JP6389241B2 - 癌を治療するためのTORキナーゼ阻害剤及びIMiD化合物を含む組合せ療法 - Google Patents
癌を治療するためのTORキナーゼ阻害剤及びIMiD化合物を含む組合せ療法 Download PDFInfo
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- JP6389241B2 JP6389241B2 JP2016509054A JP2016509054A JP6389241B2 JP 6389241 B2 JP6389241 B2 JP 6389241B2 JP 2016509054 A JP2016509054 A JP 2016509054A JP 2016509054 A JP2016509054 A JP 2016509054A JP 6389241 B2 JP6389241 B2 JP 6389241B2
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- 0 CCCC(C(CCC(*)(CCC*)N)CN1C(*)(CCC(N2)=O)C2=O)C1=O Chemical compound CCCC(C(CCC(*)(CCC*)N)CN1C(*)(CCC(N2)=O)C2=O)C1=O 0.000 description 7
- PEKBSFHTEKHSFY-UHFFFAOYSA-N CC(C(CCC(C(C)=C)=O)N(Cc1c2cccc1OCc1ccc(CN(CCN3c4ccccn4)CC3=O)cc1)C2=O)=O Chemical compound CC(C(CCC(C(C)=C)=O)N(Cc1c2cccc1OCc1ccc(CN(CCN3c4ccccn4)CC3=O)cc1)C2=O)=O PEKBSFHTEKHSFY-UHFFFAOYSA-N 0.000 description 1
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- PAILYCYKWFAMGH-UHFFFAOYSA-N COc(cc1)ccc1NC(NCc(cc1C(N2C(CCC(N3)=O)C3=O)=O)ccc1C2=O)=O Chemical compound COc(cc1)ccc1NC(NCc(cc1C(N2C(CCC(N3)=O)C3=O)=O)ccc1C2=O)=O PAILYCYKWFAMGH-UHFFFAOYSA-N 0.000 description 1
- RQOMIWCVIUKHQA-UHFFFAOYSA-N Cc1cc(CNC(Cc(cc2)ccc2Cl)=O)ccc1C(NC(CCC=O)C(N)=O)=O Chemical compound Cc1cc(CNC(Cc(cc2)ccc2Cl)=O)ccc1C(NC(CCC=O)C(N)=O)=O RQOMIWCVIUKHQA-UHFFFAOYSA-N 0.000 description 1
- DJNUTFIXAYRICK-UHFFFAOYSA-N NC(C(CCC=O)N(C(c1c2cc(CNC(c3ccc(C(F)(F)F)cc3)=O)cc1)=O)C2=O)=O Chemical compound NC(C(CCC=O)N(C(c1c2cc(CNC(c3ccc(C(F)(F)F)cc3)=O)cc1)=O)C2=O)=O DJNUTFIXAYRICK-UHFFFAOYSA-N 0.000 description 1
- GACAOIKPNDQHIU-UHFFFAOYSA-N O=C(NCc(cc1)cc(C(N2C(CCC(N3)=O)C3=O)=O)c1C2=O)Nc(cc1)ccc1Cl Chemical compound O=C(NCc(cc1)cc(C(N2C(CCC(N3)=O)C3=O)=O)c1C2=O)Nc(cc1)ccc1Cl GACAOIKPNDQHIU-UHFFFAOYSA-N 0.000 description 1
- LRGPIURPNNEALP-UHFFFAOYSA-N O=C(NCc(cc1)cc(C(N2C(CCC(N3)=O)C3=O)=O)c1C2=O)Nc1cccc(Cl)c1 Chemical compound O=C(NCc(cc1)cc(C(N2C(CCC(N3)=O)C3=O)=O)c1C2=O)Nc1cccc(Cl)c1 LRGPIURPNNEALP-UHFFFAOYSA-N 0.000 description 1
- XOMORRFRQIUYCI-UHFFFAOYSA-N O=Cc1c(C2OC2NC(CCC(N2)=O)C2=O)cc(CNC(c(cc2)ccc2OC(F)(F)F)=O)cc1 Chemical compound O=Cc1c(C2OC2NC(CCC(N2)=O)C2=O)cc(CNC(c(cc2)ccc2OC(F)(F)F)=O)cc1 XOMORRFRQIUYCI-UHFFFAOYSA-N 0.000 description 1
- JJXGBEKSKZBZEV-UHFFFAOYSA-N OC(CCCCC(NCc(cc1)cc(C(N2C(CCC(N3)=O)C3=O)=O)c1C2=O)=O)=O Chemical compound OC(CCCCC(NCc(cc1)cc(C(N2C(CCC(N3)=O)C3=O)=O)c1C2=O)=O)=O JJXGBEKSKZBZEV-UHFFFAOYSA-N 0.000 description 1
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
- A61K39/39533—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
- A61K39/39558—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against tumor tissues, cells, antigens
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/2887—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against CD20
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Immunology (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Oncology (AREA)
- Biomedical Technology (AREA)
- Genetics & Genomics (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361813094P | 2013-04-17 | 2013-04-17 | |
| US61/813,094 | 2013-04-17 | ||
| US201361908859P | 2013-11-26 | 2013-11-26 | |
| US61/908,859 | 2013-11-26 | ||
| PCT/US2014/034312 WO2014172429A1 (en) | 2013-04-17 | 2014-04-16 | Combination therapy comprising a tor kinase inhibitor and an imid compound for treating cancer |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2016516817A JP2016516817A (ja) | 2016-06-09 |
| JP2016516817A5 JP2016516817A5 (https=) | 2017-05-18 |
| JP6389241B2 true JP6389241B2 (ja) | 2018-09-12 |
Family
ID=50736198
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016509054A Active JP6389241B2 (ja) | 2013-04-17 | 2014-04-16 | 癌を治療するためのTORキナーゼ阻害剤及びIMiD化合物を含む組合せ療法 |
Country Status (15)
| Country | Link |
|---|---|
| US (2) | US20140314752A1 (https=) |
| EP (1) | EP2986318A1 (https=) |
| JP (1) | JP6389241B2 (https=) |
| KR (2) | KR102223060B1 (https=) |
| CN (1) | CN105358177B (https=) |
| AU (1) | AU2014254056B2 (https=) |
| BR (1) | BR112015026006B1 (https=) |
| CA (1) | CA2908954C (https=) |
| HK (1) | HK1221148A1 (https=) |
| IL (1) | IL241964B (https=) |
| MX (2) | MX373803B (https=) |
| NZ (1) | NZ629456A (https=) |
| TW (1) | TW201526897A (https=) |
| WO (1) | WO2014172429A1 (https=) |
| ZA (1) | ZA201507735B (https=) |
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| DK2428513T3 (en) | 2006-09-26 | 2017-08-21 | Celgene Corp | 5-substituted quinazolinone derivatives as anti-cancer agents |
| EP2536706B1 (en) | 2010-02-11 | 2017-06-14 | Celgene Corporation | Arylmethoxy isoindoline derivatives and compositions comprising and methods of using the same |
| JP5959543B2 (ja) | 2011-03-11 | 2016-08-02 | セルジーン コーポレイション | 3−(5−アミノ−2−メチル−4−オキソ−4h−キナゾリン−3−イル)−ピペリジン−2,6−ジオンの固体形態、並びにそれらの医薬組成物及び使用 |
| ES2814952T3 (es) | 2012-09-04 | 2021-03-29 | Celgene Corp | Isotopólogos de 3-(5-amino-2-metil-4-oxoquinazolin-3(4H)-il) piperidina-2-6-diona y métodos de preparación de los mismos |
| US9126950B2 (en) | 2012-12-21 | 2015-09-08 | Celgene Avilomics Research, Inc. | Heteroaryl compounds and uses thereof |
| US9695145B2 (en) | 2013-01-22 | 2017-07-04 | Celgene Corporation | Processes for the preparation of isotopologues of 3-(4-((4- morpholinomethyl)benzyl)oxy)-1-oxoisoindolin-2-yl)piperidine-2,6-dione and pharmaceutically acceptable salts thereof |
| TW201527300A (zh) | 2013-04-17 | 2015-07-16 | Signal Pharm Llc | 關於1-乙基-7-(2-甲基-6-(1H-1,2,4-三唑-3-基)吡啶-3-基)-3,4-二氫吡并[2,3-b]吡-2(1H)-酮之醫藥調配物、方法、固態型式及使用方法 |
| BR112015026297B1 (pt) * | 2013-04-17 | 2022-08-23 | Signal Pharmaceuticals, Llc | Uso de um inibidor da quinase tor e quinazolinona 5-substituída, composição farmacêutica que os compreende, e kit |
| BR112015026292B1 (pt) | 2013-04-17 | 2022-04-12 | Signal Pharmaceuticals, Llc | Uso de 1-etil-7-(2-metil-6-(1h-1,2,4-triazol-3-il)piridin-3-il)-3,4-dihidropirazino [2,3-b]pirazin-2(1h)- ona e métodos in vitro |
| AU2014254052B2 (en) | 2013-04-17 | 2019-06-06 | Signal Pharmaceuticals, Llc | Treatment of cancer with dihydropyrazino-pyrazines |
| US9937169B2 (en) | 2013-04-17 | 2018-04-10 | Signal Pharmaceuticals, Llc | Methods for treating cancer using dihydropyrazino-pyrazine compound combination therapy |
| EP3003313A1 (en) | 2013-05-29 | 2016-04-13 | Signal Pharmaceuticals, LLC | Pharmaceutical compositions of 7-(6-(2-hydroxypropan-2-yl)pyridin-3-yl)-1-((trans)-4-methoxycyclohexyl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1h)-one, a solid form thereof and methods of their use |
| IL278381B2 (en) | 2013-12-06 | 2024-08-01 | Celgene Corp | Methods for determining the effectiveness of a drug for the treatment of diffuse large B-cell lymphoma, multiple myeloma, and myeloid cancer |
| US9415049B2 (en) | 2013-12-20 | 2016-08-16 | Celgene Avilomics Research, Inc. | Heteroaryl compounds and uses thereof |
| EP3131552B1 (en) | 2014-04-16 | 2020-07-15 | Signal Pharmaceuticals, LLC | Methods for treating cancer using tor kinase inhibitor combination therapy |
| NZ714742A (en) | 2014-04-16 | 2017-04-28 | Signal Pharm Llc | Solid forms of 1-ethyl-7-(2-methyl-6-(1h-1,2,4-triazol-3-yl)pyridin-3-yl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1h)-one, compositions thereof and methods of their use |
| US9512129B2 (en) | 2014-04-16 | 2016-12-06 | Signal Pharmaceuticals, Llc | Solid forms comprising 1-ethyl-7-(2-methyl-6-(1H-1,2,4-triazol-3-yl)pyridin-3-yl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1H)-one and a coformer |
| WO2016007854A1 (en) * | 2014-07-11 | 2016-01-14 | Celgene Corporation | Combination therapy for cancer |
| JP2017538104A (ja) * | 2014-10-07 | 2017-12-21 | セルジーン コーポレイション | 癌治療に対する臨床的感応性を予測するためのバイオマーカーの使用 |
| CN106146508A (zh) * | 2015-03-19 | 2016-11-23 | 浙江导明医药科技有限公司 | 优化的联合用药及其治疗癌症和自身免疫疾病的用途 |
| US9717745B2 (en) | 2015-03-19 | 2017-08-01 | Zhejiang DTRM Biopharma Co. Ltd. | Pharmaceutical compositions and their use for treatment of cancer and autoimmune diseases |
| HK1247093A1 (zh) * | 2015-06-29 | 2018-09-21 | 阿布拉科斯生物科学有限公司 | 使用纳米颗粒mtor抑制剂联合疗法治疗实体瘤的方法 |
| US20180256551A1 (en) * | 2015-06-29 | 2018-09-13 | Abraxis Bioscience, Llc | Methods of treating hematological malignancy using nanoparticle mtor inhibitor combination therapy |
| PL3998069T3 (pl) | 2015-06-29 | 2025-03-31 | Abraxis Bioscience, Llc | Nanocząsteczki zawierające syrolimus i albuminę do zastosowania w leczeniu nowotworów z komórek nabłonkowatych |
| CN106769807A (zh) * | 2016-12-07 | 2017-05-31 | 王兰英 | 一种利用流式细胞仪检测HeLa细胞凋亡的方法 |
| EP3641772B1 (en) | 2017-06-22 | 2023-08-02 | Celgene Corporation | Treatment of hepatocellular carcinoma characterized by hepatitis b virus infection |
| TW201922256A (zh) * | 2017-10-27 | 2019-06-16 | 中國大陸商浙江導明醫藥科技有限公司 | 治療淋巴樣惡性疾病之方法 |
| AU2019284608A1 (en) | 2018-06-13 | 2020-12-17 | Biotheryx, Inc. | Aminoamide compounds |
| CN114502176A (zh) * | 2019-10-04 | 2022-05-13 | 达纳-法伯癌症研究所股份有限公司 | 作为zeta链相关蛋白激酶70(zap70)激动剂的免疫调节性酰亚胺药物及其用途 |
| CN115916191A (zh) * | 2020-06-25 | 2023-04-04 | 新基公司 | 用组合疗法治疗癌症的方法 |
| WO2022066835A1 (en) | 2020-09-23 | 2022-03-31 | St. Jude Children's Research Hospital, Inc. | Substituted n-(2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-5-yl)arylsulfonamide analogs as modulators of cereblon protein |
| JP2024504932A (ja) | 2021-01-13 | 2024-02-02 | モンテ ローザ セラピューティクス, インコーポレイテッド | イソインドリノン化合物 |
| CN117045800A (zh) * | 2022-05-06 | 2023-11-14 | 上海科技大学 | mTOR抑制剂增强靶向蛋白降解药物功效的应用 |
| AU2023301383A1 (en) * | 2022-06-27 | 2025-01-16 | Ganymede Oncology, Inc. | Nrf2 protein degraders |
| WO2024015618A2 (en) * | 2022-07-15 | 2024-01-18 | St. Jude Children's Research Hospital, Inc. | Substituted 3-(1-oxoisoindolin-2-yl)piperidine-2,6-dione/2-(2,6-dioxopiperidin-3-yl)isoindoline-1,3-dione analogs as modulators of cereblon protein |
| WO2024167423A1 (en) * | 2023-02-07 | 2024-08-15 | Captor Therapeutics S.A. | Gspt1 degrader compounds |
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| US5955476A (en) | 1997-11-18 | 1999-09-21 | Celgene Corporation | Substituted 2-(2,6-dioxo-3-fluoropiperidin-3-yl)-isoindolines and method of reducing inflammatory cytokine levels |
| US5874448A (en) | 1997-11-18 | 1999-02-23 | Celgene Corporation | Substituted 2-(2,6 dioxo-3-fluoropiperidin-3-yl)-isoindolines and method of reducing TNFα levels |
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| NZ629456A (en) | 2017-06-30 |
| MX2020003174A (es) | 2020-07-28 |
| JP2016516817A (ja) | 2016-06-09 |
| BR112015026006A2 (pt) | 2017-07-25 |
| TW201526897A (zh) | 2015-07-16 |
| BR112015026006A8 (pt) | 2020-01-14 |
| CA2908954A1 (en) | 2014-10-23 |
| CN105358177A (zh) | 2016-02-24 |
| HK1221148A1 (zh) | 2017-05-26 |
| KR102223060B1 (ko) | 2021-03-05 |
| KR102382576B1 (ko) | 2022-04-08 |
| KR20160002791A (ko) | 2016-01-08 |
| KR20210024231A (ko) | 2021-03-04 |
| CN105358177B (zh) | 2018-11-23 |
| US20200113896A1 (en) | 2020-04-16 |
| CA2908954C (en) | 2021-08-03 |
| AU2014254056B2 (en) | 2019-06-06 |
| AU2014254056A1 (en) | 2015-11-05 |
| US20140314752A1 (en) | 2014-10-23 |
| MX373803B (es) | 2020-03-24 |
| WO2014172429A1 (en) | 2014-10-23 |
| BR112015026006B1 (pt) | 2022-10-18 |
| MX2015014596A (es) | 2016-03-03 |
| EP2986318A1 (en) | 2016-02-24 |
| IL241964B (en) | 2020-01-30 |
| ZA201507735B (en) | 2017-06-28 |
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