Clinical trial
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
NCT05672966 is registered in ClinicalTrials.gov with Wuhan BravoVax Co., Ltd. as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- 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
- Lead sponsor
- Wuhan BravoVax Co., Ltd.
- Phase
- Phase 1
- Overall status
- Unknown status
- Start date
- August 1, 2023
- Completion date
- October 31, 2024
- Enrollment
- 40 (estimated)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.
human papillomavirus infection