Phase 3 DataVYD222 produced high serum virus neutralizing antibody titer levels in immunocompromised participants with a favorable safety profile including no study drug-related serious adverse events, supporting an immunobridging approach for a high probability of success in Phase 3 and subsequent FDA approval for EUA.
Product LaunchTimothy Lee takes over as Chief Commercial Officer to further support the launch of Pemgarda, leveraging his extensive commercial experience leading product launches for Alexion, Biohaven, and Amylyx.
Regulatory ProgressInvivyd continues to make progress on establishing a defined regulatory pathway to expedite the review of future monoclonal antibodies (mAbs) for the prevention and treatment of symptomatic COVID-19.