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Study identifier: NCT04422366 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Evaluate the Efficacy, Immunogenicity and Safety of 9-valent HPV Recombinant Vaccine in Chinese Healthy Females

Condition: Cervical Cancer · Vulvar Cancer · Vaginal Cancer  ·  Sponsor: Shanghai Bovax Biotechnology Co., Ltd.

PhasePhase 3
Planned participants8000
Who can joinFemale, 20 Years to 45 Years
Healthy volunteersYes

About this study

This study is designed to evaluate the vaccine 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 .

This description comes directly from the study's public registry record.

Talk to the study team

Yi Mo, Master  ·  +8613788686968  ·  moyi0415@qq.com

Always discuss trial participation with your own doctor first.

Locations (1)

Liuzhou center for disease control and preventionLiuzhou, Guangxi, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT04422366