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Clinical trial

A Phase 3 Open-Label Clinical Trial to Study the Immunogenicity, Safety and Tolerability of Recombinant Human Papillomavirus Quadrivalent (Types 6, 11, 16, 18) Vaccine (V501) in Chinese Girls Aged 9-19 Years and Young Women Aged 20-26 Years

NCT03493542 is registered in ClinicalTrials.gov with Merck Sharp & Dohme LLC as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Phase 3 Open-Label Clinical Trial to Study the Immunogenicity, Safety and Tolerability of Recombinant Human Papillomavirus Quadrivalent (Types 6, 11, 16, 18) Vaccine (V501) in Chinese Girls Aged 9-19 Years and Young Women Aged 20-26 Years
Lead sponsor
Merck Sharp & Dohme LLC
Phase
Phase 3
Overall status
Completed
Start date
August 31, 2018
Completion date
October 30, 2023
Enrollment
766 (actual)
Sites
1

Conditions

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

prevention of hpv types 16- and 18-related cervical cancer, cervical intraepithelial neoplasia (cin) 1/2/3, and cervical adenocarcinoma in situ