Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Vi-rEPA is an investigational typhoid conjugate vaccine developed by the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD). The vaccine is composed of 25 μg of the Vi capsular polysaccharide from *Salmonella typhi* covalently linked to 25 μg of recombinant exoprotein A (rEPA) from *Pseudomonas aeruginosa*, which serves as a carrier protein. This conjugation converts the Vi polysaccharide from a T-cell independent antigen into a T-cell dependent immunogen, significantly enhancing its immunogenicity and efficacy in young children and infants. Clinical trials in Vietnam demonstrated that Vi-rEPA has a 91.5% efficacy rate in preventing blood culture-confirmed typhoid fever in children aged 2 to 5 years, with protection lasting at least four years. It has also been evaluated for safety and compatibility when co-administered with routine infant vaccinations such as DTP. Despite its high efficacy, the vaccine is not currently commercially available.
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 Vi-rEPA.