Trial intelligence / Profile preview

Safety and Immunogenicity of Quadrivalent HPV Vaccine (Hansenula Polymorpha) in Chinese Females

NCT03085381Phase 1Completed

Sponsor
Shanghai Bovax Biotechnology Co., Ltd.
Start
Dec 2016
Primary completion
Oct 2017
Modality
Vaccines & Immunotherapeutics
Countries
1
01

Overview

Phase 1, randomised, double-blind trial of CERVAVAC in human papillomavirus infection (2 arms), sponsored by Shanghai Bovax Biotechnology Co., Ltd. Primary endpoints: Systemic and local adverse events and Primary Immunogenicity. Started Dec 2016; status: completed.

02

Drugs

CERVAVAC
03

Conditions

human papillomavirus infection

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