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EMA Accepts Approval for AstraZeneca MAA for Sipavibart
AstraZeneca has announced that its Marketing Authorisation 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 | 02/07/2024 | By Aishwarya | 132
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