Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
NVP-1203-R1 + NVP-1203-R2 is an experimental recombinant protein subunit vaccine candidate developed by Novartis for the prevention of Respiratory Syncytial Virus (RSV) infection. The vaccine targets the RSV fusion (F) protein, a critical surface glycoprotein that mediates viral entry and syncytia formation. The R1 and R2 designations refer to specific formulations or manufacturing releases evaluated in early-phase clinical trials (such as NCT02296359) to assess safety, tolerability, and immunogenicity in healthy adults. Development of this specific asset under the Novartis pipeline was discontinued following the 2015 divestment of Novartis's non-influenza vaccine business to GSK, which subsequently prioritized its own RSV vaccine programs.
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 NVP-1203-R1 + NVP-1203-R2.