drugset / Trial / NCT05672966

Phase I Clinical Trial of a Candidate HPV Vaccine

NCT05672966 ↗

RandomizedSequentialQuadruple-blindPrevention

Summary

This is a Phase I, first-in-human, randomized, observer-blinded, placebo-controlled, dose escalation study to evaluate the safety, tolerability, and immunogenicity of BV601 (a HPV Vaccine) in healthy adult volunteers.

Timeline

Start
2023-08-01
Primary completion
2024-07-31
Completion
2024-10-31

Drugs

EvaluationDrugModalityDoseRoute
Subject BV601 Vaccine 0.5 ml Intramuscular