JP2008540629A5 - - Google Patents

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Publication number
JP2008540629A5
JP2008540629A5 JP2008511809A JP2008511809A JP2008540629A5 JP 2008540629 A5 JP2008540629 A5 JP 2008540629A5 JP 2008511809 A JP2008511809 A JP 2008511809A JP 2008511809 A JP2008511809 A JP 2008511809A JP 2008540629 A5 JP2008540629 A5 JP 2008540629A5
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JP
Japan
Prior art keywords
compound
composition
matrix
cellulose acetate
hydroxypropylmethylcellulose
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.)
Withdrawn
Application number
JP2008511809A
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English (en)
Japanese (ja)
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JP2008540629A (ja
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Publication date
Application filed filed Critical
Priority claimed from PCT/IB2006/001295 external-priority patent/WO2006123223A1/en
Publication of JP2008540629A publication Critical patent/JP2008540629A/ja
Publication of JP2008540629A5 publication Critical patent/JP2008540629A5/ja
Withdrawn legal-status Critical Current

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JP2008511809A 2005-05-19 2006-05-08 非晶形のvegf−r阻害剤を含む医薬組成物 Withdrawn JP2008540629A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US68292805P 2005-05-19 2005-05-19
PCT/IB2006/001295 WO2006123223A1 (en) 2005-05-19 2006-05-08 Pharmaceutical compostions comprising an amorphous form of a vegf-r inhibitor

Publications (2)

Publication Number Publication Date
JP2008540629A JP2008540629A (ja) 2008-11-20
JP2008540629A5 true JP2008540629A5 (enExample) 2009-01-08

Family

ID=36933392

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2008511809A Withdrawn JP2008540629A (ja) 2005-05-19 2006-05-08 非晶形のvegf−r阻害剤を含む医薬組成物

Country Status (5)

Country Link
US (1) US20080274192A1 (enExample)
EP (1) EP1885338A1 (enExample)
JP (1) JP2008540629A (enExample)
CA (1) CA2608952A1 (enExample)
WO (1) WO2006123223A1 (enExample)

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KR20070058690A (ko) 2004-11-02 2007-06-08 화이자 인코포레이티드 인다졸 화합물의 제조방법
MX2009010761A (es) 2007-04-05 2009-10-28 Pfizer Prod Inc Formas cristalinas de 6-[2-(metilcarbamoil)fenilsulfanil]-3-e-[2-( piridin-2-il)etenil]indzol adecuadas para el tratamiento del crecimiento celular anormal en mamiferos.
EP2305263B1 (en) * 2007-06-07 2012-09-19 Novartis AG Stabilized amorphous forms of imatinib mesylate
SG174488A1 (en) * 2009-03-19 2011-10-28 Shionogi & Co Solid preparation containing npy y5 receptor antagonist
WO2012042421A1 (en) 2010-09-29 2012-04-05 Pfizer Inc. Method of treating abnormal cell growth
MX2014003886A (es) 2011-09-30 2014-05-13 Pfizer Composiciones farmaceuticas de n-metil-2-[3-((e) 2-piridin-2-il-vinil)-1h-indazol-6-ilsulfanil]benzamida.
WO2013068909A1 (en) 2011-11-11 2013-05-16 Pfizer Inc. N-methyl-2-[3-((e)-2-pyridin-2-yl-vinyl)-1h-indazol-6-ylsulfanyl]-benzamide for the treatment of chronic myelogenous leukemia
ES2946549T3 (es) 2012-01-13 2023-07-20 Xspray Pharma Ab Publ Composición farmacéutica de nilotinib
EP4450130A3 (en) * 2012-09-11 2025-01-08 Medivation Prostate Therapeutics LLC Formulations of enzalutamide
EP2956121B1 (en) * 2013-02-12 2018-05-30 Bend Research, Inc. Solid dispersions of low-water solubility actives
EP2792360A1 (en) 2013-04-18 2014-10-22 IP Gesellschaft für Management mbH (1aR,12bS)-8-cyclohexyl-11-fluoro-N-((1-methylcyclopropyl)sulfonyl)-1a-((3-methyl-3,8-diazabicyclo[3.2.1]oct-8-yl)carbonyl)-1,1a,2,2b-tetrahydrocyclopropa[d]indolo[2,1-a][2]benzazepine-5-carboxamide for use in treating HCV
CN104140414B (zh) * 2013-05-07 2018-12-11 江苏豪森药业集团有限公司 阿昔替尼晶型的制备方法
WO2015067224A1 (en) 2013-11-08 2015-05-14 Zentiva, K.S. Salts of 6-[2-(methylcarbamoyl)phenylsulfanyl]-3-e-[2-(pyridin-2-yl)ethanyl] indazole
CA2929499C (en) * 2013-11-22 2019-01-08 Merck Sharp & Dohme Corp. Composition of a non-nucleoside reverse transcriptase inhibitor
CN118286440A (zh) 2014-02-04 2024-07-05 辉瑞大药厂 用于治疗癌症的pd-1拮抗剂和vegfr抑制剂的组合
JP2017530950A (ja) 2014-08-25 2017-10-19 ファイザー・インコーポレイテッド 癌を処置するためのpd−1アンタゴニストおよびalk阻害剤の併用
IL278423B2 (en) 2015-02-26 2024-04-01 Merck Patent Gmbh Pd-1 / pd-l1 inhibitors for the treatment of cancer
KR102013440B1 (ko) * 2015-04-03 2019-08-22 임팩트 테라퓨틱스, 인코포레이티드 Parp 억제제 고체약물제형 및 그 용도
RU2766890C2 (ru) 2015-06-16 2022-03-16 Мерк Патент Гмбх Комбинированные способы лечения антагонистами pd-l1
CN106467512B (zh) * 2015-08-19 2022-03-11 浙江九洲药业股份有限公司 一种阿西替尼富马酸盐及其结晶形式和制备方法
CA3039451A1 (en) 2016-10-06 2018-04-12 Pfizer Inc. Dosing regimen of avelumab for the treatment of cancer
WO2019234581A1 (en) * 2018-06-04 2019-12-12 Glenmark Pharmaceuticals Limited Pharmaceutical compositions of axitinib
US20220370606A1 (en) 2018-12-21 2022-11-24 Pfizer Inc. Combination Treatments Of Cancer Comprising A TLR Agonist
WO2022000265A1 (zh) * 2020-06-30 2022-01-06 天津理工大学 一种阿西替尼与戊二酸共晶及其制备方法
JP7654346B2 (ja) 2022-03-03 2025-04-01 ファイザー・インク 多重特異性抗体およびその使用
WO2025157389A1 (en) 2024-01-22 2025-07-31 Iomx Therapeutics Ag Combinations of halogenated heterocyclic kinase inhibitors and vegfr inhibitors

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JPS53148542A (en) * 1977-05-27 1978-12-25 Reiichi Yamaga Pharmaceutical composition densistry
JPS59219384A (ja) * 1983-05-30 1984-12-10 Mitsui Norin Kk 天然抗酸化剤の製造方法
US5266319A (en) * 1992-03-18 1993-11-30 National Science Council Tannin derivatives and their use for treatment of hypertension
US5773419A (en) * 1995-03-03 1998-06-30 Falcon; Juan Method of treating cancer with tannic acid
US6350786B1 (en) * 1998-09-22 2002-02-26 Hoffmann-La Roche Inc. Stable complexes of poorly soluble compounds in ionic polymers
US6706283B1 (en) * 1999-02-10 2004-03-16 Pfizer Inc Controlled release by extrusion of solid amorphous dispersions of drugs
TWI262914B (en) * 1999-07-02 2006-10-01 Agouron Pharma Compounds and pharmaceutical compositions for inhibiting protein kinases
PE20010306A1 (es) * 1999-07-02 2001-03-29 Agouron Pharma Compuestos de indazol y composiciones farmaceuticas que los contienen utiles para la inhibicion de proteina kinasa
EP1120109A3 (en) * 2000-01-24 2002-07-10 Pfizer Products Inc. Rapidly disintegrating and fast dissolving solid dosage form
PT1469833T (pt) * 2002-02-01 2021-07-13 Bend Res Inc Método para produzir dispersões de fármaco amorfo sólido seco por pulverização homogéneas utilizando aparelho de secagem por pulverização modificado
US20040126448A1 (en) * 2002-08-05 2004-07-01 Nils-Olof Lindberg Sexual dysfunction compounds
WO2004092217A1 (en) * 2003-04-17 2004-10-28 Pfizer Inc. Crystal structure of vegfrkd: ligand complexes and methods of use thereof
AU2005300317A1 (en) * 2004-11-02 2006-05-11 Pfizer Inc. Polymorphic forms of 6-[2-(methylcarbamoyl)phenylsulfanyl]-3-E-[2-(pyridin-2-yl)ethenyl]indazole

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