WO2022162513 - PHARMACEUTICAL COMPOSITION

National phase entry is expected:
Publication Number WO/2022/162513
Publication Date 04.08.2022
International Application No. PCT/IB2022/050578
International Filing Date 24.01.2022
Title **
[English] PHARMACEUTICAL COMPOSITION
[French] COMPOSITION PHARMACEUTIQUE
Applicants **
NOVARTIS AG Lichtstrasse 35 4056 Basel, CH
Inventors
JUHNKE, Michael Novartis Pharma AG Postfach 4002 Basel, CH
RAPP, Karin Novartis Pharma AG Postfach 4002 Basel, CH
SIN, Kim-Hien Novartis Pharma AG Postfach 4002 Basel, CH
Priority Data
63/141,558   26.01.2021   US
63/240,438   03.09.2021   US
63/290,251   16.12.2021   US
Application details
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Entry into National Phase under
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Quotation for National Phase entry

Country StagesTotal
China Filing1999
EPO Filing, Examination7248
Japan Filing593
South Korea Filing640
USA Filing, Examination3535
MasterCard Visa

Total: 14015

The term for entry into the National Phase has expired. This quotation is for informational purposes only

Abstract[English] The present invention relates to the field of pharmacy, particularly to a pharmaceutical composition for oral administration comprising a pharmaceutical composition for oral administration comprising: (a) an inert substrate, and (b) a mixture comprising N-(3-(6-amino-5-(2-(N-methylacrylamido)ethoxy)pyrimidin-4-yl)-5-fluoro-2-methylphenyl)-4-cyclopropyl-2-fluorobenzamide, or a pharmaceutically acceptable salt thereof, or a free form thereof, and at least one binder. The present invention also relates to a process for preparing said pharmaceutical composition for oral administration; and to the use of said pharmaceutical composition in the manufacture of a medicament.[French] La présente invention concerne le domaine de la pharmacie, en particulier une composition pharmaceutique pour administration orale comprenant : (a) un substrat inerte et (b) un mélange comprenant du N-(3-(6-amino-5-(2- (N-méthylacrylamido)éthoxy)pyrimidin-4-yl)-5-fluoro-2-méthylphényl)-4-cyclopropyl-2-fluorobenzamide ou un sel pharmaceutiquement acceptable correspondant, ou une forme libre correspondante et au moins un liant. La présente invention concerne également un procédé pour préparer ladite composition pharmaceutique destinée à une administration orale ; et l'utilisation de ladite composition pharmaceutique dans la fabrication d'un médicament.
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