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Study details
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MK-4716-001 Clinical Trial

Merck Sharp & Dohme LLC
NCT IDNCT07247110ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1

Target enrollment

250

Study length

about 5 years

Ages

18+

Locations

3 sites in NJ, TX, VA

About this study

This trial is testing a treatment called MK-4716 in people with certain solid tumors. Researchers are looking to see if this treatment is safe and well-tolerated when used alone or with other treatments.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Receive Cetuximab
  • 2.Receive Pembrolizumab
  • 3.Take MK-4716
PhasePhase 1
DrugCetuximab
Routeinjection
Primary goalNumber of Participants Who Discontinue Study Intervention Due to an AE

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low11%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Drug classes

cetuximab, pembrolizumab (Immune checkpoint inhibitor; blocks PD-1 to boost T-cell attack on cancer)

Drug routes

injection (Injection), infusion

Endpoints

Primary: Number of Participants Who Discontinue Study Intervention Due to an AE, Number of Participants Who Experience One or More Dose-Limiting Toxicities (DLT), Number of Participants Who Experience an Adverse Event (AE)

Secondary: Area Under the Concentration-Time Curve (AUC) of MK-4716, Half-Life (t1/2) of MK-4716, Maximum Plasma Concentration (Cmax) of MK-4716

Body systems

Oncology