drugset / Trial / NCT03085381

A Phase I Study of Quadrivalent HPV Recombinant Vaccine

NCT03085381

Phase 1 Completed 90 enrolled Shanghai Bovax Biotechnology Co., Ltd.
RandomizedParallel-groupDouble-blindPrevention

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.

Timeline

Start
2016-12
Primary completion
2017-10
Completion
2018-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Gardasil Vaccine