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Study of MK-1697 in Participants With Advanced Solid Tumors (MK-1697-001)
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 sponsor | Merck Sharp & Dohme LLC |
|---|---|
| Phase | PHASE1 |
| Status | TERMINATED |
| Enrolment | 22 |
| Start date | Mon Aug 13 2018 00:00:00 GMT+0000 (Coordinated Universal Time) |
| Completion | Tue Feb 18 2020 00:00:00 GMT+0000 (Coordinated Universal Time) |
Conditions
- Neoplasms
- Colorectal Neoplasms
- Head and Neck Neoplasms
Interventions
- MK-1697
Countries
Hong Kong, Australia