RecruitingPhase 4NCT06162377

Methylnatrexone In Resectable Head and Neck Squamous Cell Carcinoma (MINK). A "Window of Opportunity" Pilot Study.


Sponsor

M.D. Anderson Cancer Center

Enrollment

25 participants

Start Date

Jan 10, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

To learn if OCSCC patients can be safely given methylnaltrexone for 2 weeks before surgery.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests methylnaltrexone — a drug that reverses opioid-induced constipation — to see if it can also slow the growth of head and neck squamous cell carcinoma (cancer of the mouth, throat, or larynx). The drug is given before surgery to study its effects on the tumor. **You may be eligible if...** - You are 18 or older with head and neck squamous cell carcinoma (HNSCC) - Your cancer is resectable (can be surgically removed) - You have not yet had surgery, radiation, or systemic treatment for this cancer - Your general health is adequate for surgery **You may NOT be eligible if...** - Your cancer has spread to distant organs - You have had prior treatment for this cancer (surgery, radiation, chemo) - You have a bowel obstruction or severe gastrointestinal disease - You are pregnant or breastfeeding - You have severe kidney or liver impairment Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGMethylnaltrexone

Given by SC (injection)


Locations(1)

MD Anderson Cancer Center

Houston, Texas, United States

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NCT06162377


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