Status:

COMPLETED

A Study of MK-4700 Alone or With Pembrolizumab in Participants With Advanced or Metastatic Solid Tumors (MK-4700-001)

Lead Sponsor:

Merck Sharp & Dohme LLC

Conditions:

Malignant Neoplasm

Eligibility:

All Genders

18+ years

Phase:

PHASE1

Brief Summary

The goal of this study is to learn about the safety of different doses of MK-4700 and if people tolerate them. The study will also measure what happens in a person's body over time when MK-4700 is giv...

Eligibility Criteria

Inclusion

  • The key inclusion criteria include but are not limited to the following:
  • Has histologically or cytologically confirmed advanced/metastatic solid tumor by pathology report who have experienced disease progression on or after prior anti-cancer treatments, or been intolerant to, or refused all treatment known to confer clinical benefit
  • Has head and neck squamous cell carcinoma (HNSCC), melanoma (cutaneous), non-small cell lung cancer (NSCLC), cervical cancer, triple negative breast cancer (TNBC), urothelial carcinoma (UC), or renal cell carcinoma (RCC; clear cell, papillary)
  • If human immunodeficiency virus (HIV) infected, must have well controlled HIV on antiretroviral therapy (ART)
  • Has normal cardiac function

Exclusion

  • The key exclusion criteria include but are not limited to the following:
  • If HIV-infected with a history of Kaposi's sarcoma and/or Multicentric Castleman's Disease
  • Has known additional malignancy that is progressing or has required active treatment within the past 2 years
  • Has known active central nervous system (CNS) metastases and/or carcinomatous meningitis
  • Has active autoimmune disease that has required systemic treatment in the past 2 years except replacement therapy
  • Has history of (noninfectious) pneumonitis/interstitial lung disease that required steroids
  • Has current pneumonitis/interstitial lung disease
  • Has active infection requiring systemic therapy
  • Has known history of Hepatitis B (defined as Hepatitis B surface antigen reactive) or known active Hepatitis C virus infection
  • Has had an allogeneic tissue/solid organ transplant in the last 5 years

Key Trial Info

Start Date :

April 23 2025

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

November 24 2025

Estimated Enrollment :

5 Patients enrolled

Trial Details

Trial ID

NCT06894771

Start Date

April 23 2025

End Date

November 24 2025

Last Update

December 11 2025

Active Locations (7)

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Page 1 of 2 (7 locations)

1

John Theurer Cancer Center at Hackensack University Medical Center ( Site 0301)

Hackensack, New Jersey, United States, 07601

2

NEXT Oncology ( Site 0300)

San Antonio, Texas, United States, 78229

3

Princess Margaret Cancer Center ( Site 0101)

Toronto, Ontario, Canada, M5G 2M9

4

Centre intégré de cancérologie du CHU de Québec Université Laval, Hôpital de l'Enfant-Jésus ( Site 0102)

Québec, Quebec, Canada, G1J 1Z4