JP2008538751A5 - - Google Patents

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Publication number
JP2008538751A5
JP2008538751A5 JP2008505990A JP2008505990A JP2008538751A5 JP 2008538751 A5 JP2008538751 A5 JP 2008538751A5 JP 2008505990 A JP2008505990 A JP 2008505990A JP 2008505990 A JP2008505990 A JP 2008505990A JP 2008538751 A5 JP2008538751 A5 JP 2008538751A5
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JP
Japan
Prior art keywords
nanoparticles
surfactant
particle size
formulation
average particle
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Withdrawn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
JP2008505990A
Other languages
English (en)
Japanese (ja)
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JP2008538751A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/IB2006/001094 external-priority patent/WO2006109183A1/en
Publication of JP2008538751A publication Critical patent/JP2008538751A/ja
Publication of JP2008538751A5 publication Critical patent/JP2008538751A5/ja
Withdrawn legal-status Critical Current

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JP2008505990A 2005-04-13 2006-04-10 ナノ粒子組成物を持続放出するための注射用デポ製剤および方法 Withdrawn JP2008538751A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US67112405P 2005-04-13 2005-04-13
PCT/IB2006/001094 WO2006109183A1 (en) 2005-04-13 2006-04-10 Injectable depot formulations and methods for providing sustained release of nanoparticle compositions

Publications (2)

Publication Number Publication Date
JP2008538751A JP2008538751A (ja) 2008-11-06
JP2008538751A5 true JP2008538751A5 (cg-RX-API-DMAC7.html) 2009-05-21

Family

ID=36602931

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2008505990A Withdrawn JP2008538751A (ja) 2005-04-13 2006-04-10 ナノ粒子組成物を持続放出するための注射用デポ製剤および方法

Country Status (14)

Country Link
US (1) US20080193542A1 (cg-RX-API-DMAC7.html)
EP (1) EP1874268A1 (cg-RX-API-DMAC7.html)
JP (1) JP2008538751A (cg-RX-API-DMAC7.html)
KR (1) KR20070119678A (cg-RX-API-DMAC7.html)
CN (1) CN101166514A (cg-RX-API-DMAC7.html)
AU (2) AU2006233345A1 (cg-RX-API-DMAC7.html)
BR (1) BRPI0609299A2 (cg-RX-API-DMAC7.html)
CA (1) CA2605153A1 (cg-RX-API-DMAC7.html)
IL (1) IL186131A0 (cg-RX-API-DMAC7.html)
MX (1) MX2007012103A (cg-RX-API-DMAC7.html)
NZ (1) NZ561950A (cg-RX-API-DMAC7.html)
RU (1) RU2407529C2 (cg-RX-API-DMAC7.html)
WO (1) WO2006109183A1 (cg-RX-API-DMAC7.html)
ZA (1) ZA200708188B (cg-RX-API-DMAC7.html)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1623703B1 (en) 1999-10-29 2011-10-05 Euro-Celtique S.A. Controlled release hydrocodone formulations
US10179130B2 (en) 1999-10-29 2019-01-15 Purdue Pharma L.P. Controlled release hydrocodone formulations
HU230875B1 (hu) 2000-10-30 2018-11-29 Euro-Celtique S.A. Szabályozott hatóanyag-leadású hidrokodon készítmények
TW200526221A (en) * 2003-09-02 2005-08-16 Imran Ahmed Sustained release dosage forms of ziprasidone
US20080305161A1 (en) * 2005-04-13 2008-12-11 Pfizer Inc Injectable depot formulations and methods for providing sustained release of nanoparticle compositions
JP2008546781A (ja) * 2005-06-20 2008-12-25 エラン・ファルマ・インターナショナル・リミテッド アリール−複素環式化合物を含んでなるナノ粒状及び制御放出の組成物
HK1117060A1 (en) * 2005-06-20 2009-01-09 Elan Pharma International Limited Nanoparticulate and controlled release compositions comprising aryl-heterocyclic compounds
EP2175857B1 (en) * 2007-07-12 2013-09-11 Janssen R&D Ireland Crystalline form of (e) 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]amino]-2-pyrimidinyl]amino]benzonitrile
JP5893616B2 (ja) 2010-10-18 2016-03-23 大日本住友製薬株式会社 注射用徐放性製剤
RS60651B1 (sr) 2011-04-15 2020-09-30 Janssen Pharmaceutica Nv Nanosuspenzije leka osušene zamrzavanjem
CN104814926A (zh) * 2015-04-08 2015-08-05 中国药科大学 一种鲁拉西酮纳米混悬剂及其制备方法
MX2018003380A (es) * 2015-09-21 2018-08-16 Teva Pharmaceuticals Int Gmbh Formulaciones de olanzapina de liberacion sostenida.
CA3057438A1 (en) 2017-03-20 2018-09-27 Teva Pharmaceuticals International Gmbh Sustained release olanzapine formulaitons
CN109998991A (zh) * 2019-04-28 2019-07-12 中国药科大学 一种盐酸鲁拉西酮长效肌肉注射纳米混悬液及其制备方法
KR102847306B1 (ko) * 2021-08-13 2025-08-18 단국대학교 천안캠퍼스 산학협력단 결정형 몬테루카스트를 포함하는 지속성 현탁 주사제 및 이의 제조방법

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5145684A (en) * 1991-01-25 1992-09-08 Sterling Drug Inc. Surface modified drug nanoparticles
US5346702A (en) * 1992-12-04 1994-09-13 Sterling Winthrop Inc. Use of non-ionic cloud point modifiers to minimize nanoparticle aggregation during sterilization
US6150366A (en) * 1998-06-15 2000-11-21 Pfizer Inc. Ziprasidone formulations
US6267989B1 (en) * 1999-03-08 2001-07-31 Klan Pharma International Ltd. Methods for preventing crystal growth and particle aggregation in nanoparticulate compositions
EP1575616A2 (en) * 2002-10-25 2005-09-21 Pfizer Products Inc. Novel injectable depot formulations
US7488729B2 (en) * 2002-12-04 2009-02-10 Dr. Reddy's Laboratories Limited Polymorphic forms of ziprasidone and its hydrochloride salt and process for preparation thereof
US20040121003A1 (en) * 2002-12-19 2004-06-24 Acusphere, Inc. Methods for making pharmaceutical formulations comprising deagglomerated microparticles
TW200526221A (en) * 2003-09-02 2005-08-16 Imran Ahmed Sustained release dosage forms of ziprasidone

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