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Completed Phase 1 Interventional

A Phase I Study to Evaluate the Safety, Tolerability and Efficacy of MEDI4736 (Durvalumab) With Tremelimumab in Head and Neck Cancer

ClinicalTrials.gov ID: NCT02262741

Public ClinicalTrials.gov record NCT02262741. 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 3, 2026, 11:28 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 I Study to Evaluate the Safety, Tolerability, and Efficacy of MEDI4736 in Combination With Tremelimumab in Subjects With Recurrent or Metastatic Squamous Cell Carcinoma of the Head and Neck

Brief summary

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

This is a multicenter, open-label, dose-exploration and dose-expansion study to evaluate the safety, tolerability, antitumor activity, PK, pharmacodynamics, and immunogenicity of MEDI4736 in combination with tremelimumab in subjects with recurrent/metastatic squamous cell carcinoma of the head and neck.

Study identification

NCT ID
NCT02262741
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
MedImmune LLC
Industry
Enrollment
71 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
18 Years to 99 Years
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
Oct 15, 2014 (Actual)
Primary completion
Sep 21, 2017 (Actual)
Completion
Sep 21, 2017 (Actual)
Last update posted
Oct 23, 2017

2014 – 2017

United States locations

U.S. sites
21
U.S. states
17
U.S. cities
19
Facility City State ZIP Site status
Research Site Scottsdale Arizona 85258 —
Research Site La Jolla California 92093 —
Research Site Los Angeles California 90025 —
Research Site Los Angeles California 90095 —
Research Site San Francisco California 94143 —
Research Site Aurora Colorado 80045 —
Research Site New Haven Connecticut 06520 —
Research Site Orlando Florida 32806 —
Research Site Chicago Illinois 60611 —
Research Site Fairway Kansas 66205 —
Research Site New Orleans Louisiana 70112 —
Research Site Baltimore Maryland 21287 —
Research Site Detroit Michigan 48201 —
Research Site Minneapolis Minnesota 55455 —
Research Site New York New York 10016 —
Research Site New York New York 10065 —
Research Site Portland Oregon 97213 —
Research Site Philadelphia Pennsylvania 19111 —
Research Site Greenville South Carolina 29605 —
Research Site San Antonio Texas 78229 —
Research Site Fairfax Virginia 22031 —

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 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02262741, 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 Oct 23, 2017 · Synced Oct 3, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02262741 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →