Trial Profile

A multi-center, randomised, double-blind, placebo-controlled phase III clinical trial to evaluate the protective efficacy, safety and immunogenicity of Recombinant Human Papillomavirus Quadrivalent (Types 6, 11, 16, 18) Vaccine (Hansenulapolymorpha)quadri recomb in healthy Chinese woman aged 18-45 years

Status: Recruiting

Phase of Trial: Phase III

Latest Information Update: 08 Jun 2018

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At a glance

Drugs Human papillomavirus vaccine quadrivalent Chengdu institute of biological product (Primary)
Indications Cervical cancer
Focus Registrational; Therapeutic Use
Sponsors Chengdu Institute of Biological Products

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