RU2482877C2 - Композиции и способы для лечения опухоли - Google Patents
Композиции и способы для лечения опухоли Download PDFInfo
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- RU2482877C2 RU2482877C2 RU2009126588/15A RU2009126588A RU2482877C2 RU 2482877 C2 RU2482877 C2 RU 2482877C2 RU 2009126588/15 A RU2009126588/15 A RU 2009126588/15A RU 2009126588 A RU2009126588 A RU 2009126588A RU 2482877 C2 RU2482877 C2 RU 2482877C2
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- thalidomide
- melphalan
- antibody
- bortezomib
- patient
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US87446006P | 2006-12-11 | 2006-12-11 | |
| US60/874,460 | 2006-12-11 | ||
| PCT/US2007/068300 WO2008073509A2 (en) | 2006-12-11 | 2007-05-04 | Compositions and methods for treating a neoplasm |
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| RU2482877C2 true RU2482877C2 (ru) | 2013-05-27 |
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Cited By (1)
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|---|---|---|---|---|
| RU2836995C1 (ru) * | 2024-04-18 | 2025-03-25 | Федеральное государственное бюджетное образовательное учреждение высшего образования "Самарский государственный медицинский университет" Министерства здравоохранения Российской Федерации | Способ лечения пациентов с множественной миеломой, осложненной двойной рефрактерностью, с помощью адоптивной иммунотерапии на основе натуральных киллеров |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7750124B2 (en) | 2006-09-29 | 2010-07-06 | Oncomed Pharmaceuticals, Inc. | Anti-human DLL4 antibodies and compositions |
| EP3485908B1 (en) | 2009-10-16 | 2021-08-18 | Mereo BioPharma 5, Inc. | Therapeutic combination and use of dll4 antagonist antibodies and anti-hypertensive agents |
| US8551479B2 (en) | 2010-09-10 | 2013-10-08 | Oncomed Pharmaceuticals, Inc. | Methods for treating melanoma |
| EP2655334B1 (en) | 2010-12-22 | 2018-10-03 | Eutropics Pharmaceuticals, Inc. | Compositions and methods useful for treating diseases |
| HRP20190044T1 (hr) | 2011-09-23 | 2019-02-22 | Oncomed Pharmaceuticals, Inc. | Agensi koji vežu vegf/dll4 i njihove uporabe |
| CN104244934A (zh) * | 2012-03-14 | 2014-12-24 | 印第安纳大学研究及科技有限公司 | 用于治疗白血病的化合物和方法 |
| AU2013337811A1 (en) | 2012-10-31 | 2015-05-14 | Oncomed Pharmaceuticals, Inc. | Methods and monitoring of treatment with a DLL4 antagonist |
| GB201409471D0 (en) | 2014-05-28 | 2014-07-09 | Euro Celtique Sa | Pharmaceutical composition |
| MX382902B (es) | 2014-10-31 | 2025-03-13 | Oncomed Pharm Inc | Inhibidor de la vía noth en combinación con un agente inmunoterapéutico para usarse en el tratamiento de cáncer. |
| FI3328843T3 (fi) | 2015-07-27 | 2023-01-31 | 1,3,4-oksadiatsolisulfonamidijohdannaisyhdisteitä histonideasetylaasi-6:n inhibiittoreina ja samaa käsittävä farmaseuttinen koostumus | |
| CN107980040B (zh) | 2015-07-27 | 2021-11-26 | 株式会社钟根堂 | 作为组蛋白去乙酰酶6抑制剂的1,3,4-噁二唑磺酰胺衍生物及含其的医药组合物 |
| HRP20201304T1 (hr) | 2015-07-27 | 2020-11-27 | Chong Kun Dang Pharmaceutical Corp. | Spoj derivata 1,3,4-oksadiazol-amida koji služi kao inhibitor histonske deacetilaze 6 i farmaceutski pripravak koji sadrži taj spoj |
| DK3331864T3 (da) | 2015-08-04 | 2021-12-13 | Chong Kun Dang Pharmaceutical Corp | 1,3,4-Oxadiazolderivat-forbindelser som histon-deacetylase-6-hæmmer, og den farmaceutiske sammensætning omfattende disse |
| WO2017053705A1 (en) | 2015-09-23 | 2017-03-30 | Oncomed Pharmaceuticals, Inc. | Methods and compositions for treatment of cancer |
| MY196174A (en) | 2015-10-12 | 2023-03-20 | Chong Kun Dang Pharmaceutical Corp | Oxadiazole Amine Derivative Compounds as Histone Deacetylase 6 Inhibitor, and the Pharmaceutical Composition Comprising the Same |
| GB201709406D0 (en) | 2017-06-13 | 2017-07-26 | Euro-Cletique S A | Compounds for treating TNBC |
| US11524053B2 (en) | 2018-01-26 | 2022-12-13 | The Regents Of The University Of California | Methods and compositions for treatment of angiogenic disorders using anti-VEGF agents |
| KR102316234B1 (ko) | 2018-07-26 | 2021-10-22 | 주식회사 종근당 | 히스톤 탈아세틸화효소 6 억제제로서의 1,3,4-옥사다이아졸 유도체 화합물 및 이를 포함하는 약제학적 조성물 |
| CN113874369B (zh) | 2019-05-31 | 2024-08-27 | 株式会社钟根堂 | 作为组蛋白脱乙酰酶6抑制剂的1,3,4-噁二唑高邻苯二甲酰亚胺衍生化合物及包含其的药物组合物 |
| IL293131A (en) | 2019-11-25 | 2022-07-01 | Univ California | Long-acting vegf inhibitors for intraocular neovascularization |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2197477C2 (ru) * | 1997-12-05 | 2003-01-27 | АСТРАЗЕНЕКА Ю Кей ЛИМИТЕД | Производные адамантана, способ их получения, фармацевтическая композиция на их основе, способ ее получения и способ воздействия на иммуносупрессию |
| WO2004103274A2 (en) * | 2003-05-15 | 2004-12-02 | Celgene Corporation | Methods and compositions using immunomodulatory compounds for treatment and management of cancers and other diseases |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6281230B1 (en) * | 1996-07-24 | 2001-08-28 | Celgene Corporation | Isoindolines, method of use, and pharmaceutical compositions |
| US5635517B1 (en) * | 1996-07-24 | 1999-06-29 | Celgene Corp | Method of reducing TNFalpha levels with amino substituted 2-(2,6-dioxopiperidin-3-YL)-1-oxo-and 1,3-dioxoisoindolines |
| US6169106B1 (en) * | 1998-04-15 | 2001-01-02 | Boehringer Ingelheim Pharma Kg | Indolinones having kinase inhibitory activity |
| DE59906030D1 (de) * | 1998-09-25 | 2003-07-24 | Boehringer Ingelheim Pharma | Neue substituierte indolinone mit einer inhibierenden wirkung auf verschiedene kinasen und cyclin/cdk-komplexe |
| US6762180B1 (en) * | 1999-10-13 | 2004-07-13 | Boehringer Ingelheim Pharma Kg | Substituted indolines which inhibit receptor tyrosine kinases |
| US6638965B2 (en) * | 2000-11-01 | 2003-10-28 | Boehringer Ingelheim Pharma Kg | Substituted indolinones, preparation thereof and their use as pharmaceutical compositions |
| US7758859B2 (en) * | 2003-08-01 | 2010-07-20 | Genentech, Inc. | Anti-VEGF antibodies |
| US20050106667A1 (en) * | 2003-08-01 | 2005-05-19 | Genentech, Inc | Binding polypeptides with restricted diversity sequences |
| TWI580694B (zh) * | 2007-11-30 | 2017-05-01 | 建南德克公司 | 抗-vegf抗體 |
-
2007
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Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2197477C2 (ru) * | 1997-12-05 | 2003-01-27 | АСТРАЗЕНЕКА Ю Кей ЛИМИТЕД | Производные адамантана, способ их получения, фармацевтическая композиция на их основе, способ ее получения и способ воздействия на иммуносупрессию |
| WO2004103274A2 (en) * | 2003-05-15 | 2004-12-02 | Celgene Corporation | Methods and compositions using immunomodulatory compounds for treatment and management of cancers and other diseases |
Non-Patent Citations (5)
| Title |
|---|
| BERENSON JR et al. Phase I/II trial assessing bortezomib and melphalan combination therapy for the treatment of patients with relapsed or refractory multiple myeloma // J Clin Oncol. 2006 Feb 20; 24(6):937-44. * |
| HERBST RS et al. Phase I/II trial evaluating the anti-vascular endothclial growth factor monoclonal antibody bevacizumab in combination with the HER-l/epidermal growth factor receptor tyrosine kinase inhibitor erlotinib for patients with recurrent non-small-cell lung cancer //J Clin Oncol. 2005 Apr 10; 23(11):2544-55. * |
| HIDESHIMA T et al. p38 MAPK inhibition enhances PS-341 (bortezomib)-induced cytotoxicity against multiple myeloma cells // Oncogene. 2004 Nov 18; 23(54): 8766-76. * |
| HIDESHIMA T et al. p38 MAPK inhibition enhances PS-341 (bortezomib)-induced cytotoxicity against multiple myeloma cells // Oncogene. 2004 Nov 18; 23(54): 8766-76. HERBST RS et al. Phase I/II trial evaluating the anti-vascular endothclial growth factor monoclonal antibody bevacizumab in combination with the HER-l/epidermal growth factor receptor tyrosine kinase inhibitor erlotinib for patients with recurrent non-small-cell lung cancer //J Clin Oncol. 2005 Apr 10; 23(11):2544-55. BERENSON JR et al. Phase I/II trial assessing bortezomib and melphalan combination therapy for the treatment of patients with relapsed or refractory multiple myeloma // J Clin Oncol. 2006 Feb 20; 24(6):937-44. ZANGARI M et al. Phase II study of SU5416, a small molecule vascular endothelial growth factor tyrosine kinase receptor inhibitor, in patients with refractory multiple myeloma // Clin Cancer Res. 2004 Jan 1; 10 (1 Pt 1):88-95. * |
| ZANGARI M et al. Phase II study of SU5416, a small molecule vascular endothelial growth factor tyrosine kinase receptor inhibitor, in patients with refractory multiple myeloma // Clin Cancer Res. 2004 Jan 1; 10 (1 Pt 1):88-95. * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2836995C1 (ru) * | 2024-04-18 | 2025-03-25 | Федеральное государственное бюджетное образовательное учреждение высшего образования "Самарский государственный медицинский университет" Министерства здравоохранения Российской Федерации | Способ лечения пациентов с множественной миеломой, осложненной двойной рефрактерностью, с помощью адоптивной иммунотерапии на основе натуральных киллеров |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2007333565A1 (en) | 2008-06-19 |
| CN101547705A (zh) | 2009-09-30 |
| KR101320198B1 (ko) | 2013-10-30 |
| US20100086544A1 (en) | 2010-04-08 |
| WO2008073509A3 (en) | 2009-01-08 |
| ZA200903489B (en) | 2010-08-25 |
| RU2009126588A (ru) | 2011-01-20 |
| NZ577058A (en) | 2012-04-27 |
| CA2670707A1 (en) | 2008-06-19 |
| IL198852A0 (en) | 2011-08-01 |
| EP2099489A2 (en) | 2009-09-16 |
| HK1131064A1 (en) | 2010-01-15 |
| SG177891A1 (en) | 2012-02-28 |
| KR20090087908A (ko) | 2009-08-18 |
| SI2099489T1 (sl) | 2014-09-30 |
| IL198852A (en) | 2013-06-27 |
| DK2099489T3 (da) | 2014-08-18 |
| EP2099489B1 (en) | 2014-05-21 |
| MX2009006202A (es) | 2009-06-22 |
| JP2010512407A (ja) | 2010-04-22 |
| BRPI0717688A2 (pt) | 2013-01-22 |
| WO2008073509A2 (en) | 2008-06-19 |
| CN101547705B (zh) | 2013-06-12 |
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