Active, not recruitingPhase 3NCT06465914
A Phase III Study to Evaluate the Efficacy, Immunogenicity and Safety of the 9-valent HPV Vaccine in Chinese Males
Studying Malignant tumor of penis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Shanghai Bovax Biotechnology Co., Ltd.
- Principal Investigator
- Lidong Gao, MasterHunan Provincial Center for Disease Control and Prevention
- Intervention
- 9-valent Human Papillomavirus (Types 6, 11, 16, 18, 31, 33, 45, 52 and 58) Recombinant Vaccine (Hansenula Polymorpha)(biological)
- Enrollment
- 9000 target
- Eligibility
- 18-45 years · MALE
- Timeline
- 2024 – 2030
Study locations (5)
- Guangxi Zhuang Autonomous Region Center for Disease Control and Prevention, Nanning, Guangxi, China
- Hunan Center for Disease Control and Prevention, Changsha, Hunan, China
- Shanxi Provincial Disease for Control and Prevention, Taiyuan, Shanxi, China
- Sichuan Center for Disease Control and Prevention, Chengdu, Sichuan, China
- Yunnan Center for Disease Control and Prevention, Kunming, Yunnan, China
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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