Clinical Trials Directory

Trials / Completed

CompletedNCT01433913

Metformin Hydrochloride in Treating Patients With Prostate Cancer Undergoing Surgery

Phase II Study of Metformin in a Pre-prostatectomy Prostate Cancer Cohort

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
20 (actual)
Sponsor
National Cancer Institute (NCI) · NIH
Sex
Male
Age
18 Years
Healthy volunteers
Not accepted

Summary

This randomized phase II trial studies how well metformin hydrochloride works compared to placebo in treating patients with prostate cancer undergoing surgery. Metformin hydrochloride may make some enzymes active. These enzymes may block other enzymes needed for cell growth and stop the growth of tumor cells.

Detailed description

PRIMARY OBJECTIVES: I. To determine the effect of 4-12 weeks of metformin (metformin hydrochloride) intervention on cell proliferation in the prostatectomy tissue. SECONDARY OBJECTIVES: I. To determine the effect of metformin intervention on prostate tissue bioavailability of metformin. II. To determine the effect of metformin intervention on apoptosis and angiogenesis in the prostatectomy tissue. III. To determine the effect of metformin intervention on potential molecular targets of metformin including activated protein kinase (AMPK) activation, mammalian target of rapamycin (mTOR) regulation, and cell cycle regulation in the prostatectomy tissue. IV. To determine the effect of metformin intervention on changes in systemic hormones and growth factors that have been shown to be modulated by metformin in other patient populations including fasting glucose, fasting insulin, insulin-like growth factor axis, testosterone, and sex hormone binding globulin (SHBG). V. To determine the effect of metformin intervention on changes in prostate-specific antigen (PSA) levels. OUTLINE: Patients are randomized to 1 of 2 treatment arms. ARM I: Patients receive extended-release metformin hydrochloride orally (PO) once daily (QD) for 4-12 weeks. ARM II: Patients receive placebo PO QD for 4-12 weeks. Patients in both arms undergo surgery one day after completion of treatment. After completion of study treatment, patients are followed up within 30 days of surgery.

Conditions

Interventions

TypeNameDescription
DRUGmetformin hydrochlorideGiven PO
OTHERplaceboGiven PO
OTHERlaboratory biomarker analysisCorrelative studies

Timeline

Start date
2011-11-01
Primary completion
2014-04-01
Completion
2014-04-01
First posted
2011-09-14
Last updated
2018-01-10
Results posted
2015-05-15

Locations

3 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01433913. Inclusion in this directory is not an endorsement.