)OC)C(C)=O)[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 STQGQHZAVUOBTE-VGBVRHCVSA-N 0.000 claims 4
- 229960001156 Mitoxantrone Drugs 0.000 claims 4
- KKZJGLLVHKMTCM-UHFFFAOYSA-N Mitoxantrone Chemical compound O=C1C2=C(O)C=CC(O)=C2C(=O)C2=C1C(NCCNCCO)=CC=C2NCCNCCO KKZJGLLVHKMTCM-UHFFFAOYSA-N 0.000 claims 4
- DASWEROEPLKSEI-UIJRFTGLSA-N Monomethyl auristatin E Chemical group CN[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N(C)[C@@H]([C@@H](C)CC)[C@H](OC)CC(=O)N1CCC[C@H]1[C@H](OC)[C@@H](C)C(=O)N[C@H](C)[C@@H](O)C1=CC=CC=C1 DASWEROEPLKSEI-UIJRFTGLSA-N 0.000 claims 4
- 125000004450 alkenylene group Chemical group 0.000 claims 4
- 239000003795 chemical substances by application Substances 0.000 claims 4
- 229940079593 drugs Drugs 0.000 claims 4
- 239000012216 imaging agent Substances 0.000 claims 4
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- 108010093470 monomethyl auristatin E Proteins 0.000 claims 4
- WYWHKKSPHMUBEB-UHFFFAOYSA-N tioguanine Chemical compound N1C(N)=NC(=S)C2=C1N=CN2 WYWHKKSPHMUBEB-UHFFFAOYSA-N 0.000 claims 4
- ZGXJTSGNIOSYLO-UHFFFAOYSA-N aminolevulinic acid Chemical compound NCC(=O)CCC(O)=O ZGXJTSGNIOSYLO-UHFFFAOYSA-N 0.000 claims 3
- 229960002749 aminolevulinic acid Drugs 0.000 claims 3
- 229920001577 copolymer Polymers 0.000 claims 3
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- 125000000468 ketone group Chemical group 0.000 claims 3
- 229920000642 polymer Polymers 0.000 claims 3
- FSIRXIHZBIXHKT-MHTVFEQDSA-N (2S)-2-[[4-[1-(2,4-diaminopteridin-6-yl)butan-2-yl]benzoyl]amino]pentanedioic acid Chemical compound C=1N=C2N=C(N)N=C(N)C2=NC=1CC(CC)C1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 FSIRXIHZBIXHKT-MHTVFEQDSA-N 0.000 claims 2
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- KSFOVUSSGSKXFI-GAQDCDSVSA-N CC1=C/2NC(\C=C3/N=C(/C=C4\N\C(=C/C5=N/C(=C\2)/C(C=C)=C5C)C(C=C)=C4C)C(C)=C3CCC(O)=O)=C1CCC(O)=O Chemical compound CC1=C/2NC(\C=C3/N=C(/C=C4\N\C(=C/C5=N/C(=C\2)/C(C=C)=C5C)C(C=C)=C4C)C(C)=C3CCC(O)=O)=C1CCC(O)=O KSFOVUSSGSKXFI-GAQDCDSVSA-N 0.000 claims 2
- 229920002574 CR-39 Polymers 0.000 claims 2
- VSJKWCGYPAHWDS-FQEVSTJZSA-N Camptothecin Chemical compound C1=CC=C2C=C(CN3C4=CC5=C(C3=O)COC(=O)[C@]5(O)CC)C4=NC2=C1 VSJKWCGYPAHWDS-FQEVSTJZSA-N 0.000 claims 2
- 206010008342 Cervix carcinoma Diseases 0.000 claims 2
- 229960004397 Cyclophosphamide Drugs 0.000 claims 2
- CMSMOCZEIVJLDB-UHFFFAOYSA-N Cyclophosphamide Chemical compound ClCCN(CCCl)P1(=O)NCCCO1 CMSMOCZEIVJLDB-UHFFFAOYSA-N 0.000 claims 2
- 206010014733 Endometrial cancer Diseases 0.000 claims 2
- VJJPUSNTGOMMGY-MRVIYFEKSA-N Etoposide Chemical compound COC1=C(O)C(OC)=CC([C@@H]2C3=CC=4OCOC=4C=C3[C@@H](O[C@H]3[C@@H]([C@@H](O)[C@@H]4O[C@H](C)OC[C@H]4O3)O)[C@@H]3[C@@H]2C(OC3)=O)=C1 VJJPUSNTGOMMGY-MRVIYFEKSA-N 0.000 claims 2
- 229960005420 Etoposide Drugs 0.000 claims 2
- CHPZKNULDCNCBW-UHFFFAOYSA-N Gallium nitrate Chemical compound [Ga+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O CHPZKNULDCNCBW-UHFFFAOYSA-N 0.000 claims 2
- 206010017758 Gastric cancer Diseases 0.000 claims 2
- 208000005017 Glioblastoma Diseases 0.000 claims 2
- 229960001101 Ifosfamide Drugs 0.000 claims 2
- HOMGKSMUEGBAAB-UHFFFAOYSA-N Ifosfamide Chemical compound ClCCNP1(=O)OCCCN1CCCl HOMGKSMUEGBAAB-UHFFFAOYSA-N 0.000 claims 2
- FBOZXECLQNJBKD-ZDUSSCGKSA-N L-methotrexate Chemical compound C=1N=C2N=C(N)N=C(N)C2=NC=1CN(C)C1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 FBOZXECLQNJBKD-ZDUSSCGKSA-N 0.000 claims 2
- 206010023825 Laryngeal cancer Diseases 0.000 claims 2
- 206010024324 Leukaemias Diseases 0.000 claims 2
- 206010058467 Lung neoplasm malignant Diseases 0.000 claims 2
- 206010025323 Lymphomas Diseases 0.000 claims 2
- MFRNYXJJRJQHNW-NARUGQRUSA-N Monomethyl auristatin F Chemical compound CN[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N(C)C([C@@H](C)CC)[C@H](OC)CC(=O)N1CCC[C@H]1[C@H](OC)[C@@H](C)C(=O)N[C@H](C(O)=O)CC1=CC=CC=C1 MFRNYXJJRJQHNW-NARUGQRUSA-N 0.000 claims 2
- 206010061306 Nasopharyngeal cancer Diseases 0.000 claims 2
- 206010030155 Oesophageal carcinoma Diseases 0.000 claims 2
- 206010031096 Oropharyngeal cancer Diseases 0.000 claims 2
- 206010025310 Other lymphomas Diseases 0.000 claims 2
- 206010033128 Ovarian cancer Diseases 0.000 claims 2
- 208000008443 Pancreatic Carcinoma Diseases 0.000 claims 2
- 229920001710 Polyorthoester Polymers 0.000 claims 2
- 206010060862 Prostate cancer Diseases 0.000 claims 2
- 206010038389 Renal cancer Diseases 0.000 claims 2
- 206010039491 Sarcoma Diseases 0.000 claims 2
- 210000001550 Testis Anatomy 0.000 claims 2
- 229960005454 Thioguanine Drugs 0.000 claims 2
- 231100000765 Toxin Toxicity 0.000 claims 2
- 229960004528 Vincristine Drugs 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- RJURFGZVJUQBHK-IIXSONLDSA-N actinomycin D Chemical compound C[C@H]1OC(=O)[C@H](C(C)C)N(C)C(=O)CN(C)C(=O)[C@@H]2CCCN2C(=O)[C@@H](C(C)C)NC(=O)[C@H]1NC(=O)C1=C(N)C(=O)C(C)=C2OC(C(C)=CC=C3C(=O)N[C@@H]4C(=O)N[C@@H](C(N5CCC[C@H]5C(=O)N(C)CC(=O)N(C)[C@@H](C(C)C)C(=O)O[C@@H]4C)=O)C(C)C)=C3N=C21 RJURFGZVJUQBHK-IIXSONLDSA-N 0.000 claims 2
- 230000001028 anti-proliferant Effects 0.000 claims 2
- 239000002246 antineoplastic agent Substances 0.000 claims 2
- 201000010881 cervical cancer Diseases 0.000 claims 2
- 239000003153 chemical reaction reagent Substances 0.000 claims 2
- 229950006700 edatrexate Drugs 0.000 claims 2
- 230000002708 enhancing Effects 0.000 claims 2
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- 125000004185 ester group Chemical group 0.000 claims 2
- 201000010536 head and neck cancer Diseases 0.000 claims 2
- 125000001072 heteroaryl group Chemical group 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 2
- 238000002347 injection Methods 0.000 claims 2
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- 201000002313 intestinal cancer Diseases 0.000 claims 2
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- 201000007270 liver cancer Diseases 0.000 claims 2
- 201000005202 lung cancer Diseases 0.000 claims 2
- GLVAUDGFNGKCSF-UHFFFAOYSA-N mercaptopurine Chemical compound S=C1NC=NC2=C1NC=N2 GLVAUDGFNGKCSF-UHFFFAOYSA-N 0.000 claims 2
- 229960001428 mercaptopurine Drugs 0.000 claims 2
- 229960000485 methotrexate Drugs 0.000 claims 2
- 108010059074 monomethylauristatin F Proteins 0.000 claims 2
- 230000000269 nucleophilic Effects 0.000 claims 2
- 201000006958 oropharynx cancer Diseases 0.000 claims 2
- 201000002528 pancreatic cancer Diseases 0.000 claims 2
- 239000002745 poly(ortho ester) Substances 0.000 claims 2
- 102000004169 proteins and genes Human genes 0.000 claims 2
- 108090000623 proteins and genes Proteins 0.000 claims 2
- 229950003776 protoporphyrin Drugs 0.000 claims 2
- 201000000849 skin cancer Diseases 0.000 claims 2
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- 125000001174 sulfone group Chemical group 0.000 claims 2
- 230000001225 therapeutic Effects 0.000 claims 2
- 239000003053 toxin Substances 0.000 claims 2
- 108020003112 toxins Proteins 0.000 claims 2
- 201000005112 urinary bladder cancer Diseases 0.000 claims 2
- OGWKCGZFUXNPDA-XQKSVPLYSA-N vincristine Chemical compound C([N@]1C[C@@H](C[C@]2(C(=O)OC)C=3C(=CC4=C([C@]56[C@H]([C@@]([C@H](OC(C)=O)[C@]7(CC)C=CCN([C@H]67)CC5)(O)C(=O)OC)N4C=O)C=3)OC)C[C@@](C1)(O)CC)CC1=C2NC2=CC=CC=C12 OGWKCGZFUXNPDA-XQKSVPLYSA-N 0.000 claims 2
- OYINILBBZAQBEV-UWJYYQICSA-N (17S,18S)-18-(2-carboxyethyl)-20-(carboxymethyl)-12-ethenyl-7-ethyl-3,8,13,17-tetramethyl-17,18,22,23-tetrahydroporphyrin-2-carboxylic acid Chemical compound N1C2=C(C)C(C=C)=C1C=C(N1)C(C)=C(CC)C1=CC(C(C)=C1C(O)=O)=NC1=C(CC(O)=O)C([C@@H](CCC(O)=O)[C@@H]1C)=NC1=C2 OYINILBBZAQBEV-UWJYYQICSA-N 0.000 claims 1
- ZROHGHOFXNOHSO-BNTLRKBRSA-L (1R,2R)-cyclohexane-1,2-diamine;oxalate;platinum(2+) Chemical compound [H][N]([C@@H]1CCCC[C@H]1[N]1([H])[H])([H])[Pt]11OC(=O)C(=O)O1 ZROHGHOFXNOHSO-BNTLRKBRSA-L 0.000 claims 1
- FLWWDYNPWOSLEO-HQVZTVAUSA-N (2S)-2-[[4-[1-(2-amino-4-oxo-1H-pteridin-6-yl)ethyl-methylamino]benzoyl]amino]pentanedioic acid Chemical compound C=1N=C2NC(N)=NC(=O)C2=NC=1C(C)N(C)C1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 FLWWDYNPWOSLEO-HQVZTVAUSA-N 0.000 claims 1
- NRUKOCRGYNPUPR-QBPJDGROSA-N (5S,5aR,8aR,9R)-5-[[(2R,4aR,6R,7R,8R,8aS)-7,8-dihydroxy-2-thiophen-2-yl-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxin-6-yl]oxy]-9-(4-hydroxy-3,5-dimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[6,5-f][1,3]benzodioxol-8-one Chemical compound COC1=C(O)C(OC)=CC([C@@H]2C3=CC=4OCOC=4C=C3[C@@H](O[C@H]3[C@@H]([C@@H](O)[C@@H]4O[C@@H](OC[C@H]4O3)C=3SC=CC=3)O)[C@@H]3[C@@H]2C(OC3)=O)=C1 NRUKOCRGYNPUPR-QBPJDGROSA-N 0.000 claims 1
- OMJKFYKNWZZKTK-POHAHGRESA-N (5Z)-5-(dimethylaminohydrazinylidene)imidazole-4-carboxamide Chemical compound CN(C)N\N=C1/N=CN=C1C(N)=O OMJKFYKNWZZKTK-POHAHGRESA-N 0.000 claims 1
- JXVAMODRWBNUSF-KZQKBALLSA-N (7S,9R,10R)-7-[(2R,4S,5S,6S)-5-[[(2S,4aS,5aS,7S,9S,9aR,10aR)-2,9-dimethyl-3-oxo-4,4a,5a,6,7,9,9a,10a-octahydrodipyrano[4,2-a:4',3'-e][1,4]dioxin-7-yl]oxy]-4-(dimethylamino)-6-methyloxan-2-yl]oxy-10-[(2S,4S,5S,6S)-4-(dimethylamino)-5-hydroxy-6-methyloxan-2 Chemical compound O([C@@H]1C2=C(O)C=3C(=O)C4=CC=CC(O)=C4C(=O)C=3C(O)=C2[C@@H](O[C@@H]2O[C@@H](C)[C@@H](O[C@@H]3O[C@@H](C)[C@H]4O[C@@H]5O[C@@H](C)C(=O)C[C@@H]5O[C@H]4C3)[C@H](C2)N(C)C)C[C@]1(O)CC)[C@H]1C[C@H](N(C)C)[C@H](O)[C@H](C)O1 JXVAMODRWBNUSF-KZQKBALLSA-N 0.000 claims 1
- KMSKQZKKOZQFFG-YXRRJAAWSA-N (7S,9S)-7-[(2R,4S,5S,6S)-4-amino-6-methyl-5-[(2R)-oxan-2-yl]oxyoxan-2-yl]oxy-6,9,11-trihydroxy-9-(2-hydroxyacetyl)-4-methoxy-8,10-dihydro-7H-tetracene-5,12-dione Chemical compound O([C@H]1[C@@H](N)C[C@@H](O[C@H]1C)O[C@H]1C[C@@](O)(CC=2C(O)=C3C(=O)C=4C=CC=C(C=4C(=O)C3=C(O)C=21)OC)C(=O)CO)[C@@H]1CCCCO1 KMSKQZKKOZQFFG-YXRRJAAWSA-N 0.000 claims 1
- BTOTXLJHDSNXMW-POYBYMJQSA-N 1-[(2R,5S)-5-(hydroxymethyl)oxolan-2-yl]pyrimidine-2,4-dione Chemical compound O1[C@H](CO)CC[C@@H]1N1C(=O)NC(=O)C=C1 BTOTXLJHDSNXMW-POYBYMJQSA-N 0.000 claims 1
- SVUOLADPCWQTTE-UHFFFAOYSA-N 1H-1,2-benzodiazepine Chemical compound N1N=CC=CC2=CC=CC=C12 SVUOLADPCWQTTE-UHFFFAOYSA-N 0.000 claims 1
- BOMZMNZEXMAQQW-UHFFFAOYSA-N 2,5,11-trimethyl-6H-pyrido[4,3-b]carbazol-2-ium-9-ol;acetate Chemical compound CC([O-])=O.C[N+]1=CC=C2C(C)=C(NC=3C4=CC(O)=CC=3)C4=C(C)C2=C1 BOMZMNZEXMAQQW-UHFFFAOYSA-N 0.000 claims 1
- ODJVLHDVEGAIAW-USOGPTGWSA-N 2-(1-Hexyloxyethyl)-2-devinyl pyropheophorbide-a Chemical compound N1C(C=C2C(C(C)OCCCCCC)=C(C)C(N2)=C2)=C(C)C(CC)=C1C=C(N=C13)C(C)=C3C(=O)CC1=C1[C@@H](CCC(O)=O)[C@H](C)C2=N1 ODJVLHDVEGAIAW-USOGPTGWSA-N 0.000 claims 1
- CTRPRMNBTVRDFH-UHFFFAOYSA-N 2-N-methyl-1,3,5-triazine-2,4,6-triamine Chemical compound CNC1=NC(N)=NC(N)=N1 CTRPRMNBTVRDFH-UHFFFAOYSA-N 0.000 claims 1
- QCXJFISCRQIYID-IAEPZHFASA-N 2-amino-1-N-[(3S,6S,7R,10S,16S)-3-[(2S)-butan-2-yl]-7,11,14-trimethyl-2,5,9,12,15-pentaoxo-10-propan-2-yl-8-oxa-1,4,11,14-tetrazabicyclo[14.3.0]nonadecan-6-yl]-4,6-dimethyl-3-oxo-9-N-[(3S,6S,7R,10S,16S)-7,11,14-trimethyl-2,5,9,12,15-pentaoxo-3,10-di(propa Chemical compound C[C@H]1OC(=O)[C@H](C(C)C)N(C)C(=O)CN(C)C(=O)[C@@H]2CCCN2C(=O)[C@H](C(C)C)NC(=O)[C@H]1NC(=O)C1=C(N=C2C(C(=O)N[C@@H]3C(=O)N[C@H](C(N4CCC[C@H]4C(=O)N(C)CC(=O)N(C)[C@@H](C(C)C)C(=O)O[C@@H]3C)=O)[C@@H](C)CC)=C(N)C(=O)C(C)=C2O2)C2=C(C)C=C1 QCXJFISCRQIYID-IAEPZHFASA-N 0.000 claims 1
- FDAYLTPAFBGXAB-UHFFFAOYSA-N 2-chloro-N,N-bis(2-chloroethyl)ethanamine Chemical compound ClCCN(CCCl)CCCl FDAYLTPAFBGXAB-UHFFFAOYSA-N 0.000 claims 1
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- PWMYMKOUNYTVQN-UHFFFAOYSA-N 3-(8,8-diethyl-2-aza-8-germaspiro[4.5]decan-2-yl)-N,N-dimethylpropan-1-amine Chemical compound C1C[Ge](CC)(CC)CCC11CN(CCCN(C)C)CC1 PWMYMKOUNYTVQN-UHFFFAOYSA-N 0.000 claims 1
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- ROBVIMPUHSLWNV-UHFFFAOYSA-N Aminoglutethimide Chemical compound C=1C=C(N)C=CC=1C1(CC)CCC(=O)NC1=O ROBVIMPUHSLWNV-UHFFFAOYSA-N 0.000 claims 1
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- XREUEWVEMYWFFA-CSKJXFQVSA-N CARUBICIN Chemical compound C1[C@H](N)[C@H](O)[C@H](C)O[C@H]1O[C@@H]1C2=C(O)C(C(=O)C3=C(O)C=CC=C3C3=O)=C3C(O)=C2C[C@@](O)(C(C)=O)C1 XREUEWVEMYWFFA-CSKJXFQVSA-N 0.000 claims 1
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- GAGWJHPBXLXJQN-UORFTKCHSA-N Capecitabine Chemical compound C1=C(F)C(NC(=O)OCCCCC)=NC(=O)N1[C@H]1[C@H](O)[C@H](O)[C@@H](C)O1 GAGWJHPBXLXJQN-UORFTKCHSA-N 0.000 claims 1
- MKQWTWSXVILIKJ-LXGUWJNJSA-N Chlorozotocin Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](C=O)NC(=O)N(N=O)CCCl MKQWTWSXVILIKJ-LXGUWJNJSA-N 0.000 claims 1
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- CIORWBWIBBPXCG-SXZCQOKQSA-N α-amanitin Chemical compound O=C1N[C@@H](CC(N)=O)C(=O)N2C[C@H](O)C[C@H]2C(=O)N[C@@H]([C@@H](C)[C@@H](O)CO)C(=O)N[C@@H](C2)C(=O)NCC(=O)N[C@@H]([C@@H](C)CC)C(=O)NCC(=O)N[C@H]1C[S@@](=O)C1=C2C2=CC=C(O)C=C2N1 CIORWBWIBBPXCG-SXZCQOKQSA-N 0.000 claims 1
Claims (16)
- 治療剤及びグロボ系列の抗原に結合する抗体又は抗原結合性断片を含む抗体−薬物コンジュゲート(ADC)であって、
治療剤が、リンカーにより、抗体又は抗原結合性断片へと、共有結合的にコンジュゲートされ、
抗体が、モノクローナル抗体、抗原結合性断片、キメラ抗体及びヒト化抗体から選択され、
抗原結合性断片が、Fab断片、F(ab’) 2 断片、Fv断片又はscFv断片である、
ADC。 - 式:
Ab−(L−D)n (I)
[式中、1つ以上の治療用薬物部分(D)は、リンカー(L)により、グロボ系列の抗原をターゲティングする抗体である抗体(Ab)へと共有結合的に連結され、nは、1〜8の整数である]
を有する、請求項1に記載のADC化合物の混合物を含む組成物であって、
薬物部分(D)は、化学療法剤、光力学療法剤又は生物学的薬剤または抗増殖剤であり、
リンカー(L)は、任意選択的にジスルフィド架橋の還元によって生成される、チオ基を含む、組成物。 - グロボ系列の抗原が、SSEA−4(Neu5Acα2→3Galβ1→3GalNAcβ1→3Galα1→4Galβ1→4Glcβ1)、SSEA−3(Galβ1→3GalNAcβ1→3Galα1→4Galβ1→4Glcβ1)及び/又はグロボH(Fucα1→2Galβ1→3GalNAcβ1→3Galα1→4Galβ1→4Glc)である、請求項1に記載のADC。
- 抗体が、任意選択的にOBI−888である抗グロボH抗体、抗SSEA3抗体又は任意選択的にOBI−898である抗SSEA4抗体であり、
治療剤が、モノメチルアウリスタチンE(MMAE)である、請求項1に記載のADC。 - 請求項1に記載のADC又は薬学的に許容されるその塩、及び薬学的に許容される希釈剤、担体又は賦形剤を含み、
グロボ系列の抗原をターゲティングする、他のADCの組合せをさらに含む、医薬組成物。 - 請求項2に記載の組成物を作製する方法であって、
Abを、式IIまたは式IIIのリンカー試薬と反応させて、抗体−リンカー中間体であるAb−Lを形成し、次いで、Ab−Lを、薬物部分と反応させて、ADCの混合物を形成するステップ;又は
薬物部分であるDを、リンカー試薬と反応させて、薬物−リンカー中間体であるD−Lを形成し、次いで、D−Lを、Abと反応させて、ADCの混合物を形成するステップ
を含み、
式IIが、以下の構造:
[式中、X及びX’のうちの一方は、ポリマー(とりわけ、毒素)を表し、他方は、水素原子を表す;各Qは、独立に連結基を表し;Wは、電子求引性部分又は電子求引性部分の還元により調製可能な部分を表す;又は、X’がポリマーを表す場合、X−Q−W−は、一緒になって、電子求引性基を表す場合もあり;加えて、Xがポリマーを表す場合、X’及び電子求引性基であるWは、介在原子と一緒になって、環を形成する場合もあり;Z 1 及びZ 2 の各々は、独立に各々が、求核部分を介して、A及びBへと連結された生物学的分子に由来する基を表す;又はZ 1 及びZ 2 は、一緒になって、2つの求核部分を介して、A及びBへと連結された生物学的分子に由来する、単一の基を表し;Aは、C 1〜5 アルキレン又はアルケニレン鎖であり;Bは、結合又はC 1〜4 アルキレン若しくはアルケニレン鎖である]を有し、
式IIIが、以下の構造:
[式中、Xは、ポリアルキレングリコール、ポリビニルピロリドン、ポリアクリレート、ポリメタクリレート、ポリオキサゾリン、ポリビニルアルコール、ポリアクリルアミド、ポリメタクリルアミド、HPMAコポリマー、ポリエステル、ポリアセタール、ポリ(オルトエステル)、ポリカーボネート、ポリ(イミノカーボネート)、ポリアミド、ジビニルエーテル−無水マレイン酸のコポリマー及びスチレン−無水マレイン酸のコポリマー、多糖並びにポリグルタミン酸からなる群から選択される、ホモポリマー又はコポリマー(とりわけ、毒素)であり;Qは、直接的な結合、アルキレン、任意選択的に置換されたアリール及び任意選択的に置換されたヘテロアリールからなる群から選択される連結基であり、この場合、アルキレン、アリール又はヘテロアリールは、1つ以上の酸素原子、硫黄原子、ケト基、−O−CO−基、−CO−O−基又は−NR基[式中、Rは、アルキル又はアリール群である]により終結する場合もあり、これらにより中断される場合もあり;Wは、ケト基、エステル基、スルホン基、還元ケト基、還元エステル基及び還元スルホン基からなる群から選択され;X’−Qは、水素であり;Aは、C 1〜5 アルキレン又はアルケニレン鎖であり;Bは、結合又はC 1〜4 アルキレン若しくはアルケニレン鎖であり;Zは、ジスルフィド架橋の還元により、タンパク質において生成された、2つのチオール基を介して、A及びBへと連結された、単一のタンパク質である]を有する、方法。 - 光力学療法剤が、フォトフリン、レザフィリン、アミノレブリン酸(ALA)、シリコンフタロシアニンPc4、m−テトラヒドロキシフェニルクロリン(mTHPC)、クロリンe6(Ce6)、アルメラ、レブラン、フォスカン、メトビックス、ヘクスビックス、フォトクロール、フォトセンス、フォトレックス、ルマカン、ビソナック、アムフィネックス、ベルテポルフィン、プルリチン、ATMPn、アエンフタロシアニン(ZnPc)、プロトポルフィリンIX(PpIX)、ピロフェオフォルバイドa(PPa)又はフェオフォルバイド(PhA)から選択される、請求項2に記載の組成物。
- 抗増殖剤が、モノメチルアウリスタチンE(MMAE)、モノメチルアウリスタチンF(MMAF)、メルタンシン(DM1)、アントラサイクリン、ピロロベンゾジアゼピン、α−アマニチン、ツブリシン、ベンゾジアゼピン、エルロチニブ、ボルテゾミブ、フルベストラント、スニチニブ、レトロゾール、メシル酸イマチニブ、PTK787/ZK 222584、オキサリプラチン、ロイコボリン、ラパマイシン、ラパチニブ、ロナファルニブ、ソラファニブ、ゲフィチニブ、AG1478、AG1571、アルキル化剤;スルホン酸アルキル;アジリジン;エチレンイミン;メチルメラミン;アセトゲニン;カンプトテシン;ブリオスタチン;カリスタチン;CC−1065;クリプトフィシン;ドラスタチン;デュオカルマイシン;エリュテロビン;パンクラチスタチン;サルコチクチイン;スポンジスタチン;クロランブシル;クロルナファジン;シクロホスファミド;エストラムスチン;イホスファミド;メクロレタミン;塩酸メクロレタミンオキシド;メルファラン;ノベムビシン;フェネステリン;プレドニムスチン;トロホスファミド;ウラシルマスタード;カルムスチン;クロロゾトシン;ホテムスチン;ロムスチン;ニムスチン;ラニムスチン;カリケアミシン;ジネミシン;クロドロネート;エスペラミシン;ネオカルチノスタチン発色団;アクラシノマイシン;アクチノマイシン;アントラマイシン;アザセリン;ブレオマイシン;カクチノマイシン;カラビシン;カルミノマイシン;カルジノフィリン;クロモマイシン;ダクチノマイシン;ダウノルビシン;デトルビシン;6−ジアゾ−5−オキソ−L−ノルロイシン;ドキソルビシン;エピルビシン;エソルビシン;イダルビシン;マルセロマイシン;マイトマイシン;ミコフェノール酸;ノガラマイシン;オリボマイシン;ペプロマイシン;ポトフィロマイシン;ピューロマイシン;ケラマイシン;ロドルビシン;ストレプトニグリン;ストレプトゾシン、ツベルシジン、ウベニメクス、ジノスタチン、ゾルビシン;メトトレキサート;5−フルオロウラシル(5−FU);デノプテリン;プテロプテリン;トリメトレキサート;フルダラビン;6−メルカプトプリン;チアミプリン;チオグアニン;アンシタビン;アザシチジン;6−アザウリジン;カルモフール;シタラビン;ジデオキシウリジン;ドキシフルリジン;エノシタビン;フロクスウリジン;カルステロン;プロピオン酸ドロモスタノロン;エピチオスタノール;メピチオスタン;テストラクトン;アミノグルテチミド;ミトタン;トリロスタン;フォリン酸;アセグラトン;アルドホスファミドグリコシド;アミノレブリン酸;エニルウラシル;アムサクリン;ベストラブシル;ビサントレン;エダトレキサート;デフォファミン;デメコルシン;ジアジコン;エルフォルミチン;酢酸エリプチニウム;エポチロン;エトグルシド;硝酸ガリウム;ヒドロキシウレア;レンチナン;ロニダイニン;メイタンシン;アンサマイトシン;ミトグアゾン;ミトキサントロン;モピダンモール;ニトラエリン;ペントスタチン;フェナメト;ピラルビシン;ロソキサントロン;ポドフィリン酸;2−エチルヒドラジド;プロカルバジン;ラゾキサン;リゾキシン;シゾフィラン;スピロゲルマニウム;テヌアゾン酸;トリアジコン;2,2’,2’’−トリクロロトリエチルアミン;トリコテセン;ウレタン;ビンデシン;ダカルバジン;マンノムスチン;ミトブロニトール;ミトラクトール;ピポブロマン;ガシトシン;アラビノシド;シクロホスファミド;チオテパ;タキソイド;パクリタキセル;ドセタキセル;クロランブシル;ゲムシタビン;6−チオグアニン;メルカプトプリン;メトトレキサート;シスプラチン;カルボプラチン;ビンブラスチン;白金;エトポシド;イホスファミド;ミトキサントロン;ビンクリスチン;ビノレルビン;ノバントロン;テニポシド;エダトレキサート;ダウノマイシン;アミノプテリン;ゼローダ;イバンドロネート;トポイソメラーゼ阻害剤;ジフルオロメチルオルニチン(DMFO);レチノイド又はカペシタビンから選択される、請求項2に記載の組成物。
- 治療を必要とするヒト対象におけるグロボ系列の抗原を発現しているがんの治療に使用するための、治療有効量の請求項1に記載のADCを含む、医薬組成物であって、
がんが、肉腫、皮膚がん、白血病、リンパ腫、脳腫瘍、神経膠芽腫、肺がん、乳がん、口腔がん、頭頸部がん、鼻咽頭がん、食道がん、胃がん、肝臓がん、胆管がん、胆嚢がん、膀胱がん、膵臓がん、腸がん、結腸直腸がん、腎臓がん、子宮頸がん、子宮内膜がん、卵巣がん、睾丸がん、口腔がん、口腔咽頭がん、喉頭がん及び前立腺がんからなる群から選択され、
治療有効量が、任意選択的に、0.01μg〜250mgまたは0.001μg/kg〜250mg/kgである、医薬組成物。 - 前記使用が、有効量の、グロボ系列の抗原をターゲティングする、他のADCの組合せを、処置を必要とするヒト対象に投与するステップを含み、
前記組合せが、がん処置における相乗効果及び治療有効性の増強をもたらす、請求項9に記載の医薬組成物。 - 免疫反応の誘導又は増強を必要とするヒト対象における免疫反応の誘導又は増強に使用するための、免疫学的有効量の、請求項2に記載の医薬組成物であって、
免疫反応を誘導又は増強する方法が、
(a)請求項1に記載のADCを、2回以上投与する手順;
(b)2回の逐次的投与の間の時間間隔及び/若しくは用量レジメンを調整する手順;
(c)投与経路を調整する手順及び/若しくは投与の注射部位を変更する手順;又は
(d)グロボ系列の抗原をターゲティングする他のADCを組み合わせる手順
から選択される手順のうちの1つ以上を含み、
注射を、免疫応答追加剤の添加により、変更及び/又は補充することができ、
免疫学的有効量が、任意選択的に、0.01μg〜250mg又は0.001μg/kg〜250mg/kgである、医薬組成物。 - 肉腫、皮膚がん、白血病、リンパ腫、脳腫瘍、神経膠芽腫、肺がん、乳がん、口腔がん、頭頸部がん、鼻咽頭がん、食道がん、胃がん、肝臓がん、胆管がん、胆嚢がん、膀胱がん、膵臓がん、腸がん、結腸直腸がん、腎臓がん、子宮頸がん、子宮内膜がん、卵巣がん、睾丸がん、口腔がん、口腔咽頭がん、喉頭がん及び前立腺がんからなる群から選択されるがんの処置における使用のための、抗がん剤、免疫抑制剤及び抗感染剤からなる群から選択される、有効量の、さらなる薬剤と組み合わせた使用のための、請求項1に記載のADC。
- ヒト対象のイメージングに使用するための、請求項1に記載のADCを含む組成物であって、前記使用が、
(a)ヒト対象においてイメージング剤を検出するステップを含み、
(b)ここで、ヒト対象は、イメージング剤及びグロボ系列の抗原に結合する抗体又は抗原結合性断片を含む、有効量の、ADCを投与されており、
イメージング剤が、リンカーにより、抗体又は抗原結合性断片へと、共有結合的にコンジュゲートされている、組成物。 - イメージング剤が、フルオロフォア、色素、MRI造影剤又は放射性核種であり、
ヒト対象が、がんを有し、任意選択的に、前記使用が、がんの転移を検出する使用としてさらに規定される、請求項13に記載の組成物。 - グロボHに結合する抗体−薬物コンジュゲート(ADC)であって、
重鎖可変ドメインが、
配列番号1のアミノ酸配列を有する、第1の重鎖相補性決定領域(HCDR1);
配列番号2のアミノ酸配列を有する、第2の重鎖相補性決定領域(HCDR2);
配列番号3のアミノ酸配列を有する、第3の重鎖相補性決定領域(HCDR3)
を含み、軽鎖可変ドメインが、
配列番号7のアミノ酸配列を有する、第1の軽鎖相補性決定領域(LCDR1);
配列番号8のアミノ酸配列を有する、第2の軽鎖相補性決定領域(LCDR2);
配列番号9のアミノ酸配列を有する、第3の軽鎖相補性決定領域(LCDR3)
を含む抗体を含むADC。 - SSEA−4に結合する抗体−薬物コンジュゲート(ADC)であって、
重鎖可変ドメインが、
配列番号29のアミノ酸配列を有する、第1の重鎖相補性決定領域(HCDR1);
配列番号31のアミノ酸配列を有する、第2の重鎖相補性決定領域(HCDR2);
配列番号33のアミノ酸配列を有する、第3の重鎖相補性決定領域(HCDR3)
を含み、軽鎖可変ドメインが、
配列番号22のアミノ酸配列を有する、第1の軽鎖相補性決定領域(LCDR1);
配列番号24のアミノ酸配列を有する、第2の軽鎖相補性決定領域(LCDR2);
配列番号26のアミノ酸配列を有する、第3の軽鎖相補性決定領域(LCDR3)
を含む抗体を含むADC。
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2017
- 2017-11-21 JP JP2019527170A patent/JP2019535731A/ja active Pending
- 2017-11-21 EP EP17871220.4A patent/EP3541414B1/en active Active
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- 2017-11-21 CN CN201780071980.6A patent/CN110290800A/zh active Pending
- 2017-11-21 WO PCT/US2017/062886 patent/WO2018094414A1/en active Application Filing
- 2017-11-21 BR BR112019010356A patent/BR112019010356A2/pt not_active Application Discontinuation
- 2017-11-21 TW TW106140308A patent/TWI767959B/zh active
- 2017-11-21 KR KR1020197017395A patent/KR20190077103A/ko not_active Application Discontinuation
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- 2017-11-21 AU AU2017361549A patent/AU2017361549B2/en active Active
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