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Active, not recruiting Phase 3 Interventional

A Study of Pembrolizumab (MK-3475) in Combination With Belzutifan (MK-6482) and Lenvatinib (MK-7902), or Pembrolizumab/Quavonlimab (MK-1308A) in Combination With Lenvatinib, Versus Pembrolizumab and Lenvatinib, for Treatment of Advanced Clear Cell Renal Cell Carcinoma (MK-6482-012)

ClinicalTrials.gov ID: NCT04736706

Public ClinicalTrials.gov record NCT04736706. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 18, 2026, 12:08 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Open-label, Randomized Phase 3 Study to Evaluate Efficacy and Safety of Pembrolizumab (MK-3475) in Combination With Belzutifan (MK-6482) and Lenvatinib (MK-7902), or MK-1308A in Combination With Lenvatinib, Versus Pembrolizumab and Lenvatinib, as First-Line Treatment in Participants With Advanced Clear Cell Renal Cell Carcinoma (ccRCC)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The goal of this study is to evaluate the efficacy and safety of pembrolizumab plus belzutifan plus lenvatinib or pembrolizumab/quavonlimab plus lenvatinib versus pembrolizumab plus lenvatinib as first-line treatment in participants with advanced clear cell renal cell carcinoma (ccRCC). The primary hypotheses are (1) pembrolizumab plus belzutifan plus lenvatinib is superior to pembrolizumab plus lenvatinib with respect to progression-free survival (PFS) and overall survival (OS), in advanced ccRCC participants; and (2) pembrolizumab/quavonlimab plus lenvatinib is superior to pembrolizumab plus lenvatinib with respect to PFS and OS, in advanced ccRCC participants.

Study identification

NCT ID
NCT04736706
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Merck Sharp & Dohme LLC
Industry
Enrollment
1,688 participants

Conditions and interventions

Interventions

Biological · Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 14, 2021 (Actual)
Primary completion
Feb 4, 2026 (Actual)
Completion
Apr 22, 2027 (Estimated)
Last update posted
Oct 2, 2026

2021 – 2027

United States locations

U.S. sites
33
U.S. states
21
U.S. cities
31
Facility City State ZIP Site status
The University of Alabama at Birmingham ( Site 0010) Birmingham Alabama 35294-3300 —
UC San Diego ( Site 0050) La Jolla California 92037 —
Cedars Sinai Medical Center ( Site 0027) Los Angeles California 90048 —
University of California Irvine ( Site 0029) Orange California 92868 —
UCLA Hematology Oncology Santa Monica ( Site 0048) Santa Monica California 90404 —
Hartford Hospital ( Site 0024) Hartford Connecticut 06102 —
Advent Health Hematology & Oncology ( Site 0003) Orlando Florida 32804 —
University Cancer & Blood Center, LLC ( Site 0057) Athens Georgia 30607 —
Emory University Winship Cancer Institute ( Site 0012) Atlanta Georgia 30322 —
Rush University Medical Center ( Site 0040) Chicago Illinois 60607 —
Parkview Cancer Institute ( Site 0088) Fort Wayne Indiana 46845 —
Norton Cancer Institute - St. Matthews ( Site 0065) Louisville Kentucky 40207 —
Ochsner Medical Center ( Site 0049) New Orleans Louisiana 70121 —
New England Cancer Specialists ( Site 0082) Scarborough Maine 04074 —
Massachusetts General Hospital ( Site 0094) Boston Massachusetts 02114 —
Beth Israel Deaconess Medical Center ( Site 0089) Boston Massachusetts 02215 —
Dana Farber Cancer Institute ( Site 0093) Boston Massachusetts 02215 —
Lahey Hospital & Medical Center ( Site 0090) Burlington Massachusetts 01805 —
Henry Ford Hospital ( Site 0038) Detroit Michigan 48202 —
Cancer & Hematology Centers of Western Michigan ( Site 0018) Grand Rapids Michigan 49503 —
HealthPartners Cancer Research Center-HealthPartners Frauenshuh Cancer Center ( Site 0005) Saint Louis Park Minnesota 55426 —
Regions Hospital ( Site 0095) Saint Paul Minnesota 55101 —
University of Mississippi Medical Center ( Site 0037) Jackson Mississippi 39216 —
Dartmouth Hitchcock Medical Center ( Site 0075) Lebanon New Hampshire 03756 —
Roswell Park Cancer Institute ( Site 0032) Buffalo New York 14263 —
R.J. Zuckerberg Cancer Center-Medical Oncology ( Site 0013) Lake Success New York 11042 —
Sidney Kimmel Center for Prostate and Urologic Cancers ( Site 0055) New York New York 10065 —
Oregon Health & Science University ( Site 0071) Portland Oregon 97239 —
Ralph H. Johnson VA Center ( Site 0073) Charleston South Carolina 29401 —
University of Tennessee Medical Center Knoxville ( Site 0019) Knoxville Tennessee 37920 —
Vanderbilt University Medical Center ( Site 0069) Nashville Tennessee 37232 —
UTSW Medical Center ( Site 0015) Dallas Texas 75390 —
Central Washington Health Services Association d/b/a Confluence Health ( Site 0061) Wenatchee Washington 98801 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 229 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04736706, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 2, 2026 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04736706 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →