A Study of Nivolumab in Patients With Head and Neck Cancer.

Sponsor
Bristol-Myers Squibb
Study ID
NCT04050761
Status
Completed

Conditions

  • Squamous Cell Carcinoma of the Head and Neck; Head and Neck Cancer; Head and Neck Carcinoma; Cancer of the Head and Neck

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Nivolumab — BIOLOGICAL
    Specified dose on Specific Days

Study Details

A prospective real world evidence study of Nivolumab use in France in patient with recurrent or metastatic squamous cell carcinoma of the Head and Neck progressing on or after a platinum based therapy

Key Dates

Start date
Jun 26, 2019
Status verified
Jun 2025
Primary completion
Jul 8, 2024
Completion
Jul 8, 2024

Study Design

Enrollment
502 participants (actual)

Arms

  • Arm: Monotherapy
    Participants diagnosed with recurrent or metastatic squamous cell carcinoma of the Head and Neck and whose physician has decided to initiate a treatment with Nivolumab for the first time for the treatment of SCCHN.

Primary Outcome Measure

Overall Survival [ Time Frame: 3 Years ]