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A Phase I Study of Quadrivalent HPV Recombinant Vaccine

HPV Infections Clinical Trial

Official title:
A Randomized, Double-Blind and Placebo-Controlled Phase I Study to Evaluate the Safety and Primary Immunogenicity of the Quadrivalent Human Papillomavirus (Types 6, 11, 16, 18) Recombinant Vaccine (Hansenula Polymorpha) in Chinese Female Subjects Aged 9-45 Years

Clinical Trial Summary

To evaluate the safety and primary immunogenicity of the quadrivalent human papillomavirus (types 6, 11, 16, 18) recombinant vaccine (hansenula polymorpha) in Chinese female subjects aged 9-45 years.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03085381
Study type Interventional
Source Shanghai Bovax Biotechnology Co., Ltd.
Contact
Status Completed
Phase Phase 1
Start date December 2016
Completion date August 2018
View Details
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