Trial Profile

A Randomized, Double-Blind and Placebo-Controlled Phase I Study to Evaluate the Safety and Immunogenicity of a 9-valent Human Papillomavirus (Types 6, 11, 16, 18,31,33,45,52 and 58) Recombinant Vaccine (Pichia Pastoris) in 9 to 45 Year Old Chinese Females

Status: Completed

Phase of Trial: Phase I

Latest Information Update: 18 Apr 2023

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At a glance

Drugs Human papillomavirus vaccine recombinant 9 valent Shanghai Zerun Biotechnology (Primary)
Indications Human polyomavirus infections
Focus Adverse reactions
Sponsors Shanghai Zerun Biotechnology Co

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