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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT03477162
Other study ID # D17188
Secondary ID
Status Terminated
Phase Early Phase 1
First received
Last updated
Start date May 15, 2018
Est. completion date November 30, 2021

Study information

Verified date November 2022
Source Dartmouth-Hitchcock Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a presurgical (proof of principle, window of opportunity) study in patients with surgically resectable thoracic tumors to determine steady-state tissue and plasma concentrations of metformin.


Description:

To understand the variability in clinical results testing metformin as an anti-cancer agent, it is important to determine the concentrations of metformin that are achievable in tissue. Clinical effects of metformin develop gradually over several days of treatment. Steady-state plasma metformin concentrations are correlated with anti-hyperglycemic response. Thus, achieving steady-state concentrations in this study will allow accurate determination of the most representative concentrations of metformin in normal and cancerous tissues, as well as determine AMP-activated protein kinase (AMPK) signaling differences in these tissues. As tha Primary Objective is to determine the concentration of metformin in tumors, patients will be treated with metformin extended release (ER) (Glucophage® XR), starting at 750 milligrams (mg) oral (PO) once daily (QD) for 4 days, then escalating to 750 mg PO twice daily (BID) for 3-6 days prior to surgery. FDA prescribing information indicates that metformin reaches steady-state plasma concentrations within 24-48 hours after the start of dosing in humans; thus, the 7-to-10-day time frame of this study will allow sufficient time for metformin to reach steady-state plasma concentrations, in addition to time allotted for potential accumulation in tissues. Metformin concentrations will be measured using a validated liquid chromatography-mass spectrometry (LC-MS/MS) assay.


Recruitment information / eligibility

Status Terminated
Enrollment 18
Est. completion date November 30, 2021
Est. primary completion date November 30, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Invasive malignant solid tumor of thoracic origin (e.g., lung, esophageal, thymus, mesothelioma, chest wall, mediastinum, trachea, pleura) with the intent to treat or biopsy by surgery as standard of care. Tumor must be =2 centimeters (cm). - Patients with multicentric disease are eligible. Samples from all available tumors are requested for research purposes. - Patients with Type 2 diabetes mellitus being treated with metformin (any dose) for a clinical indication at the time of study enrollment are eligible, and will continue metformin treatment as clinically indicated during the presurgical study period. Their dose of metformin will NOT be changed. - Patients not on metformin at the time of study entry must be willing to take metformin extended release (Glucophage® XR, 750 mg QD for 4 days, then 750 mg BID for 3-6 days) for a total of 7-10 days prior to surgery. - Patients do not require a diagnosis of diabetes to be enrolled in the study. - All patients must be willing to keep a drug diary indicating the dates and times of metformin administration. Patients must meet the following clinical laboratory criteria: - Absolute neutrophil count (ANC) greater than or equal to 1,500/mm3 and platelet count greater than or equal to 75,000/mm3. - Total bilirubin less than or equal to 1.5x the upper limit of the normal range (ULN). - Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) less than or equal to 3x ULN. - Estimated glomerular filtration rate (eGFR) > 60 mL/min/1.73m2 or estimated creatinine clearance (eCrCL) > 60 mL/min - Ability to give informed consent. - Patients must be willing to provide 20 milliliters (mL) of blood for research use. - Patient must be willing to provide consent for use of archived tissue for research. Exclusion Criteria: - History of diabetes that is currently being treated without metformin. - Patients who, at the time of study entry, are not taking metformin for a clinical indication, and who will need a radiographic analysis with an iodinated contrast agent during the metformin study treatment period. - This criterion does not apply to patients taking clinically indicated metformin at the time of study entry. - History of liver disease as defined with liver function tests (LFTs) above those in the inclusion - Known hypersensitivity to metformin. - History of reactive hypoglycemia. - Active or history of lactic acidosis, metabolic acidosis, or diabetic ketoacidosis.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Metformin
Metformin will be given to patients prior to surgery.

Locations

Country Name City State
United States Dartmouth Hitchcock Medical Center Lebanon New Hampshire

Sponsors (1)

Lead Sponsor Collaborator
Dartmouth-Hitchcock Medical Center

Country where clinical trial is conducted

United States, 

References & Publications (38)

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Glucophage XR product insert. https://www.google.com/url?sa=t&rct=j&q=&esrc=s&source=web&cd=1&ved=0ahUKEwjcrMLO8cPXAhWGZiYKHVe1DoMQFggrMAA&url=https%3A%2F%2Fpackageinserts.bms.com%2Fpi%2Fpi_glucophage.pdf&usg=AOvVaw2zAbyMgwlF7wxaXv60vtv3.

Graham GG, Punt J, Arora M, Day RO, Doogue MP, Duong JK, Furlong TJ, Greenfield JR, Greenup LC, Kirkpatrick CM, Ray JE, Timmins P, Williams KM. Clinical pharmacokinetics of metformin. Clin Pharmacokinet. 2011 Feb;50(2):81-98. doi: 10.2165/11534750-000000000-00000. — View Citation

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Tucker GT, Casey C, Phillips PJ, Connor H, Ward JD, Woods HF. Metformin kinetics in healthy subjects and in patients with diabetes mellitus. Br J Clin Pharmacol. 1981 Aug;12(2):235-46. doi: 10.1111/j.1365-2125.1981.tb01206.x. — View Citation

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Wright JL, Stanford JL. Metformin use and prostate cancer in Caucasian men: results from a population-based case-control study. Cancer Causes Control. 2009 Nov;20(9):1617-22. doi: 10.1007/s10552-009-9407-y. Epub 2009 Aug 4. — View Citation

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* Note: There are 38 references in allClick here to view all references

Outcome

Type Measure Description Time frame Safety issue
Other AMPK Activity Alterations. To determine whether metformin alters AMPK activity in tumor cells. Within 7 days from surgery.
Primary Lung Tumor Tissue Concentration of Metformin To determine the intra-tumor concentrations of metformin, with a standard deviation =25% of the mean, in patients with solid tumors of thoracic origin administered metformin extended release. Within 7 days from surgery
Secondary Concentration of Metformin in Adipose Tissue To determine the concentration of metformin in adipose tissue. Within 7 days from surgery
Secondary Concentration of Metformin in Tumor-adjacent Normal Tissue To determine the concentration of metformin in tumor-adjacent normal tissue. Within 7 days from surgery
Secondary Concentration of Metformin in Plasma. To determine the concentration of metformin in plasma. Within 7 days from surgery
Secondary Concentration of Metformin in Whole Blood. To determine the concentration of metformin in whole blood. Within 7 days from surgery
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