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Express News | Shanghai Fosun Pharma - Clinical Trial of 24-Valent Pneumococcal Polysaccharide Conjugate Vaccine Got Approval From China's Nmpa
FOSUN PHARMA (600196.SH): The controlling subsidiary has received approval for vaccine clinical trials.
On March 4th, Glodon reported that FOSUN PHARMA (600196.SH) announced that its holding subsidiary FOSUN ANTIGEN (Chengdu) Pharmaceutical Co., Ltd. (hereinafter referred to as "FOSUN ANTIGEN") recently received approval from the National Medical Products Administration for the clinical trial of the 24-valent pneumococcal polysaccharide conjugate vaccine (Registration Classification: Preventive Biological Products Category 1.4; hereinafter referred to as "24-valent pneumococcal vaccine" or "the vaccine"). FOSUN ANTIGEN plans to conduct Phase I clinical trials of the vaccine in mainland China (excluding Hong Kong, Macao, and Taiwan) once conditions are met. This vaccine is part of the Group (that is, the Company and its holding subsidiaries).
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