[go: up one dir, main page]

PE20040091A1 - Formulaciones farmaceuticas de liberacion controlada - Google Patents

Formulaciones farmaceuticas de liberacion controlada

Info

Publication number
PE20040091A1
PE20040091A1 PE2003000670A PE2003000670A PE20040091A1 PE 20040091 A1 PE20040091 A1 PE 20040091A1 PE 2003000670 A PE2003000670 A PE 2003000670A PE 2003000670 A PE2003000670 A PE 2003000670A PE 20040091 A1 PE20040091 A1 PE 20040091A1
Authority
PE
Peru
Prior art keywords
inhibitor
pharmaceutically acceptable
acceptable salt
release
pde4d
Prior art date
Application number
PE2003000670A
Other languages
English (en)
Inventor
Avinash Govind Thombre
Kenneth Craig Waterman
Alfred Berchielli
Sheri Lynn Shamblin
Original Assignee
Pfizer Prod Inc
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 Pfizer Prod Inc filed Critical Pfizer Prod Inc
Publication of PE20040091A1 publication Critical patent/PE20040091A1/es

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4433Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with oxygen as a ring hetero atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0002Galenical forms characterised by the drug release technique; Application systems commanded by energy
    • A61K9/0004Osmotic delivery systems; Sustained release driven by osmosis, thermal energy or gas
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/08Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/08Antiallergic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Chemical & Material Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Epidemiology (AREA)
  • Pulmonology (AREA)
  • Otolaryngology (AREA)
  • Hospice & Palliative Care (AREA)
  • Immunology (AREA)
  • Medicinal Preparation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

QUE COMPRENDE: A)UN NUCLEO, QUE COMPRENDE: a)UNA COMPOSICION MEDICAMENTOSA; Y, b)UNA COMPOSICION HIDROHINCHABLE, TAL COMO UN AGENTE DE HINCHAMIENTO POLIMERICO IONICO O NO IONICO, OCUPANDO CADA UNO (a) Y (b) REGIONES SEPARADAS DENTRO DEL MISMO; Y, 2)UNA CUBIERTA ALREDEDOR DE (A), PERMEABLE AL AGUA, INSOLUBLE EN AGUA Y QUE TIENE AL MENOS UN PORO DE LIBERACION. DONDE, (a) COMPRENDE UN INHIBIDOR DE FOSFODIESTERASA TIPO 4D (PDE4D), O UNA SAL FARMACEUTICAMENTE ACEPTABLE DEL MISMO, EN LA QUE DICHA FORMULACION PRESENTA AL MENOS UNA DE LAS SIGUIENTES CARACTERISTICAS: i)UN Tmax MAYOR A 1,5 h CUANDO SE DOSIFICA IN VIVO; ii)MENOS DE 80% DE UN INHIBIDOR PDE4D O UNA SAL FARMACEUTICAMENTE ACEPTABLE DEL MISMO, SE LIBERA IN VIVO APROXIMADAMENTE EN 1,5 h; iii)MENOS DE 80% DE UN INHIBIDOR PDE4D O UNA SAL FARMACEUTICAMENTE ACEPTABLE DEL MISMO, SE LIBERA IN VITRO APROXIMADAMENTE EN 1,5 h; iv)UN RETRASO EN EL TIEMPO DE LIBERACION IN VITRO PREVIO A LA INICIACION DE LA LIBERACION DEL INHIBIDOR PDE4D, O UNA SAL FARMACEUTICAMENTE ACEPTABLE DEL MISMO, ENTRE 0,5 h A 4 h; v)UN RETRASO EN EL TIEMPO DE LIBERACION IN VIVO PREVIO A LA INICIACION DE LA LIBERACION DE DICHO INHIBIDOR O SU SAL, DE ENTRE 0,5 h A 4 h. SIENDO DICHO INHIBIDOR ACIDO(R)-2-[4-({[2-(BENZO[1,3]DIOXOL-5-ILOXI)-PIRIDINA-3-CARBONIL]-AMINO}-METIL)-3-FLUORO-FENOXIL]-PROPIONICO, SU SAL FARMACEUTICAMENTE ACEPTABLE; o 2-(4-FLUOROFENOXI)-N-[4-(1-HIDROXI-1-METIL-ETIL)-BENCIL]-NICOTINAMIDA, O SU SAL
PE2003000670A 2002-07-03 2003-07-02 Formulaciones farmaceuticas de liberacion controlada PE20040091A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US39380102P 2002-07-03 2002-07-03

Publications (1)

Publication Number Publication Date
PE20040091A1 true PE20040091A1 (es) 2004-02-17

Family

ID=30115647

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2003000670A PE20040091A1 (es) 2002-07-03 2003-07-02 Formulaciones farmaceuticas de liberacion controlada

Country Status (13)

Country Link
US (1) US20040076668A1 (es)
EP (1) EP1519711A1 (es)
JP (1) JP2006502108A (es)
AR (1) AR040378A1 (es)
AU (1) AU2003244942A1 (es)
BR (1) BR0312410A (es)
CA (1) CA2490978A1 (es)
MX (1) MXPA05000303A (es)
PA (1) PA8576801A1 (es)
PE (1) PE20040091A1 (es)
TW (1) TW200404580A (es)
UY (1) UY27880A1 (es)
WO (1) WO2004004684A1 (es)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050186276A1 (en) * 2003-07-17 2005-08-25 Pfizer Inc Pharmaceutical formulations
US20100209489A1 (en) * 2009-02-04 2010-08-19 Supernus Pharmaceuticals, Inc. Formulations of desvenlafaxine
WO2011039686A1 (en) * 2009-09-30 2011-04-07 Pfizer Inc. Latrepirdine oral sustained release dosage forms
RU2607595C2 (ru) 2010-02-03 2017-01-10 Фарма Ту Б Лтд. Составы разагилина с пролонгированным высвобождением и их применение
WO2015119848A1 (en) * 2014-02-05 2015-08-13 Merck Sharp & Dohme Corp. Tablet formulation for cgrp-active compounds
US12168004B2 (en) 2014-02-05 2024-12-17 Merck Sharp & Dohme Llc Treatment of migraine
US11717515B2 (en) 2020-12-22 2023-08-08 Allergan Pharmaceuticals International Limited Treatment of migraine
US12383545B1 (en) 2018-06-08 2025-08-12 Allergan Pharmaceuticals International Limited Treatment of migraine
CA3190176A1 (en) 2020-07-29 2022-02-03 Allergan Pharmaceuticals International Limited Treatment of migraine
EP4408418A1 (en) 2021-09-27 2024-08-07 Allergan Pharmaceuticals International Limited Combination comprising atogepant for treating migraine
GB202202297D0 (en) 2022-02-21 2022-04-06 Verona Pharma Plc Formulation production process
TW202506117A (zh) 2023-06-26 2025-02-16 英商維羅納製藥Plc公司 顆粒組成物

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE58906173D1 (de) * 1989-03-31 1993-12-16 Walhalla Kalk Entwicklungs Und Verfahren zur Abtrennung von Arsen aus Abwässern.
TR200001847T2 (tr) * 1997-04-04 2002-06-21 Pfizer Products Inc. Nikotinamid Türevleri
CZ20022046A3 (cs) * 1999-12-23 2002-11-13 Pfizer Products Inc. Hydrogelem hnaná dávková forma účinné sloľky

Also Published As

Publication number Publication date
CA2490978A1 (en) 2004-01-15
JP2006502108A (ja) 2006-01-19
US20040076668A1 (en) 2004-04-22
WO2004004684A8 (en) 2004-12-29
PA8576801A1 (es) 2005-02-04
MXPA05000303A (es) 2005-03-31
TW200404580A (en) 2004-04-01
UY27880A1 (es) 2004-02-27
AU2003244942A1 (en) 2004-01-23
BR0312410A (pt) 2005-04-26
EP1519711A1 (en) 2005-04-06
WO2004004684A1 (en) 2004-01-15
AR040378A1 (es) 2005-03-30

Similar Documents

Publication Publication Date Title
PE20040091A1 (es) Formulaciones farmaceuticas de liberacion controlada
PE20020307A1 (es) Forma de dosificacion de farmaco activada por hidrogel
DK1246622T3 (da) Nye substituerede benzimidazol dosisformer og metoder til deres anvendelse
ATE355065T1 (de) Therapeutische zusammensetzungen bestehend aus antihypotensiva und antiangiogenika
ES2159591T3 (es) Composicion de liberacion controlada.
AR013117A1 (es) Una composicion farmaceutica solida en forma de comprimido que comprende un derivado de benzofurano con actividad antiarritmica adaptada para administracion oral
MX2007006212A (es) Medicamento oral para liberacion modificada de al menos un principio activo bajo forma multimicrocapsular.
AR053731A1 (es) Aromatizacion de gomas de mascar que contienen farmacos
AR026745A1 (es) Composiciones de eplerenona nanoparticulada
TR200100931T2 (tr) Yeni sürekli salınımlı oral formülasyonlar
CO6241105A2 (es) "composiciones farmaceuticas que comprende {4-(6-fluoro-7-metilamino-2,4-dioxo-1,4-dihidro-2h-quinazolin-3-il)-fenil}-5-cloro-tiofen-2-il-sulfonilurea y un anticoagulante u otro agente antiplaquetario"
JP2005532372A5 (es)
AR027391A1 (es) Composiciones farmaceuticas de toxina botulinica
TR200200561T2 (tr) Mesalazin içeren ve vücut içinde kontrollü bir şekilde salgılanabilen ağızdan alınan farmasötik bileşimler
JP2014512390A5 (es)
PE20030527A1 (es) Formulacion farmaceutica con liberacion retardada que contiene 3-(3-dimetilamino-1-etil-2-metil-propil) fenol o una sal farmaceuticamente aceptable del mismo y tabletas para administracion oral que la contienen
PE20080613A1 (es) Derivados de pirazol como agentes antiagregantes plaquetarios y antitromboticos
IL158899A0 (en) Pharmaceutical compositions for inhibiting angiogenesis containing oleuropein and derivatives thereof
DK2170857T3 (da) 3',4',5-trimethoxyflavonderivater som stimulerende middel ved slimafsondring, tilsvarende fremgangsmåde og farmaceutisk præparat, der indeholder disse
WO2002026191A3 (en) Methods, compositions and devices utilizing stinging cells/capsules for delivering a therapeutic or a cosmetic agent into a tissue
UY27588A1 (es) Lactamas como antagonistas de taquiquininas
EP1284265A4 (en) BENZOTHIOPHENE DERIVATIVES AND MEDICINAL USE THEREOF
AR046036A1 (es) Composiciones de risedronato y metodos para su uso
PE17897A1 (es) Formulacion transdermica en parche del 3-(4-butiltio)-1,2,5-tiadiazol-3-il)-1-azabiciclo (2,2,2) octano
PE20051163A1 (es) Formas de dosificacion oral de acido n-(2-(2-ftalimido-etoxi)-acetil)-l-alanil-d-glutamico (lk 423)

Legal Events

Date Code Title Description
FD Application declared void or lapsed