Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
A recombinant subunit vaccine designed to protect against plague caused by *Yersinia pestis*. It consists of two primary antigens: the natural Fraction 1 (F1) capsular protein and a recombinant version of the V (LcrV) antigen. These antigens are critical for the virulence of *Y. pestis* and are known to provide synergistic protection against both bubonic and pneumonic plague. The vaccine is being developed by the Jiangsu Provincial Center for Disease Control and Prevention and has been evaluated in Phase 2 clinical trials using various immunization regimens (e.g., 0-1-6 and 0-2-6 months). The formulation typically includes an adjuvant to enhance immunogenicity.
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 plague vaccine F1 + rV.