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Pfizer and BioNTech Receive EMA’s CHMP Positive Opinion Recommending Marketing Authorization for Omicron BA.4/BA.5- Bivalent Booster Vaccine

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Pfizer and BioNTech Receive EMA’s CHMP Positive Opinion Recommending Marketing Authorization for Omicron BA.4/BA.5- Bivalent Booster Vaccine

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  • The EMA’s CHMP has adopted the positive opinion recommending marketing authorization for a booster dose of Omicron BA.4/BA.5-adapted bivalent COVID-19 vaccine in children aged 5-11yrs. The EC’s final decision is expected shortly
  • The recommendation was based on safety & immunogenicity data from the Omicron BA.1-adapted bivalent vaccine in individuals aged ≥12yrs., initially approved 10µg pediatric formulations of the COVID-19 vaccine, manufacturing data from pediatric formulation & preclinical data from Omicron BA.4/BA.5-adapted bivalent vaccine
  • The P-II/III trial results showed that booster vaccine in adults aged ≥18yrs. elicited a strong immune response against BA.4 & BA.5 sublineages, safety & tolerability profile similar to the COVID-19 vaccine

Ref: Globenewswire | Image: BioNTech

Click here to­ read the full press release 

Senior Editor

Neha is a Senior Editor at PharmaShots. She is passionate and very enthusiastic about recent updates and developments in the life sciences and pharma industry. She covers Biopharma, MedTech, and Digital health segments along with different reports at PharmaShots. She can be contacted at connect@pharmashots.com.

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