Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
SeVRSV is a live-attenuated, recombinant viral vector vaccine candidate designed to provide bivalent protection against respiratory syncytial virus (RSV) and human parainfluenza virus type 1 (hPIV1). Developed by St. Jude Children's Research Hospital, the vaccine utilizes the Sendai virus (SeV)—a murine parainfluenza virus—as a vector to express the RSV fusion (F) protein. Because SeV is antigenically related to hPIV1, the vector backbone itself induces cross-reactive immunity against hPIV1, while the expressed F protein induces neutralizing antibodies and T-cell responses against RSV. The vaccine is typically administered intranasally to stimulate mucosal immunity in the upper respiratory tract, mimicking natural infection to prevent lower respiratory tract disease in infants and children.
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 SeVRSV.