Goliath has submitted to the State Drug Administration an application for the listing of the original oral hepatitis C cure program
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Last Update: 2020-06-11
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Source: Internet
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Author: User
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recently, Goli announced that theCompany's(to the StateMedicines(the Supervisory Authority submitted China's first original research full oral hepatitis C treatment program to the market application, is expected to be available within 5 working days of feedback.)the program consists of Ravidasvir (Ravidasvir, RDV, ASC16) united with the Gonowei ® (Danorivir, Danoprevir, DNV) with a 12-week cure rate of 99%Ravidawe is the second anti-hepatitis Cnew drugdeveloped independently by Golii (supported by the 13th Five-Year National Science and Technology Major Special "Major New Drug Creation" project, and its clinicaltest(application was also included in the priority review process by the State Drug Administration)about the New Generation of Trans-Genotype Direct Anti-CVIRUSDrugdeveloped by The Unda
we for NS5A Targets (combined with goliath's first innovative anti-Chepatitis ®, which was approved in early June, to form China's first total oral interferon-free hepatitis C treatment (RDV/DNV treatment regimen)the results of phase II/III clinical trials completed in Chinese mainland showed that after 12 weeks of treatment, the RDV/DNV treatment was 99% in patients with genotype 1 non-cirrhosis (SVR12) and 100% SVR12 was achieved in patients with NS5A drug-resistant mutations at baseline
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