Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
V-01D-351 is a bivalent recombinant protein subunit COVID-19 vaccine booster developed as an updated formulation of the original V-01 vaccine. It contains receptor-binding domain (RBD) proteins from both the Beta (K417N, E484K, N501Y mutations) and Delta (L452R, T478K mutations) variants of SARS-CoV-2 in a 1:1 mixture. The vaccine is designed to enhance cross-neutralizing antibody responses against multiple SARS-CoV-2 variants of concern, including prototype, Delta, and Omicron strains. Clinical studies have shown that V-01D-351 induces robust and durable neutralizing antibody titers superior to those achieved with monovalent boosters or inactivated vaccines such as CoronaVac. The safety profile has been favorable with mostly mild or moderate adverse reactions[1][2][3][5][6].
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 V-01D-351.