Active, not recruitingPhase 3NCT03553836

Safety and Efficacy of Pembrolizumab Compared to Placebo in Resected High-risk Stage II Melanoma (MK-3475-716/KEYNOTE-716)

Studying Autosomal dominant multiple pterygium syndrome

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Key facts

Sponsor
Merck Sharp & Dohme LLC
Principal Investigator
Medical Director
Merck Sharp & Dohme LLC
Intervention
Pembrolizumab(biological)
Enrollment
976 target
Eligibility
12 years · All sexes
Timeline
20182033

Study locations (30)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT03553836 on ClinicalTrials.gov

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