MX2010004292A - Producto de dispersion solida que contiene un compuesto a base de n-aril urea. - Google Patents

Producto de dispersion solida que contiene un compuesto a base de n-aril urea.

Info

Publication number
MX2010004292A
MX2010004292A MX2010004292A MX2010004292A MX2010004292A MX 2010004292 A MX2010004292 A MX 2010004292A MX 2010004292 A MX2010004292 A MX 2010004292A MX 2010004292 A MX2010004292 A MX 2010004292A MX 2010004292 A MX2010004292 A MX 2010004292A
Authority
MX
Mexico
Prior art keywords
solid dispersion
dispersion product
based compound
product containing
aryl urea
Prior art date
Application number
MX2010004292A
Other languages
English (en)
Inventor
Rudolf Schroeder
Tanja Heitermann
Original Assignee
Abbott Gmbh & Co Kg
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Abbott Gmbh & Co Kg filed Critical Abbott Gmbh & Co Kg
Publication of MX2010004292A publication Critical patent/MX2010004292A/es

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605Excipients; Inactive ingredients
    • A61K9/1629Organic macromolecular compounds
    • A61K9/1635Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/337Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having four-membered rings, e.g. taxol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605Excipients; Inactive ingredients
    • A61K9/1617Organic compounds, e.g. phospholipids, fats
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605Excipients; Inactive ingredients
    • A61K9/1629Organic macromolecular compounds
    • A61K9/1652Polysaccharides, e.g. alginate, cellulose derivatives; Cyclodextrin

Abstract

Un producto que comprende al menos un agente farmacéuticamente activo a base de N-aril urea o un agente de estructura relacionada que es obtenido mediante a) la preparación de una mezcla líquida que contiene el al menos un agente activo, el al menos un agente formador de matriz aceptable para uso farmacéutico, el al menos un agente tensoactivo aceptable para uso farmacéutico y el al menos un solvente, y b) la eliminación del o de los solventes de la mezcla líquida para obtener el producto de dispersión sólida.
MX2010004292A 2007-10-19 2008-10-17 Producto de dispersion solida que contiene un compuesto a base de n-aril urea. MX2010004292A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US99961307P 2007-10-19 2007-10-19
PCT/EP2008/064073 WO2009050289A2 (en) 2007-10-19 2008-10-17 Solid dispersion product containing n-aryl urea-based compound

Publications (1)

Publication Number Publication Date
MX2010004292A true MX2010004292A (es) 2010-08-02

Family

ID=40089072

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2010004292A MX2010004292A (es) 2007-10-19 2008-10-17 Producto de dispersion solida que contiene un compuesto a base de n-aril urea.

Country Status (23)

Country Link
US (1) US20090143423A1 (es)
EP (1) EP2197426A2 (es)
JP (1) JP2011500647A (es)
KR (1) KR20100090689A (es)
CN (1) CN101827585A (es)
AR (1) AR068916A1 (es)
AU (1) AU2008313620A1 (es)
BR (1) BRPI0818339A2 (es)
CA (1) CA2699335A1 (es)
CL (1) CL2008003092A1 (es)
CO (1) CO6270303A2 (es)
CR (1) CR11441A (es)
DO (1) DOP2010000114A (es)
EC (1) ECSP10010184A (es)
GT (1) GT201000095A (es)
MX (1) MX2010004292A (es)
PE (1) PE20091041A1 (es)
RU (1) RU2010119924A (es)
TW (1) TW200922549A (es)
UA (1) UA100866C2 (es)
UY (1) UY31406A1 (es)
WO (1) WO2009050289A2 (es)
ZA (1) ZA201002130B (es)

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WO2010045402A1 (en) * 2008-10-17 2010-04-22 Abbott Laboratories Trpv1 antagonists
AR073631A1 (es) * 2008-10-17 2010-11-17 Abbott Lab Antagonistas del receptor transitorio potencial de vanilloides 1 ( trpv1) utiles para tratar inflamacion y dolor
US20100210682A1 (en) * 2009-02-19 2010-08-19 Abbott Laboratories Repeated Dosing of TRPV1 Antagonists
WO2011032860A1 (de) * 2009-09-18 2011-03-24 Basf Se Verfahren zur herstellung von zubereitungen von in wasser schwerlöslichen substanzen
EP2654731B1 (en) * 2010-12-23 2016-07-27 AbbVie Deutschland GmbH & Co. KG Solid retard formulations based on solid dispersions
CN103391770A (zh) 2011-01-10 2013-11-13 细胞基因公司 环丙烷羧酸{2-[(1s)-1-(3-乙氧基-4-甲氧基-苯基)-2-甲烷磺酰基-乙基]-3-氧代-2,3-二氢-1h-异吲哚-4-基}-酰胺的口服剂型
EP2907505A3 (en) * 2011-12-29 2015-12-30 Abbvie Inc. Solid compositions comprising an HCV inhibitor
US9034832B2 (en) 2011-12-29 2015-05-19 Abbvie Inc. Solid compositions
TW201431570A (zh) 2012-11-22 2014-08-16 Ucb Pharma Gmbh 用於經皮投服羅替戈汀(Rotigotine)之多天式貼片
PL2950786T3 (pl) 2013-01-31 2020-05-18 Gilead Pharmasset Llc Formulacja skojarzona dwóch związków przeciwwirusowych
EA032322B1 (ru) 2013-03-15 2019-05-31 Бёрингер Ингельхайм Интернациональ Гмбх Твердая пероральная дозированная композиция ингибитора hcv в аморфном состоянии
US10046151B2 (en) 2013-07-03 2018-08-14 Lts Lohmann Therapie-Systeme, Ag Transdermal therapeutic system with electronic component
PL3038601T3 (pl) 2013-08-27 2020-08-24 Gilead Pharmasset Llc Formulacja złożona dwóch związków przeciwwirusowych
CN106456567A (zh) 2014-05-20 2017-02-22 Lts勒曼治疗系统股份公司 在经皮递送系统中调节活性剂释放的方法
CN106456566B (zh) * 2014-05-20 2020-06-16 Lts勒曼治疗系统股份公司 含罗替戈汀的经皮递送系统
CA2948221C (en) 2014-05-20 2022-11-22 Lts Lohmann Therapie-Systeme Ag Transdermal delivery system including an interface mediator
CA3039767C (en) * 2015-12-22 2023-11-14 Arizona Board Of Regents On Behalf Of The University Of Arizona Compositions and methods for treatment, amelioration, and prevention of anesthesia-induced hypothermia
CA3117563A1 (en) * 2018-10-30 2020-05-07 Peloton Therapeutics, Inc. Solid dispersions and pharmaceutical compositions comprising a substituted indane and methods for the preparation and use thereof
WO2021039023A1 (ja) 2019-08-23 2021-03-04 持田製薬株式会社 ヘテロシクリデンアセトアミド誘導体の製造方法
JP6830569B1 (ja) 2019-08-23 2021-02-17 持田製薬株式会社 ヘテロシクリデンアセトアミド誘導体の製造方法

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US5362878A (en) * 1991-03-21 1994-11-08 Pfizer Inc. Intermediates for making N-aryl and N-heteroarylamide and urea derivatives as inhibitors of acyl coenzyme A: cholesterol acyl transferase (ACAT)
EP0642498A1 (en) * 1992-05-28 1995-03-15 Pfizer Inc. NEW $i(N)-ARYL AND $i(N)-HETEROARYLUREA DERIVATIVES AS INHIBITORS OF ACYL COENZYME A:CHOLESTEROL ACYL TRANSFERASE (ACAT)
CA2302735A1 (en) * 1998-07-14 2000-01-27 Em Industries, Inc. Microdisperse drug delivery systems
US7015233B2 (en) * 2003-06-12 2006-03-21 Abbott Laboratories Fused compounds that inhibit vanilloid subtype 1 (VR1) receptor
BRPI0511900A (pt) * 2004-06-08 2008-01-22 Vertex Pharma composições farmacêuticas
JP5128948B2 (ja) * 2004-08-27 2013-01-23 ニッポネックス インコーポレイテッド 癌の治療のための新規な薬剤組成物
MX2007012947A (es) * 2005-04-18 2008-04-09 Rubicon Res Pvt Ltd Composiciones biomejoradas.
KR100715355B1 (ko) * 2005-09-30 2007-05-07 주식회사유한양행 프란루카스트를 함유하는 분무-건조 과립 및 그의 제조방법
US20070104780A1 (en) * 2005-10-25 2007-05-10 Lipari John M Formulation comprising a drug of low water solubility and method of use thereof
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US7745448B2 (en) * 2005-12-28 2010-06-29 Abbott Laboratories Inc. Crystalline N-(4-(4-aminothieno[2,3-d]pyrimidin-5-yl)phenyl)-N′-(2-fluoro-5-(trifluoromethyl)phenyl)urea ethanolate
JP5773560B2 (ja) * 2006-02-09 2015-09-02 メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. Cetp阻害剤のポリマー製剤

Also Published As

Publication number Publication date
UY31406A1 (es) 2009-05-29
CL2008003092A1 (es) 2009-11-27
JP2011500647A (ja) 2011-01-06
CN101827585A (zh) 2010-09-08
RU2010119924A (ru) 2011-11-27
BRPI0818339A2 (pt) 2015-04-22
ZA201002130B (en) 2011-11-30
PE20091041A1 (es) 2009-08-22
DOP2010000114A (es) 2010-05-15
CR11441A (es) 2010-10-25
CO6270303A2 (es) 2011-04-20
ECSP10010184A (es) 2010-06-29
GT201000095A (es) 2012-04-03
KR20100090689A (ko) 2010-08-16
UA100866C2 (ru) 2013-02-11
CA2699335A1 (en) 2009-04-23
AR068916A1 (es) 2009-12-16
TW200922549A (en) 2009-06-01
WO2009050289A3 (en) 2010-03-25
WO2009050289A2 (en) 2009-04-23
US20090143423A1 (en) 2009-06-04
AU2008313620A1 (en) 2009-04-23
EP2197426A2 (en) 2010-06-23

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