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HPV 16/18 Bivalent Vaccine (Cecolin) in Healthy Females (18-25 Years)

NCT01356823Phase 2Completed

Sponsor
Xiamen University
Start
Mar 2011
Primary completion
Dec 2011
Countries
1
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Overview

Phase 2, randomised, double-blind trial of human papillomavirus 16/18 bivalent vaccine in Cervical Cancer (CC) and cervical intraepithelial neoplasia (CIN) (4 arms), sponsored by Xiamen University. Primary endpoint: Seroconversion of anti-HPV 16 and anti-HPV 18 neutralizing antibody at 7 months. Started Mar 2011; status: completed.

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Drugs

human papillomavirus 16/18 bivalent vaccine
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Conditions

Cervical Cancer (CC)cervical intraepithelial neoplasia (CIN)

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