Methotrexate, Erlotinib, and Celecoxib for the Treatment of Recurrent/Metastatic Head and Neck Cancer in a Rural Midwest United States Population

This phase II trial gathers information on the feasibility, safety, and effect of giving methotrexate, erlotinib, and celecoxib in treating head and neck cancer that has come back after a period of improvement (recurrent) or that has spread from where it first started (primary site) to other places in the body (metastatic) among rural Midwest patients. Methotrexate is in a class of medications called antimetabolites. It is also a type of antifolate. Methotrexate stops cells from using folic acid to make deoxyribonucleic acid and may kill tumor cells. Erlotinib is in a class of medications call

Trial Details

NCT ID
NCT06997068
Phase
PHASE2
Sponsor
Mayo Clinic
Status
RECRUITING
Cancer Type
HPV Positive Head and Neck Cancer
Interventions
  • Celecoxib
  • Erlotinib Hydrochloride
  • Imaging Procedure
  • Interview
  • Methotrexate
  • Questionnaire Administration
Locations (sample)
  • Rochester, Minnesota, United States|44.02163,-92.4699

Key Eligibility Criteria

  • Age ≥ 18 years
  • Histologically confirmed diagnosis of relapsed/metastatic head and neck cancer, including oral cavity, oropharynx \[human papillomavirus (HPV) posi…
  • Measurable or non-measurable disease is allowed
  • Measurable disease as defined by Response Evaluation Criteria in Solid Tumors (RECIST) criteria

For full eligibility, visit ClinicalTrials.gov.

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