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Clinical Trial Summary

This study is designed to evaluate the vaccine efficacy, immunogenicity and safety of the 4-valent Human Papillomavirus (Types 6, 11, 16, and 18) Recombinant Vaccine (Hansenula Polymorpha) in Chinese Female Subjects Aged 18-45 Years .


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05584332
Study type Interventional
Source Shanghai Bovax Biotechnology Co., Ltd.
Contact
Status Terminated
Phase Phase 3
Start date December 9, 2022
Completion date March 23, 2023

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