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WO2010008719A3 - Formulations pharmaceutiques orales d’antagonistes de vla-4 - Google Patents

Formulations pharmaceutiques orales d’antagonistes de vla-4 Download PDF

Info

Publication number
WO2010008719A3
WO2010008719A3 PCT/US2009/047353 US2009047353W WO2010008719A3 WO 2010008719 A3 WO2010008719 A3 WO 2010008719A3 US 2009047353 W US2009047353 W US 2009047353W WO 2010008719 A3 WO2010008719 A3 WO 2010008719A3
Authority
WO
WIPO (PCT)
Prior art keywords
vla
pharmaceutical formulations
oral pharmaceutical
antagonists
antagonist
Prior art date
Application number
PCT/US2009/047353
Other languages
English (en)
Other versions
WO2010008719A9 (fr
WO2010008719A2 (fr
Inventor
David Harris
Ramya Kumbale
Original Assignee
Schering Corporation
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 Schering Corporation filed Critical Schering Corporation
Publication of WO2010008719A2 publication Critical patent/WO2010008719A2/fr
Publication of WO2010008719A3 publication Critical patent/WO2010008719A3/fr
Publication of WO2010008719A9 publication Critical patent/WO2010008719A9/fr

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605—Excipients; Inactive ingredients
    • A61K9/1617—Organic compounds, e.g. phospholipids, fats
    • A61K9/1623—Sugars or sugar alcohols, e.g. lactose; Derivatives thereof; Homeopathic globules
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4412—Non condensed pyridines; Hydrogenated derivatives thereof having oxo groups directly attached to the heterocyclic ring
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605—Excipients; Inactive ingredients
    • A61K9/1629—Organic macromolecular compounds
    • A61K9/1652—Polysaccharides, e.g. alginate, cellulose derivatives; Cyclodextrin

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Biophysics (AREA)
  • Molecular Biology (AREA)
  • Medicinal Preparation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

La présente invention concerne des formulations pharmaceutiques orales comprenant un antagonistes de VLA-4 et un tensioactif. Dans un mode de réalisation préféré, l’antagoniste de VLA-4 est le sel monosodique d’acide (3S)-3-[({[1-(2-chlorobenzyl)-4-hydroxy-5-méthyl-2-oxo-1,2-dihydropyridin-3-yl]amino}carbonyl)amino]-3-(4-méthylphényl)propanoïque. La présente invention concerne en outre des procédés pour traiter et/ou prévenir et/ou inhiber la progression d’une maladie inflammatoire utilisant de telles formulations pharmaceutiques.
PCT/US2009/047353 2008-06-16 2009-06-15 Formulations pharmaceutiques orales d’antagonistes de vla-4 WO2010008719A2 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US6185708P 2008-06-16 2008-06-16
US61/061,857 2008-06-16

Publications (3)

Publication Number Publication Date
WO2010008719A2 WO2010008719A2 (fr) 2010-01-21
WO2010008719A3 true WO2010008719A3 (fr) 2010-03-11
WO2010008719A9 WO2010008719A9 (fr) 2010-07-01

Family

ID=41395474

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2009/047353 WO2010008719A2 (fr) 2008-06-16 2009-06-15 Formulations pharmaceutiques orales d’antagonistes de vla-4

Country Status (1)

Country Link
WO (1) WO2010008719A2 (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20230033021A1 (en) 2018-06-20 2023-02-02 Progenity, Inc. Treatment of a disease of the gastrointestinal tract with an integrin inhibitor

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2761266A1 (fr) * 1997-03-28 1998-10-02 Sanofi Sa Composition pharmaceutique formee par granulation humide pour l'administration orale d'un derive du n-piperidino-3- pyrazolecarboxamide, de ses sels et de leurs solvates
US6238695B1 (en) * 1998-04-07 2001-05-29 Dupont Pharmaceuticals Company Formulation of fast-dissolving efavirenz capsules or tablets using super-disintegrants
WO2004044046A2 (fr) * 2002-11-08 2004-05-27 Encysive Pharmaceuticals Produits de combinaison comprenant des derives d'acide carboxylique inhibant la liaison des integrines a leurs recepteurs et autres composes therapeutiques
US20050003001A1 (en) * 2001-11-07 2005-01-06 Hisami Yamaguchi Method for improving dissolution of poorly dispersible medicaments

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2761266A1 (fr) * 1997-03-28 1998-10-02 Sanofi Sa Composition pharmaceutique formee par granulation humide pour l'administration orale d'un derive du n-piperidino-3- pyrazolecarboxamide, de ses sels et de leurs solvates
US6238695B1 (en) * 1998-04-07 2001-05-29 Dupont Pharmaceuticals Company Formulation of fast-dissolving efavirenz capsules or tablets using super-disintegrants
US20050003001A1 (en) * 2001-11-07 2005-01-06 Hisami Yamaguchi Method for improving dissolution of poorly dispersible medicaments
WO2004044046A2 (fr) * 2002-11-08 2004-05-27 Encysive Pharmaceuticals Produits de combinaison comprenant des derives d'acide carboxylique inhibant la liaison des integrines a leurs recepteurs et autres composes therapeutiques

Also Published As

Publication number Publication date
WO2010008719A9 (fr) 2010-07-01
WO2010008719A2 (fr) 2010-01-21

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