Diabetes Mellitus, Type 2
Conditions
Keywords
T2DM, Pharmacodynamics, GSK256073
Brief summary
The aim of this study is to verify whether a significant decrease in glucose levels can be achieved with the HM74A agonist GSK256073 in type 2 diabetic patients. Several dose levels and a placebo will be evaluated in a three period crossover study with two active doses and one placebo dose per subject, in order to determine whether there is a dose that produces glucose lowering in the target population. In addition, this study will investigate the optimal dosing regimen for full manifestation of any metabolic effect of GSK256073 by comparing once a day versus twice a day regimens.
Detailed description
This is a multi-center study that will enroll approximately 36 subjects. The study consists of three periods of two days of dosing each. The study will evaluate 5 potential dose regimens. Each subject will receive a randomized sequence of treatments over three periods, with placebo treatment in one period and two different active dose regimens in the other two periods. There will be 5 to 12 days of outpatient washout between treatment periods. Subjects will continue their current treatment on metformin throughout the study. Subjects will monitor blood glucose levels daily via glucometer during oupatient washout periods. A follow-up visit will occur between 5 and 10 days after the last period of the study.
Interventions
DRUGGSK256073
5mg in the AM and 5mg in the PM
OTHERPlacebo
2 placebo tablets in the AM and 2 placebo tablets in the PM
Sponsors
GlaxoSmithKline
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Subject)
Eligibility
Sex/Gender
ALL
Age
20 Years to 70 Years
Healthy volunteers
No
Inclusion criteria
* Subjects with documented (not less than 6 months prior to screening) type 2 diabetes mellitus diagnosis with: * HbA1c levels greater than 6.5 percent and less than or equal to 9.5 percent at screening, * On monotherapy with metformin at the time of screening, and at a todal daily dose greater than or equal to 1000 mg at the time of dosing, * Fasting plasma glucose level less than 270 mg/dl at screening * Male or female between 20 and 70 years of age inclusive, at the time of signing the informed consent * Waist circumference above 102cm (40 inches) for men, and 88cm (35 inches) for women * Fasting triglycerides between 150 mg/dl and 500 mg/dl, inclusive * BMI within the range of 22-37 kg/meter squared, inclusive
Exclusion criteria
A subject will not eligible for inclusion in this study if any of the following criteria apply: * Requiring insulin therapy or use of combination oral antidiabetic medications or use of monotherapy other than metformin within the 3 months prior to screening * Past or present disease (other than type 2 diabetes mellitus) that in the opinion of the Investigator may affect the outcome of this study. These diseases include the following but are not limited to, cardiovascular disease, malignancy, hepatic disease, renal disease, hematological disease, neurological disease, gastrointestinal disease and endocrine disease * A positive pre-study Hepatitis B surface antigen, or positive Hepatitis C or HIV antibody result within 3 months of screening * Renal impairment as defined by a calculated GFR less than 60 ml/min * Any concurrent serious illness (e.g., severe COPD, history of malignancy other than skin cancer within 5 years of initial diagnosis or with evidence of recurrence) that may interfere with a subject completing the study * Clinical laboratory values as defined per protocol * ECG parameters as defined per protocol * History of gout and/or hyperuricemia/uric acid kidney stone or treated with drugs for hyperuricemia: allopurinol and/or probenecid * Current or chronic history of liver disease, or known hepatic or biliary abnormalities (with the exception of Gilbert's syndrome or asymptomatic gallstones) * Use of the following blood pressure medications or other medications renally excreted via OAT is prohibited: Enalapril (at any dose), Losartan (at any dose), Captopril (at any dose) * Pregnant females as determined by positive serum hCG test at screening or positive urine hCG test prior to dosing * Lactating females
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Weighted mean AUC for glucose | 24 hours |
Secondary
| Measure | Time frame |
|---|---|
| Weighted mean AUC for NEFA, glycerol, triglycerides, insulin, and C-peptide | 24 hours |
Countries
United States
Outcome results
None listed