Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
RSV-F vaccine + seasonal TIV refers to the coadministration of a respiratory syncytial virus (RSV) prefusion F protein-based subunit vaccine and a seasonal trivalent or quadrivalent inactivated influenza (TIV/QIV) vaccine. The RSV-F component is a protein subunit or recombinant protein that contains stabilized prefusion F antigens from both RSV A and B strains. It stimulates active immunity by inducing neutralizing antibodies against the fusion glycoprotein of the virus, thereby preventing lower respiratory tract disease caused by RSV[5][6]. The most widely used brands for this are Abrysvo (Pfizer) and Arexvy (GSK), both approved for adults over 60 years old and certain high-risk populations[3][5]. Seasonal TIV is an inactivated influenza virus vaccine targeting circulating strains of influenza A and B viruses. Coadministration studies show that giving these vaccines together is immunologically non-inferior for most strains but may result in slightly lower antibody titers; clinical significance remains unclear[8].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on RSV-F vaccine + seasonal TIV.