drugset / Trial / NCT06190509

Assessing the Safety, Immune Response, and Early Efficacy of a Candida Vaccine in Women With Recurrent Vulvovaginal Candidiasis: A Randomized Controlled Study

NCT06190509 ↗

Phase 1/2 Active not recruiting 251 enrolled LimmaTech Biologics AG GlaxoSmithKline · collab
RandomizedParallel-groupTriple-blindPrevention

Summary

In this study, the pentavalent bioconjugate candidate vaccine (Candi5V) against Candida will be tested to obtain first-time-in-human (FTIH) data on its safety, immunogenicity, and preliminary efficacy in women with recurrent vulvovaginal candidiasis.

Timeline

Start
2023-12-06
Primary completion
2027-04-30
Completion
2027-04-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Candi5V Vaccine — —