CI

At a glance

ClinicalIndex Comparison Record
Phase 1Active· 23 enrolled / 23 target
Drug / intervention
Cetuximab +2 morebiological
Likely dose
Not stated in 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/NCT01468896
NCT01468896Phase 1ActiveUpdate Overdue (0.1/mo)Completion was 129mo ago

A Phase I/II Trial of Cetuximab in Combination With Interleukin-12 Administered to Patients With Unresectable Primary or Recurrent Squamous Cell Carcinoma of the Head and Neck

National Cancer Institute (NCI)·interventional·Posted Nov 10, 2011·Updated Jun 25, 2026

In Brief

A Phase 1 clinical trial evaluating Cetuximab, Edodekin alfa, and 1 other intervention for Metastatic Head and Neck Squamous Cell Carcinoma and 2 related conditions. Active but no longer recruiting, targeting 23 participants across 2 sites.

Signals

Enrollment appears stalled

Detailed Summary

This phase I/II trial studies the side effects and best dose of recombinant interleukin-12 when given together with cetuximab and to see how well they work in treating patients with squamous cell carcinoma of the head and neck that has come back, spread to another place in the body, or cannot be removed by surgery. Recombinant interleukin-12 may stimulate the white blood cells to kill tumor cells. Immunotherapy with monoclonal antibodies, such as cetuximab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread Giving recombinant interleukin-12 together with cetuximab may kill more tumor cells.

Study Details

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

Timeline

Phase 1Active
2012201320142015201620172018201920202021202220232024202520262027
First PostedNov 10, 2011
Enrollment StartOct 26, 2011
Primary CompletionSep 29, 2015
Study CompletionMar 31, 2027
TodayJul 2, 2026
Enrollment to primary: 3.9 yearsPosted 14.6 years ago

Arms & Interventions

Treatment (cetuximab and recombinant interleukin-12)experimental

Patients receive cetuximab IV over 1-2 hours on day 1 and recombinant interleukin-12 SC on days 2 and 5 beginning in course 2. Treatment repeats every 2 weeks for 12 courses in the absence of disease progression or unacceptable toxicity. Patients achieving clinical response or stable disease may continue with therapy until disease progression.

Biological: CetuximabBiological: Edodekin alfaOther: Laboratory Biomarker Analysis

Interventions

Cetuximabbiological

Given IV

Edodekin alfabiological

Given SC

Laboratory Biomarker Analysisother

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