Trial Profile

A Multicenter,Randomized,Blind and Positive-Controlled Phase Ⅲ Study to Evaluate the Efficacy, Immunogenicity and Safety of the 9-valent Human Papillomavirus (Types 6, 11, 16, 18,31,33,45,52 and 58) Recombinant Vaccine (Hansenula Polymorpha) in Chinese Female Subjects Aged 20-45 Years

Status: Recruiting

Phase of Trial: Phase III

Latest Information Update: 19 Apr 2024

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At a glance

Drugs Human papillomavirus recombinant vaccine nonavalent - Shanghai Bovax Biotechnology (Primary) ; Human papillomavirus vaccine recombinant quadrivalent Merck
Indications Human papillomavirus infections
Focus Adverse reactions; Registrational
Sponsors Shanghai Bovax Biotechnology

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