Trial Profile

A Phase I Trial in Healthy Chinese Women Ages 18-45 to Evaluate the Safety and Tolerability Profile of Recombinant Nonavalent (Types 6/11/16/18/31/33/45/52/58) Human Papillomavirus (HPV) Vaccine (Escherichia Coli)

Status: Completed

Phase of Trial: Phase I

Latest Information Update: 18 Jan 2023

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At a glance

Drugs Nonavalent-human-papillomavirus-vaccine-Beijing-Health-Guard-Biotechnology (Primary) ; Human papillomavirus vaccine recombinant quadrivalent Merck
Indications Human papillomavirus infections
Focus Adverse reactions
Sponsors Beijing Health Guard Biotechnology

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