Skip to main content
OpenTrials
Completed

NCT Number: NCT02083692

Pilot Study of Metformin in Head and Neck Squamous Cell Cancer and Its Effects on Stromal-epithelial Metabolic Uncoupling

The purpose of this study is to assess the effect of metformin in tumor metabolism in patients with head and neck cancer by evaluating metformin's ability to decrease TOMM20 expression in squamous carcinoma cells and decrease MCT4 expression in fibroblasts.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

Thomas Jefferson University

Philadelphia, Pennsylvania, 19107, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of head and neck cancer biopsy proven, and who have a scheduled appointment for definitive resection of the tumor at TJUH
  • Age ≥ 18 years of age and ≤80 years old.
  • Newly diagnosed with HNSCC cancer.
  • No prior therapy for HNSCC cancer is permitted for enrollment in the trial.
  • All subjects must be able to comprehend and sign a written informed consent document.

Exclusion criteria

  • Pregnant or may become pregnant during metformin administration.
  • On metformin for any reason during the preceding 4 weeks.
  • Diabetic patients are eligible if they are not taking metformin, insulin or sulfonylureas.
  • Received iodinated contrast dye less than 48 hours prior to screening meet a temporary exclusion criteria to receive metformin. These patients cannot start investigational metformin until 48 hours have elapsed from contrast administration. Subjects who are scheduled for iodinated contrast dye administration within 48 hours of definitive surgery are excluded.
  • Plasma alanine aminotransferase greater than 40 IU/dL.
  • Plasma aspartate aminotransferase greater than 45 IU/dL.
  • Plasma creatinine level greater than 1.3 mg/dL.
  • Plasma alkaline phosphatase greater than 190 IU/dL.
  • Plasma bicarbonate less than 22 mEq/L or history of lactic or any other metabolic acidosis.
  • History of congestive heart failure.
  • Myocardial ischemia or peripheral muscle ischemia.
  • Sepsis or severe infection.
  • History of lung disease currently requiring any pharmacologic or supplemental oxygen treatment.
  • Scheduled for definitive HNSCC cancer surgical resection less than two weeks from enrollment or greater than five weeks from enrollment.
  • History of hepatic dysfunction or hepatic disease.
  • Excessive alcohol intake which is defined in accordance with CDC definitions as more than 1 drink per day for women and more than 2 drinks per day for men.

All medications are permitted except those that are contraindicated with metformin under current FDA recommendations.

Treatment and study plan

metformin

Drug

Primary outcomes

  1. Change in TOMM20 and MCT4 expression from tumor cells from date of biopsy and date of surgery

    Time frame: date of biopsy and date of surgery (9-28 days)

Sponsors and collaborators

Lead sponsor

Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University

Other

Registry information

Official study title

Pilot Study of Metformin in Head and Neck Squamous Cell Cancer and Its Effects on Stromal-epithelial Metabolic Uncoupling.

Important dates

Study start
2013
Primary completion
2016
Study completion
2017
First posted
Mar 11, 2014
Registry last updated
May 15, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.