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China NMPA Approves PARP Inhibitor Pamiparib for Patients with Previously Treated Advanced Ovarian Cancer


Published: May 07, 2021
May 7, 2021 04:00 UTC
Pamiparib becomes the first PARP inhibitor approved in both platinum-sensitive and platinum-resistant relapsed ovarian cancer in China
This marks the first approval of pamiparib and the third BeiGene-discovered medicine to receive regulatory approval
BeiGene, Ltd. (NASDAQ: BGNE; HKEX: 06160), a global biotechnology company focused on developing and commercializing innovative medicines worldwide, today announced that its PARP inhibitor pamiparib has received conditional approval from the China National Medical Products Administration (NMPA) for the treatment of patients with germline
BRCA (
gBRCA) mutation-associated recurrent advanced ovarian, fallopian tube, or primary peritoneal cancer who have been treated with two or more lines of chemotherapy. The new drug application was previously granted priority review by the Center for Drug Evaluation (CDE) in July 2020. BeiGene is preparing to launch pamiparib t ....

United States , Yong Ben , Xiaobin Wu , Xiaohua Wu , Ovarian Cancer Research Alliance , Beigene Ltd , Exchange Commission , China National Medical Products Administration , Bristol Myers Squibb , Pamiparib Clinical Program , Drug Evaluation , Chief Operating Officer , General Manager , Chief Medical Officer , Gynecologic Oncology Department , Fudan University Shanghai Cancer Center , Pamiparib Clinical , Bristol Myers , Mirati Therapeutics , Novartis Pharma , North America , Private Securities Litigation Reform Act , Ovarian Cancer Research , Accessed April , Hina Nmpa Approves Parp Inhibitor Pamiparib For Patients With Previously Treated Advanced Ovarian Cancer , ஒன்றுபட்டது மாநிலங்களில் ,