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BioNTech SE and Pfizer Inc. announced that the European Medicines Agency's (EMA) Committee for Medicinal Products for Human Use (CHMP) has recommended marketing authorization for their LP.8.1-adapted monovalent COVID-19 vaccine (COMIRNATY LP.8.1) for individuals 6 months of age and older. The vaccine is designed to prevent COVID-19 caused by SARS-CoV-2. The companies are developing a COVID-19 vaccine, the BNT162b2 mRNA vaccine program, and the Pfizer-BioNTech COVID-19 Vaccine, also known as COMIRNATY (COVID-19 Vaccine, mRNA) (BNT162b2).
The European Medicines Agency's (EMA) Committee for Medicinal Products for Human Use (CHMP) has recommended marketing authorization for Pfizer Inc. (PFE) and BioNTech SE (BNTX)'s LP.8.1-adapted monovalent COVID-19 vaccine, COMIRNATY LP.8.1, for individuals aged 6 months and older [1]. The recommendation is based on the EMA's Emergency Task Force (ETF) recommendation to update COVID-19 vaccines to target the LP.8.1 variant for the 2025-2026 season.
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