JP2016535756A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2016535756A5 JP2016535756A5 JP2016528821A JP2016528821A JP2016535756A5 JP 2016535756 A5 JP2016535756 A5 JP 2016535756A5 JP 2016528821 A JP2016528821 A JP 2016528821A JP 2016528821 A JP2016528821 A JP 2016528821A JP 2016535756 A5 JP2016535756 A5 JP 2016535756A5
- Authority
- JP
- Japan
- Prior art keywords
- cancer
- pharmaceutical composition
- composition according
- group
- therapy
- 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.)
- Granted
Links
- 239000008194 pharmaceutical composition Substances 0.000 claims 15
- 239000003795 chemical substances by application Substances 0.000 claims 8
- 206010028980 Neoplasm Diseases 0.000 claims 6
- 201000011510 cancer Diseases 0.000 claims 6
- 201000008325 diseases of cellular proliferation Diseases 0.000 claims 5
- 238000002560 therapeutic procedure Methods 0.000 claims 5
- -1 y-27632 Chemical compound 0.000 claims 5
- BIIVYFLTOXDAOV-YVEFUNNKSA-N Alvocidib Chemical compound O[C@@H]1CN(C)CC[C@@H]1C1=C(O)C=C(O)C2=C1OC(C=1C(=CC=CC=1)Cl)=CC2=O BIIVYFLTOXDAOV-YVEFUNNKSA-N 0.000 claims 4
- ZVHNDZWQTBEVRY-UHFFFAOYSA-N CYT387 Chemical compound C1=CC(C(NCC#N)=O)=CC=C1C1=CC=NC(NC=2C=CC(=CC=2)N2CCOCC2)=N1 ZVHNDZWQTBEVRY-UHFFFAOYSA-N 0.000 claims 4
- KTEIFNKAUNYNJU-GFCCVEGCSA-N Crizotinib Chemical compound O([C@H](C)C=1C(=C(F)C=CC=1Cl)Cl)C(C(=NC=1)N)=CC=1C(=C1)C=NN1C1CCNCC1 KTEIFNKAUNYNJU-GFCCVEGCSA-N 0.000 claims 4
- 239000002136 L01XE07 - Lapatinib Substances 0.000 claims 4
- 239000002146 L01XE16 - Crizotinib Substances 0.000 claims 4
- BCFGMOOMADDAQU-UHFFFAOYSA-N Lapatinib Chemical compound O1C(CNCCS(=O)(=O)C)=CC=C1C1=CC=C(N=CN=C2NC=3C=C(Cl)C(OCC=4C=C(F)C=CC=4)=CC=3)C2=C1 BCFGMOOMADDAQU-UHFFFAOYSA-N 0.000 claims 4
- 229960005061 crizotinib Drugs 0.000 claims 4
- 229960004891 lapatinib Drugs 0.000 claims 4
- 229960001686 Afatinib Drugs 0.000 claims 3
- MLDQJTXFUGDVEO-UHFFFAOYSA-N BAY-43-9006 Chemical compound C1=NC(C(=O)NC)=CC(OC=2C=CC(NC(=O)NC=3C=C(C(Cl)=CC=3)C(F)(F)F)=CC=2)=C1 MLDQJTXFUGDVEO-UHFFFAOYSA-N 0.000 claims 3
- UBPYILGKFZZVDX-UHFFFAOYSA-N Bosutinib Chemical compound C1=C(Cl)C(OC)=CC(NC=2C3=CC(OC)=C(OCCCN4CCN(C)CC4)C=C3N=CC=2C#N)=C1Cl UBPYILGKFZZVDX-UHFFFAOYSA-N 0.000 claims 3
- 108010022830 Cetuximab Proteins 0.000 claims 3
- ZBNZXTGUTAYRHI-UHFFFAOYSA-N Dasatinib Chemical compound C=1C(N2CCN(CCO)CC2)=NC(C)=NC=1NC(S1)=NC=C1C(=O)NC1=C(C)C=CC=C1Cl ZBNZXTGUTAYRHI-UHFFFAOYSA-N 0.000 claims 3
- 229960001433 Erlotinib Drugs 0.000 claims 3
- AAKJLRGGTJKAMG-UHFFFAOYSA-N Erlotinib Chemical compound C=12C=C(OCCOC)C(OCCOC)=CC2=NC=NC=1NC1=CC=CC(C#C)=C1 AAKJLRGGTJKAMG-UHFFFAOYSA-N 0.000 claims 3
- XGALLCVXEZPNRQ-UHFFFAOYSA-N Gefitinib Chemical compound C=12C=C(OCCCN3CCOCC3)C(OC)=CC2=NC=NC=1NC1=CC=C(F)C(Cl)=C1 XGALLCVXEZPNRQ-UHFFFAOYSA-N 0.000 claims 3
- KTUFNOKKBVMGRW-UHFFFAOYSA-N Imatinib Chemical compound C1CN(C)CCN1CC1=CC=C(C(=O)NC=2C=C(NC=3N=C(C=CN=3)C=3C=NC=CC=3)C(C)=CC=2)C=C1 KTUFNOKKBVMGRW-UHFFFAOYSA-N 0.000 claims 3
- 239000005517 L01XE01 - Imatinib Substances 0.000 claims 3
- 239000005411 L01XE02 - Gefitinib Substances 0.000 claims 3
- 239000005551 L01XE03 - Erlotinib Substances 0.000 claims 3
- 239000002147 L01XE04 - Sunitinib Substances 0.000 claims 3
- 239000005511 L01XE05 - Sorafenib Substances 0.000 claims 3
- 239000002067 L01XE06 - Dasatinib Substances 0.000 claims 3
- 239000002118 L01XE12 - Vandetanib Substances 0.000 claims 3
- 239000002145 L01XE14 - Bosutinib Substances 0.000 claims 3
- 206010058467 Lung neoplasm malignant Diseases 0.000 claims 3
- CYOHGALHFOKKQC-UHFFFAOYSA-N Selumetinib Chemical compound OCCONC(=O)C=1C=C2N(C)C=NC2=C(F)C=1NC1=CC=C(Br)C=C1Cl CYOHGALHFOKKQC-UHFFFAOYSA-N 0.000 claims 3
- WINHZLLDWRZWRT-ATVHPVEESA-N Sunitinib Chemical compound CCN(CC)CCNC(=O)C1=C(C)NC(\C=C/2C3=CC(F)=CC=C3NC\2=O)=C1C WINHZLLDWRZWRT-ATVHPVEESA-N 0.000 claims 3
- 108010010691 Trastuzumab Proteins 0.000 claims 3
- UHTHHESEBZOYNR-UHFFFAOYSA-N Vandetanib Chemical compound COC1=CC(C(/N=CN2)=N/C=3C(=CC(Br)=CC=3)F)=C2C=C1OCC1CCN(C)CC1 UHTHHESEBZOYNR-UHFFFAOYSA-N 0.000 claims 3
- ULXXDDBFHOBEHA-CWDCEQMOSA-N afatinib Chemical compound N1=CN=C2C=C(O[C@@H]3COCC3)C(NC(=O)/C=C/CN(C)C)=CC2=C1NC1=CC=C(F)C(Cl)=C1 ULXXDDBFHOBEHA-CWDCEQMOSA-N 0.000 claims 3
- 230000000118 anti-eoplastic Effects 0.000 claims 3
- 229960003005 axitinib Drugs 0.000 claims 3
- RITAVMQDGBJQJZ-FMIVXFBMSA-N axitinib Chemical compound CNC(=O)C1=CC=CC=C1SC1=CC=C(C(\C=C\C=2N=CC=CC=2)=NN2)C2=C1 RITAVMQDGBJQJZ-FMIVXFBMSA-N 0.000 claims 3
- 229960003736 bosutinib Drugs 0.000 claims 3
- 229960005395 cetuximab Drugs 0.000 claims 3
- 229960002448 dasatinib Drugs 0.000 claims 3
- 229960002584 gefitinib Drugs 0.000 claims 3
- 229960002411 imatinib Drugs 0.000 claims 3
- 201000005202 lung cancer Diseases 0.000 claims 3
- 239000003757 phosphotransferase inhibitor Substances 0.000 claims 3
- 229960003787 sorafenib Drugs 0.000 claims 3
- 229960001796 sunitinib Drugs 0.000 claims 3
- 229960000575 trastuzumab Drugs 0.000 claims 3
- 229960000241 vandetanib Drugs 0.000 claims 3
- JOGKUKXHTYWRGZ-UHFFFAOYSA-N BEZ235 Chemical compound O=C1N(C)C2=CN=C3C=CC(C=4C=C5C=CC=CC5=NC=4)=CC3=C2N1C1=CC=C(C(C)(C)C#N)C=C1 JOGKUKXHTYWRGZ-UHFFFAOYSA-N 0.000 claims 2
- 208000009899 Burkitt Lymphoma Diseases 0.000 claims 2
- 206010012818 Diffuse large B-cell lymphoma Diseases 0.000 claims 2
- 206010017758 Gastric cancer Diseases 0.000 claims 2
- SDUQYLNIPVEERB-QPPQHZFASA-N Gemcitabine Chemical compound O=C1N=C(N)C=CN1[C@H]1C(F)(F)[C@H](O)[C@@H](CO)O1 SDUQYLNIPVEERB-QPPQHZFASA-N 0.000 claims 2
- 239000005536 L01XE08 - Nilotinib Substances 0.000 claims 2
- 239000003798 L01XE11 - Pazopanib Substances 0.000 claims 2
- 239000002144 L01XE18 - Ruxolitinib Substances 0.000 claims 2
- WOSKHXYHFSIKNG-UHFFFAOYSA-N Lenvatinib Chemical compound C=12C=C(C(N)=O)C(OC)=CC2=NC=CC=1OC(C=C1Cl)=CC=C1NC(=O)NC1CC1 WOSKHXYHFSIKNG-UHFFFAOYSA-N 0.000 claims 2
- 229950002212 Mubritinib Drugs 0.000 claims 2
- 239000005462 Mubritinib Substances 0.000 claims 2
- ZTFBIUXIQYRUNT-MDWZMJQESA-N Mubritinib Chemical compound C1=CC(C(F)(F)F)=CC=C1\C=C\C1=NC(COC=2C=CC(CCCCN3N=NC=C3)=CC=2)=CO1 ZTFBIUXIQYRUNT-MDWZMJQESA-N 0.000 claims 2
- HHZIURLSWUIHRB-UHFFFAOYSA-N Nilotinib Chemical compound C1=NC(C)=CN1C1=CC(NC(=O)C=2C=C(NC=3N=C(C=CN=3)C=3C=NC=CC=3)C(C)=CC=2)=CC(C(F)(F)F)=C1 HHZIURLSWUIHRB-UHFFFAOYSA-N 0.000 claims 2
- 108010061219 Panitumumab Proteins 0.000 claims 2
- 206010038038 Rectal cancer Diseases 0.000 claims 2
- 206010038389 Renal cancer Diseases 0.000 claims 2
- CBPNZQVSJQDFBE-FUXHJELOSA-N Temsirolimus Chemical compound C1C[C@@H](OC(=O)C(C)(CO)CO)[C@H](OC)C[C@@H]1C[C@@H](C)[C@H]1OC(=O)[C@@H]2CCCCN2C(=O)C(=O)[C@](O)(O2)[C@H](C)CC[C@H]2C[C@H](OC)/C(C)=C/C=C/C=C/[C@@H](C)C[C@@H](C)C(=O)[C@H](OC)[C@H](O)/C(C)=C/[C@@H](C)C(=O)C1 CBPNZQVSJQDFBE-FUXHJELOSA-N 0.000 claims 2
- 230000002424 anti-apoptotic Effects 0.000 claims 2
- 239000002246 antineoplastic agent Substances 0.000 claims 2
- 229960005277 gemcitabine Drugs 0.000 claims 2
- 201000010982 kidney cancer Diseases 0.000 claims 2
- 229960003784 lenvatinib Drugs 0.000 claims 2
- 229960001346 nilotinib Drugs 0.000 claims 2
- 229960001972 panitumumab Drugs 0.000 claims 2
- 229960000639 pazopanib Drugs 0.000 claims 2
- CUIHSIWYWATEQL-UHFFFAOYSA-N pazopanib Chemical compound C1=CC2=C(C)N(C)N=C2C=C1N(C)C(N=1)=CC=NC=1NC1=CC=C(C)C(S(N)(=O)=O)=C1 CUIHSIWYWATEQL-UHFFFAOYSA-N 0.000 claims 2
- 201000001275 rectum cancer Diseases 0.000 claims 2
- 229960000215 ruxolitinib Drugs 0.000 claims 2
- HFNKQEVNSGCOJV-OAHLLOKOSA-N ruxolitinib Chemical compound C1([C@@H](CC#N)N2N=CC(=C2)C=2C=3C=CNC=3N=CN=2)CCCC1 HFNKQEVNSGCOJV-OAHLLOKOSA-N 0.000 claims 2
- 201000011549 stomach cancer Diseases 0.000 claims 2
- 229960000235 temsirolimus Drugs 0.000 claims 2
- 229960003862 vemurafenib Drugs 0.000 claims 2
- GPXBXXGIAQBQNI-UHFFFAOYSA-N vemurafenib Chemical compound CCCS(=O)(=O)NC1=CC=C(F)C(C(=O)C=2C3=CC(=CN=C3NC=2)C=2C=CC(Cl)=CC=2)=C1F GPXBXXGIAQBQNI-UHFFFAOYSA-N 0.000 claims 2
- 229920000160 (ribonucleotides)n+m Polymers 0.000 claims 1
- LQBVNQSMGBZMKD-UHFFFAOYSA-N 4-[4-[[2-(4-chlorophenyl)-4,4-dimethylcyclohexen-1-yl]methyl]piperazin-1-yl]-N-[3-nitro-4-(oxan-4-ylmethylamino)phenyl]sulfonyl-2-(1H-pyrrolo[2,3-b]pyridin-5-yloxy)benzamide Chemical compound C=1C=C(Cl)C=CC=1C=1CC(C)(C)CCC=1CN(CC1)CCN1C(C=C1OC=2C=C3C=CNC3=NC=2)=CC=C1C(=O)NS(=O)(=O)C(C=C1[N+]([O-])=O)=CC=C1NCC1CCOCC1 LQBVNQSMGBZMKD-UHFFFAOYSA-N 0.000 claims 1
- HPLNQCPCUACXLM-PGUFJCEWSA-N 4-[4-[[2-(4-chlorophenyl)phenyl]methyl]piperazin-1-yl]-N-[4-[[(2R)-4-(dimethylamino)-1-phenylsulfanylbutan-2-yl]amino]-3-nitrophenyl]sulfonylbenzamide Chemical compound C([C@@H](CCN(C)C)NC=1C(=CC(=CC=1)S(=O)(=O)NC(=O)C=1C=CC(=CC=1)N1CCN(CC=2C(=CC=CC=2)C=2C=CC(Cl)=CC=2)CC1)[N+]([O-])=O)SC1=CC=CC=C1 HPLNQCPCUACXLM-PGUFJCEWSA-N 0.000 claims 1
- WLCZTRVUXYALDD-IBGZPJMESA-N 7-[[(2S)-2,6-bis(2-methoxyethoxycarbonylamino)hexanoyl]amino]heptoxy-methylphosphinic acid Chemical compound COCCOC(=O)NCCCC[C@H](NC(=O)OCCOC)C(=O)NCCCCCCCOP(C)(O)=O WLCZTRVUXYALDD-IBGZPJMESA-N 0.000 claims 1
- AOJJSUZBOXZQNB-TZSSRYMLSA-N ADRIAMYCIN 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(=O)CO)[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 AOJJSUZBOXZQNB-TZSSRYMLSA-N 0.000 claims 1
- 206010004146 Basal cell carcinoma Diseases 0.000 claims 1
- 108010005144 Bevacizumab Proteins 0.000 claims 1
- 206010005003 Bladder cancer Diseases 0.000 claims 1
- 206010005949 Bone cancer Diseases 0.000 claims 1
- 206010006187 Breast cancer Diseases 0.000 claims 1
- 206010008342 Cervix carcinoma Diseases 0.000 claims 1
- 208000006332 Choriocarcinoma Diseases 0.000 claims 1
- 206010009944 Colon cancer Diseases 0.000 claims 1
- 229940115080 Doxil Drugs 0.000 claims 1
- 206010014733 Endometrial cancer Diseases 0.000 claims 1
- 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 1
- 229960005420 Etoposide Drugs 0.000 claims 1
- 229950005309 Fostamatinib Drugs 0.000 claims 1
- GKDRMWXFWHEQQT-UHFFFAOYSA-N Fostamatinib Chemical compound COC1=C(OC)C(OC)=CC(NC=2N=C(NC=3N=C4N(COP(O)(O)=O)C(=O)C(C)(C)OC4=CC=3)C(F)=CN=2)=C1 GKDRMWXFWHEQQT-UHFFFAOYSA-N 0.000 claims 1
- 208000002250 Hematologic Neoplasms Diseases 0.000 claims 1
- HOMGKSMUEGBAAB-UHFFFAOYSA-N Ifosfamide Chemical compound ClCCNP1(=O)OCCCN1CCCl HOMGKSMUEGBAAB-UHFFFAOYSA-N 0.000 claims 1
- 229960001101 Ifosfamide Drugs 0.000 claims 1
- 206010023825 Laryngeal cancer Diseases 0.000 claims 1
- 206010024324 Leukaemias Diseases 0.000 claims 1
- 206010025323 Lymphomas Diseases 0.000 claims 1
- 206010025650 Malignant melanoma Diseases 0.000 claims 1
- 241000124008 Mammalia Species 0.000 claims 1
- JLYAXFNOILIKPP-KXQOOQHDSA-N Navitoclax Chemical compound C([C@@H](NC1=CC=C(C=C1S(=O)(=O)C(F)(F)F)S(=O)(=O)NC(=O)C1=CC=C(C=C1)N1CCN(CC1)CC1=C(CCC(C1)(C)C)C=1C=CC(Cl)=CC=1)CSC=1C=CC=CC=1)CN1CCOCC1 JLYAXFNOILIKPP-KXQOOQHDSA-N 0.000 claims 1
- 206010029260 Neuroblastoma Diseases 0.000 claims 1
- 206010030155 Oesophageal carcinoma Diseases 0.000 claims 1
- FAQDUNYVKQKNLD-UHFFFAOYSA-N Olaparib Chemical compound FC1=CC=C(CC2=C3[CH]C=CC=C3C(=O)N=N2)C=C1C(=O)N(CC1)CCN1C(=O)C1CC1 FAQDUNYVKQKNLD-UHFFFAOYSA-N 0.000 claims 1
- 206010025310 Other lymphomas Diseases 0.000 claims 1
- 206010033128 Ovarian cancer Diseases 0.000 claims 1
- 208000008443 Pancreatic Carcinoma Diseases 0.000 claims 1
- 102000030951 Phosphotransferases Human genes 0.000 claims 1
- 108091000081 Phosphotransferases Proteins 0.000 claims 1
- 206010035226 Plasma cell myeloma Diseases 0.000 claims 1
- XOFYZVNMUHMLCC-ZPOLXVRWSA-N Prednisone Chemical compound O=C1C=C[C@]2(C)[C@H]3C(=O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 XOFYZVNMUHMLCC-ZPOLXVRWSA-N 0.000 claims 1
- 206010060862 Prostate cancer Diseases 0.000 claims 1
- 108010062724 Ranibizumab Proteins 0.000 claims 1
- 229960003876 Ranibizumab Drugs 0.000 claims 1
- 108010001645 Rituximab Proteins 0.000 claims 1
- 206010039491 Sarcoma Diseases 0.000 claims 1
- AYUNIORJHRXIBJ-TXHRRWQRSA-N Tanespimycin Chemical compound N1C(=O)\C(C)=C\C=C/[C@H](OC)[C@@H](OC(N)=O)\C(C)=C\[C@H](C)[C@@H](O)[C@@H](OC)C[C@H](C)CC2=C(NCC=C)C(=O)C=C1C2=O AYUNIORJHRXIBJ-TXHRRWQRSA-N 0.000 claims 1
- 229950007866 Tanespimycin Drugs 0.000 claims 1
- 206010057644 Testis cancer Diseases 0.000 claims 1
- 206010046766 Uterine cancer Diseases 0.000 claims 1
- 229960004528 Vincristine Drugs 0.000 claims 1
- 238000009098 adjuvant therapy Methods 0.000 claims 1
- 229960000397 bevacizumab Drugs 0.000 claims 1
- 201000009036 biliary tract cancer Diseases 0.000 claims 1
- 201000005216 brain cancer Diseases 0.000 claims 1
- 201000010881 cervical cancer Diseases 0.000 claims 1
- 238000002512 chemotherapy Methods 0.000 claims 1
- 201000010918 connective tissue cancer Diseases 0.000 claims 1
- 229920003013 deoxyribonucleic acid Polymers 0.000 claims 1
- 210000002249 digestive system Anatomy 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 229940079593 drugs Drugs 0.000 claims 1
- 201000004101 esophageal cancer Diseases 0.000 claims 1
- 238000001415 gene therapy Methods 0.000 claims 1
- 201000010536 head and neck cancer Diseases 0.000 claims 1
- 238000009169 immunotherapy Methods 0.000 claims 1
- 239000003112 inhibitor Substances 0.000 claims 1
- 230000002401 inhibitory effect Effects 0.000 claims 1
- 201000007270 liver cancer Diseases 0.000 claims 1
- 201000001441 melanoma Diseases 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 201000000050 myeloid neoplasm Diseases 0.000 claims 1
- 229960000572 olaparib Drugs 0.000 claims 1
- 201000002528 pancreatic cancer Diseases 0.000 claims 1
- 229960003407 pegaptanib Drugs 0.000 claims 1
- 229960004618 prednisone Drugs 0.000 claims 1
- 238000001959 radiotherapy Methods 0.000 claims 1
- 230000000241 respiratory Effects 0.000 claims 1
- 201000000582 retinoblastoma Diseases 0.000 claims 1
- 201000009410 rhabdomyosarcoma Diseases 0.000 claims 1
- 229960004641 rituximab Drugs 0.000 claims 1
- 201000000849 skin cancer Diseases 0.000 claims 1
- 238000001356 surgical procedure Methods 0.000 claims 1
- 201000003120 testicular cancer Diseases 0.000 claims 1
- 201000002510 thyroid cancer Diseases 0.000 claims 1
- 230000002485 urinary Effects 0.000 claims 1
- 201000005112 urinary bladder cancer Diseases 0.000 claims 1
- 229960001183 venetoclax Drugs 0.000 claims 1
- 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 1
- 230000003612 virological Effects 0.000 claims 1
Claims (16)
- JQ1およびそのアナログから選択される1以上の第一の剤および1以上の第二の剤を含む、それを必要とする対象において新生物を処置することにおける使用のための医薬組成物であって、1以上の第二の剤が、
MK2206、ダサチニブ、AZD6244、クリゾチニブ、CYT387、ラパチニブ、フラボピリドール、y−27632、エルロチニブ、アファチニブ、アキシチニブ、ボスチニブ、セツキシマブ、フォスタマチニブ、ゲフィチニブ、イマチニブ、ラパチニブ、レンバチニブ、ムブリチニブ、ニロチニブ、パニツムマブ、パゾパニブ、ルクソリチニブ、ソラフェニブ、スニチニブ、トラスツズマブ、バンデタニブ、およびベムラフェニブからなる群から選択されるキナーゼインヒビター;
抗アポトーシス剤;
ビンクリスチン、エトポシド、17−AAG、アドルシル、SAHA、ドキシル、ゲムシタビン、AZD2281、DBZ、イホスファミド、レブリミド、プレドニゾン、リツキシマブ、ベバシズマブ、ペガプタニブ、およびラニビズマブからなる群から選択される抗新生物剤;
テムシロリムスまたはBEZ235、ここでテムシロリムスまたはBEZ235は単独では抗新生物効果を有しない用量で投与される;
から選択される、前記医薬組成物。 - キナーゼインヒビターが、クリゾチニブ、CYT387、ラパチニブ、およびフラボピリドールからなる群から選択される、請求項1に記載の医薬組成物。
- JQ1および/またはそのアナログが、1以上の第二の剤と別々に、連続的に、または同時に投与される、請求項1または2に記載の医薬組成物。
- 抗アポトーシス剤が、ABT263、ABT199、ABT737、およびオバトクラックスからなる群から選択される、請求項1に記載の医薬組成物。
- 抗新生物剤がゲムシタビンである、請求項1に記載の医薬組成物。
- 対象が哺乳動物である、請求項1〜5のいずれか一項に記載の医薬組成物。
- 対象がヒト患者である、請求項6に記載の医薬組成物。
- 対象が、肺がん、びまん性大細胞型B細胞リンパ腫およびバーキットリンパ腫を含むリンパ腫、前立腺がん、基底細胞癌、胆道がん、膀胱がん、骨がん、脳がん、CNSがん、乳がん、子宮頸がん、絨毛癌、大腸がん、直腸がん、結合組織がん、消化器系のがん、子宮内膜がん、食道がん、眼がん、頭頸部のがん、胃のがん、上皮内新生物、腎臓がん、喉頭がん、白血病、肝がん、肺がん、血液新生物、メラノーマ、ミエローマ、神経芽細胞腫、口腔がん、卵巣がん、膵がん、網膜芽細胞腫、横紋筋肉腫、直腸のがん、腎がん、呼吸器系のがん、肉腫、皮膚がん、胃がん、精巣がん、甲状腺がん、子宮がん、および泌尿器系のがんからなる群から選択される新生物を有する、請求項1に記載の医薬組成物。
- 新生物が肺がんである、請求項8に記載の医薬組成物。
- 新生物がびまん性大細胞型B細胞リンパ腫である、請求項8に記載の医薬組成物。
- 新生物がバーキットリンパ腫である、請求項8に記載の医薬組成物。
- 対象が追加の抗新生物療法でさらに処置される、請求項1に記載の医薬組成物。
- 追加の抗新生物療法が、手術、放射線療法、化学療法、遺伝子療法、DNA療法、ウイルス療法、RNA療法、アジュバント療法、免疫療法またはそれらの組み合わせである、請求項12に記載の医薬組成物。
- JQ1および/またはそのアナログがJQ1である、請求項1に記載の医薬組成物。
- (a)JQ1およびそのアナログから選択される第一の剤、および
(b)MK2206、ダサチニブ、AZD6244、クリゾチニブ、CYT387、ラパチニブ、フラボピリドール、y−27632、エルロチニブ、アファチニブ、アキシチニブ、ボスチニブ、セツキシマブ、フォスタマチニブ、ゲフィチニブ、イマチニブ、レンバチニブ、ムブリチニブ、ニロチニブ、パニツムマブ、パゾパニブ、ルクソリチニブ、ソラフェニブ、スニチニブ、トラスツズマブ、バンデタニブ、およびベムラフェニブからなる群から選択されるキナーゼインヒビター
の有効量を含む、医薬組成物。 - (a)JQ1およびそのアナログから選択される第一の剤を含有する容器、および
(b)MK2206、ダサチニブ、AZD6244、クリゾチニブ、CYT387、ラパチニブ、フラボピリドール、y−27632、エルロチニブ、アファチニブ、アキシチニブ、ボスチニブ、セツキシマブ、フォスタマチニブ、ゲフィチニブ、イマチニブ、レンバチニブ、ムブリチニブ、ニロチニブ、パニツムマブ、パゾパニブ、ルクソリチニブ、ソラフェニブ、スニチニブ、トラスツズマブ、バンデタニブ、およびベムラフェニブからなる群から選択されるキナーゼインヒビターを含有する容器
を含有する包装を含む、キット。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201361901908P | 2013-11-08 | 2013-11-08 | |
US61/901,908 | 2013-11-08 | ||
PCT/US2014/064549 WO2015070020A2 (en) | 2013-11-08 | 2014-11-07 | Combination therapy for cancer using bromodomain and extra-terminal (bet) protein inhibitors |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2016535756A JP2016535756A (ja) | 2016-11-17 |
JP2016535756A5 true JP2016535756A5 (ja) | 2017-12-14 |
JP6637884B2 JP6637884B2 (ja) | 2020-01-29 |
Family
ID=53042332
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2016528821A Active JP6637884B2 (ja) | 2013-11-08 | 2014-11-07 | ブロモドメインおよびエクストラターミナル(bet)タンパク質インヒビターを使用するがんのための併用療法 |
Country Status (9)
Country | Link |
---|---|
US (2) | US11446309B2 (ja) |
EP (1) | EP3066101B1 (ja) |
JP (1) | JP6637884B2 (ja) |
KR (1) | KR20160072261A (ja) |
CN (1) | CN105849110B (ja) |
CA (1) | CA2929652A1 (ja) |
MX (1) | MX2016005980A (ja) |
RU (1) | RU2016122654A (ja) |
WO (1) | WO2015070020A2 (ja) |
Families Citing this family (35)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105582014B (zh) | 2010-05-14 | 2019-06-14 | 达那-法伯癌症研究所 | 用于治疗白血病的组合物和方法 |
BR122014024883A2 (pt) | 2010-05-14 | 2019-08-20 | Dana-Farber Cancer Institute, Inc. | Compostos no tratamento de neoplasia |
CA2929652A1 (en) | 2013-11-08 | 2015-05-14 | Dana-Farber Cancer Institute, Inc. | Combination therapy for cancer using bromodomain and extra-terminal (bet) protein inhibitors |
JP2017506666A (ja) | 2014-02-28 | 2017-03-09 | テンシャ セラピューティクス,インコーポレイテッド | 高インスリン血症に関連した症状の処置 |
US20150345047A1 (en) * | 2014-05-29 | 2015-12-03 | Memorial Sloan Kettering Cancer Center | Systems and methods for identifying drug combinations for reduced drug resistance in cancer treatment |
US10124009B2 (en) | 2014-10-27 | 2018-11-13 | Tensha Therapeutics, Inc. | Bromodomain inhibitors |
EP3215135B1 (en) * | 2014-11-07 | 2020-05-13 | Tolero Pharmaceuticals, Inc. | Methods to target transcriptional control at super-enhancer regions |
US10813939B2 (en) | 2014-12-05 | 2020-10-27 | H. Lee Moffitt Cancer Center And Research Institute, Inc. | Bromodomain inhibitor as adjuvant in cancer immunotherapy |
WO2016172214A1 (en) | 2015-04-20 | 2016-10-27 | Tolero Pharmaceuticals, Inc. | Predicting response to alvocidib by mitochondrial profiling |
EP4086264B1 (en) | 2015-05-18 | 2023-10-25 | Sumitomo Pharma Oncology, Inc. | Alvocidib prodrugs having increased bioavailability |
WO2017015027A1 (en) * | 2015-07-20 | 2017-01-26 | Mayo Foundation For Medical Education And Research | Methods and materials for treating cancer |
MX2018001289A (es) | 2015-08-03 | 2018-04-30 | Tolero Pharmaceuticals Inc | Terapias de combinacion para el tratamiento del cancer. |
EP3334725A4 (en) | 2015-08-10 | 2019-07-31 | Dana-Farber Cancer Institute, Inc. | RESISTANCE MECHANISM VERSUS BET BROMDOMÄNEN INHIBITORS |
SG11201800865WA (en) * | 2015-08-19 | 2018-02-27 | Eisai R&D Man Co Ltd | Therapeutic agent for biliary tract cancer |
CN109462980B (zh) | 2016-03-15 | 2022-02-08 | 奥莱松基因组股份有限公司 | 用于治疗血液恶性肿瘤的lsd1抑制剂的组合 |
EP3532059B1 (en) | 2016-10-27 | 2022-01-26 | Celgene Quanticel Research, Inc. | Bromodomain and extra-terminal protein inhibitor combination therapy |
US20180133212A1 (en) * | 2016-11-03 | 2018-05-17 | Gilead Sciences, Inc. | Combination of a bcl-2 inhibitor and a bromodomain inhibitor for treating cancer |
US11279694B2 (en) | 2016-11-18 | 2022-03-22 | Sumitomo Dainippon Pharma Oncology, Inc. | Alvocidib prodrugs and their use as protein kinase inhibitors |
WO2018106988A1 (en) * | 2016-12-09 | 2018-06-14 | Smet Pharmaceutical Inc. | Biologically active compositions containing two different classes of chemical compounds for treating solid tumors |
KR20190099260A (ko) | 2016-12-19 | 2019-08-26 | 톨레로 파마수티컬스, 인크. | 프로파일링 펩티드 및 감도 프로파일링을 위한 방법 |
JP7300394B2 (ja) | 2017-01-17 | 2023-06-29 | ヘパリジェニックス ゲーエムベーハー | 肝再生の促進又は肝細胞死の低減もしくは予防のためのプロテインキナーゼ阻害 |
EP3658188A1 (en) * | 2017-07-26 | 2020-06-03 | H. Hoffnabb-La Roche Ag | Combination therapy with a bet inhibitor and a bcl-2 inhibitor |
EP3664807A4 (en) * | 2017-08-09 | 2021-05-05 | Mayo Foundation for Medical Education and Research | METHODS AND MATERIALS FOR IDENTIFYING AND TREATING BET INHIBITOR RESISTANT CANCER |
US11497756B2 (en) | 2017-09-12 | 2022-11-15 | Sumitomo Pharma Oncology, Inc. | Treatment regimen for cancers that are insensitive to BCL-2 inhibitors using the MCL-1 inhibitor alvocidib |
WO2019103238A1 (ko) * | 2017-11-23 | 2019-05-31 | 한국과학기술원 | Pi3k/mtor 저해제 저항성 암 치료제 |
US20190240198A1 (en) * | 2018-02-05 | 2019-08-08 | Dean G. Tang | Formulations and methods for the treatment of cancers |
CA3092003A1 (en) * | 2018-02-27 | 2019-09-06 | Pfizer Inc. | Combination of a cyclin dependent kinase inhibitor and a bet-bromodomain inhibitor |
CZ308400B6 (cs) * | 2018-04-11 | 2020-07-29 | Univerzita Karlova | Farmaceutický přípravek pro léčení maligního melanomu |
MX2021006544A (es) | 2018-12-04 | 2021-07-07 | Sumitomo Pharma Oncology Inc | Inhibidores de cinasa dependiente de ciclina 9 (cdk9) y polimorfos de los mismos para uso como agentes para el tratamiento de cancer. |
WO2020191326A1 (en) | 2019-03-20 | 2020-09-24 | Sumitomo Dainippon Pharma Oncology, Inc. | Treatment of acute myeloid leukemia (aml) with venetoclax failure |
CN113018301A (zh) * | 2019-12-09 | 2021-06-25 | 中国科学院大连化学物理研究所 | JQ1与Erlotinib组合物在制备治疗肝癌药物中应用和治疗肝癌药物 |
CN111012774A (zh) * | 2020-03-02 | 2020-04-17 | 南通大学附属医院 | 一种jq-1在制备胰腺癌治疗药物中的应用及其抑制胰腺癌外泌体分泌的验证方法 |
WO2022111390A1 (zh) * | 2020-11-24 | 2022-06-02 | 广州君赫生物科技有限公司 | 化合物在制备调降 runx2 表达试剂中的应用 |
CN113082037B (zh) * | 2021-04-23 | 2022-09-13 | 浙江大学 | 小分子组合物在制备治疗肝内胆管细胞癌药物中的应用 |
CA3228524A1 (en) * | 2021-08-10 | 2023-02-16 | Bryan William STROUSE | Momelotinib combination therapy |
Family Cites Families (141)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2951540A (en) | 1956-11-05 | 1960-09-06 | Gen Motors Corp | Propeller brake |
US3709898A (en) | 1971-02-09 | 1973-01-09 | Upjohn Co | Process for the production of triazolobenzodiazepines and intermediates |
US3681343A (en) | 1971-05-11 | 1972-08-01 | Upjohn Co | 6-phenyl-s-triazolo{8 4,3-a{9 {8 1,4{9 {0 benzodiazepines |
US3812259A (en) | 1971-08-09 | 1974-05-21 | Upjohn Co | Animal feed and process |
CH622019A5 (en) | 1975-10-23 | 1981-03-13 | Upjohn Co | Process for the preparation of aminotriazolobenzodiazepines |
FR2329668A1 (fr) | 1975-10-27 | 1977-05-27 | Upjohn Co | Procede de preparation d'aminotriazolobenzodiazepines |
EP0087850A1 (en) | 1982-01-04 | 1983-09-07 | The Upjohn Company | Benzodiazepines for anti-hypertensive use |
DE3435973A1 (de) | 1984-10-01 | 1986-04-10 | Boehringer Ingelheim KG, 6507 Ingelheim | Diazepine enthaltende pharmazeutische zusammensetzungen mit paf-antagonistischer wirkung |
DE3724164A1 (de) | 1986-07-25 | 1988-01-28 | Boehringer Ingelheim Kg | Neue 1,4-benzodiazepine, ihre herstellung und verwendung |
ATE86256T1 (de) | 1987-05-28 | 1993-03-15 | Yoshitomi Pharmaceutical | Thieno(triazolo)diazepinverbindungen, und medizinische verwendung derselben. |
JPH0676326B2 (ja) | 1988-05-24 | 1994-09-28 | 吉富製薬株式会社 | 循環器系疾患治療薬 |
EP0368175A1 (de) | 1988-11-06 | 1990-05-16 | Boehringer Ingelheim Kg | 3S,7S-3-(Morpholinocarbonyl)-5-(2-chlorphenyl)-7,10-dimethyl-3,4-dihydro-2H,7H-cyclopenta[4,5]thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin. |
EP0387613A1 (de) | 1989-03-03 | 1990-09-19 | Boehringer Ingelheim Kg | Neue Thienodiazepine |
CA2020806A1 (en) | 1989-07-12 | 1991-01-13 | Karl-Heinz Weber | Thienodiazepine derivatives |
DE4010528A1 (de) | 1990-04-02 | 1991-10-17 | Boehringer Ingelheim Kg | Praeparativ chromatographisches trennverfahren zur herstellung enantiomerenreiner hetrazepine |
CA2120939A1 (en) | 1991-10-11 | 1993-04-15 | Tetsuya Tahara | Therapeutic agent for osteoporosis and diazepine compound |
WO1994006802A1 (en) | 1992-09-18 | 1994-03-31 | Yoshitomi Pharmaceutical Industries, Ltd. | Thienodiazepine compound and medicinal use thereof |
EP0692483A1 (en) | 1993-03-30 | 1996-01-17 | Yoshitomi Pharmaceutical Industries, Ltd. | Cell adhesion inhibitor and thienotriazolodiazepine compound |
WO1995032963A1 (fr) | 1994-06-01 | 1995-12-07 | Yoshitomi Pharmaceutical Industries, Ltd. | Compose de thienylazole et compose de thienotriazolodiazepine |
JP3001979B2 (ja) | 1995-01-06 | 2000-01-24 | エフ・ホフマン−ラ ロシュ アーゲー | ヒドロキシメチル−イミダゾジアゼピン類及びそれらのエステル |
US5730723A (en) | 1995-10-10 | 1998-03-24 | Visionary Medical Products Corporation, Inc. | Gas pressured needle-less injection device and method |
DK0853480T3 (da) | 1995-09-09 | 2003-05-05 | Hoffmann La Roche | Anvendelse af en thienotriazolodiazepin til forøgelse af apolipoprotein A-I-niveauer |
GB9607549D0 (en) | 1996-04-11 | 1996-06-12 | Weston Medical Ltd | Spring-powered dispensing device |
AU3106197A (en) | 1996-06-12 | 1998-01-07 | Japan Tobacco Inc. | Cytokine production inhibitors, triazepine compounds, and intermediates there of |
US5693641A (en) | 1996-08-16 | 1997-12-02 | Berlex Laboratories Inc. | Bicyclic pyrimidine derivatives and their use as anti-coagulants |
CN1109037C (zh) | 1996-09-13 | 2003-05-21 | 三菱制药株式会社 | 噻吩并-三唑并二氮杂䓬化合物及其医药用途 |
US6444664B1 (en) | 1997-04-18 | 2002-09-03 | Nederlandse Organisatie Voor Toegepast - Natuurweten Schappelijk Onderzoek (Tno) | Method for controlling the plasma level of lipoproteins to treat alzheimeris disease |
JPH11228576A (ja) | 1997-12-10 | 1999-08-24 | Japan Tobacco Inc | アポトーシス抑制剤 |
IT1298087B1 (it) | 1998-01-08 | 1999-12-20 | Fiderm S R L | Dispositivo per il controllo della profondita' di penetrazione di un ago, in particolare applicabile ad una siringa per iniezioni |
FR2779652B1 (fr) | 1998-06-15 | 2001-06-08 | Sod Conseils Rech Applic | Utilisation de diazepines pour la preparation de medicaments destines a traiter les etats pathologiques ou les maladies dans lesquels un des recepteurs de la somatostatine est implique |
KR20000016732A (en) | 1998-12-12 | 2000-03-25 | Japan Tobacco Inc | Cytokine production inhibitors, triazepine compounds, and intermediates thereof |
KR20020000223A (ko) | 1999-05-14 | 2002-01-05 | 존 비. 랜디스 | 표피성장인자 수용체 길항제를 사용한 인간 난치성 종양의치료 방법 |
US6312215B1 (en) | 2000-02-15 | 2001-11-06 | United Technologies Corporation | Turbine engine windmilling brake |
US7589167B2 (en) | 2000-02-22 | 2009-09-15 | J. David Gladstone Institutes | ZA loops of bromodomains |
KR100838686B1 (ko) | 2000-06-16 | 2008-06-16 | 미쯔비시 웰 파마 가부시키가이샤 | 방출 pH 범위 및/또는 속도 제어 조성물 |
AU2001270297A1 (en) | 2000-06-30 | 2002-01-14 | Neurogen Corporation | 2-phenylimidazo(1,2-a)pyridine derivatives: a new class of gaba brain receptor ligands |
US20060142257A1 (en) | 2001-01-19 | 2006-06-29 | Eberhard Nieschlag | Male contraceptive formulation comprising norethisterone |
US6979682B2 (en) | 2001-02-23 | 2005-12-27 | Board Of Supervisors Of Louisiana State University And Agricultural And Mechanical College | Platelet-activating factor antagonist inhibition of angiogenesis and tumor growth induced by basic fibroblast |
US20030216758A1 (en) | 2001-12-28 | 2003-11-20 | Angiotech Pharmaceuticals, Inc. | Coated surgical patches |
GB0206215D0 (en) | 2002-03-15 | 2002-05-01 | Novartis Ag | Organic compounds |
US6861422B2 (en) | 2003-02-26 | 2005-03-01 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Dihydropteridinones, processes for preparing them and their use as pharmaceutical compositions |
PL378116A1 (pl) | 2003-02-27 | 2006-03-06 | Abbott Laboratories | Heterocykliczne inhibitory kinazy |
GB0305929D0 (en) | 2003-03-14 | 2003-04-23 | Novartis Ag | Organic compounds |
EP1656155A2 (en) | 2003-06-02 | 2006-05-17 | Ohio University | Use of genes differentially expressed during aging of liver for treatment and diagnosis |
WO2005002526A2 (en) | 2003-07-01 | 2005-01-13 | President And Fellows Of Harvard College | Method and compositions for treatment of viral infections |
AU2004272288B2 (en) | 2003-09-18 | 2008-11-13 | Novartis Ag | 2,4-di (phenylamino) pyrimidines useful in the treatment of proliferative disorders |
EP1528056A1 (en) | 2003-10-29 | 2005-05-04 | Academisch Ziekenhuis bij de Universiteit van Amsterdam | Deoxynojirimycin analogues and their uses as glucosylceramidase inhibitors |
US20060074088A1 (en) | 2004-08-14 | 2006-04-06 | Boehringer Ingelheim International Gmbh | Dihydropteridinones for the treatment of cancer diseases |
US7759485B2 (en) | 2004-08-14 | 2010-07-20 | Boehringer Ingelheim International Gmbh | Process for the manufacture of dihydropteridinones |
US20060035903A1 (en) | 2004-08-14 | 2006-02-16 | Boehringer Ingelheim International Gmbh | Storage stable perfusion solution for dihydropteridinones |
US20060058311A1 (en) | 2004-08-14 | 2006-03-16 | Boehringer Ingelheim International Gmbh | Combinations for the treatment of diseases involving cell proliferation |
CN1759834B (zh) | 2004-09-17 | 2010-06-23 | 中国医学科学院医药生物技术研究所 | 黄连素或其与辛伐他汀联合在制备用于预防或治疗与血脂有关疾病或症状的产品中用途 |
US8624027B2 (en) | 2005-05-12 | 2014-01-07 | Abbvie Inc. | Combination therapy for treating cancer and diagnostic assays for use therein |
JP5159305B2 (ja) | 2005-05-30 | 2013-03-06 | 田辺三菱製薬株式会社 | チエノトリアゾロジアゼピン化合物及びその医薬としての用途 |
WO2007014838A1 (en) | 2005-08-03 | 2007-02-08 | Boehringer Ingelheim International Gmbh | Dihydropteridinones in the treatment of respiratory diseases |
US8604042B2 (en) | 2005-11-01 | 2013-12-10 | Targegen, Inc. | Bi-aryl meta-pyrimidine inhibitors of kinases |
US8133900B2 (en) | 2005-11-01 | 2012-03-13 | Targegen, Inc. | Use of bi-aryl meta-pyrimidine inhibitors of kinases |
WO2007053452A1 (en) | 2005-11-01 | 2007-05-10 | Targegen, Inc. | Bi-aryl meta-pyrimidine inhibitors of kinases |
TW200803842A (en) | 2005-11-04 | 2008-01-16 | Wyeth Corp | Antineoplastic combinations of temsirolimus and sunitinib malate |
PT1962830E (pt) | 2005-12-23 | 2013-05-29 | Glaxosmithkline Llc | Inibidores azaindólicos de cinases aurora |
KR101062583B1 (ko) | 2006-01-17 | 2011-09-06 | 에프. 호프만-라 로슈 아게 | Gaba 수용체에 의해 알츠하이머병의 치료에 유용한아릴-아이속사졸-4-일-이미다조[1,2-a]피리딘 |
JP5243970B2 (ja) | 2006-02-14 | 2013-07-24 | バーテックス ファーマシューティカルズ インコーポレイテッド | タンパク質キナーゼの阻害剤として有用なジヒドロジアゼピン |
US20070218135A1 (en) | 2006-03-14 | 2007-09-20 | Glenmark Pharmaceuticals Limited | Sustained release matrix pharmaceutical composition |
CA2649701A1 (en) | 2006-05-03 | 2007-11-15 | Novartis Ag | Use of organic compounds |
US7621117B2 (en) | 2006-06-19 | 2009-11-24 | Pratt & Whitney Canada Corp. | Apparatus and method for controlling engine windmilling |
BRPI0717767A2 (pt) | 2006-10-19 | 2013-11-12 | Signal Pharm Llc | Composto, composição farmacêutica, e, métodos para tratar ou prevenir câncer, uma condição inflamatória, uma condição imunológica ou uma condição metabólica, e para inibir uma quinase em uma célula de expressa a dita quinase |
WO2008066887A2 (en) | 2006-11-30 | 2008-06-05 | Albert Einstein College Of Medicine Of Yeshiva University | Small molecule inhibitors of bcl6 |
TWI618544B (zh) | 2006-12-26 | 2018-03-21 | 藍瑟斯醫學影像公司 | 使心臟神經分布顯像之配位體 |
JP2008156311A (ja) | 2006-12-26 | 2008-07-10 | Institute Of Physical & Chemical Research | Brd2ブロモドメイン結合剤 |
WO2008137081A1 (en) | 2007-05-02 | 2008-11-13 | The Trustees Of Columbia University In The City Of New York | Substituted ( 5, 6 ) -dihydronaphraalenyl compounds as reversible male contraceptives |
KR20080107050A (ko) | 2007-06-05 | 2008-12-10 | 울산대학교 산학협력단 | 항-cd137 단일클론 항체를 포함하는 만성이식편대숙주 질환의 예방 또는 치료용 약학적 조성물 |
CA2710118A1 (en) | 2007-12-20 | 2009-07-02 | Cellzome Limited | Sulfamides as zap-70 inhibitors |
JP5478262B2 (ja) | 2007-12-28 | 2014-04-23 | 田辺三菱製薬株式会社 | 抗癌剤 |
EP2276747A1 (en) | 2008-03-11 | 2011-01-26 | Cellzome Limited | Sulfonamides as zap-70 inhibitors |
WO2010015340A1 (en) | 2008-08-06 | 2010-02-11 | Bayer Schering Pharma Aktiengesellschaft | Daa-pyridine as peripheral benzodiazepine receptor ligand for diagnostic imaging and pharmaceutical treatment |
EA018620B1 (ru) | 2008-10-30 | 2013-09-30 | Сёркомед Ллк | ПРОИЗВОДНЫЕ ТИЕНОТРИАЗОЛОДИАЗЕПИНА, АКТИВНЫЕ В ОТНОШЕНИИ Apo A1 |
US9266890B2 (en) | 2009-01-06 | 2016-02-23 | Dana-Farber Cancer Institute, Inc. | Pyrimido-diazepinone kinase scaffold compounds and methods of treating disorders |
MA33053B1 (fr) | 2009-01-23 | 2012-02-01 | Tadeka Pharmaceutical Company Ltd | Inhibiteurs de la poly(adp-ribose) polymerase (parp) |
GB0919431D0 (en) | 2009-11-05 | 2009-12-23 | Glaxosmithkline Llc | Novel compounds |
GB0919426D0 (en) | 2009-11-05 | 2009-12-23 | Glaxosmithkline Llc | Novel compounds |
EA023441B1 (ru) | 2009-11-05 | 2016-06-30 | ГЛАКСОСМИТКЛАЙН ЭлЭлСи | Бензодиазепиновый ингибитор бромодомена |
GB0919423D0 (en) | 2009-11-05 | 2009-12-23 | Glaxosmithkline Llc | Novel compounds |
GB0919432D0 (en) | 2009-11-05 | 2009-12-23 | Glaxosmithkline Llc | Use |
JP5524343B2 (ja) | 2009-11-05 | 2014-06-18 | グラクソスミスクライン エルエルシー | ベンゾジアゼピンブロモドメイン阻害剤 |
GB0919434D0 (en) | 2009-11-05 | 2009-12-23 | Glaxosmithkline Llc | Novel compounds |
US8862173B2 (en) | 2009-12-10 | 2014-10-14 | Motorola Solutions, Inc. | Method for selecting media for delivery to users at an incident |
WO2011101369A1 (en) | 2010-02-17 | 2011-08-25 | Boehringer Ingelheim International Gmbh | Dihydropteridinones, method for production and use thereof |
EP2553251B1 (en) | 2010-03-26 | 2018-11-07 | Rolls-Royce North American Technologies, Inc. | Adaptive fan system for a variable cycle turbofan engine |
JP5715241B2 (ja) | 2010-05-14 | 2015-05-07 | ダナ−ファーバー キャンサー インスティテュート, インコーポレイテッド | 新生物、炎症性疾患、およびその他の障害を治療するための組成物および方法 |
CN103119160B (zh) | 2010-05-14 | 2016-06-01 | 达那-法伯癌症研究所 | 用于调节代谢的组合物和方法 |
CN105582014B (zh) | 2010-05-14 | 2019-06-14 | 达那-法伯癌症研究所 | 用于治疗白血病的组合物和方法 |
CN103180318B (zh) | 2010-05-14 | 2017-05-10 | 达那-法伯癌症研究所 | 雄性避孕组合物以及使用方法 |
BR122014024883A2 (pt) | 2010-05-14 | 2019-08-20 | Dana-Farber Cancer Institute, Inc. | Compostos no tratamento de neoplasia |
JP5844358B2 (ja) | 2010-06-22 | 2016-01-13 | グラクソスミスクライン エルエルシー | ベンゾトリアゾロジアゼピン化合物を含むブロモドメイン阻害剤 |
RU2012154576A (ru) | 2010-06-25 | 2014-07-27 | Шир Хьюман Дженетик Терапис, Инк. | Способы и композиции для доставки к цнс гепаран-n-сульфатазы |
US20120014979A1 (en) | 2010-07-16 | 2012-01-19 | Alexander Dent | Use of bcl6 inhibitors for treating autoimmune diseases |
TWI583689B (zh) | 2010-08-04 | 2017-05-21 | 達納 法柏癌症學院有限公司 | 治療腫瘤形成、發炎疾病及其他病症之組成物及方法 |
CN103228142A (zh) | 2010-09-28 | 2013-07-31 | 加利福尼亚大学董事会 | 治疗代谢综合征相关疾病的gaba激动剂和治疗或预防i型糖尿病的gaba组合 |
AR084070A1 (es) * | 2010-12-02 | 2013-04-17 | Constellation Pharmaceuticals Inc | Inhibidores del bromodominio y usos de los mismos |
US9249161B2 (en) | 2010-12-02 | 2016-02-02 | Constellation Pharmaceuticals, Inc. | Bromodomain inhibitors and uses thereof |
US20130004481A1 (en) | 2011-01-12 | 2013-01-03 | Boehringer Ingelheim International Gmbh | Anticancer therapy |
EP2677865A4 (en) | 2011-02-23 | 2015-04-22 | Icahn School Med Mount Sinai | BROMODOMAIN INHIBITORS AS MODULATORS OF GENE EXPRESSION |
EP3323820B1 (en) | 2011-02-28 | 2023-05-10 | Epizyme, Inc. | Substituted 6,5-fused bicyclic heteroaryl compounds |
EP2741784B1 (en) | 2011-03-02 | 2017-05-17 | Board Of Regents, The University Of Texas System | Tusc2 therapies |
JP2014524409A (ja) | 2011-07-29 | 2014-09-22 | ザ・チルドレンズ・ホスピタル・オブ・フィラデルフィア | Hivの治療のための組成物および方法 |
FI20110279A0 (fi) | 2011-08-29 | 2011-08-29 | Outotec Oyj | Menetelmä metallien talteenottamiseksi niitä sisältävästä materiaalista |
WO2013033269A1 (en) | 2011-08-29 | 2013-03-07 | Coferon, Inc. | Bioorthogonal monomers capable of dimerizing and targeting bromodomains and methods of using same |
WO2013033270A2 (en) | 2011-08-29 | 2013-03-07 | Coferon, Inc. | Bromodomain ligands capable of dimerizing in an aqueous solution, and methods of using same |
WO2013033420A1 (en) * | 2011-08-30 | 2013-03-07 | Whitehead Institute For Biomedical Research | Methods of downregulating translocated oncogene expression using bromodomain inhibitors |
DE102011082013A1 (de) * | 2011-09-01 | 2013-03-07 | Bayer Pharma AG | 6H-Thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine |
WO2013097052A1 (en) | 2011-12-30 | 2013-07-04 | Abbott Laboratories | Bromodomain inhibitors |
WO2013123521A1 (en) | 2012-02-17 | 2013-08-22 | Nexbio, Inc. | Methods, Compounds and Compositions for Treatment of Parainfluenza Virus in Immunocompromised Patients |
EP2830629A4 (en) | 2012-03-28 | 2016-01-20 | Icahn School Of Medicine Mount Sinai | COMPOSITIONS AND METHODS FOR REACTING LATENT IMMUNODEFICIENCY VIRUS |
WO2013192274A2 (en) * | 2012-06-19 | 2013-12-27 | The Broad Institute, Inc. | Diagnostic and treatment methods in subjects having or at risk of developing resistance to cancer therapy |
JP2015531365A (ja) | 2012-09-28 | 2015-11-02 | オンコエシックス エスエー | チエノトリアゾロジアゼピン化合物を含む医薬製剤 |
WO2014071247A1 (en) | 2012-11-02 | 2014-05-08 | Dana-Farber Cancer Institute, Inc. | Pyrrol-1 -yl benzoic acid derivates useful as myc inhibitors |
CN105189514A (zh) | 2013-02-22 | 2015-12-23 | 拜耳医药股份有限公司 | 作为bet-蛋白抑制剂用于治疗过度增殖性疾病的吡咯并-和吡唑并-三唑并二氮杂卓 |
JP2016513118A (ja) | 2013-02-22 | 2016-05-12 | バイエル ファーマ アクチエンゲゼルシャフト | 4−置換されたピロロ−およびピラゾロジアゼピン類 |
AU2014223990A1 (en) | 2013-02-28 | 2015-09-10 | Washington University | Methods of treatment of human cytomegalovirus infection and diseases with bromodomain inhibitors |
WO2014159392A1 (en) | 2013-03-14 | 2014-10-02 | Dana-Farber Cancer Institute, Inc. | Bromodomain binding reagents and uses thereof |
WO2014144721A2 (en) | 2013-03-15 | 2014-09-18 | Genentech, Inc. | Treating th2-mediated diseases by inhibition of bromodomains |
CN105358150A (zh) | 2013-05-28 | 2016-02-24 | 达纳-法伯癌症研究所有限公司 | 用于心脏病的bet抑制疗法 |
WO2015013635A2 (en) | 2013-07-25 | 2015-01-29 | Dana-Farber Cancer Institute, Inc. | Inhibitors of transcription factors and uses thereof |
WO2015018522A1 (en) | 2013-08-06 | 2015-02-12 | Oncoethix Sa | Bet-bromodomain inhibitor shows synergism with several anti-cancer agents in pre-clinical models of diffuse large b-cell lymphoma (dlbcl) |
EP3030242A1 (en) | 2013-08-06 | 2016-06-15 | Oncoethix GmbH | Method of treating diffuse large b-cell lymphoma (dlbcl) using a bet-bromodomain inhibitor |
WO2015023938A1 (en) | 2013-08-16 | 2015-02-19 | Rana Therapeutics, Inc. | Epigenetic regulators of frataxin |
US8988212B2 (en) | 2013-08-22 | 2015-03-24 | GM Global Technology Operations LLC | Electric vehicle pedestrian warning system |
JP6663852B2 (ja) | 2013-09-19 | 2020-03-13 | デイナ ファーバー キャンサー インスティチュート,インコーポレイテッド | Bh3プロファイリングの方法 |
AU2014331697A1 (en) | 2013-10-11 | 2016-05-05 | Constellation Pharmaceuticals, Inc. | Use of CBP/EP300 bromodomain inhibitors for cancer immunotherapy |
CA2929652A1 (en) | 2013-11-08 | 2015-05-14 | Dana-Farber Cancer Institute, Inc. | Combination therapy for cancer using bromodomain and extra-terminal (bet) protein inhibitors |
US20160256458A1 (en) | 2013-11-18 | 2016-09-08 | Forma Therapeutics, Inc. | Benzopiperazine compositions as bet bromodomain inhibitors |
WO2015081284A1 (en) | 2013-11-26 | 2015-06-04 | Coferon, Inc. | Bivalent bromodomain ligands, and methods of using same |
BR112016013744B1 (pt) | 2013-12-24 | 2022-08-30 | Bristol-Myers Squibb Company | Compostos tricíclicos e seu uso como agentes anticâncer |
JP2017504653A (ja) | 2014-01-31 | 2017-02-09 | ダナ−ファーバー キャンサー インスティテュート, インコーポレイテッド | ジアミノピリミジンベンゼンスルホン誘導体およびその使用 |
JP2017504651A (ja) | 2014-01-31 | 2017-02-09 | ダナ−ファーバー キャンサー インスティテュート, インコーポレイテッド | ジアゼパン誘導体の使用 |
EP3099696A4 (en) | 2014-01-31 | 2017-07-05 | Dana-Farber Cancer Institute, Inc. | Diazepane derivatives and uses thereof |
JP2017506666A (ja) | 2014-02-28 | 2017-03-09 | テンシャ セラピューティクス,インコーポレイテッド | 高インスリン血症に関連した症状の処置 |
US10124009B2 (en) | 2014-10-27 | 2018-11-13 | Tensha Therapeutics, Inc. | Bromodomain inhibitors |
US10813939B2 (en) * | 2014-12-05 | 2020-10-27 | H. Lee Moffitt Cancer Center And Research Institute, Inc. | Bromodomain inhibitor as adjuvant in cancer immunotherapy |
MX2017016337A (es) | 2015-06-26 | 2018-11-22 | Tensha Therapeutics Inc | Tratamiento de carcinoma de linea media nut. |
MA43037A (fr) | 2015-10-02 | 2018-08-08 | Dana Farber Cancer Inst Inc | Polythérapie par inhibiteurs de bromodomaine et blocage de point de contrôle |
-
2014
- 2014-11-07 CA CA2929652A patent/CA2929652A1/en not_active Abandoned
- 2014-11-07 MX MX2016005980A patent/MX2016005980A/es unknown
- 2014-11-07 WO PCT/US2014/064549 patent/WO2015070020A2/en active Application Filing
- 2014-11-07 US US15/034,922 patent/US11446309B2/en active Active
- 2014-11-07 RU RU2016122654A patent/RU2016122654A/ru not_active Application Discontinuation
- 2014-11-07 CN CN201480066883.4A patent/CN105849110B/zh active Active
- 2014-11-07 JP JP2016528821A patent/JP6637884B2/ja active Active
- 2014-11-07 EP EP14860080.2A patent/EP3066101B1/en active Active
- 2014-11-07 KR KR1020167014189A patent/KR20160072261A/ko not_active Application Discontinuation
-
2020
- 2020-07-16 US US16/931,170 patent/US20210100813A1/en not_active Abandoned
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP2016535756A5 (ja) | ||
RU2016122654A (ru) | Комбинированная терапия злокачественной опухоли с использованием ингибиторов бромодоменового и экстратерминального (вет) белка | |
JP2016528251A5 (ja) | ||
ES2881048T3 (es) | Bisaminoquinolinas asimétricas y bisaminoquinolinas con enlazadores variados como inhibidores de la autofagia para el cáncer y otras terapias | |
JP2014512354A5 (ja) | ||
HRP20221152T1 (hr) | Spojevi korisni u inhibiranju cdk7 | |
JP2015532292A5 (ja) | ||
JP2014512356A5 (ja) | ||
BR112016012506A8 (pt) | combinações farmacêuticas, seus usos, e uso de um portador de dados | |
JP2015536964A5 (ja) | ||
JP2020510032A5 (ja) | ||
JP2018534289A5 (ja) | ||
JP2016528162A5 (ja) | ||
NZ703940A (en) | Pharmaceutical combinations comprising a b-raf inhibitor, an egfr inhibitor and optionally a pi3k-alpha inhibitor | |
BR112019021032A2 (pt) | terapia combinada anticâncer | |
EA201591781A1 (ru) | Химические соединения | |
Giancola et al. | Osteonecrosis of the jaw related to everolimus and bisphosphonate: a unique case report? | |
JP2014512355A5 (ja) | ||
BR112019016737A2 (pt) | Terapia anticâncer combinada | |
MX2014013039A (es) | Uso de laquinimod de dosis alta para el tratamiento de esclerosis multiple. | |
CA3081750A1 (en) | Anticancer agents | |
CN105263484A (zh) | 包含二甲双胍和二氢槲皮素的药物组合及其用于治疗癌症的用途 | |
HRP20201681T1 (hr) | Inhibitor aurora a kinaze | |
JP2018503697A5 (ja) | ||
RU2014144254A (ru) | Комбинированные продукты, содержащие ингибиторы тирозинкиназ, и их применение |