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Phase I Clinical Trial of a Candidate HPV Vaccine

Human Papillomavirus Infection Clinical Trial

Official title:
A Phase I, First-in-human, Randomized, Observer-blinded, Placebo-controlled, Dose Escalation Study to Evaluate the Safety, Tolerability, and Immunogenicity of BV601 in Healthy Adult Volunteers

Clinical Trial 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.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05672966
Study type Interventional
Source Wuhan BravoVax Co., Ltd.
Contact Long Xu, Ph.D.
Phone +86 27 8798 8585 ext. 8251
Email ct@bravovax.com
Status Not yet recruiting
Phase Phase 1
Start date August 1, 2023
Completion date October 31, 2024
View Details
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