WO2024028902 - ORAL FORMULATIONS OF ABIRATERONE ACETATE AND METHOD OF MANUFACTURING THEREOF

National phase entry:
Publication Number WO/2024/028902
Publication Date 08.02.2024
International Application No. PCT/IN2023/050753
International Filing Date 05.08.2023
Title **
[English] ORAL FORMULATIONS OF ABIRATERONE ACETATE AND METHOD OF MANUFACTURING THEREOF
[French] FORMULATIONS ORALES D'ACÉTATE D'ABIRATÉRONE ET LEUR PROCÉDÉ DE FABRICATION
Applicants **
BDR PHARMACEUTICALS INTERNATIONAL PRIVATE LIMITED
Inventors
DHARMESH MAHENDRABHAI, Shah
ARAVIND MANAPPA, Badiger
MUKESHKUMAR SUBHASHCHANDRA, Sharma
MADHAVKUMAR DILIPBHAI, Trivedi
SAMIRKUMAR BABULAL, Panchal
NILAY MANIKANT, Jayaswal
AKSHAYKUMAR SAMPATSINH, Jadav
Priority Data
202221044843   05.08.2022   IN
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Quotation for National Phase entry

Country StagesTotal
China Filing, Examination, Granting1958
EPO Filing, Examination, Granting11551
Japan Filing, Examination, Granting1937
South Korea Filing, Examination, Granting1669
USA Filing, Examination, Granting4740
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Total: 21,855

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 oral suspension dosage form of Abiraterone Acetate. The invention also relates to provide patient-compliant, economical and technically advanced dosage form over existing dosage form. Moreover, the solubility and stability of the patient compliant Abiraterone Acetate formulation, prepared as per the present invention, is proven higher when compared to prior art inventions. Furthermore, the present invention also provides a suspension composition prepared by a process which is relatively simple, easy to commercially manufacture, and functionally reproducible.[French] La présente invention concerne une forme galénique de suspension orale d'acétate d'abiratérone. L'invention concerne également la fourniture d'une forme galénique adaptée au patient, économique et techniquement avancée par rapport à une forme galénique existante. De plus, la solubilité et la stabilité de la formulation d'acétate d'abiratérone adaptée au patient, préparée selon la présente invention, s'avère être plus élevée par rapport aux inventions de l'état de la technique. En outre, la présente invention concerne également une composition de suspension préparée selon un procédé qui est relativement simple, facile à mettre en oeuvre dans le commerce, et fonctionnellement reproductible.