drugset / Trial / NCT04422366

Evaluate the Efficacy, Immunogenicity and Safety of 9-valent HPV Recombinant Vaccine in Chinese Healthy Females

NCT04422366 ↗

Phase 3 Recruiting 8000 enrolled Shanghai Bovax Biotechnology Co., Ltd.
RandomizedParallel-groupDouble-blindPrevention

Summary

This study is designed to evaluate the vaccine efficacy, immunogenicity and safety of the 9-valent Human Papillomavirus (Types 6, 11, 16, 18,31,33,45,52 and 58) Recombinant Vaccine (Hansenula Polymorpha) in Chinese Female Subjects Aged 20-45 Years .

Timeline

Start
2020-04-28
Primary completion
2027-09-15
Completion
2029-09-15