WO2024172778 - NOVEL POLYMORPH OF RUXOLITINIB HEMIFUMARATE AND METHOD OF PREPARATION

National phase entry is expected:
Publication Number WO/2024/172778
Publication Date 22.08.2024
International Application No. PCT/TR2023/050151
International Filing Date 16.02.2023
Title **
[English] NOVEL POLYMORPH OF RUXOLITINIB HEMIFUMARATE AND METHOD OF PREPARATION
[French] NOUVEAU POLYMORPHE D'HÉMIFUMARATE DE RUXOLITINIB ET PROCÉDÉ DE PRÉPARATION
Applicants **
DEVA HOLDING Halkali Merkez Mah. Basin Ekspres Cad. No:1 34303 Kucukcekmece/Istanbul, TR
Inventors
HAAS, Philipp Daniel Halkali Merkez Mah. Basin Ekspres Cad. No:1 34303 Kucukcekmece/Istanbul, TR
STECKEL, Hartwig Andreas Halkali Merkez Mah. Basin Ekspres Cad. No:1 34303 Kucukcekmece/Istanbul, TR
BELLUR ATİCİ, Esen Halkali Merkez Mah. Basin Ekspres Cad. No:1 34303 Kucukcekmece/Istanbul, TR
BOSTANCIOĞLU, Gamze Halkali Merkez Mah. Basin Ekspres Cad. No:1 34303 Kucukcekmece/Istanbul, TR
SOYER CAN, Okşan Halkali Merkez Mah. Basin Ekspres Cad. No:1 34303 Kucukcekmece/Istanbul, TR
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Quotation for National Phase entry

Country StagesTotal
China Filing862
EPO Filing, Examination4880
Japan Filing540
South Korea Filing483
USA Filing, Examination3835
MasterCard Visa

Total: 10600

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

Abstract[English] The present invention relates to a new crystalline polymorphic form of ruxolitinib hemifumarate, namely Form III, and methods for its preparation. The new crystalline polymorph Form III of ruxolitinib hemifumarate is characterized by an XRPD pattern having characteristic peaks (2-theta ± 0.2º) at 13.7, 19.3, 21.5 and 22.7. The present invention also provides pharmaceutical compositions comprising Form III of ruxolitinib hemifumarate, and medical use of Form III.[French] La présente invention concerne une nouvelle forme polymorphe cristalline d'hémifumarate de ruxolitinib, à savoir la forme III, et des procédés pour sa préparation. La nouvelle forme polymorphe cristalline III d'hémifumarate de ruxolitinib est caractérisée par un diagramme XRPD ayant des pics caractéristiques (2-thêta ± 0,2°) à 13,7,19,3, 21,5 et 22,7. La présente invention concerne également des compositions pharmaceutiques comprenant la forme III d'hémifumarate de ruxolitinib, et l'utilisation médicale de la forme III.
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