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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02125305
Other study ID # ME01
Secondary ID
Status Completed
Phase Phase 1
First received April 25, 2014
Last updated April 28, 2014
Start date August 2013

Study information

Verified date April 2014
Source Seoul National University Hospital
Contact n/a
Is FDA regulated No
Health authority Korea: Ministry for Health and Welfare
Study type Interventional

Clinical Trial Summary

This study aims to investigate the pharmacokinetics/pharmacodynamics metformin IR after oral administration in healthy elderly male volunteers.


Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date
Est. primary completion date January 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 65 Years to 85 Years
Eligibility Inclusion Criteria:

- Males aged 65-85 years with a body mass index (BMI) of 18-28 kg/m2

- Good health based on complete medical history, physical examinations, vital signs, electrocardiography (ECG), and clinical laboratory evaluations including hematology (blood cell count, hemoglobin, and platelet count), liver function test (aspartate aminotransferase (AST), alanine aminotransferase (ALT), and bilirubin), serum creatinine, blood glucose and urinalysis

Exclusion Criteria:

- If they had clinically relevant disorders

- Past history of diabetes or clinical findings to suspect diabetes

- Abnormal clinical laboratory values (i.e., platelets = 75,000/mm3, hemoglobin = 9 g/dL, neutrophils absolute = 1000/mm3, fasting glucose > 126mg/dL, creatinine = 1.5 mg/dL, or AST, ALT > 3 × upper limit of normal)

Study Design

Endpoint Classification: Pharmacokinetics/Dynamics Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Metformin


Locations

Country Name City State
Korea, Republic of Seoul National University Bundang Hospital Seoul

Sponsors (1)

Lead Sponsor Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary AUC(area under the plasma concentration-time curve) AUC(area under the plasma concentration-time curve), Cmax(maximum plasma concentration), t1/2 Predose and 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 10, 12h postdose No
Secondary AUGC(total area under the serum concentration-time curve for glucose concentration) AUG (total area under the serum concentration-time curve for glucose) Gmax(maximum serum glucose concentration) predose and 15, 30, 45, 60, 90, 120 min oral glucose tolerance test No
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