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The FDA approved Moderna’s mFlusiva on August 6, 2026, making it the first mRNA-based influenza vaccine authorized in the United States. The agency granted traditional approval for adults aged 50 to 64 but used accelerated approval for those 65 and
The FDA granted accelerated approval to Replimune’s Tudriqev with nivolumab on August 6, 2026, for advanced melanoma after anti-PD-1 therapy. The decision is significant because FDA had previously rejected the application twice over efficacy concerns. For Regulatory Affairs and clinical