Melanoma Clinical Trial
Official title:
Phase Ib Study of MK-3475 in Subjects With Advanced Melanoma
This study will assess the safety, tolerability, and efficacy of every-3-week dosing (Q3W) of pembrolizumab (MK-3475) in participants with advanced melanoma; participants may receive pembrolizumab for up to 2 years if deriving clinical benefit. The primary study hypothesis is that treatment with single agent pembrolizumab will result in a clinically meaningful overall response rate.
Participants who discontinue pembrolizumab after achieving a complete response (CR) and
subsequently develop progressive disease (PD) may be eligible to enter a Second Course Phase
and receive pembrolizumab again.
The end of the study for each participant will occur with: 1) the marketing approval of
pembrolizumab for melanoma, 2) the completion of safety follow up or 3) the time when a
possibility of entry to second course of treatment is lost, whichever occurs last.
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