Active, not recruitingPHASE1, PHASE2NCT04305054

Substudy 02B: Safety and Efficacy of Pembrolizumab in Combination With Investigational Agents or Pembrolizumab Alone in Participants With First Line (1L) Advanced Melanoma (MK-3475-02B/KEYMAKER-U02)

Studying Neuroendocrine neoplasm

Last synced from ClinicalTrials.gov

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Key facts

Sponsor
Merck Sharp & Dohme LLC
Principal Investigator
Medical Director
Merck Sharp & Dohme LLC
Intervention
Pembrolizumab(biological)
Enrollment
315 target
Eligibility
18-120 years · All sexes
Timeline
20202026

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 NCT04305054 on ClinicalTrials.gov

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