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Active, not recruiting Phase 1Phase 2 Interventional

Substudy 03A: A Study of Immune and Targeted Combination Therapies in Participants With First Line (1L) Renal Cell Carcinoma (MK-3475-03A)

ClinicalTrials.gov ID: NCT04626479

Public ClinicalTrials.gov record NCT04626479. 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 Sep 12, 2026, 3:59 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

A Phase 1b/2 Study of Immune and Targeted Combination Therapies in Participants With RCC (U03): Substudy 03A in First Line Metastatic Participants

Brief summary

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

Substudy 03A is part of a larger research study that is testing experimental treatments for renal cell carcinoma (RCC). The larger study is the umbrella study (U03). The goal of substudy 03A is to evaluate the safety and efficacy of experimental combinations of investigational agents in participants with advanced first line (1L) clear cell renal cell carcinoma (ccRCC). This substudy will have two phases: a safety lead-in phase and an efficacy phase. The safety lead-in phase will be used to demonstrate a tolerable safety profile for the combination of investigational agents. There will be no hypothesis testing in this study.

Study identification

NCT ID
NCT04626479
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Merck Sharp & Dohme LLC
Industry
Enrollment
400 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 120 Years
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
Dec 15, 2020
Primary completion
Aug 20, 2026
Completion
Aug 20, 2026
Last update posted
Jul 29, 2026

2020 – 2026

United States locations

U.S. sites
10
U.S. states
9
U.S. cities
9
Facility City State ZIP Site status
University of California at San Francisco ( Site 1008) San Francisco California 94158
Yale-New Haven Hospital-Yale Cancer Center ( Site 1011) New Haven Connecticut 06510
University of Chicago ( Site 1013) Chicago Illinois 60637
University of Iowa ( Site 1012) Iowa City Iowa 52242
Henry Ford Health System ( Site 1014) Detroit Michigan 48202
Laura and Isaac Perlmutter Cancer Center ( Site 1016) New York New York 10016
Memorial Sloan Kettering Cancer Center ( Site 1002) New York New York 10065
Duke Cancer Institute ( Site 1015) Durham North Carolina 27710
UPMC Cancer Center/Hillman Cancer Center ( Site 1017) Pittsburgh Pennsylvania 15232
UTSW Medical Center ( Site 1003) Dallas Texas 75390

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 45 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04626479, 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 Jul 29, 2026 · Synced Sep 12, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04626479 live on ClinicalTrials.gov.

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