Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**Euvichol-S** is a ready-to-use, non-adjuvanted, preservative-free oral cholera vaccine jointly developed by the International Vaccine Institute and EuBiologics for prevention of cholera caused by *Vibrio cholerae* serogroup O1. It contains formalin-inactivated whole cells of *V. cholerae* O1 Inaba El Tor strain Phil 6973 and O1 Ogawa classical strain Cairo 50. Oral administration induces protective mucosal and systemic immune responses against O1 cholera antigens, including lipopolysaccharide-associated antigens. It is a simplified, higher-productivity successor formulation to Euvichol-Plus, supplied as a 1.5 mL oral suspension and administered as two doses two weeks apart. WHO prequalified Euvichol-S on April 12, 2024. ([extranet.who.int](https://extranet.who.int/prequal/sites/default/files/vwa_vaccine/FVP-P-456_Euvichol-S_1dose_Eubiologics_WHOPAR-2025.pdf))
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 Euvichol-S.