JP2005530784A5 - - Google Patents
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- JP2005530784A5 JP2005530784A5 JP2004505051A JP2004505051A JP2005530784A5 JP 2005530784 A5 JP2005530784 A5 JP 2005530784A5 JP 2004505051 A JP2004505051 A JP 2004505051A JP 2004505051 A JP2004505051 A JP 2004505051A JP 2005530784 A5 JP2005530784 A5 JP 2005530784A5
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- 239000008194 pharmaceutical composition Substances 0.000 claims 28
- 150000001875 compounds Chemical class 0.000 claims 12
- 206010035226 Plasma cell myeloma Diseases 0.000 claims 6
- 239000003795 chemical substances by application Substances 0.000 claims 5
- 201000000050 myeloid neoplasm Diseases 0.000 claims 4
- UREBDLICKHMUKA-CXSFZGCWSA-N Dexamethasone Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@@H](C)[C@@](C(=O)CO)(O)[C@@]1(C)C[C@@H]2O UREBDLICKHMUKA-CXSFZGCWSA-N 0.000 claims 3
- 229960003957 Dexamethasone Drugs 0.000 claims 3
- GOTYRUGSSMKFNF-UHFFFAOYSA-N Lenalidomide Chemical compound C1C=2C(N)=CC=CC=2C(=O)N1C1CCC(=O)NC1=O GOTYRUGSSMKFNF-UHFFFAOYSA-N 0.000 claims 3
- 201000011510 cancer Diseases 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- 239000011780 sodium chloride Substances 0.000 claims 3
- 239000012453 solvate Substances 0.000 claims 3
- 208000003950 B-Cell Lymphoma Diseases 0.000 claims 2
- 102000004269 Granulocyte Colony-Stimulating Factor Human genes 0.000 claims 2
- 108010017080 Granulocyte Colony-Stimulating Factor Proteins 0.000 claims 2
- 102000015696 Interleukins Human genes 0.000 claims 2
- 108010063738 Interleukins Proteins 0.000 claims 2
- 206010058467 Lung neoplasm malignant Diseases 0.000 claims 2
- 108010001645 Rituximab Proteins 0.000 claims 2
- 229960000390 fludarabine Drugs 0.000 claims 2
- GIUYCYHIANZCFB-FJFJXFQQSA-N fludarabine phosphate Chemical compound C1=NC=2C(N)=NC(F)=NC=2N1[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@@H]1O GIUYCYHIANZCFB-FJFJXFQQSA-N 0.000 claims 2
- 201000005202 lung cancer Diseases 0.000 claims 2
- 239000000203 mixture Substances 0.000 claims 2
- 201000009251 multiple myeloma Diseases 0.000 claims 2
- 201000006417 multiple sclerosis Diseases 0.000 claims 2
- 229960004641 rituximab Drugs 0.000 claims 2
- 238000002560 therapeutic procedure Methods 0.000 claims 2
- 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
- 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
- 206010002022 Amyloidosis Diseases 0.000 claims 1
- 206010002023 Amyloidosis Diseases 0.000 claims 1
- GXJABQQUPOEUTA-RDJZCZTQSA-N Bortezomib Chemical compound C([C@@H](C(=O)N[C@@H](CC(C)C)B(O)O)NC(=O)C=1N=CC=NC=1)C1=CC=CC=C1 GXJABQQUPOEUTA-RDJZCZTQSA-N 0.000 claims 1
- 102100006400 CSF2 Human genes 0.000 claims 1
- 229960004562 Carboplatin Drugs 0.000 claims 1
- OLESAACUTLOWQZ-UHFFFAOYSA-L Carboplatin Chemical compound O=C1O[Pt]([N]([H])([H])[H])([N]([H])([H])[H])OC(=O)C11CCC1 OLESAACUTLOWQZ-UHFFFAOYSA-L 0.000 claims 1
- MYSWGUAQZAJSOK-UHFFFAOYSA-N Ciprofloxacin Chemical compound C12=CC(N3CCNCC3)=C(F)C=C2C(=O)C(C(=O)O)=CN1C1CC1 MYSWGUAQZAJSOK-UHFFFAOYSA-N 0.000 claims 1
- CMSMOCZEIVJLDB-UHFFFAOYSA-N Cyclophosphamide Chemical compound ClCCN(CCCl)P1(=O)NCCCO1 CMSMOCZEIVJLDB-UHFFFAOYSA-N 0.000 claims 1
- 229960004397 Cyclophosphamide Drugs 0.000 claims 1
- 102000004127 Cytokines Human genes 0.000 claims 1
- 108090000695 Cytokines Proteins 0.000 claims 1
- ZDZOTLJHXYCWBA-VCVYQWHSSA-N Docetaxel Chemical compound O([C@H]1[C@H]2[C@@](C([C@H](O)C3=C(C)[C@@H](OC(=O)[C@H](O)[C@@H](NC(=O)OC(C)(C)C)C=4C=CC=CC=4)C[C@]1(O)C3(C)C)=O)(C)[C@@H](O)C[C@H]1OC[C@]12OC(=O)C)C(=O)C1=CC=CC=C1 ZDZOTLJHXYCWBA-VCVYQWHSSA-N 0.000 claims 1
- 229960004679 Doxorubicin Drugs 0.000 claims 1
- 102000003951 Erythropoietin Human genes 0.000 claims 1
- 108090000394 Erythropoietin Proteins 0.000 claims 1
- 108010017213 Granulocyte-Macrophage Colony-Stimulating Factor Proteins 0.000 claims 1
- RCINICONZNJXQF-MZXODVADSA-N Intaxel Chemical compound O([C@@H]1[C@@]2(C[C@@H](C(C)=C(C2(C)C)[C@H](C([C@]2(C)[C@@H](O)C[C@H]3OC[C@]3([C@H]21)OC(C)=O)=O)OC(=O)C)OC(=O)[C@H](O)[C@@H](NC(=O)C=1C=CC=CC=1)C=1C=CC=CC=1)O)C(=O)C1=CC=CC=C1 RCINICONZNJXQF-MZXODVADSA-N 0.000 claims 1
- 102000014150 Interferons Human genes 0.000 claims 1
- 108010050904 Interferons Proteins 0.000 claims 1
- UWKQSNNFCGGAFS-XIFFEERXSA-N Irinotecan Chemical compound C1=C2C(CC)=C3CN(C(C4=C([C@@](C(=O)OC4)(O)CC)C=4)=O)C=4C3=NC2=CC=C1OC(=O)N(CC1)CCC1N1CCCCC1 UWKQSNNFCGGAFS-XIFFEERXSA-N 0.000 claims 1
- 208000003543 Lymphoma, T-Cell, Cutaneous Diseases 0.000 claims 1
- SGDBTWWWUNNDEQ-LBPRGKRZSA-N Melphalan Chemical compound OC(=O)[C@@H](N)CC1=CC=C(N(CCCl)CCCl)C=C1 SGDBTWWWUNNDEQ-LBPRGKRZSA-N 0.000 claims 1
- 206010029592 Non-Hodgkin's lymphomas Diseases 0.000 claims 1
- 208000002154 Non-Small-Cell Lung Carcinoma Diseases 0.000 claims 1
- 108009000071 Non-small cell lung cancer Proteins 0.000 claims 1
- 206010033128 Ovarian cancer Diseases 0.000 claims 1
- 229960001592 Paclitaxel Drugs 0.000 claims 1
- 208000008443 Pancreatic Carcinoma Diseases 0.000 claims 1
- BYPFEZZEUUWMEJ-UHFFFAOYSA-N Pentoxifylline Chemical compound O=C1N(CCCCC(=O)C)C(=O)N(C)C2=C1N(C)C=N2 BYPFEZZEUUWMEJ-UHFFFAOYSA-N 0.000 claims 1
- 229960001476 Pentoxifylline Drugs 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
- 206010038389 Renal cancer Diseases 0.000 claims 1
- 208000000587 Small Cell Lung Carcinoma Diseases 0.000 claims 1
- 206010041067 Small cell lung cancer Diseases 0.000 claims 1
- 229940063683 Taxotere Drugs 0.000 claims 1
- UCFGDBYHRUNTLO-QHCPKHFHSA-N Topotecan Chemical compound C1=C(O)C(CN(C)C)=C2C=C(CN3C4=CC5=C(C3=O)COC(=O)[C@]5(O)CC)C4=NC2=C1 UCFGDBYHRUNTLO-QHCPKHFHSA-N 0.000 claims 1
- GCPXMJHSNVMWNM-UHFFFAOYSA-N Trihydroxyarsenite(Iii) Chemical compound O[As](O)O GCPXMJHSNVMWNM-UHFFFAOYSA-N 0.000 claims 1
- 229960004528 Vincristine Drugs 0.000 claims 1
- 239000002246 antineoplastic agent Substances 0.000 claims 1
- 229960002594 arsenic trioxide Drugs 0.000 claims 1
- GOLCXWYRSKYTSP-UHFFFAOYSA-N arsenic trioxide Inorganic materials O1[As]2O[As]1O2 GOLCXWYRSKYTSP-UHFFFAOYSA-N 0.000 claims 1
- 229960001467 bortezomib Drugs 0.000 claims 1
- 239000002775 capsule Substances 0.000 claims 1
- 238000002512 chemotherapy Methods 0.000 claims 1
- 229960003405 ciprofloxacin Drugs 0.000 claims 1
- 201000007241 cutaneous T cell lymphoma Diseases 0.000 claims 1
- 229960003901 dacarbazine Drugs 0.000 claims 1
- 229960003668 docetaxel Drugs 0.000 claims 1
- -1 doxetaxol Chemical compound 0.000 claims 1
- 229940105423 erythropoietin Drugs 0.000 claims 1
- 239000003102 growth factor Substances 0.000 claims 1
- 230000003394 haemopoietic Effects 0.000 claims 1
- 201000005787 hematologic cancer Diseases 0.000 claims 1
- 238000001794 hormone therapy Methods 0.000 claims 1
- 238000009169 immunotherapy Methods 0.000 claims 1
- 229940079322 interferon Drugs 0.000 claims 1
- 229960004768 irinotecan Drugs 0.000 claims 1
- 201000010982 kidney cancer Diseases 0.000 claims 1
- 229960001924 melphalan Drugs 0.000 claims 1
- 201000005962 mycosis fungoide Diseases 0.000 claims 1
- MIMNFCVQODTQDP-NDLVEFNKSA-N oblimersen Chemical group O=C1NC(=O)C(C)=CN1[C@@H]1O[C@H](COP(S)(=O)O[C@@H]2[C@H](O[C@H](C2)N2C3=NC=NC(N)=C3N=C2)COP(O)(=S)O[C@@H]2[C@H](O[C@H](C2)N2C(N=C(N)C=C2)=O)COP(O)(=S)O[C@@H]2[C@H](O[C@H](C2)N2C(N=C(N)C=C2)=O)COP(O)(=S)O[C@@H]2[C@H](O[C@H](C2)N2C3=C(C(NC(N)=N3)=O)N=C2)COP(O)(=S)O[C@@H]2[C@H](O[C@H](C2)N2C(N=C(N)C=C2)=O)COP(O)(=S)O[C@@H]2[C@H](O[C@H](C2)N2C3=C(C(NC(N)=N3)=O)N=C2)COP(O)(=S)O[C@@H]2[C@H](O[C@H](C2)N2C(NC(=O)C(C)=C2)=O)COP(O)(=S)O[C@@H]2[C@H](O[C@H](C2)N2C3=C(C(NC(N)=N3)=O)N=C2)COP(O)(=S)O[C@@H]2[C@H](O[C@H](C2)N2C(N=C(N)C=C2)=O)COP(O)(=S)O[C@@H]2[C@H](O[C@H](C2)N2C3=C(C(NC(N)=N3)=O)N=C2)COP(O)(=S)O[C@@H]2[C@H](O[C@H](C2)N2C3=NC=NC(N)=C3N=C2)COP(O)(=S)O[C@@H]2[C@H](O[C@H](C2)N2C(N=C(N)C=C2)=O)COP(O)(=S)O[C@@H]2[C@H](O[C@H](C2)N2C(N=C(N)C=C2)=O)COP(O)(=S)O[C@@H]2[C@H](O[C@H](C2)N2C(N=C(N)C=C2)=O)COP(O)(=S)O[C@@H]2[C@H](O[C@H](C2)N2C(NC(=O)C(C)=C2)=O)COP(O)(=S)O[C@@H]2[C@H](O[C@H](C2)N2C(N=C(N)C=C2)=O)COP(O)(=S)O[C@@H]2[C@H](O[C@H](C2)N2C(NC(=O)C(C)=C2)=O)CO)[C@@H](O)C1 MIMNFCVQODTQDP-NDLVEFNKSA-N 0.000 claims 1
- 229960000435 oblimersen Drugs 0.000 claims 1
- 201000002528 pancreatic cancer Diseases 0.000 claims 1
- 229960004618 prednisone Drugs 0.000 claims 1
- 230000002265 prevention Effects 0.000 claims 1
- 238000001959 radiotherapy Methods 0.000 claims 1
- 230000000306 recurrent Effects 0.000 claims 1
- 230000004936 stimulating Effects 0.000 claims 1
- 229930003347 taxol Natural products 0.000 claims 1
- 229960000303 topotecan 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
- GBABOYUKABKIAF-IELIFDKJSA-N vinorelbine Chemical compound C1N(CC=2C3=CC=CC=C3NC=22)CC(CC)=C[C@H]1C[C@]2(C(=O)OC)C1=CC([C@]23[C@H]([C@@]([C@H](OC(C)=O)[C@]4(CC)C=CCN([C@H]34)CC2)(O)C(=O)OC)N2C)=C2C=C1OC GBABOYUKABKIAF-IELIFDKJSA-N 0.000 claims 1
- 229960002066 vinorelbine Drugs 0.000 claims 1
Claims (26)
- 治療上または予防上有効な量の化合物3-(4-アミノ-1-オキソ-1,3-ジヒドロ-イソインドール-2-イル)-ピペリジン-2,6-ジオンまたはその製薬上許容される塩、溶媒和物もしくは立体異性体を含む癌の予防または治療のための医薬組成物であって、癌が、多発性硬化症、血液の癌、非ホジキンリンパ腫、卵巣癌、膵臓癌、腎癌、アミロイドーシス、皮膚T細胞リンパ腫、皮膚B細胞リンパ腫、大細胞型B細胞リンパ腫および肺癌からなる群より選択される、上記医薬組成物。
- 化合物が3-(4-アミノ-1-オキソ-1,3-ジヒドロ-イソインドール-2-イル)-ピペリジン-2,6-ジオンである、請求項１に記載の医薬組成物。
- 化合物が製薬上許容される塩である、請求項１に記載の医薬組成物。
- 化合物が製薬上許容される溶媒和物である、請求項１に記載の医薬組成物。
- 化合物が製薬上許容される立体異性体である、請求項１に記載の医薬組成物。
- 立体異性体がエナンチオマー的に純粋なＲ体である、請求項５に記載の医薬組成物。
- 立体異性体がエナンチオマー的に純粋なＳ体である、請求項５に記載の医薬組成物。
- 治療上または予防上有効な量の第2の活性剤であって、造血増殖因子、サイトカインおよび抗癌剤からなる群より選択される第2の活性剤をさらに含む、請求項１〜７のいずれか１項に記載の医薬組成物。
- 第2の活性剤が顆粒球コロニー刺激因子（G-CSF）、顆粒球-マクロファージジコロニー刺激因子（GM-CSF）、エリスロポエチン（EPO）、インターロイキン（IL）、インターフェロン（IFN）、またはそれらの薬理学的に活性な突然変異体もしくは誘導体である、請求項８に記載の医薬組成物。
- 第2の活性剤が、オブリマーセン、メルファラン、トポテカン、ペントキシフィリン、タキソテール、イリノテカン、シプロフロキサシン、デキサメタゾン、ドキソルビシン、ビンクリスチン、ダカルバジン、Ara-C、ビノレルビン、プレドニゾン、シクロホスファミド、ボルテゾミブ、三酸化ヒ素、カルボプラチン、パクリタキセル、ドキセタキソール、フルダラビン、リツキシマブまたはそれらの組合せである、請求項８に記載の医薬組成物。
- 第2の活性剤がフルダラビンまたはリツキシマブである、請求項１０に記載の医薬組成物。
- 放射線療法、ホルモン療法、生物学的療法または免疫療法とともに投与される、請求項１〜１１のいずれか１項に記載の医薬組成物。
- 肺癌が小細胞肺癌または非小細胞肺癌である、請求項１〜１２のいずれか１項に記載の医薬組成物。
- 多発性骨髄腫が、くすぶり型骨髄腫、無痛無症候性骨髄腫、化学療法応答性多発性骨髄腫、不応性骨髄腫、再発骨髄腫、または再発もしくは不応性のDune-Salmon第III期多発性骨髄腫である、請求項１〜１２のいずれか１項に記載の医薬組成物。
- 癌が再発、または従来療法に不応性もしくは抵抗性である、請求項１〜１２のいずれか１項に記載の医薬組成物。
- 経口投与される、請求項１〜１５のいずれか１項に記載の医薬組成物。
- カプセル剤または錠剤の形態である、請求項１６に記載の医薬組成物。
- 1〜150mg/日の量の化合物を含む、請求項１〜１７のいずれか１項に記載の医薬組成物。
- 1〜50mg/日の量の化合物を含む、請求項１８に記載の医薬組成物。
- 5〜25mg/日の量の化合物を含む、請求項１８に記載の医薬組成物。
- 1日おきに10〜50mgの量の化合物を含む、請求項１〜１７のいずれか１項に記載の医薬組成物。
- 周期的に投与される、請求項１〜２１のいずれか１項に記載の医薬組成物。
- １サイクルが4〜6週間を含む、請求項２２に記載の医薬組成物。
- １サイクルが21日間の化合物の投与と7日間の休止期間を含む、請求項２２に記載の医薬組成物。
- 28日サイクルで、21日間にわたり１日当たり5〜25mgの量が投与され、7日間の休止期間が設けられる、請求項２２に記載の医薬組成物。
- 治療上または予防上有効な量の化合物3-(4-アミノ-1-オキソ-1,3-ジヒドロ-イソインドール-2-イル)-ピペリジン-2,6-ジオンまたはその製薬上許容される塩、溶媒和物もしくは立体異性体とデキサメタゾンとの組み合わせを含む多発性硬化症の予防または治療のための医薬組成物であって、該化合物は各28日サイクルの1〜21日目に１日１回25mgの量で投与され、デキサメタゾンは、最初の4サイクルについては各28日サイクルの1〜4、9〜12及び17〜20日目に１日１回40mgの量で投与され、その最初の4サイクル以後は各28日サイクルの1〜4日目に１日１回40mgの量で投与される、上記医薬組成物。
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US38084202P | 2002-05-17 | 2002-05-17 | |
| US42460002P | 2002-11-06 | 2002-11-06 | |
| PCT/US2003/015470 WO2003097052A2 (en) | 2002-05-17 | 2003-05-16 | Methods and compositions using immunomodulatory compounds for treatment and management of cancers and other diseases |
Related Child Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006288966A Division JP2007008966A (ja) | 2002-05-17 | 2006-10-24 | 癌および他の疾患を治療および管理するための免疫調節性化合物を用いた方法および組成物 |
| JP2009116363A Division JP2009191072A (ja) | 2002-05-17 | 2009-05-13 | 癌および他の疾患を治療および管理するための免疫調節性化合物を用いた方法および組成物 |
| JP2009116367A Division JP5839770B2 (ja) | 2002-05-17 | 2009-05-13 | 癌および他の疾患を治療および管理するための免疫調節性化合物を用いた方法および組成物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2005530784A JP2005530784A (ja) | 2005-10-13 |
| JP2005530784A5 true JP2005530784A5 (ja) | 2006-12-14 |
Family
ID=29553516
Family Applications (8)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004505051A Pending JP2005530784A (ja) | 2002-05-17 | 2003-05-16 | 癌および他の疾患を治療および管理するための免疫調節性化合物を用いた方法および組成物 |
| JP2006288966A Pending JP2007008966A (ja) | 2002-05-17 | 2006-10-24 | 癌および他の疾患を治療および管理するための免疫調節性化合物を用いた方法および組成物 |
| JP2009116363A Withdrawn JP2009191072A (ja) | 2002-05-17 | 2009-05-13 | 癌および他の疾患を治療および管理するための免疫調節性化合物を用いた方法および組成物 |
| JP2009116367A Expired - Lifetime JP5839770B2 (ja) | 2002-05-17 | 2009-05-13 | 癌および他の疾患を治療および管理するための免疫調節性化合物を用いた方法および組成物 |
| JP2012273326A Expired - Lifetime JP5830005B2 (ja) | 2002-05-17 | 2012-12-14 | 癌および他の疾患を治療および管理するための免疫調節性化合物を用いた方法および組成物 |
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| JP2009116363A Withdrawn JP2009191072A (ja) | 2002-05-17 | 2009-05-13 | 癌および他の疾患を治療および管理するための免疫調節性化合物を用いた方法および組成物 |
| JP2009116367A Expired - Lifetime JP5839770B2 (ja) | 2002-05-17 | 2009-05-13 | 癌および他の疾患を治療および管理するための免疫調節性化合物を用いた方法および組成物 |
| JP2012273326A Expired - Lifetime JP5830005B2 (ja) | 2002-05-17 | 2012-12-14 | 癌および他の疾患を治療および管理するための免疫調節性化合物を用いた方法および組成物 |
| JP2013038222A Withdrawn JP2013126999A (ja) | 2002-05-17 | 2013-02-28 | 癌および他の疾患を治療および管理するための免疫調節性化合物を用いた方法および組成物 |
| JP2015125342A Expired - Lifetime JP6194335B2 (ja) | 2002-05-17 | 2015-06-23 | 癌および他の疾患を治療および管理するための免疫調節性化合物を用いた方法および組成物 |
| JP2017095838A Pending JP2017132817A (ja) | 2002-05-17 | 2017-05-12 | 癌および他の疾患を治療および管理するための免疫調節性化合物を用いた方法および組成物 |
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| SI (1) | SI1505973T1 (ja) |
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