Sipavibart closer to offering COVID-19 protection to immunocompromised in Europe
AstraZeneca’s (LSE: AZN) Marketing Authorization Application (MAA) for sipavibart has been accepted under an accelerated assessment procedure by the European Medicines Agency (EMA), for the pre-exposure prophylaxis (prevention) of COVID-19 in immunocompromised patients.
Sipavibart is an investigational long-acting antibody designed to provide COVID-19 protection for immunocompromised patients who often do not respond adequately to vaccination alone and remain at high risk of serious outcomes from the virus.
The MAA is based on positive results from the SUPERNOVA Phase III trial.
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