VidPrevtyn Beta
Withdrawn
This medicine's authorisation has been withdrawn
COVID-19 Vaccine (recombinant, adjuvanted)
Medicine
Human
Withdrawn
- Rolling review
- Application under evaluation
- CHMP opinion
- European Commission decision
Overview
The marketing authorisation for Vidprevtyn Beta has been withdrawn at the request of the marketing-authorisation holder.
Product information
Latest procedure affecting product information:II/0007/G
11/03/2024
This medicine’s product information is available in all official EU languages.
Select 'available languages' to access the language you need.
Product information documents contain:
- summary of product characteristics (annex I);
- manufacturing authorisation holder responsible for batch release (annex IIA);
- conditions of the marketing authorisation (annex IIB);
- labelling (annex IIIA);
- package leaflet (annex IIIB).
Product details
- Name of medicine
- VidPrevtyn Beta
- Active substance
- SARS-CoV-2 prefusion Spike delta TM protein, recombinant (B.1.351 strain)
- International non-proprietary name (INN) or common name
- COVID-19 Vaccine (recombinant, adjuvanted)
- Therapeutic area (MeSH)
- COVID-19 virus infection
- Anatomical therapeutic chemical (ATC) code
- J07BN04
Pharmacotherapeutic group
VaccinesTherapeutic indication
VidPrevtyn Beta is indicated as a booster for active immunisation to prevent COVID-19 in adults who have previously received an mRNA or adenoviral vector COVID-19 vaccine (see sections 4.2 and 5.1 in product information document).
The use of this vaccine should be in accordance with official recommendations.
News on VidPrevtyn Beta
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