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PE20071037A1 - SALTS AND FORMULATIONS OF 1- [5- (4-AMINO-7-ISOPROPYL-7H-PYRROLO [2,3-d] PYRIMIDIN-5-CARBONYL) -2-METOXY-PHENYL] -3- (2,4-DICHLORO -PHENIL) -UREA - Google Patents

SALTS AND FORMULATIONS OF 1- [5- (4-AMINO-7-ISOPROPYL-7H-PYRROLO [2,3-d] PYRIMIDIN-5-CARBONYL) -2-METOXY-PHENYL] -3- (2,4-DICHLORO -PHENIL) -UREA

Info

Publication number
PE20071037A1
PE20071037A1 PE2006001565A PE2006001565A PE20071037A1 PE 20071037 A1 PE20071037 A1 PE 20071037A1 PE 2006001565 A PE2006001565 A PE 2006001565A PE 2006001565 A PE2006001565 A PE 2006001565A PE 20071037 A1 PE20071037 A1 PE 20071037A1
Authority
PE
Peru
Prior art keywords
phenyl
urea
metoxy
pyrrolo
pyrimidin
Prior art date
Application number
PE2006001565A
Other languages
Spanish (es)
Inventor
Tracy Lee Boyden
Feng Guo
Susan Deborah Lagreca
Douglas Alan Lorenz
Shanker Ravy Mysore
Franzanne Vreeland
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 PE20071037A1 publication Critical patent/PE20071037A1/en

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
    • A61K9/1652Polysaccharides, e.g. alginate, cellulose derivatives; Cyclodextrin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents

Landscapes

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

Abstract

REFERIDA A UNA COMPOSICION FARMACEUTICA QUE COMPRENDE UNA DISPERSION SOLIDA AMORFA DE 1-[5-(4-AMINO-7-ISOPROPIL-7H-PIRROLO[2,3-d]PIRIMIDIN-5-CARBONIL)-2-METOXI-FENIL]-3-(2,4-DICLORO-FENIL)-UREA Y UN POLIMERO PARA AUMENTAR LA CONCENTRACION TAL COMO ACETATO SUCCINATO DE HIDROXIPROPIL METILCELULOSA, EN DONDE DICHO COMPUESTO DE UREA COMPRENDE ENTRE 10% Y 40% EN PESO DE LA DISPERSION SOLIDA AMORFA. DICHA DISPERSION SOLIDA AMORFA ESTA MEZCLADA CON MAS POLIMEROS PARA AUMENTAR LA CONCENTRACION TALES COMO ACETATO DE HIDROXIPROPIL METIL CELULOSA, HIDROXIPROPIL METIL CELULOSA, HIDROXIPROPIL CELULOSA, METIL CELULOSA, HIDROXIETIL METIL CELULOSA, ENTRE OTROS. DICHA COMPOSICION FARMACEUTICA ES UTIL PARA EL TRATAMIENTO DE TRASTORNOS HIPERPROLIFERATIVOSREFERRING TO A PHARMACEUTICAL COMPOSITION INCLUDING AN AMORPHOUS SOLID DISPERSION OF 1- [5- (4-AMINO-7-ISOPROPIL-7H-PYRROLO [2,3-d] PYRIMIDIN-5-CARBONYL) -2-METOXY-PHENYL] - 3- (2,4-DICHLORO-PHENYL) -UREA AND A POLYMER TO INCREASE THE CONCENTRATION SUCH AS HYDROXYPROPYL METHYLCELLULOSE ACETATE SUCCINATE, WHERE SAID UREA COMPOUND INCLUDES BETWEEN 10% AND 40% BY WEIGHT OF THE DISPERSION SOLID. SAID AMORPHOUS SOLID DISPERSION IS MIXED WITH MORE POLYMERS TO INCREASE THE CONCENTRATION SUCH AS HYDROXYPROPYL METHYL CELLULOSE ACETATE, HYDROXYPROPYL METHYL CELLULOSE, HYDROXYPROPYL CELLULOSE, METHYL CELLULOSE, METHYL CELLULOSE. SAID PHARMACEUTICAL COMPOSITION IS USEFUL FOR THE TREATMENT OF HYPERPROLIFERATIVE DISORDERS

PE2006001565A 2005-12-09 2006-12-06 SALTS AND FORMULATIONS OF 1- [5- (4-AMINO-7-ISOPROPYL-7H-PYRROLO [2,3-d] PYRIMIDIN-5-CARBONYL) -2-METOXY-PHENYL] -3- (2,4-DICHLORO -PHENIL) -UREA PE20071037A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US74907005P 2005-12-09 2005-12-09

Publications (1)

Publication Number Publication Date
PE20071037A1 true PE20071037A1 (en) 2007-11-19

Family

ID=38123252

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2006001565A PE20071037A1 (en) 2005-12-09 2006-12-06 SALTS AND FORMULATIONS OF 1- [5- (4-AMINO-7-ISOPROPYL-7H-PYRROLO [2,3-d] PYRIMIDIN-5-CARBONYL) -2-METOXY-PHENYL] -3- (2,4-DICHLORO -PHENIL) -UREA

Country Status (8)

Country Link
AR (1) AR058293A1 (en)
DO (1) DOP2006000271A (en)
GT (1) GT200600496A (en)
NL (1) NL2000337A1 (en)
PE (1) PE20071037A1 (en)
TW (1) TW200733965A (en)
UY (1) UY29991A1 (en)
WO (1) WO2007066189A2 (en)

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* Cited by examiner, † Cited by third party
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US20090143423A1 (en) * 2007-10-19 2009-06-04 Abbott Gmbh & Co. Kg Solid dispersion product containing n-aryl urea-based compound
AU2008313622A1 (en) * 2007-10-19 2009-04-23 Abbott Gmbh & Co. Kg Solid dispersion product of N-aryl urea-based drugs
WO2010045542A2 (en) * 2008-10-16 2010-04-22 The Regents Of The University Of California Fused ring heteroaryl kinase inhibitors
KR20120124428A (en) 2009-12-30 2012-11-13 아르퀼 인코포레이티드 Substituted pyrrolo-aminopyrimidine compounds
CN103037843A (en) * 2010-06-23 2013-04-10 麦它波莱克斯股份有限公司 Compositions of 5-ethyl-2-{4-[4-(4-tetrazol-1-Yl-phenoxymethyl)-thiazol-2-Yl]-piperidin-1-Yl}-pyrimidine
US8754114B2 (en) 2010-12-22 2014-06-17 Incyte Corporation Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3
EP2751112B1 (en) 2011-09-02 2019-10-09 The Regents of The University of California Substituted pyrazolo[3,4-d]pyrimidines and uses thereof
US20140004192A1 (en) * 2012-04-13 2014-01-02 Ziopharm Oncology, Inc. Pharmaceutical formulations of indibulin and uses thereof
US9611267B2 (en) 2012-06-13 2017-04-04 Incyte Holdings Corporation Substituted tricyclic compounds as FGFR inhibitors
US9388185B2 (en) 2012-08-10 2016-07-12 Incyte Holdings Corporation Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors
MX2015003874A (en) 2012-09-26 2015-12-16 Univ California Modulation of ire1.
US9266892B2 (en) 2012-12-19 2016-02-23 Incyte Holdings Corporation Fused pyrazoles as FGFR inhibitors
TWI715901B (en) 2013-04-19 2021-01-11 美商英塞特控股公司 Bicyclic heterocycles as fgfr inhibitors
US10851105B2 (en) 2014-10-22 2020-12-01 Incyte Corporation Bicyclic heterocycles as FGFR4 inhibitors
ES2751669T3 (en) 2015-02-20 2020-04-01 Incyte Corp Bicyclic heterocycles as FGFR inhibitors
MA41551A (en) 2015-02-20 2017-12-26 Incyte Corp BICYCLIC HETEROCYCLES USED AS FGFR4 INHIBITORS
US9580423B2 (en) 2015-02-20 2017-02-28 Incyte Corporation Bicyclic heterocycles as FGFR4 inhibitors
CN107722012B (en) * 2016-08-11 2020-05-29 斯福瑞(南通)制药有限公司 Process for preparing 4-chloro-7H-pyrrolo [2,3-d ] pyrimidines
AR111960A1 (en) 2017-05-26 2019-09-04 Incyte Corp CRYSTALLINE FORMS OF A FGFR INHIBITOR AND PROCESSES FOR ITS PREPARATION
SG11202010636VA (en) 2018-05-04 2020-11-27 Incyte Corp Solid forms of an fgfr inhibitor and processes for preparing the same
KR20210018264A (en) 2018-05-04 2021-02-17 인사이트 코포레이션 Salts of FGFR inhibitors
US11628162B2 (en) 2019-03-08 2023-04-18 Incyte Corporation Methods of treating cancer with an FGFR inhibitor
WO2021007269A1 (en) 2019-07-09 2021-01-14 Incyte Corporation Bicyclic heterocycles as fgfr inhibitors
WO2021067374A1 (en) 2019-10-01 2021-04-08 Incyte Corporation Bicyclic heterocycles as fgfr inhibitors
PE20221085A1 (en) 2019-10-14 2022-07-05 Incyte Corp BICYCLIC HETEROCYCLES AS FGFR INHIBITORS
WO2021076728A1 (en) 2019-10-16 2021-04-22 Incyte Corporation Bicyclic heterocycles as fgfr inhibitors
BR112022010664A2 (en) 2019-12-04 2022-08-16 Incyte Corp DERIVATIVES OF A FGFR INHIBITOR
EP4069696A1 (en) 2019-12-04 2022-10-12 Incyte Corporation Tricyclic heterocycles as fgfr inhibitors
WO2021146424A1 (en) 2020-01-15 2021-07-22 Incyte Corporation Bicyclic heterocycles as fgfr inhibitors
TW202304459A (en) 2021-04-12 2023-02-01 美商英塞特公司 Combination therapy comprising an fgfr inhibitor and a nectin-4 targeting agent
JP2024522189A (en) 2021-06-09 2024-06-11 インサイト・コーポレイション Tricyclic Heterocycles as FGFR Inhibitors
JP2025015449A (en) * 2023-07-18 2025-01-30 信越化学工業株式会社 Composition for solid dispersion, solid dispersion, and method of manufacturing solid dispersion

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE364374T1 (en) * 1997-08-11 2007-07-15 Pfizer Prod Inc SOLID PHARMACEUTICAL DISPERSIONS WITH INCREASED BIOAVAILABILITY
UA80171C2 (en) * 2002-12-19 2007-08-27 Pfizer Prod Inc Pyrrolopyrimidine derivatives

Also Published As

Publication number Publication date
GT200600496A (en) 2007-07-17
UY29991A1 (en) 2007-07-31
TW200733965A (en) 2007-09-16
WO2007066189A3 (en) 2008-08-14
DOP2006000271A (en) 2007-08-15
WO2007066189A2 (en) 2007-06-14
AR058293A1 (en) 2008-01-30
NL2000337A1 (en) 2007-06-12

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