MA27075A1 - Formulations pharmaceutiques pour la liberation controlee de la 4-amino-6,7-dimethoxy-2-(5-methanesulfonamido-1,2,3,4-tetrahydroisoquinol-2-yl)-5-(2-pyridyl) - quinazoline - Google Patents

Formulations pharmaceutiques pour la liberation controlee de la 4-amino-6,7-dimethoxy-2-(5-methanesulfonamido-1,2,3,4-tetrahydroisoquinol-2-yl)-5-(2-pyridyl) - quinazoline

Info

Publication number
MA27075A1
MA27075A1 MA27623A MA27623A MA27075A1 MA 27075 A1 MA27075 A1 MA 27075A1 MA 27623 A MA27623 A MA 27623A MA 27623 A MA27623 A MA 27623A MA 27075 A1 MA27075 A1 MA 27075A1
Authority
MA
Morocco
Prior art keywords
tetrahydroisoquinol
quinazoline
dimethoxy
pyridyl
amino
Prior art date
Application number
MA27623A
Other languages
English (en)
Inventor
Douglas Davis John
James Macrae Ross
John Humphrey Michael
Sarah Smith Janet
Original Assignee
Pfizer
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 filed Critical Pfizer
Publication of MA27075A1 publication Critical patent/MA27075A1/fr

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • 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
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/2004Excipients; Inactive ingredients
    • A61K9/2013Organic 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
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/2004Excipients; Inactive ingredients
    • A61K9/2022Organic macromolecular compounds
    • A61K9/205Polysaccharides, e.g. alginate, gums; Cyclodextrin
    • A61K9/2054Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/48Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/50Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
    • A61K9/5005Wall or coating material
    • A61K9/5021Organic macromolecular compounds
    • A61K9/5026Organic 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
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/08Drugs for disorders of the urinary system of the prostate

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Urology & Nephrology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biophysics (AREA)
  • Molecular Biology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

DEPOSANT Société dite: PFIZER INC. REVENDICATION DE PRIORITES GB 11 Octobre 2001 0124455.7 Voir en annexe le titre de l'invention et le texte de l'abrégé Formulations pharmaceutiques pour la libération contrôlée de la 4-amino-6,7-diméthoxy-2-(5-méthanesulfonamido-1,2,3, 4-tétrahydroisoquinol-2-yl)-5-(2-pyridyl)-quinazoline La présente invention propose une formulation pharmaceutique à libération contrôlée pour administration orale, comprenant de la 4-amino-6,7-diméthoxy-2-(5-méthanesulfonamido-1,2,3,4-tétrahydroisoquinol-2-yl)-5-(2-pyridyl)-quinazoline, ou un de ses sels pharmaceutiquement acceptables, et un adjuvant, diluant ou support pharmaceutiquement acceptable, ladite formulation étant caractérisée en ce qu'elle est adaptée a libérer au moins 50 % en poids de la 4-amino-6,7-diméthoxy-2-(5-méthane-sulfonamido-1,2,3,4-tétrahydroisoquinol-2-yl)-5-(2-pyridyl)-quinazoline, ou de son sel pharmaceutiquement acceptable, au bout de 6 heures dans l'Appareil 1 décrit dans la Pharmacopée des Etats-Unis d'Amérique 24 (2000), pages 1941-1943, comprenant des récipients de 1 litre, des paniers à mailles no. 40 (ouvertures de 0,4 mm), à une vitesse de rotation de 100 tr/min, et avec un milieu de dissolution consistant en 900 ml d'acide chlorhydrique 0,01 M contenant 0,7 % en poids / volume de chlorure de sodium à 37o.C. Les formulations conformes à la présente invention conviennent au traitement de l'hyperplasie prostatique bénigne (HPB).
MA27623A 2001-10-11 2004-04-08 Formulations pharmaceutiques pour la liberation controlee de la 4-amino-6,7-dimethoxy-2-(5-methanesulfonamido-1,2,3,4-tetrahydroisoquinol-2-yl)-5-(2-pyridyl) - quinazoline MA27075A1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB0124455.7A GB0124455D0 (en) 2001-10-11 2001-10-11 Pharmaceutical formulations

Publications (1)

Publication Number Publication Date
MA27075A1 true MA27075A1 (fr) 2004-12-20

Family

ID=9923660

Family Applications (1)

Application Number Title Priority Date Filing Date
MA27623A MA27075A1 (fr) 2001-10-11 2004-04-08 Formulations pharmaceutiques pour la liberation controlee de la 4-amino-6,7-dimethoxy-2-(5-methanesulfonamido-1,2,3,4-tetrahydroisoquinol-2-yl)-5-(2-pyridyl) - quinazoline

Country Status (32)

Country Link
EP (1) EP1434570B8 (fr)
JP (1) JP4131471B2 (fr)
KR (1) KR20050032510A (fr)
CN (1) CN1568180A (fr)
AP (1) AP2004003001A0 (fr)
AR (1) AR036782A1 (fr)
AT (1) ATE303135T1 (fr)
BR (1) BR0213196A (fr)
CA (1) CA2461168A1 (fr)
CO (1) CO5560534A2 (fr)
DE (1) DE60205925T2 (fr)
DK (1) DK1434570T3 (fr)
DO (1) DOP2002000464A (fr)
EA (1) EA006168B1 (fr)
ES (1) ES2246017T3 (fr)
GB (1) GB0124455D0 (fr)
GT (1) GT200200184A (fr)
HR (1) HRP20040261A2 (fr)
HU (1) HUP0600064A3 (fr)
IL (1) IL160969A0 (fr)
IS (1) IS7179A (fr)
MA (1) MA27075A1 (fr)
MX (1) MXPA04003293A (fr)
NO (1) NO20041520L (fr)
OA (1) OA12709A (fr)
PA (1) PA8556001A1 (fr)
PE (1) PE20030551A1 (fr)
PL (1) PL369666A1 (fr)
SV (1) SV2004001279A (fr)
UY (1) UY27477A1 (fr)
WO (1) WO2003032956A1 (fr)
ZA (1) ZA200401976B (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0317663D0 (en) * 2003-07-29 2003-09-03 Astrazeneca Ab Pharmaceutical composition
MY186048A (en) 2013-03-14 2021-06-17 Cytokinetics Inc Heterocyclic compounds and their uses
KR101943592B1 (ko) 2017-08-31 2019-01-30 조현우 데이터 마이닝 기법을 이용한 전자가계부 시스템

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE69008526T2 (de) * 1990-07-02 1994-08-18 Bend Res Inc Asymmetrische mikroporöse Kügelchen für regulierbare Freigabe.
FR2752737B1 (fr) * 1996-08-29 1998-10-02 Synthelabo Comprime a liberation controlee de chlorhydrate d'alfuzosine
GB9700504D0 (en) * 1997-01-11 1997-02-26 Pfizer Ltd Pharmaceutical compounds
IL141235A (en) * 2000-02-09 2012-04-30 Novartis Int Pharm Ltd Combined use of an alpha-adrenoceptor antagonist and a muscarinic antagonist in the preparation of a drug for the treatment of non-malignant prostatic hyperplasia
CN1214029C (zh) * 2000-03-03 2005-08-10 辉瑞大药厂 4-氨基-6,7-二甲氧基-2-(5-甲磺酰氨基-1,2,3,4-四氢异喹啉-2-基)-5-(2-吡啶基)喹唑啉甲磺酸盐及多晶形物

Also Published As

Publication number Publication date
ZA200401976B (en) 2004-07-12
EA006168B1 (ru) 2005-10-27
GT200200184A (es) 2003-05-23
NO20041520L (no) 2004-04-05
AR036782A1 (es) 2004-10-06
HRP20040261A2 (en) 2004-08-31
GB0124455D0 (en) 2001-12-05
EP1434570B8 (fr) 2005-10-26
EP1434570B1 (fr) 2005-08-31
DK1434570T3 (da) 2005-11-07
WO2003032956A1 (fr) 2003-04-24
HUP0600064A3 (en) 2007-02-28
KR20050032510A (ko) 2005-04-07
CO5560534A2 (es) 2005-09-30
PL369666A1 (en) 2005-05-02
OA12709A (en) 2006-06-26
IS7179A (is) 2004-03-11
HUP0600064A2 (en) 2006-06-28
CA2461168A1 (fr) 2003-04-24
ES2246017T3 (es) 2006-02-01
JP2005507909A (ja) 2005-03-24
SV2004001279A (es) 2004-02-19
PA8556001A1 (es) 2003-07-28
DE60205925D1 (de) 2005-10-06
EA200400431A1 (ru) 2004-08-26
EP1434570A1 (fr) 2004-07-07
MXPA04003293A (es) 2004-07-23
BR0213196A (pt) 2004-08-31
IL160969A0 (en) 2004-08-31
UY27477A1 (es) 2003-05-30
DOP2002000464A (es) 2003-04-15
CN1568180A (zh) 2005-01-19
AP2004003001A0 (en) 2004-03-31
JP4131471B2 (ja) 2008-08-13
ATE303135T1 (de) 2005-09-15
PE20030551A1 (es) 2003-06-26
DE60205925T2 (de) 2006-06-08

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