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GSK Reports the MHLW’s sNDA Acceptance of Arexvy to Prevent Respiratory Syncytial Virus (RSV) Disease

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  • Japan’s MHLW has accepted sNDA of Arexvy RSV vaccine for adults aged 18-49yrs. at increased risk, expanding its use beyond those aged ≤50yrs.
  • Submission was based on P-IIIb trial (n=1458) assessing non-inferiority & safety of Arexvy RSV vaccine in individuals (18-49yrs.; n=426) compared to adults (≥60yrs.; n=429); an additional cohort (18-49yrs.; n=603) was followed for AEs separate to safety follow up of the initial cohort
  • Trial showed non-inferior immunogenicity in individuals (18-49yrs.) who are at increased risk of RSV-LRTD. Safety & reactogenicity aligned with P-III study data that supported initial approval

Ref: GSK| Image: GSK| Press Release

Related News:- Merck and Daiichi Sankyo Report First Patient Dosing with Ifinatamab DXd in P-III (IDeate-Prostate01) Trial for mCRPC

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