drugset / Trial / NCT01895855

Safety and Efficacy Challenge Study of Live Oral Cholera Vaccine Candidate,PXVX0200, to Prevent Cholera

NCT01895855 ↗

Phase 3 Completed 197 enrolled Bavarian Nordic Emergent BioSolutions · collab
RandomizedParallel-groupQuadruple-blindPrevention

Summary

The purpose of the study is to determine if PXVX0200 is safe and effective in preventing cholera infection

Timeline

Start
2013-09
Primary completion
2014-11
Completion
2014-11

Outcome

Met primary endpoint

paper only 2 of 35 (5.7%) vaccinees at 10 days (vaccine efficacy, 90.3%; P < .0001) PMID 27001804 ↗

paper 4 of 33 (12.1%) vaccinees at 3 months (vaccine efficacy, 79.5%; P < .0001) PMID 27001804 ↗

release “a Phase 3 challenge study, where Vaxchora demonstrated 90.3% efficacy at 10 days and 79.5% efficacy at 3 months” emergentbiosolutions.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject PXVX0200 Vaccine 5e+08 unknown Oral

Indications