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Completed Phase 3 Interventional Results available

Coformulation of Pembrolizumab/Vibostolimab (MK-7684A) Versus Pembrolizumab (MK-3475) Monotherapy for Programmed Cell Death 1 Ligand 1 (PD-L1) Positive Metastatic Non-Small Cell Lung Cancer (MK-7684A-003, KEYVIBE-003)

ClinicalTrials.gov ID: NCT04738487

Public ClinicalTrials.gov record NCT04738487. 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 Jun 25, 2026, 7:56 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 3, Multicenter, Randomized, Double-Blind Study of MK-7684 With Pembrolizumab as a Coformulation (MK-7684A) Versus Pembrolizumab Monotherapy as First Line Treatment for Participants With PD-L1 Positive Metastatic Non-Small Cell Lung Cancer

Study identification

NCT ID
NCT04738487
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Merck Sharp & Dohme LLC
Industry
Enrollment
1,264 participants

Conditions and interventions

Interventions

  • Pembrolizumab/Vibostolimab Biological
  • Pembrolizumab Biological

Biological

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 6, 2021
Primary completion
Sep 4, 2024
Completion
Jan 26, 2026
Last update posted
Feb 19, 2026

2021 – 2026

United States locations

U.S. sites
7
U.S. states
5
U.S. cities
7
Facility City State ZIP Site status
Boca Raton Regional Hospital ( Site 0004) Boca Raton Florida 33486
Illinois Cancer Care ( Site 0026) Peoria Illinois 61615
Mercy Research - Cancer and Hematology Center ( Site 0032) Springfield Missouri 65804
Mercy Research - David C. Pratt Cancer Center ( Site 0025) St Louis Missouri 63141
Perlmutter Cancer Center at NYU Langone Hospital - Long Island ( Site 0022) Mineola New York 11501
Memorial Sloan Kettering Cancer Center ( Site 0013) New York New York 10065
Fox Chase Cancer Center-Hematology/Oncology ( Site 0030) Philadelphia Pennsylvania 19111

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 181 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04738487, 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 Feb 19, 2026 · Synced Jun 25, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04738487 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →