Phase 2 data demonstrated positive immune responses to A and B strains, with acceptable safety and reactogenicity profile, meeting all pre-defined study endpoints
Vaccine candidate based on CureVac's proprietary second-generation mRNA backbone
GSK confirmed data support advancing program to Phase 3; dosing of first Phase 3 participant is associated with a significant milestone payment for CureVac
In July 2024, GSK assumed full control for the development, manufacturing and commercialization of influenza vaccines through new licensing agreement
No comments:
Post a Comment
Note: Only a member of this blog may post a comment.