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BioWorld - Monday, February 23, 2026
Home » Topics » Asia-Pacific » China

China
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Brii’s SARS-CoV-2 monoclonal antibody cocktail therapy positive in phase III trial

Aug. 25, 2021
By Doris Yu
Brii Biosciences Ltd. made strides toward getting its SARS-CoV-2 neutralizing monoclonal antibody combination therapy, BRII-196/BRII-198, to market with positive interim phase III data that show high-risk outpatients may benefit from the combination therapy up to 10 days following symptom onset.
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Abogen raises $700M to help fund first Chinese COVID-19 mRNA vaccine

Aug. 24, 2021
By David Ho, Gina Lee, and Doris Yu
Suzhou Abogen Biosciences Co. Ltd.’s $700 million series C fundraising provides tailwinds for the development of its messenger ribonucleic acid (mRNA) platform. The company plans to accelerate its COVID-19 mRNA vaccine clinical trial, develop other vaccine candidates and oncology programs.
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Chinese flag

China clarifies rules for registration and classification of drug-device combinations

Aug. 24, 2021
By Doris Yu
An update from China’s NMPA clarifying registration requirements and classification methods for drug-device combination products has been welcomed by industry as the regulator seeks to keep pace with fast-moving developments in the sector.
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Hong Kong stock market illustration

Shanghai Heartcare stumbles in Hong Kong debut, but lineup for similar listings continues

Aug. 23, 2021
By Gina Lee and Doris Yu
Shanghai Heartcare Medical Technology Co. Ltd. shares took a hard fall in their Aug. 20 debut on the Hong Kong Stock Exchange (HKSE), closing at HK$129 (US$107.47) after tumbling all the way down to HK$127.8 earlier in the day.
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Abogen raises $700M to help fund first Chinese COVID-19 mRNA vaccine

Aug. 20, 2021
By Doris Yu, David Ho, and Gina Lee
Suzhou Abogen Biosciences Co. Ltd.’s $700 million series C fundraising provides tailwinds for the development of its messenger ribonucleic acid (mRNA) platform. The company plans to accelerate its COVID-19 mRNA vaccine clinical trial, develop other vaccine candidates and oncology programs.
Read More
Chinese flag

China clarifies rules for registration and classification of drug-device combinations

Aug. 19, 2021
By Doris Yu
An update from China’s NMPA clarifying registration requirements and classification methods for drug-device combination products has been welcomed by industry as the regulator seeks to keep pace with fast-moving developments in the sector.
Read More
Artery and plaque

Innovent’s PCSK9 inhibitor meets primary endpoint in phase III HeFH study in China

Aug. 17, 2021
By Doris Yu
Innovent Biologics Inc.’s PCSK9 inhibitor, IBI-306, intended for the treatment of heterozygous familial hypercholesterolemia (HeFH), has met its primary endpoint in a phase III study in Chinese patients.
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Inmagene gains rights to Syk inhibitor fostamatinib in Chinese markets

Aug. 17, 2021
By Gina Lee
Inmagene Biopharmaceuticals Co. Ltd. has licensed rights from Kissei Pharmaceutical Co. Ltd. to develop and commercialize the spleen tyrosine kinase (Syk) inhibitor fostamatinib for all potential indications in China.
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Innovent’s sintilimab combo heads toward sNDA filing in gastric cancer

Aug. 17, 2021
By Doris Yu
Following an interim analysis of phase III gastric cancer data, Innovent Biologics Inc. said it’s planning to seek an expanded label the company’s Eli Lilly and Co.-partnered PD-1 inhibitor, Tyvyt (sintilimab), in the indication. According to Innovent, a combination of the drug with chemotherapy met the primary endpoint of overall survival in the study, delivering a statistically significant improvement in the measure vs. placebo, also with chemotherapy.
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Blood sample, DNA

Belief Biomed’s BBM-H901 wins first Chinese IND approval in gene therapy for hemophilia B

Aug. 17, 2021
By Doris Yu
China’s NMPA has given Belief Biomed Inc. the official go-ahead to start testing its investigational gene therapy, BBM-H901, for the potential treatment of hemophilia B in the country, marking the first time an I.V. gene therapy for a rare disease has been approved in China. The company plans to advance the phase I/II trial for the candidate shortly, it said.
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