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Study of MK-1697 in Participants With Advanced Solid Tumors (MK-1697-001)

NCT03515824 PHASE1 TERMINATED Results posted

The purpose of this study is to evaluate the safety and preliminary efficacy of MK-1697. There are 2 parts in this study: dose escalation to determine the recommended phase 2 dose (RP2D) and confirm the RP2D (Part A) and cohort expansion to determine preliminary efficacy in participants with colorectal cancer (CRC) or head and neck squamous cell cancer (HNSCC) (Part B). No formal hypothesis testing will be done in this study.

Details

Lead sponsorMerck Sharp & Dohme LLC
PhasePHASE1
StatusTERMINATED
Enrolment22
Start dateMon Aug 13 2018 00:00:00 GMT+0000 (Coordinated Universal Time)
CompletionTue Feb 18 2020 00:00:00 GMT+0000 (Coordinated Universal Time)

Conditions

Interventions

Countries

Hong Kong, Australia