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Completed Phase 3 Interventional Results available

Safety and Efficacy of Pembrolizumab (MK-3475) Versus Placebo as Adjuvant Therapy in Participants With Hepatocellular Carcinoma (HCC) and Complete Radiological Response After Surgical Resection or Local Ablation (MK-3475-937 / KEYNOTE-937)

ClinicalTrials.gov ID: NCT03867084

Public ClinicalTrials.gov record NCT03867084. 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 30, 2026, 11:27 PM 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 Double-blinded, Two-arm Study to Evaluate the Safety and Efficacy of Pembrolizumab (MK-3475) Versus Placebo as Adjuvant Therapy in Participants With Hepatocellular Carcinoma and Complete Radiological Response After Surgical Resection or Local Ablation (KEYNOTE-937)

Brief summary

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

This study will evaluate the safety and efficacy of pembrolizumab (MK-3475) versus placebo as adjuvant therapy in participants with hepatocellular carcinoma (HCC) and complete radiological response after surgical resection or local ablation. The primary hypotheses of this study are that adjuvant pembrolizumab is superior to placebo with respect to: 1) recurrence-free survival (RFS) as assessed by blinded independent central review (BICR); and 2) overall survival (OS).

Study identification

NCT ID
NCT03867084
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Merck Sharp & Dohme LLC
Industry
Enrollment
959 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
May 28, 2019 (Actual)
Primary completion
Mar 20, 2025 (Actual)
Completion
Sep 30, 2025 (Actual)
Last update posted
Apr 24, 2026

2019 – 2025

United States locations

U.S. sites
24
U.S. states
17
U.S. cities
21
Facility City State ZIP Site status
Banner MD Anderson Cancer Center ( Site 0026) Gilbert Arizona 85234 —
The University of Arizona Cancer Center - North Campus ( Site 0039) Tucson Arizona 85719 —
City of Hope Medical Center ( Site 0027) Duarte California 91010 —
Smilow Cancer Hospital at Yale New Haven ( Site 0042) New Haven Connecticut 06510 —
Regional Cancer Center ( Site 0054) Fort Myers Florida 33905 —
Indiana University Simon Cancer Center ( Site 0075) Indianapolis Indiana 46202 —
University of Iowa ( Site 0067) Iowa City Iowa 52242 —
James Graham Brown Cancer Center ( Site 0088) Louisville Kentucky 40202 —
University of Louisville ( Site 0059) Louisville Kentucky 40202 —
University Medical Center New Orleans ( Site 0014) New Orleans Louisiana 70112 —
Massachusetts General Hospital ( Site 0062) Boston Massachusetts 02114 —
Boston Medical Center ( Site 0025) Boston Massachusetts 02118 —
Beth Israel Deaconess Medical Ctr. ( Site 0033) Boston Massachusetts 02215 —
University of Massachusetts Worcester ( Site 0017) Worcester Massachusetts 01655 —
Henry Ford Hospital-GI/Hepatology Research ( Site 0047) Detroit Michigan 48202 —
University of New Mexico ( Site 0041) Albuquerque New Mexico 87131 —
North Shore-Long Island Jewish Health System ( Site 0068) Lake Success New York 11042 —
Miami Valley Hospital South ( Site 0093) Centerville Ohio 45459 —
University of Cincinnati Medical Center ( Site 0084) Cincinnati Ohio 45219 —
ProMedica Flower Hospital ( Site 0090) Sylvania Ohio 43560 —
Stephenson Cancer Center ( Site 0045) Oklahoma City Oklahoma 73104 —
Vanderbilt Ingram Cancer Center ( Site 0006) Nashville Tennessee 37232 —
Baylor Scott & White Medical Center - Temple ( Site 0089) Temple Texas 76508 —
Virginia Mason Medical Center ( Site 0028) Seattle Washington 98101 —

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 225 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03867084, 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 Apr 24, 2026 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03867084 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →