WO2024214120 - PHARMACEUTICAL COMPOSITIONS OF NILOTINIB

National phase entry is expected:
Publication Number WO/2024/214120
Publication Date 17.10.2024
International Application No. PCT/IN2024/050382
International Filing Date 12.04.2024
Title **
[English] PHARMACEUTICAL COMPOSITIONS OF NILOTINIB
[French] COMPOSITION PHARMACEUTIQUE DU NILOTINIB
Applicants **
DR. REDDY'S LABORATORIES LIMITED
Inventors
PURAMDAS, Eslavath
KUMAR, Singh Sanjay
MALLIKARJUN, Chaudhari Sangmesh
AVIJIT, Choudhury Anup
Priority Data
202341026974   12.04.2023   IN
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Quotation for National Phase entry

Country StagesTotal
China Filing, Examination, Granting1951
EPO Filing, Examination, Granting11561
Japan Filing, Examination, Granting2026
South Korea Filing, Examination, Granting1765
USA Filing, Examination, Granting4740
MasterCard Visa
Total: 22,043

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

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Abstract[English] The present invention relates to immediate release pharmaceutical composition comprising amorphous solid dispersions of the protein kinase inhibitor, nilotinib or a pharmaceutically acceptable salt thereof, and pharmaceutical compositions comprising the same. More particularly, the present invention relates to improved pharmaceutical compositions of nilotinib, or a pharmaceutically acceptable salt thereof, that can be administered without regard to food 5 consumption and that can be administered at a significantly lower dose as compared to a commercially available immediate-release nilotinib formulation, while providing a comparable therapeutic effect. A method of preparation of the said compositions is also dislcosed.[French] La présente invention concerne une composition pharmaceutique à libération immédiate comprenant des dispersions solides amorphes de l'inhibiteur de protéine kinase, du nilotinib ou un sel pharmaceutiquement acceptable de celui-ci, et des compositions pharmaceutiques les comprenant. Plus particulièrement, la présente invention concerne des compositions pharmaceutiques améliorées de nilotinib, ou d'un sel pharmaceutiquement acceptable de celui-ci, qui peuvent être administrées sans tenir compte de la consommation d'aliments et qui peuvent être administrées à une dose significativement inférieure par rapport à une formulation de nilotinib à libération immédiate disponible dans le commerce, tout en fournissant un effet thérapeutique comparable. L'invention concerne également un procédé de préparation desdites compositions.

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