In general, VRBPAC almost always recommends the same influenza strains as the World Health Organization (WHO) for egg-based ...
The FDA has granted approval for the IND application of Everest Medicines’ tumour-associated antigen (TAA) vaccine, EVM14.
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Vietnam Investment Review on MSNAIM Vaccine's mRNA Shingles Vaccine Approved by the US FDA to Begin Clinical Trials, AI-Enabled mRNA Major Vaccine Product Development AcceleratesAIM Vaccine Co., Ltd. (06660.HK), a leading PRC vaccine company, published an announcement on March 23, 2025, the company's independently developed mRNA shingles vaccine has recently received clinical ...
Apathy about shots, diseases like flu may be just as big a threat to public health efforts as vaccine mistrust.
THE Food and Drug Administration (FDA) on Friday, March 21, 2025, warned the public against the presence of counterfeit ...
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Vietnam Investment Review on MSNEverest Medicines Announces FDA Clearance of IND Application for Tumor Associated Antigen Vaccine EVM14EVM14 received U.S. FDA clearance for its IND application, becoming Everest's first internally discovered program, and the first mRNA therapeutic cancer vaccine to be cleared for global clinical ...
In this week’s edition of InnovationRx, we look at the policy uncertainty around vaccines, sex differences in GLP-1 drug side ...
Novavax reached a settlement with Gavi, the Vaccine Alliance, after t | International vaccine partnership Gavi has ...
Rep. Marjorie Taylor Greene calls for yanking FDA approval of COVID-19 vaccines, says that "COVID-19 vaccines are causing ...
The FDA has released its recommendations on the ... meet to discuss the strains that should be included in the seasonal vaccine yesterday but was abruptly cancelled by new Health and Human ...
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Vietnam Investment Review on MSNClover Announces U.S. IND Clearance and Initiation of Revaccination Clinical Study for RSV Vaccine Candidate SCB-1019Clover Biopharmaceuticals, Ltd.today announced IND clearance by U.S. FDA and that enrollment of the first participants has ...
The recommendations were made following a meeting that included experts from the FDA, the Centers for Disease Control and Prevention, and the Department of Defense.
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