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Completed Phase 2 Interventional Results available

Study of REGN2810 in Patients With Advanced Cutaneous Squamous Cell Carcinoma

ClinicalTrials.gov ID: NCT02760498

Public ClinicalTrials.gov record NCT02760498. 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 21, 2026, 7:02 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 2 Study of REGN2810, a Fully Human Monoclonal Antibody to Programmed Death-1 (PD-1), in Patients With Advanced Cutaneous Squamous Cell Carcinoma

Study identification

NCT ID
NCT02760498
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Regeneron Pharmaceuticals
Industry
Enrollment
432 participants

Conditions and interventions

Interventions

  • cemiplimab Drug

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 6, 2016
Primary completion
Oct 17, 2023
Completion
Oct 17, 2023
Last update posted
May 27, 2025

2016 – 2023

United States locations

U.S. sites
26
U.S. states
16
U.S. cities
22
Facility City State ZIP Site status
University of Arizona Cancer Center Phoenix Arizona 85004
Mayo Clinic Phoenix Arizona 85054
City of Hope Hospital Duarte California 91010
University of California, Los Angeles Los Angeles California 90095
Stanford University Redwood City California 94063
University of California, San Diego San Diego California 92161
University of Colorado, Denver Aurora Colorado 80045
Mount Sinai Comprehensive Cancer Center Miami Beach Florida 33140
H. Lee Moffitt Cancer Center Tampa Florida 33612
Northwestern University Chicago Illinois 60611
Norton Cancer Institute Louisville Kentucky 40202
Massachusetts General Hospital Boston Massachusetts 02114
Dana-Farber Cancer Institute Boston Massachusetts 02130
Barbara Ann Karmanos Cancer Institute Detroit Michigan 48201
St. Louis University St Louis Missouri 63104
Washington University in St. Louis St Louis Missouri 63110
Nebraska Methodist Hospital Omaha Nebraska 68114
New York University New York New York 10016
Memorial Sloan Kettering Cancer Center New York New York 10021
University of Rochester Medical Center Rochester New York 14623
Cleveland Clinic Cleveland Ohio 44195
St. Luke's Hematology Oncology Specialists Easton Pennsylvania 18015
Penn State Hershey Medical Center Hershey Pennsylvania 17033
Dermatology and Laser Center of Charleston Charleston South Carolina 29407
MD Anderson Cancer Center Houston Texas 77030
Huntsman Cancer Institute Salt Lake City Utah 84112

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 52 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02760498, 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 May 27, 2025 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02760498 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →