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Quadrivalent HPV Vaccine (Yeast-Derived) in Chinese Women 18-45 Years

CTR20171662Phase 3Completed

Sponsor
Sinopharm
Start
Jan 2018
Modality
Vaccines & Immunotherapeutics, Recombinant Proteins and Enzymes
Countries
1
01

Overview

Phase 3, randomised, double-blind trial of human papillomavirus 6/11/16/18 vaccine, recombinant in human papillomavirus infection, HPV16 infection (HPV16), human papillomavirus infection type 18 and 4 more (2 arms), sponsored by Sinopharm. Primary endpoints: Vaccine efficacy against 12-month persistent infection with HPV 6/11/16/18 and Vaccine efficacy against CIN2+ cervical lesions associated with HPV 6/11/16/18 infection. Started Jan 2018; status: completed.

02

Drugs

human papillomavirus 6/11/16/18 vaccine, recombinant
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Conditions

human papillomavirus infectionHPV16 infection (HPV16)human papillomavirus infection type 18cervical intraepithelial neoplasia (CIN)anogenital warts

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