CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 50 enrolled / 50 target
Drug / intervention
Nivolumabdrug
Likely dose
Nivolumab 3mg/kgfrom 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/NCT04603248
NCT04603248N/ACompletedOn Track (0.8/mo)Completion was 3mo ago

A Study for Identification of Immune Determinants for Response to Nivolumab in Recurrent and/or Metastatic Head and Neck Squamous Cell Carcinoma

Yonsei University·interventional·Posted Oct 26, 2020·Updated Jun 10, 2026

In Brief

A clinical study evaluating Nivolumab for Head and Neck Squamous Cell Carcinoma (HNSCC). Completed, enrolled 50 participants across 1 site.

Detailed Summary

A study for identification of immune determinants for response to Nivolumab in Recurrent /Metastatic HNSCC(Head and neck squamous cell carcinoma) patients. Recurrent and metastatic head and neck squamous cell carcinoma is incurable and requires aggressive treatment, resulting in functional disability, dismal prognosis, and high mortality rate. Prognosis of Recurrent and metastatic head and neck squamous cell carcinoma is poor, with limited treatment options and survival rates of 6-9 months following standard-of-care (SOC) therapies. Clinical trials have demonstrated promising clinical activity of anti PD-1(programmed death-1) therapy in head and neck squamous cell carcinoma. Currently, nivolumab were approved for head and neck squamous cell carcinoma refractory to platinum-based therapy. However, the response rate of anti PD-1(programmed death-1) therapy is relatively low and durable clinical benefit is limited to the minority of patients. Moreover, the presence of PD-1(programmed death-1) did not clearly predict response and treatment survival outcome, reflecting imperfection of this biomarker. Actually, PD-1(programmed death-1) negativity cannot preclude the therapeutic benefit of PD-1(programmed death-1) blockade, and vice versa. Hence, development of reliable predictive biomarkers is essential for proper patient selection to maximize clinical benefit of PD-1(programmed death-1) blockade in head and neck squamous cell carcinoma patients. Therefore, we need to select patients who are most likely to benefit from anti PD-1(programmed death-1) therapy and identify the better biomarker to predict the response to PD-1(programmed death-1) blockade in head and neck squamous cell carcinoma patients. patients earlier than tumor assessment by imaging scan. In the current study, we aimed to elucidate immune-related biomarkers to predict response with tumor tissue and peripheral blood from Recurrent /Metastatic HNSCC(Head and neck squamous cell carcinoma) patients treated with nivolumab.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesSouth Korea
Collaborators--

Timeline

N/ACompletedFinished
202120222023202420252026
First PostedOct 26, 2020
Enrollment StartDec 3, 2020
Primary CompletionMar 18, 2026
TodayJul 2, 2026
Enrollment to primary: 5.3 yearsPosted 5.7 years ago

Arms & Interventions

Single Armexperimental

Drug: Nivolumab

Interventions

Nivolumabdrug

Nivolumab 3mg/kg treatment will be given every 2 weeks up to progression or unacceptable toxicity