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NCT05672966

Phase I Clinical Trial of a Candidate HPV Vaccine

Status unknown Phase 1 Last updated 6 January 2023
What this trial tests

Phase 1 trial testing Human papillomavirus (HPV) Vaccine in Human Papillomavirus Infection in 40 participants. Status unknown.

Timeline
1 August 2023
Primary endpoint
31 July 2024
31 October 2024

Quick facts

Lead sponsorWuhan BravoVax Co., Ltd.
PhasePhase 1
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designsequential
Maskingquadruple
Primary purposeprevention
Enrollment40
Start date1 August 2023
Primary completion31 July 2024
Estimated completion31 October 2024
Sites1 location across Australia

Drugs / interventions tested

Conditions studied

Sponsor

Wuhan BravoVax Co., Ltd. — full company profile →

Who can join

Adults 18 to 35, any sex, with Human Papillomavirus Infection. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Vaccination with a Human Papillomavirus L2 Multimer Provides Broad Protection against 17 Human Papillomavirus Types in the Mouse Cervicovaginal Challenge Model.
    Han Z, Wang S, Mu T, Zhao P, et al · · 2024 · cited 1× · PMID 38932417 · DOI 10.3390/vaccines12060689

Verify or expand the search:

Other recruiting trials for Human Papillomavirus Infection

Currently open trials in the same condition.

Other Wuhan BravoVax Co., Ltd. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05672966.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing