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Completed Phase 1 Interventional

Safety Testing of Adding Nivolumab to Chemotherapy in Patients With Intermediate and High-Risk Local-Regionally Advanced Head and Neck Cancer

ClinicalTrials.gov ID: NCT02764593

Public ClinicalTrials.gov record NCT02764593. 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 23, 2026, 2:35 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

Safety Evaluations of Nivolumab (Anti-PD-1) Added To Chemotherapy (CRT) Platforms In Patients With Intermediate And High-Risk Local-Regionally Advanced Head and Neck Squamous Cell Carcinoma

Brief summary

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

This study will evaluate the safety of adding nivolumab to several chemotherapy platforms with weekly cisplatin, high-dose cisplatin, cetuximab or radiation therapy alone.

Study identification

NCT ID
NCT02764593
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
RTOG Foundation, Inc.
Other
Enrollment
40 participants

Conditions and interventions

Interventions

Drug · Radiation

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
Jun 2016 (Type not available)
Primary completion
Sep 25, 2018 (Actual)
Completion
Feb 21, 2022 (Actual)
Last update posted
Nov 29, 2022

2016 – 2022

United States locations

U.S. sites
11
U.S. states
10
U.S. cities
11
Facility City State ZIP Site status
Stanford Cancer Institute Palo Alto California 94304 —
University of Florida Cancer Center at Orlando Health Orlando Florida 32806 —
Emory University/Winship Cancer Institute Atlanta Georgia 30322 —
University of Louisville Louisville Kentucky 40202 —
University Hospitals Cleveland Medical Center Cleveland Ohio 44106 —
Ohio State University Columbus Ohio 43210 —
Providence Portland Medical Center Portland Oregon 97213 —
UPMC - Shadyside Hospital Pittsburgh Pennsylvania 15232 —
MD Anderson Cancer Center Houston Texas 77030 —
Inova Fairfax Hospital Falls Church Virginia 22042 —
University of Wisconsin Hospital and Clinics Madison Wisconsin 53792 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02764593, 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 Nov 29, 2022 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02764593 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →