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Clinical trial

A Multicenter,Randomized, Placebo-Controlled, and Double-blind Phase Ⅲ Study to Evaluate the Efficacy, Immunogenicity and Safety of Quadrivalent Human Papillomavirus (Types 6, 11, 16, and 18) Recombinant Vaccine (Hansenula Polymorpha) in Chinese Female Aged 18-45 Years

NCT05584332 is registered in ClinicalTrials.gov with Shanghai Bovax Biotechnology Co., Ltd. as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Multicenter,Randomized, Placebo-Controlled, and Double-blind Phase Ⅲ Study to Evaluate the Efficacy, Immunogenicity and Safety of Quadrivalent Human Papillomavirus (Types 6, 11, 16, and 18) Recombinant Vaccine (Hansenula Polymorpha) in Chinese Female Aged 18-45 Years
Lead sponsor
Shanghai Bovax Biotechnology Co., Ltd.
Phase
Phase 3
Overall status
Terminated
Start date
December 9, 2022
Completion date
March 23, 2023
Enrollment
3,131 (actual)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

ais, cervical cancer, cin1, cin2, cin3, genital wart, vain - vaginal intraepithelial neoplasia 2, vain i, vain iii, vin i, vin ii, vin iii