CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 35 enrolled / 35 target
Drug / intervention
Durvalumab +1 moredrug
Likely dose
500mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03691714
NCT03691714Phase 2CompletedUpdate Overdue (0.4/mo)Completion was 18mo ago

An Open-label, Phase II Study of Durvalumab (MEDI4736) in Combination With Cetuximab in Previously Treated Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma (HNSCC)

Trisha Wise-Draper·interventional·Posted Oct 2, 2018·Updated Jun 26, 2026

In Brief

A Phase 2 clinical trial evaluating Durvalumab and Cetuximab for Recurrent Head and Neck Cancer and 3 related conditions. Completed, enrolled 35 participants across 1 site.

Signals

Enrollment appears stalled

Detailed Summary

The purpose of this research study is to test the combination of the anti-cancer drugs durvalumab, the study drug, and cetuximab as a treatment for metastatic or recurrent head and neck cancer. Participants will receive both durvalumab and cetuximab.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
CollaboratorsAstraZeneca

Timeline

Phase 2CompletedFinished
20192020202120222023202420252026
First PostedOct 2, 2018
Enrollment StartOct 23, 2018
Primary CompletionDec 1, 2024
TodayJul 2, 2026
Enrollment to primary: 6.1 yearsPosted 7.8 years ago

Arms & Interventions

Durvalumab and Cetuximabexperimental

Durvalumab 500mg as a 120-minute intravenous infusion every two weeks. Cetuximab 400mg/m2 IV loading dose followed by weekly Cetuximab 250mg/m2 IV Treatment with Durvalumab continues until progression and Cetuximab may continue as maintenance

Drug: DurvalumabDrug: Cetuximab

Interventions

Durvalumabdrug

Two hour infusion

Cetuximabdrug

Two hour infusion for loading dose followed by weekly one hour infusion