M4OC-Prevent: Metformin for Oral Cancer Prevention

Who is this study for? Patients with an oral premalignant lesion
What treatments are being studied? Metformin Hydrochloride
Status: Active_not_recruiting
Location: See all (4) locations...
Intervention Type: Drug, Other
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This phase IIa trial studies how well metformin hydrochloride works in preventing oral cancer in patients with an oral premalignant lesion (oral leukoplakia or erythroplakia). Oral premalignant lesions look like red or whitish plaques or lesions in the mouth that do not rub off and can be associated with a higher risk of cancer. Metformin hydrochloride may help prevent oral cancer from forming in patients with an oral premalignant lesion.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Participants with oral leukoplakia or erythroplakia with mild, moderate, or severe histologic dysplasia, or hyperplasia not associated with mechanical factors such as ill-fitted dentures

• Measurable disease - minimum lesion size of 8 x 3 mm before initial biopsy

• Karnofsky performance status \>= 70%

• Leukocytes \>= 3,000/microliter

• Absolute neutrophil count \>= 1,000/microliter

• Platelets \>= 100,000/microliter

• Total bilirubin =\< 1.5 × institutional upper limit of normal (ULN)

• Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase \[SGOT\])/alanine aminotransferase (ALT) (serum glutamate pyruvate transaminase \[SGPT\]) =\<1.5 × institutional ULN

• eGFR \> 40 mL/min using the Cockcroft-Gault equation

• Life expectancy \> 3 months

• Willing to use adequate contraception (barrier method, abstinence, subject has had a vasectomy or partner is using effective birth control or is postmenopausal) for the duration of study participation

• Ability to take oral medication

• Ability to understand and the willingness to sign a written informed consent document

Locations
United States
California
UC San Diego Medical Center - Hillcrest
San Diego
Minnesota
University of Minnesota/Masonic Cancer Center
Minneapolis
Other Locations
Canada
BC Cancer Research Centre
Vancouver
University of British Columbia Hospital
Vancouver
Time Frame
Start Date: 2016-06-10
Completion Date: 2025-12-20
Participants
Target number of participants: 26
Treatments
Experimental: Prevention (extended-release metformin hydrochloride)
Patients receive extended-release metformin hydrochloride PO QD for 2 weeks and then BID for 10-12 weeks. Treatment continues in the absence of disease progression or unacceptable toxicity.
Related Therapeutic Areas
Sponsors
Leads: National Cancer Institute (NCI)

This content was sourced from clinicaltrials.gov