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

Status
Recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2023-507527-28-00
Acronym
Candi5V01
Enrollment
251
Registered
2023-11-21
Start date
2024-09-16
Completion date
Unknown
Last updated
2025-12-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Recurrent vulvovaginal candidiasis

Interventions

None listed

Sponsors

LimmaTech Biologics AG
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Countries

Belgium, Poland

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026