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Gardasil (V501)

HPV vaccine quadrivalent · Merck Sharp & Dohme LLC
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1 regulatory and trial event tracked for Gardasil (V501), covering 2020-05-04 to 2020-05-04. Get the full timeline:

Most recent: Clinical Trial Update: A Study to Evaluate the Immunogenicity, Safety and Tolerability of Quadrivalent Human Papillomavirus Vaccine (V501) in Chinese Girls Aged 9-19 Years and Young Women Aged 20-26 Years (V501-213) [Phase 3]

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