JP2010531877A - 安定化したピコプラチン投与形態 - Google Patents
安定化したピコプラチン投与形態 Download PDFInfo
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- JP2010531877A JP2010531877A JP2010514837A JP2010514837A JP2010531877A JP 2010531877 A JP2010531877 A JP 2010531877A JP 2010514837 A JP2010514837 A JP 2010514837A JP 2010514837 A JP2010514837 A JP 2010514837A JP 2010531877 A JP2010531877 A JP 2010531877A
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- Prior art keywords
- cancer
- picoplatin
- dosage form
- solution
- chloride
- 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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- IIMIOEBMYPRQGU-UHFFFAOYSA-L picoplatin Chemical compound N.[Cl-].[Cl-].[Pt+2].CC1=CC=CC=N1 IIMIOEBMYPRQGU-UHFFFAOYSA-L 0.000 title claims abstract description 220
- 229950005566 picoplatin Drugs 0.000 title claims abstract description 218
- 239000002552 dosage form Substances 0.000 title claims abstract description 119
- 238000000034 method Methods 0.000 claims abstract description 89
- 239000000243 solution Substances 0.000 claims abstract description 56
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims abstract description 50
- 239000007864 aqueous solution Substances 0.000 claims abstract description 21
- 238000001990 intravenous administration Methods 0.000 claims abstract description 19
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- 238000006731 degradation reaction Methods 0.000 claims abstract description 9
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- 206010028980 Neoplasm Diseases 0.000 claims description 75
- 238000011282 treatment Methods 0.000 claims description 71
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 52
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 46
- 201000011510 cancer Diseases 0.000 claims description 45
- VVIAGPKUTFNRDU-UHFFFAOYSA-N 6S-folinic acid Natural products C1NC=2NC(N)=NC(=O)C=2N(C=O)C1CNC1=CC=C(C(=O)NC(CCC(O)=O)C(O)=O)C=C1 VVIAGPKUTFNRDU-UHFFFAOYSA-N 0.000 claims description 38
- 239000011672 folinic acid Substances 0.000 claims description 38
- VVIAGPKUTFNRDU-ABLWVSNPSA-N folinic acid Chemical compound C1NC=2NC(N)=NC(=O)C=2N(C=O)C1CNC1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 VVIAGPKUTFNRDU-ABLWVSNPSA-N 0.000 claims description 38
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- ZDZOTLJHXYCWBA-VCVYQWHSSA-N N-debenzoyl-N-(tert-butoxycarbonyl)-10-deacetyltaxol 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 description 24
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- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical compound CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 claims description 4
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- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/26—Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharides; Derivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin
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Families Citing this family (19)
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| GB0011903D0 (en) * | 2000-05-18 | 2000-07-05 | Astrazeneca Ab | Combination chemotherapy |
| US8168662B1 (en) | 2006-11-06 | 2012-05-01 | Poniard Pharmaceuticals, Inc. | Use of picoplatin to treat colorectal cancer |
| WO2010132596A1 (en) * | 2009-05-12 | 2010-11-18 | Poniard Pharmaceuticals, Inc. | Use of picoplatin to treat colorectal cancer |
| US8178564B2 (en) | 2006-11-06 | 2012-05-15 | Poniard Pharmaceuticals, Inc. | Use of picoplatin to treat colorectal cancer |
| US8173686B2 (en) | 2006-11-06 | 2012-05-08 | Poniard Pharmaceuticals, Inc. | Use of picoplatin to treat colorectal cancer |
| US8168661B2 (en) | 2006-11-06 | 2012-05-01 | Poniard Pharmaceuticals, Inc. | Use of picoplatin to treat colorectal cancer |
| US20110033528A1 (en) * | 2009-08-05 | 2011-02-10 | Poniard Pharmaceuticals, Inc. | Stabilized picoplatin oral dosage form |
| MX2009008487A (es) * | 2007-02-09 | 2010-01-15 | Poniard Pharmaceuticals Inc | Picoplatino encapsulado. |
| TW200916094A (en) * | 2007-06-27 | 2009-04-16 | Poniard Pharmaceuticals Inc | Stabilized picoplatin dosage form |
| US20100260832A1 (en) * | 2007-06-27 | 2010-10-14 | Poniard Pharmaceuticals, Inc. | Combination therapy for ovarian cancer |
| CN101809024A (zh) * | 2007-07-16 | 2010-08-18 | 铂雅制药公司 | 吡铂的口服制剂 |
| US20110053879A1 (en) * | 2008-02-08 | 2011-03-03 | Poniard Pharmaceuticals, Inc. | Picoplatin and amrubicin to treat lung cancer |
| EP2418955A4 (en) * | 2009-04-15 | 2012-11-21 | Poniard Pharmaceuticals Inc | ORBIOTIC ANTICANCER THERAPY BASED ON HIGH BIODISIBILITY PICOPLATIN |
| CN101804025B (zh) * | 2010-03-31 | 2011-09-21 | 昆明贵研药业有限公司 | 甲啶铂的一种水溶液注射剂 |
| CN102590385B (zh) * | 2012-02-14 | 2013-09-11 | 昆明贵研药业有限公司 | 一种甲啶铂及其杂质的检测方法 |
| AU2016260785B2 (en) * | 2015-05-13 | 2022-06-02 | Monopar Therapeutics Inc. | Clonidine and/or Clonidine derivatives for use in the prevention of skin injury resulting from radiotherapy |
| CN106943343B (zh) * | 2016-01-06 | 2020-05-12 | 山东新时代药业有限公司 | 一种甲啶铂注射液及其制备方法 |
| CN107773538B (zh) * | 2016-08-27 | 2022-09-13 | 鲁南制药集团股份有限公司 | 稳定的甲啶铂无菌冻干粉末及其制备工艺 |
| CN117940164A (zh) * | 2022-04-26 | 2024-04-26 | 石药集团中奇制药技术（石家庄）有限公司 | 米托蒽醌脂质体联合抗血管生成靶向药治疗卵巢癌的用途 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05501264A (ja) * | 1989-10-20 | 1993-03-11 | シキュース ファーマシューティカルズ，インコーポレイテッド | 充実性腫瘍治療法及び組成物 |
| JPH10509143A (ja) * | 1994-11-14 | 1998-09-08 | バイオニューメリック ファーマシューティカルズ インク | ２，２′−ジチオ−ビス（エタンスルホネート）（ジメスナ）と組み合わせたシスプラチン組成物 |
| WO2006104668A2 (en) * | 2005-03-11 | 2006-10-05 | Temple University - Of The Commonwealth System Of Higher Education | Composition and methods for the treatment of proliferative diseases |
Family Cites Families (96)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1432562A (en) * | 1972-04-10 | 1976-04-22 | Rustenburg Platinum Mines Ltd | Platinum co-ordination compounds |
| GB2060615B (en) * | 1979-08-23 | 1983-06-22 | Johnson Matthey Co Ltd | Platinum-amine complexes |
| US4302446A (en) * | 1979-10-02 | 1981-11-24 | Bristol-Myers Company | Pharmaceutical compositions |
| GR75317B (enExample) * | 1980-09-03 | 1984-07-13 | Johnson Matthey Plc | |
| US4533502A (en) * | 1983-02-22 | 1985-08-06 | Rochon Fernande D | Platinum (II) compounds and their preparation |
| EP0167310B1 (en) * | 1984-06-27 | 1991-05-29 | Johnson Matthey Public Limited Company | Platinum co-ordination compounds |
| US5082655A (en) * | 1984-07-23 | 1992-01-21 | Zetachron, Inc. | Pharmaceutical composition for drugs subject to supercooling |
| CA1327039C (en) * | 1986-12-18 | 1994-02-15 | Tetsushi Totani | Ammine-alicyclic amine-platinum complexes and antitumor agents |
| MX9203808A (es) * | 1987-03-05 | 1992-07-01 | Liposome Co Inc | Formulaciones de alto contenido de medicamento: lipido, de agentes liposomicos-antineoplasticos. |
| GB9105037D0 (en) * | 1991-03-09 | 1991-04-24 | Johnson Matthey Plc | Improvements in chemical compounds |
| US5244991A (en) * | 1991-10-15 | 1993-09-14 | Phillips Petroleum Company | Olefin polymerization process |
| MX9206577A (es) * | 1991-11-15 | 1993-05-01 | Smithkline Beecham Corp | COMPOSICIóN FARMACEUTICA PARA INHIBIR EL CRECIMIENTO DE CELULAS TUMORALES |
| EP0672181B1 (en) * | 1992-04-01 | 2003-11-05 | The Johns Hopkins University School Of Medicine | Methods of detecting mammalian nucleic acids isolated from stool specimen and reagents therefor |
| SK279684B6 (sk) * | 1993-06-14 | 1999-02-11 | Janssen Pharmaceutica N.V. | Tableta a spôsob jej výroby |
| US5624919A (en) * | 1993-09-14 | 1997-04-29 | The University Of Vermont And State Agricultural College | Trans platinum (IV) complexes |
| GB9408218D0 (en) * | 1994-04-26 | 1994-06-15 | Johnson Matthey Plc | Improvements in platinum complexes |
| WO1996001638A1 (en) * | 1994-07-11 | 1996-01-25 | Hoechst Marion Roussel, Inc. | Method of treating a neoplastic disease state by conjunctive therapy with 2'-fluoromethylidene derivatives and radiation or chemotherapy |
| US5626862A (en) * | 1994-08-02 | 1997-05-06 | Massachusetts Institute Of Technology | Controlled local delivery of chemotherapeutic agents for treating solid tumors |
| US5919816A (en) * | 1994-11-14 | 1999-07-06 | Bionumerik Pharmaceuticals, Inc. | Formulations and methods of reducing toxicity of antineoplastic agents |
| GB9502799D0 (en) * | 1995-02-14 | 1995-04-05 | Johnson Matthey Plc | Improvements in platinum complexes |
| US6245349B1 (en) * | 1996-02-23 | 2001-06-12 | éLAN CORPORATION PLC | Drug delivery compositions suitable for intravenous injection |
| US6441025B2 (en) * | 1996-03-12 | 2002-08-27 | Pg-Txl Company, L.P. | Water soluble paclitaxel derivatives |
| US5919815A (en) * | 1996-05-22 | 1999-07-06 | Neuromedica, Inc. | Taxane compounds and compositions |
| EA001517B1 (ru) * | 1996-06-25 | 2001-04-23 | Глаксо Груп Лимитед | Комбинации, содержащие vx478, зидовудин и 3tc, для применения при лечении вич |
| WO1998007409A1 (en) * | 1996-08-23 | 1998-02-26 | Sequus Pharmaceuticals, Inc. | Liposomes containing a cisplatin compound |
| DE19847618A1 (de) * | 1998-10-15 | 2000-04-20 | Basf Ag | Verfahren zur Herstellung von festen Dosierungsformen |
| US6235782B1 (en) * | 1998-11-12 | 2001-05-22 | Rifat Pamukcu | Method for treating a patient with neoplasia by treatment with a platinum coordination complex |
| US6413953B1 (en) * | 1999-04-13 | 2002-07-02 | Anormed Inc. | Pt(IV) antitumor agent |
| HUP0200748A3 (en) * | 1999-04-13 | 2010-01-28 | Anormed Inc | Process for preparing amine platinum complexes |
| GB9925127D0 (en) * | 1999-10-22 | 1999-12-22 | Pharmacia & Upjohn Spa | Oral formulations for anti-tumor compounds |
| US20020102301A1 (en) * | 2000-01-13 | 2002-08-01 | Joseph Schwarz | Pharmaceutical solid self-emulsifying composition for sustained delivery of biologically active compounds and the process for preparation thereof |
| WO2001060370A1 (en) * | 2000-02-16 | 2001-08-23 | Yamanouchi Pharmaceutical Co., Ltd. | Remedies for endothelin-induced diseases |
| CA2397657A1 (en) * | 2000-02-29 | 2001-09-07 | Janssen Pharmaceutica Inc. | Farnesyl protein transferase inhibitor combinations with platinum compounds |
| US20020156033A1 (en) * | 2000-03-03 | 2002-10-24 | Bratzler Robert L. | Immunostimulatory nucleic acids and cancer medicament combination therapy for the treatment of cancer |
| US6545010B2 (en) * | 2000-03-17 | 2003-04-08 | Aventis Pharma S.A. | Composition comprising camptothecin or a camptothecin derivative and a platin derivative for the treatment of cancer |
| US20020110601A1 (en) * | 2000-03-31 | 2002-08-15 | Roman Perez-Soler | Antineoplastic platinum therapeutic method and composition |
| EE200200565A (et) * | 2000-03-31 | 2004-06-15 | Angiogene Pharmaceuticals Ltd. | Vaskulaarse kahjustava toimega kombinatsioonravi |
| GB0011903D0 (en) * | 2000-05-18 | 2000-07-05 | Astrazeneca Ab | Combination chemotherapy |
| US6806289B1 (en) * | 2000-07-14 | 2004-10-19 | Stephen J. Lippard | Coordination complexes, and methods for preparing by combinatorial methods, assaying and using the same |
| WO2002013817A1 (en) * | 2000-08-11 | 2002-02-21 | Sumitomo Pharmaceuticals Co., Ltd. | Remedies for cisplatin-tolerant cancer |
| US6894049B1 (en) * | 2000-10-04 | 2005-05-17 | Anormed, Inc. | Platinum complexes as antitumor agents |
| CA2326004A1 (en) * | 2000-11-02 | 2002-05-02 | Richard E. Jones | Methods for treating cellular proliferative disorders |
| SE0004671D0 (sv) * | 2000-12-15 | 2000-12-15 | Amarin Dev Ab | Pharmaceutical formulation |
| AR035227A1 (es) * | 2001-02-20 | 2004-05-05 | Oncolytics Biotech Inc | Uso de un agente quimioterapeutico para la manufactura de un medicamento para la sensibilizacion de celulas neoplasicas resistentes a agentes quimioterapeuticos con reovirus |
| US6673370B2 (en) * | 2001-05-15 | 2004-01-06 | Biomedicines, Inc. | Oxidized collagen formulations for use with non-compatible pharmaceutical agents |
| PT1416917E (pt) * | 2001-08-06 | 2007-08-16 | Astrazeneca Ab | ''dispersão aquosa compreendendo nanopartículas estáveis de um triglicérido de cadeia média (mct) activo insolúvel em água e um do tipo excipiente'' |
| WO2003015778A1 (en) * | 2001-08-17 | 2003-02-27 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
| US20030059375A1 (en) * | 2001-08-20 | 2003-03-27 | Transave, Inc. | Method for treating lung cancers |
| DE10141528B4 (de) * | 2001-08-24 | 2006-08-10 | Faustus Forschungs Cie. Translational Cancer Research Gmbh | Platin(II)- und Platin(IV)-Komplexe und ihre Verwendung |
| US20030144312A1 (en) * | 2001-10-30 | 2003-07-31 | Schoenhard Grant L. | Inhibitors of ABC drug transporters in multidrug resistant cancer cells |
| AU2002353118A1 (en) * | 2001-12-11 | 2003-07-24 | Dor Biopharma, Inc. | Lipid particles and suspensions and uses thereof |
| AU2003220022A1 (en) * | 2002-03-01 | 2003-09-16 | Trustees Of Dartmouth College | Compositions and methods for preventing sporadic neoplasia in colon |
| US20040010553A1 (en) * | 2002-07-15 | 2004-01-15 | International Business Machines Corporation | Peer to peer location based services |
| WO2004006859A2 (en) * | 2002-07-16 | 2004-01-22 | Sonus Pharmaceuticals, Inc. | Platinum compound |
| WO2004012680A2 (en) * | 2002-08-06 | 2004-02-12 | Lyotropic Therapeutics, Inc. | Lipid-drug complexes in reversed liquid and liquid crystalline phases |
| AU2002951833A0 (en) * | 2002-10-02 | 2002-10-24 | Novogen Research Pty Ltd | Compositions and therapeutic methods invloving platinum complexes |
| US8217010B2 (en) * | 2002-10-24 | 2012-07-10 | The Board Of Trustees Of The University Of Illinois | Methods, compositions and articles of manufacture for contributing to the treatment of solid tumors |
| TWI323662B (en) * | 2002-11-15 | 2010-04-21 | Telik Inc | Combination cancer therapy with a gst-activated anticancer compound and another anticancer therapy |
| DE10256182A1 (de) * | 2002-12-02 | 2004-06-24 | Merck Patent Gmbh | 2-Oxadiazolchromonderivate |
| US7109337B2 (en) * | 2002-12-20 | 2006-09-19 | Pfizer Inc | Pyrimidine derivatives for the treatment of abnormal cell growth |
| DE502004006542D1 (de) * | 2003-04-30 | 2008-04-30 | Merck Patent Gmbh | Chromenonderivate |
| US20050020556A1 (en) * | 2003-05-30 | 2005-01-27 | Kosan Biosciences, Inc. | Method for treating diseases using HSP90-inhibiting agents in combination with platinum coordination complexes |
| US20070065522A1 (en) * | 2004-03-18 | 2007-03-22 | Transave, Inc. | Administration of high potency platinum compound formulations by inhalation |
| WO2005111016A1 (en) * | 2004-05-14 | 2005-11-24 | Pfizer Products Inc. | Pyrimidine derivatives for the treatment of abnormal cell growth |
| JP2007537235A (ja) * | 2004-05-14 | 2007-12-20 | ファイザー・プロダクツ・インク | 異常細胞増殖の治療用ピリミジン誘導体 |
| TW200538149A (en) * | 2004-05-20 | 2005-12-01 | Telik Inc | Sensitization to another anticancer therapy and/or amelioration of a side effect of another anticancer therapy by treatment with a GST-activated anticancer compound |
| TW200600091A (en) * | 2004-05-21 | 2006-01-01 | Telik Inc | Sulfonylethyl phosphorodiamidates |
| US7378423B2 (en) * | 2004-06-11 | 2008-05-27 | Japan Tobacco Inc. | Pyrimidine compound and medical use thereof |
| US20080146555A1 (en) * | 2004-06-18 | 2008-06-19 | Gpc Biotech, Inc | Uses of Kinase Inhibitors and Compositions Thereof |
| US20060003950A1 (en) * | 2004-06-30 | 2006-01-05 | Bone Care International, Inc. | Method of treating prostatic diseases using a combination of vitamin D analogues and other agents |
| US20060058311A1 (en) * | 2004-08-14 | 2006-03-16 | Boehringer Ingelheim International Gmbh | Combinations for the treatment of diseases involving cell proliferation |
| JP2008513435A (ja) * | 2004-09-22 | 2008-05-01 | ファイザー・インク | ポリ（ａｄｐ−リボース）ポリメラーゼ阻害剤を含む治療用組成物 |
| US20060205810A1 (en) * | 2004-11-24 | 2006-09-14 | Schering Corporation | Platinum therapeutic combinations |
| WO2006071812A2 (en) * | 2004-12-23 | 2006-07-06 | H. Lee Moffitt Cancer Center And Research Institute | Platinum iv complex inhibitor |
| US20090047365A1 (en) * | 2005-02-28 | 2009-02-19 | Eisai R & D Management Co., Ltd. | Novel Concomitant Use of Sulfonamide Compound with Anti-Cancer Agent |
| DK1888550T3 (da) * | 2005-05-12 | 2014-09-29 | Abbvie Bahamas Ltd | Apoptosepromotorer |
| US8034765B2 (en) * | 2005-08-31 | 2011-10-11 | Abraxis Bioscience, Llc | Compositions and methods for preparation of poorly water soluble drugs with increased stability |
| WO2007056236A2 (en) * | 2005-11-08 | 2007-05-18 | Transave, Inc. | Methods of treating cancer with lipid-based platinum compound formulations administered intravenously |
| US20070190182A1 (en) * | 2005-11-08 | 2007-08-16 | Pilkiewicz Frank G | Methods of treating cancer with high potency lipid-based platinum compound formulations administered intraperitoneally |
| US20070190180A1 (en) * | 2005-11-08 | 2007-08-16 | Pilkiewicz Frank G | Methods of treating cancer with high potency lipid-based platinum compound formulations administered intravenously |
| US8158152B2 (en) * | 2005-11-18 | 2012-04-17 | Scidose Llc | Lyophilization process and products obtained thereby |
| WO2007064658A2 (en) * | 2005-11-30 | 2007-06-07 | Transave, Inc. | Safe and effective methods of administering therapeutic agents |
| US8143236B2 (en) * | 2005-12-13 | 2012-03-27 | Bionumerik Pharmaceuticals, Inc. | Chemoprotective methods |
| WO2007109184A2 (en) * | 2006-03-16 | 2007-09-27 | Bionumerik Pharmaceuticals, Inc. | Anti-cancer activity augmentation compounds and formulations and methods of use thereof |
| EP2502628B1 (en) * | 2006-06-23 | 2016-12-14 | Alethia Biotherapeutics Inc. | Polynucleotides and polypeptide sequences involved in cancer |
| US8178564B2 (en) * | 2006-11-06 | 2012-05-15 | Poniard Pharmaceuticals, Inc. | Use of picoplatin to treat colorectal cancer |
| US20100297216A1 (en) * | 2006-12-20 | 2010-11-25 | Gabizon Alberto A | Method for administration of pegylated liposomal doxorubicin |
| US20110033528A1 (en) * | 2009-08-05 | 2011-02-10 | Poniard Pharmaceuticals, Inc. | Stabilized picoplatin oral dosage form |
| MX2009008487A (es) * | 2007-02-09 | 2010-01-15 | Poniard Pharmaceuticals Inc | Picoplatino encapsulado. |
| US7687487B2 (en) * | 2007-04-19 | 2010-03-30 | Bionumerik Pharmaceuticals, Inc. | Camptothecin-analog with a novel, “flipped” lactone-stable, E-ring and methods for making and using same |
| EP2152076A4 (en) * | 2007-05-31 | 2011-02-16 | Ascenta Therapeutics Inc | PULSATIVE DOSE OF GOSSYPOL FOR THE TREATMENT OF A DISEASE |
| TW200916094A (en) * | 2007-06-27 | 2009-04-16 | Poniard Pharmaceuticals Inc | Stabilized picoplatin dosage form |
| US20100260832A1 (en) * | 2007-06-27 | 2010-10-14 | Poniard Pharmaceuticals, Inc. | Combination therapy for ovarian cancer |
| CN101809024A (zh) * | 2007-07-16 | 2010-08-18 | 铂雅制药公司 | 吡铂的口服制剂 |
| ES2376175T3 (es) * | 2007-09-28 | 2012-03-09 | Bind Biosciences, Inc. | Direccionamiento a células de c�?ncer usando nanopart�?culas. |
| US20110053879A1 (en) * | 2008-02-08 | 2011-03-03 | Poniard Pharmaceuticals, Inc. | Picoplatin and amrubicin to treat lung cancer |
-
2008
- 2008-06-26 TW TW097124033A patent/TW200916094A/zh unknown
- 2008-06-27 CA CA2691115A patent/CA2691115A1/en not_active Abandoned
- 2008-06-27 EP EP08828991.3A patent/EP2157864A4/en not_active Withdrawn
- 2008-06-27 BR BRPI0811816-7A2A patent/BRPI0811816A2/pt not_active IP Right Cessation
- 2008-06-27 JP JP2010514837A patent/JP2010531877A/ja active Pending
- 2008-06-27 CN CN200880022248A patent/CN101801198A/zh active Pending
- 2008-06-27 AU AU2008295576A patent/AU2008295576A1/en not_active Abandoned
- 2008-06-27 KR KR1020107001745A patent/KR20100051797A/ko not_active Withdrawn
- 2008-06-27 WO PCT/US2008/008076 patent/WO2009032034A2/en not_active Ceased
- 2008-06-27 MX MX2009013835A patent/MX2009013835A/es not_active Application Discontinuation
-
2009
- 2009-12-10 US US12/635,534 patent/US20100178328A1/en not_active Abandoned
- 2009-12-10 US US12/635,517 patent/US20100215727A1/en not_active Abandoned
- 2009-12-15 IL IL202743A patent/IL202743A0/en unknown
-
2017
- 2017-03-15 IL IL251175A patent/IL251175A0/en unknown
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05501264A (ja) * | 1989-10-20 | 1993-03-11 | シキュース ファーマシューティカルズ，インコーポレイテッド | 充実性腫瘍治療法及び組成物 |
| JPH10509143A (ja) * | 1994-11-14 | 1998-09-08 | バイオニューメリック ファーマシューティカルズ インク | ２，２′−ジチオ−ビス（エタンスルホネート）（ジメスナ）と組み合わせたシスプラチン組成物 |
| WO2006104668A2 (en) * | 2005-03-11 | 2006-10-05 | Temple University - Of The Commonwealth System Of Higher Education | Composition and methods for the treatment of proliferative diseases |
Non-Patent Citations (3)
| Title |
|---|
| JPN5010011084; Ｐｕｊｏｌ Ｃｕｂｅｌｌｓ Ｍ ｅｔ ａｌ．: 'Ｓｔａｂｉｌｉｔｙ ｏｆ ｃｉｓｐｌａｔｉｎ ｉｎ ｓｏｄｉｕｍ ｃｈｌｏｒｉｄｅ ０．９％ ｉｎｔｒａｖｅｎｏｕｓ ｓｏｌｕｔｉｏｎ ｒｅｌａｔｅｄ ｔｏ ｔｈｅ ｃｏｎｔａｉｎｅｒ'ｓ ｍａｔｅｒ' Ｐｈａｒｍ Ｗｏｒｌｄ Ｓｃｉ． Ｖｏｌ．１５ Ｎｏ．１, 19930219, ｐｐ．３４-３６ * |
| JPN6013023415; Ｖｅｒｓｔｒａｅｔｅ Ｓ ｅｔ ａｌ．: 'Ｃｏｍｐａｒｉｓｏｎ ｏｆ ｔｈｅ ｒｅａｃｔｉｖｉｔｙ ｏｆ ｏｘａｌｉｐｌａｔｉｎ， Ｐｔ（ｄｉａｍｉｎｏｃｙｃｌｏｈｅｘａｎｅ）Ｃｌ２ ａｎｄ Ｐｔ（ｄｉａｍｉｎｏｃｙｃｌｏｈｅｘａｎｅ１）（Ｏ' Ｊ Ｉｎｏｒｇ Ｂｉｏｃｈｅｍ． Ｖｏｌ．８４ Ｎｏ．１-２, 200103, ｐｐ．１２９-１３５ * |
| JPN6013023416; Ｍｅｄｉｎａ-Ｇｕｎｄｒｕｍ Ｌ ｅｔ ａｌ．: 'ＺＤ０４７３ ｅｘｈｉｂｉｔｓ ｍａｒｋｅｄ ｉｎ ｖｉｔｒｏ ａｎｔｉｃａｎｃｅｒ ａｃｔｉｖｉｔｙ ｉｎ ｈｕｍａｎ ｔｕｍｏｒ ｓｐｅｃｉｍｅｎｓ' Ｅｕｒｏｐｅａｎ Ｊｏｕｒｎａｌ ｏｆ Ｃａｎｃｅｒ Ｖｏｌ．３７ Ｓｕｐｐｌｅｍｅｎｔ ６, 200110, ｐｐ．Ｓ１２４ * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2019509253A (ja) * | 2015-12-23 | 2019-04-04 | ニューカナ パブリック リミテッド カンパニー | 併用療法 |
Also Published As
| Publication number | Publication date |
|---|---|
| US20100178328A1 (en) | 2010-07-15 |
| MX2009013835A (es) | 2010-05-17 |
| TW200916094A (en) | 2009-04-16 |
| CN101801198A (zh) | 2010-08-11 |
| IL202743A0 (en) | 2010-06-30 |
| BRPI0811816A2 (pt) | 2014-12-30 |
| IL251175A0 (en) | 2017-04-30 |
| KR20100051797A (ko) | 2010-05-18 |
| AU2008295576A1 (en) | 2009-03-12 |
| CA2691115A1 (en) | 2009-03-12 |
| WO2009032034A3 (en) | 2009-04-30 |
| EP2157864A4 (en) | 2013-09-11 |
| WO2009032034A2 (en) | 2009-03-12 |
| EP2157864A2 (en) | 2010-03-03 |
| US20100215727A1 (en) | 2010-08-26 |
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