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 + Matrix-M1 adjuvant is a recombinant subunit nanoparticle vaccine developed by Novavax to prevent respiratory syncytial virus (RSV) infection. The vaccine consists of a recombinant RSV fusion (F) protein antigen, stabilized in its prefusion conformation, and is formulated with Novavax's proprietary saponin-based Matrix-M1 adjuvant. The Matrix-M1 adjuvant is designed to enhance the immune response by stimulating both humoral and cellular (Th1-biased) immunity. Despite showing promise in early trials, the vaccine failed to meet its primary endpoints in large-scale Phase 3 clinical trials for both older adults (Resolve trial) and maternal immunization (Prepare trial), leading to the discontinuation of its development in these specific forms.
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 + matrix-m1 adjuvant.