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ZF2001 (brand name Zifivax) is a recombinant protein subunit vaccine developed by Anhui Zhifei Longcom Biopharmaceutical in collaboration with the Institute of Microbiology of the Chinese Academy of Sciences. The vaccine is produced in Chinese Hamster Ovary (CHO) cells and utilizes a tandem repeat dimeric form of the SARS-CoV-2 spike protein receptor-binding domain (RBD) as its antigen, adjuvanted with aluminum hydroxide. It is administered via intramuscular injection, typically following a three-dose schedule at 0, 28, and 56 days. ZF2001 was the first protein subunit COVID-19 vaccine to receive emergency use authorization (EUA) globally, initially in Uzbekistan and subsequently in China. The Sichuan Center for Disease Control and Prevention served as a primary sponsor for its international multicenter Phase III clinical trial (ChiCTR2100050849 / NCT04646525), which evaluated the vaccine's efficacy, safety, and immunogenicity in adults aged 18 and older.
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