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BioWorld - Friday, February 13, 2026
Home » Topics » Regulatory » NMPA

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Drug capsules in petri dish

Micurx wins China approval for antibacterial contezolid

June 8, 2021
By Elise Mak
Micurx Pharmaceuticals Inc. has won marketing approval from China's NMPA for its lead antibacterial, contezolid, for treating adults with complicated skin and soft tissue infection (cSSTI), marking the first NDA for the Shanghai drugmaker. Set to be marketed as Youxitai in China, Micurx discovered the new-generation oral oxazolidinone antibiotic, developing it over 12 years. It’s designed to treat multidrug-resistant gram-positive bacteria such as methicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococci.
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China's NMPA clears IND for FXR agonist ASC-42 for chronic hepatitis B

June 7, 2021

China's NMPA accepts IND application for CT-120, a dual-antigen specific CAR-T therapy

June 4, 2021
Drug capsules in petri dish

Micurx wins China approval for antibacterial contezolid

June 3, 2021
By Elise Mak
Micurx Pharmaceuticals Inc. has won marketing approval from China's NMPA for its lead antibacterial, contezolid, for treating adults with complicated skin and soft tissue infection (cSSTI), marking the first NDA for the Shanghai drugmaker. Set to be marketed as Youxitai in China, Micurx discovered the new-generation oral oxazolidinone antibiotic, developing it over 12 years. It’s designed to treat multidrug-resistant gram-positive bacteria such as methicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococci.
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China takes action against counterfeits, but is it enough?

June 1, 2021
By Mari Serebrov
Drug regulators throughout China cracked down last year on companies manufacturing and selling counterfeit and substandard drugs and active pharmaceutical ingredients.
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China's NMPA approves initiation of phase I/II trial of AK-117 for medium- to high-risk MDS

May 20, 2021

China's NMPA approves phase I trial of InnoCare's TYK2 inhibitor ICP-332

May 19, 2021

China's NMPA issues clinical trial approval for JS-103 for gout

May 13, 2021
Ovarian cancer illustration

Beigene’s PARP inhibitor approved for recurrent ovarian cancer in China

May 11, 2021
By Elise Mak
Beigene Ltd.’s PARP inhibitor, pamiparib, won conditional approval from China’s National Medical Products Administration for treating patients with germline BRCA mutation-associated recurrent advanced ovarian, fallopian tube or primary peritoneal cancer who have been treated with two or more lines of chemotherapy.
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China accelerates drug approvals, development since joining ICH

May 11, 2021
By Elise Mak
Since joining the International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use in 2017, China has approved clinical trials and marketing of drugs a lot faster with simultaneous clinical development at home and abroad.
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