WO2023027671 - A SOLID PHARMACEUTICAL COMPOSITION COMPRISING SACUBITRIL AND VALSARTAN

National phase entry is expected:
Publication Number WO/2023/027671
Publication Date 02.03.2023
International Application No. PCT/TR2022/050885
International Filing Date 22.08.2022
Title [English] A SOLID PHARMACEUTICAL COMPOSITION COMPRISING SACUBITRIL AND VALSARTAN [French] COMPOSITION PHARMACEUTIQUE SOLIDE COMPRENANT DU SACUBITRIL ET DU VALSARTAN
Applicants ** SANOVEL ILAC SANAYI VE TICARET ANONIM SIRKETI Istınye Mahallesı Balabandere Caddesı No:14 34460 Sarıyer/Istanbul, TR
Inventors ** KARABULUT, Serif Istınye Mahallesı Balabandere Caddesı No:14 34460 Sarıyer/Istanbul, TR ERDOGAN, Akif Istınye Mahallesı Balabandere Caddesı No:14 34460 Sarıyer/Istanbul, TR ATAK, Fadime Bilgehan Istınye Mahallesı Balabandere Caddesı No:14 34460 Sarıyer/Istanbul, TR SUNEL, Fatih Istınye Mahallesı Balabandere Caddesı No:14 34460 Sarıyer/Istanbul, TR
Priority Data 2021/013354  24.08.2021  TR
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Quotation for National Phase entry

Country Stages Total
China Filing 1033
EPO Filing, Examination 4917
Japan Filing 570
South Korea Filing 578
USA Filing, Examination 2635
MasterCard Visa
Total: 9733
Abstract [English] The present invention relates to a solid pharmaceutical composition comprises sacubitril in the form of the free base or in the form of pharmaceutically acceptable salts, crystalline polymorph thereof and valsartan in the form of the free base or in the form of pharmaceutically acceptable salts, crystalline polymorph thereof and at least one pharmaceutically acceptable excipient wherein the amount of binder is 0.1% to 20.0% by weight of the total composition. Further, the present invention also relates [French] La présente invention concerne une composition pharmaceutique solide comprenant du sacubitril sous la forme de la base libre ou sous la forme de sels pharmaceutiquement acceptables, un polymorphe cristallin correspondant et du valsartan sous la forme de la base libre ou sous la forme de sels pharmaceutiquement acceptables, un polymorphe cristallin correspondant et au moins un excipient pharmaceutiquement acceptable, la quantité de liant étant de 0,1 % à 20,0 % en poids de la composition totale. En outre, la présente invention concerne également un procédé.