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Active, not recruiting Phase 3 Interventional Results available

Pembrolizumab/Vibostolimab (MK-7684A) or Atezolizumab in Combination With Chemotherapy in First Line Treatment of Extensive-Stage Small Cell Lung Cancer (MK-7684A-008/KEYVIBE-008)

ClinicalTrials.gov ID: NCT05224141

Public ClinicalTrials.gov record NCT05224141. 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 Jul 20, 2026, 1:07 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, Randomized, Double-Blind Study of MK-7684A in Combination With Etoposide and Platinum Followed by MK-7684A vs Atezolizumab in Combination With Etoposide and Platinum Followed by Atezolizumab for the First-Line Treatment of Participants With Extensive-Stage Small Cell Lung Cancer (KEYVIBE-008)

Study identification

NCT ID
NCT05224141
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Merck Sharp & Dohme LLC
Industry
Enrollment
460 participants

Conditions and interventions

Interventions

  • Pembrolizumab/Vibostolimab Co-Formulation Biological
  • Saline placebo Drug
  • Etoposide Drug
  • Cisplatin Drug
  • Atezolizumab Biological
  • Carboplatin Drug

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
Mar 23, 2022
Primary completion
Jun 3, 2024
Completion
Jun 6, 2027
Last update posted
Jul 7, 2025

2022 – 2027

United States locations

U.S. sites
11
U.S. states
9
U.S. cities
10
Facility City State ZIP Site status
Infirmary Cancer Care ( Site 0022) Mobile Alabama 36607
Los Angeles Hematology Oncology Medical Group ( Site 0006) Los Angeles California 90017
VA West Los Angeles Medical Center ( Site 0004) Los Angeles California 90073
Boca Raton Regional Hospital-Lynn Cancer Institute ( Site 0014) Boca Raton Florida 33486
Fort Wayne Medical Oncology and Hematology ( Site 0013) Fort Wayne Indiana 46804
Dana-Farber Cancer Institute ( Site 0018) Boston Massachusetts 02215
Cancer and Hematology Centers of Western Michigan ( Site 0001) Grand Rapids Michigan 49503
Hattiesburg Clinic Hematology/Oncology ( Site 0003) Hattiesburg Mississippi 39401
Lancaster General Hospital - Ann B Barshinger Cancer Institute ( Site 0005) Lancaster Pennsylvania 17601
Blue Ridge Cancer Care ( Site 0015) Blacksburg Virginia 24060
University of Virginia Cancer Center ( Site 0019) Charlottesville Virginia 22903

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 129 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05224141, 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 7, 2025 · Synced Jul 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05224141 live on ClinicalTrials.gov.

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