Trial intelligence / Profile preview

Efficacy, Immunogenicity and Safety of the 9vHPV Vaccine in Japanese Males

NCT04635423Phase 3Completed

Sponsor
Merck & Co.
Start
Nov 2020
Primary completion
Dec 2023
Modality
Vaccines & Immunotherapeutics
Countries
1
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Overview

Phase 3, randomised, double-blind trial of recombinant human papillomavirus 9-valent vaccine in human papillomavirus infection, genital warts and anal neoplasms (4 arms), sponsored by Merck & Co. Primary endpoints: Combined Incidence of Human Papillomavirus (HPV) 6/11/16/18-related Anogenital Persistent Infection at 36 months, Percentage of Participants With Solicited Injection-site Adverse Events (AEs) at 5 days and 3 more. Started Nov 2020; status: completed.

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Drugs

recombinant human papillomavirus 9-valent vaccine
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Conditions

human papillomavirus infectiongenital wartsanal neoplasms

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