May 20, 2025
Source: drugdu
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On May 19, Aimi Vaccine (06660) announced that its mRNA shingles vaccine has recently obtained the "Drug Clinical Trial Approval Notice" from the National Medical Products Administration, which corresponds to the approval of the U.S. Food and Drug Administration for clinical trials in March 2025. This dual approval fully verifies the strength of the company's mRNA technology platform.
In preclinical trials, results from third-party testing units showed that the vaccine developed by the company was significantly higher than the internationally marketed recombinant subunit control vaccine in terms of specific T cell immunity, specific IgG antibody titer and membrane antigen fluorescent antibody (FAMA) titer.
Currently, no mRNA shingles vaccine has been approved for marketing internationally, and the market potential is huge. It is estimated that by 2030, the Chinese market size will reach about 20 billion yuan, and the global market size will reach about 23.9 billion US dollars. The launch of this product is expected to bring considerable performance growth to the company and reshape the market landscape.
https://finance.eastmoney.com/a/202505193407950828.html
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