NCT06894771CompletedPhase 1
A Study of MK-4700 Alone or With Pembrolizumab in Participants With Advanced or Metastatic Solid Tumors (MK-4700-001)
A Phase 1 Open-label, Multicenter Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of MK-4700 as Monotherapy and in Combination With Pembrolizumab in Participants With Advanced or Metastatic Solid Tumors
Source: ClinicalTrials.gov · Last updated 16 Mar 2026
Brief summary (registry, in English)
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 given alone or with pembrolizumab (MK-3475) in order to find a dose that is safe, tolerated, and may work to treat certain types of cancer.
- Status (registry)
- Completed
- Phase (registry)
- Phase 1
- Study type
- Interventional
- Enrollment
- 5 (actual)
- First submitted
- 3 Mar 2025
- Start date
- 23 Apr 2025
- Primary completion date
- 8 Dec 2025
- Lead sponsor
- Merck Sharp & Dohme LLC
- Diseases
- Triple-negative breast cancer, Head and neck cancer, Kidney cancer, Bladder cancer, Melanoma, Cervical cancer, Lung cancer
- NCT number
- NCT06894771
What you commit to
- Study type: Interventional · Phase 1
- Participants enrolled: 5
- From 23 Apr 2025 to the primary completion date, 8 Dec 2025
- 7 sites in 3 countries
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study design.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Has had an allogeneic tissue/solid organ transplant in the last 5 years
Other illness
- 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 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
Other
- The key exclusion criteria include but are not limited to the following:
- Has known active central nervous system (CNS) metastases and/or carcinomatous meningitis
Who the study is looking for
- 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
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (7)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Centre intégré de cancérologie du CHU de Québec Université Laval, Hôpital de l'Enfant-Jésus ( Site 0102) Coordinator of this site? Confirm its status | Québec | Canada | Unknown status |
| Princess Margaret Cancer Center ( Site 0101) Coordinator of this site? Confirm its status | Toronto | Canada | Unknown status |
| Rambam Health Care Campus ( Site 0201) Coordinator of this site? Confirm its status | Haifa | Israel | Unknown status |
| Rabin Medical Center ( Site 0202) Coordinator of this site? Confirm its status | Petah Tikva | Israel | Unknown status |
| Sheba Medical Center ( Site 0200) Coordinator of this site? Confirm its status | Ramat Gan | Israel | Unknown status |
| John Theurer Cancer Center at Hackensack University Medical Center ( Site 0301) Coordinator of this site? Confirm its status | Hackensack | United States | Unknown status |
| NEXT Oncology ( Site 0300) Coordinator of this site? Confirm its status | San Antonio | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.