JP2004521897A5 - - Google Patents

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Publication number
JP2004521897A5
JP2004521897A5 JP2002562325A JP2002562325A JP2004521897A5 JP 2004521897 A5 JP2004521897 A5 JP 2004521897A5 JP 2002562325 A JP2002562325 A JP 2002562325A JP 2002562325 A JP2002562325 A JP 2002562325A JP 2004521897 A5 JP2004521897 A5 JP 2004521897A5
Authority
JP
Japan
Prior art keywords
itraconazole
particles
dosage form
particle
strong acid
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.)
Pending
Application number
JP2002562325A
Other languages
English (en)
Japanese (ja)
Other versions
JP2004521897A (ja
Filing date
Publication date
Priority claimed from US09/933,032 external-priority patent/US6663897B2/en
Application filed filed Critical
Publication of JP2004521897A publication Critical patent/JP2004521897A/ja
Publication of JP2004521897A5 publication Critical patent/JP2004521897A5/ja
Pending legal-status Critical Current

Links

JP2002562325A 2001-02-06 2002-02-01 経口イトラコナゾール調製物およびその製造法 Pending JP2004521897A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US26665301P 2001-02-06 2001-02-06
US09/933,032 US6663897B2 (en) 2001-02-06 2001-08-20 Oral itraconazole formulations and methods of making the same
PCT/NL2002/000080 WO2002062318A2 (en) 2001-02-06 2002-02-01 Oral itraconazole formulations and methods of making the same

Publications (2)

Publication Number Publication Date
JP2004521897A JP2004521897A (ja) 2004-07-22
JP2004521897A5 true JP2004521897A5 (enExample) 2005-12-22

Family

ID=26951964

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2002562325A Pending JP2004521897A (ja) 2001-02-06 2002-02-01 経口イトラコナゾール調製物およびその製造法

Country Status (9)

Country Link
US (1) US6663897B2 (enExample)
EP (1) EP1357899B1 (enExample)
JP (1) JP2004521897A (enExample)
AT (1) ATE369840T1 (enExample)
AU (1) AU2002233822A1 (enExample)
CA (1) CA2437372A1 (enExample)
DE (1) DE60221795T2 (enExample)
MX (1) MXPA03006980A (enExample)
WO (1) WO2002062318A2 (enExample)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0015239D0 (en) * 2000-06-21 2000-08-16 Biochemie Gmbh Organic compounds
US8071133B2 (en) 2001-08-20 2011-12-06 Stiefel Laboratories, Inc. Oral dosage forms of water insoluble drugs and methods of making the same
US20040115266A1 (en) * 2002-02-01 2004-06-17 Namburi Ranga Raju Oral itraconazole formulations and methods of making the same
WO2003101392A2 (en) 2002-05-31 2003-12-11 Transform Pharmaceuticals, Inc. Novel conazole crystalline forms and related processes, pharmaceutical compositions and methods
US7446107B2 (en) 2002-02-15 2008-11-04 Transform Pharmaceuticals, Inc. Crystalline forms of conazoles and methods of making and using the same
WO2003074474A2 (en) 2002-03-01 2003-09-12 University Of South Florida Multiple-component solid phases containing at least one active pharmaceutical ingredient
US7927613B2 (en) 2002-02-15 2011-04-19 University Of South Florida Pharmaceutical co-crystal compositions
US7790905B2 (en) 2002-02-15 2010-09-07 Mcneil-Ppc, Inc. Pharmaceutical propylene glycol solvate compositions
WO2004000284A1 (en) 2002-06-21 2003-12-31 Transform Pharmaceuticals, Inc. Pharmaceutical compositions with improved dissolution
GB0205253D0 (en) * 2002-03-06 2002-04-17 Univ Gent Immediate release pharmaceutical granule compositions and a continuous process for making them
WO2004012714A1 (en) * 2002-08-05 2004-02-12 Dsm Ip Assets B.V. Oral dosage forms of water insoluble drugs and methods of making the same
US8183290B2 (en) 2002-12-30 2012-05-22 Mcneil-Ppc, Inc. Pharmaceutically acceptable propylene glycol solvate of naproxen
US20050074494A1 (en) * 2003-10-06 2005-04-07 Xiu-Xiu Cheng Itraconazole immediate release formulation
US20050118265A1 (en) * 2003-11-28 2005-06-02 Anandi Krishnan Antifungal oral dosage forms and the methods for preparation
GB0612695D0 (en) * 2006-06-27 2006-08-09 Univ Gent Process for preparing a solid dosage form

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4791111A (en) 1985-12-23 1988-12-13 Janssen Pharmaceutica, N.V. [[4-[4-(4-phenyl-1-piperazinyl)phenoxymethyl]-1,3-dioxolan-2-yl]methyl]-1H-imidazoles and 1H-1,2,4-triazoles having anti-microbial properties
PH30929A (en) 1992-09-03 1997-12-23 Janssen Pharmaceutica Nv Beads having a core coated with an antifungal and a polymer.
IT1263831B (it) 1993-01-29 1996-09-04 Paolo Chiesi Complessi di inclusione multicomponente ad elevata solubilita' costituiti da un farmaco di tipo basico, un acido ed una ciclodestrina
CZ421498A3 (cs) * 1996-06-28 1999-06-16 Schering Corporation Orální prostředek obsahující triazolovou antifungální sloučeninu
FR2758461A1 (fr) 1997-01-17 1998-07-24 Pharma Pass Composition pharmaceutique presentant une biodisponibilite elevee et son procede de preparation
JP3608800B2 (ja) * 1997-03-26 2005-01-12 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ 抗真菌剤およびポリマーでコートされたコアを有するペレット剤
NZ505245A (en) * 1998-07-17 2001-12-21 Janssen Pharmaceutica Nv Pharmaceutical compositions of itraconazole and a water-soluble polymer to treat fungal infection
BR9915738A (pt) 1998-11-20 2001-10-02 Rtp Pharma Inc Micropartìculas estabilizadas em fosfolipìdeos dispersìveis
AU3900300A (en) 1999-03-24 2000-10-09 Fmc Corporation Improved aqueous solubility pharmaceutical formulations
US6383471B1 (en) * 1999-04-06 2002-05-07 Lipocine, Inc. Compositions and methods for improved delivery of ionizable hydrophobic therapeutic agents
KR100331529B1 (ko) 1999-06-16 2002-04-06 민경윤 난용성 항진균제의 경구투여용 조성물 및 그의 제조 방법

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