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BioWorld - Tuesday, May 5, 2026
Home » Topics » Regulatory » NMPA

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China approves Sincere Biotech’s oral HIV-1 drug azvudine

July 27, 2021
By Elise Mak
China’s NMPA gave conditional approval to Henan Sincere Biotech Co. Ltd.’s dual-targeting, oral HIV drug, azvudine, to treat HIV-1-infected adult patients with high viral loads. Azvudine could challenge lamivudine, a drug extensively used for treating HIV infection.
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Red blood cells

Sinocelltech’s SCT-800 wins NMPA approval; first homegrown drug for hemophilia A

July 26, 2021
By Doris Yu
Sinocelltech Group Ltd. won market approval from China’s NMPA for SCT-800, a B-domain deleted recombinant human coagulation factor VIII, for the prophylactic treatment of severe hemophilia A in adolescent and adult patients. This marks the first homegrown drug for treating hemophilia A in China.
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China's NMPA clears initiation of clinical trials with ESG-401 for solid tumors

July 23, 2021

China approves Sincere Biotech’s oral HIV-1 drug azvudine

July 22, 2021
By Elise Mak
China’s NMPA gave conditional approval to Henan Sincere Biotech Co. Ltd.’s dual-targeting, oral HIV drug, azvudine, to treat HIV-1-infected adult patients with high viral loads. Azvudine could challenge lamivudine, a drug extensively used for treating HIV infection.
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Chinese flag and microscopes

China now wants quality, not just quantity

July 20, 2021
By Doris Yu
China’s Center for Drug Evaluation has released the guideline on developing oncology drugs with a clinical value-oriented approach, part of its ongoing efforts to encourage the development of truly innovative oncology drugs in China.
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Lepu’s NDA for anti-PD-1 antibody accepted ahead of Hong Kong IPO

July 20, 2021
By Doris Yu
The China NMPA’s Center for Drug Evaluation accepted Lepu Biopharma Co. Ltd.’s new drug application (NDA) for anti-PD-1 antibody candidate HX-008 (pucotenlimab). That comes after the company filed for an IPO in Hong Kong.
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Chinese flag and microscopes

China now wants quality, not just quantity

July 16, 2021
By Doris Yu
China’s Center for Drug Evaluation has released the guideline on developing oncology drugs with a clinical value-oriented approach, part of its ongoing efforts to encourage the development of truly innovative oncology drugs in China.
Read More

Lepu’s NDA for anti-PD-1 antibody accepted ahead of Hong Kong IPO

July 15, 2021
By Doris Yu
The China NMPA’s Center for Drug Evaluation accepted Lepu Biopharma Co. Ltd.’s new drug application (NDA) for anti-PD-1 antibody candidate HX-008 (pucotenlimab). That comes after the company filed for an IPO in Hong Kong.
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NMPA accepts IND application for TST-002 anti-sclerostin monoclonal antibody

July 7, 2021
Green approved stamp

China grants first CAR T approval to Fosun Kite

June 29, 2021
By Elise Mak
China’s drug regulator granted a first CAR T therapy approval to Fosun Kite Biotechnology Co. Ltd.’s FKC-876. Marketed as Yescarta (axicabtagene ciloleucel) in the U.S. and EU, the approval by the National Medical Production Administration for the CD19-directed CAR T therapy came 3.5 years after the FDA nod.
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