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Characterization of the Variability of Insulin Secretory Parameters in the Meal Tolerance and the Maximal Stimulation Tests of Subjects With Type 2 Diabetes Mellitus
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ClinicalTrials.gov Identifier: NCT01663220
: August 13, 2012
Last Update Posted
: August 14, 2013
Foundation for the National Institutes of Health
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Juvenile Diabetes Research Foundation
Amylin Pharmaceuticals, LLC.
Merck Sharp & Dohme Corp.
Eli Lilly and Company
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
A multi-year clinical study to improve tools for measuring the function of insulin-producing beta cells in people with type 2 diabetes mellitus.
Condition or disease
Type 2 Diabetes
A three-year observational study to standardize the meal tolerance and maximum stimulational tests for measuring beta cell function in the clinical setting. It also aims to improve methods for the early prediction of the long-term response to an intervention and for identification of patients at risk for rapid beta cell function deterioration, thereby enabling future clinical studies that examine diabetes progression.
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Ages Eligible for Study:
30 Years to 65 Years (Adult)
Sexes Eligible for Study:
Accepts Healthy Volunteers:
obese individuals with type 2 diabetes mellitus
Ability to give informed consent and comply with all study requirements
Overweight and obese men and women. Healthy is defined as no clinically relevant abnormalities identified by a detailed medical history (with the exception of glucose, see below), full physical examination, including blood pressure and pulse rate measurement, 12 lead ECG and clinical laboratory tests.
T2D diagnosis by ADA criteria 2011
Fasting glucose 126-270 mg/dL
Diabetes medications allowed: metformin only: stable dose (8 weeks or longer) and 500-2000 mg/day ;
Estimated creatinine clearance, by Cockcroft-Gault, >60 cc/min
No washout of medications allowed
Women of child-bearing potential are allowed (but must agree to use non-hormonal contraception and not plan to become pregnant for the duration of the study). Must agree to maintain the same contraceptive measures throughout the study. Acceptable contraceptive methods for female subjects of childbearing potential include one of the following:
One (1) of the following methods:
Copper-containing intrauterine device (IUD)
Condom AND spermicidal foam/gel/film/cream/suppository
Male partner who has had a vasectomy for at least 6 months.
It is required that all male subjects use an acceptable method of contraception (as outlined below), starting from the first dose of study medication and continuing for at least 28 days after the last dose of study drug:
A condom AND one of the following:
Vasectomy for more than 6 months.
Female partner who meets one of the following conditions:
Has had a tubal ligation, hysterectomy, or bilateral oophorectomy; or
Is post menopausal (menopause is defined as over the age of 60 years, or between 45 and 60 years being amenorrheic for at least 2 years with plasma (FSH) level > 30 UI/L) or
Or for female partners of the male participants, in addition to hysterectomy, oophorectorectomy, or post-menopausal status, that the use of a spermicidal gel or foam will constitute adequate protection in conjunction with use of a condom by the male.
BMI 27-40; stable weight (less than 3% change in past 3 months)
Age Range: 30-65
Other conditions may be allowed, if medically stable and controlled for at least four weeks within clinically acceptable limits, including: hypertension, dyslipidemia, osteoarthritis, osteoporosis
Smokers allowed, but must be able to participate on inpatient stay and not smoke
Subjects presenting with any of the following will not be included in the study:
Evidence or history of clinically significant hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurologic, neoplastic, or allergic or clinical findings at Screening (seasonal allergies allowed).
Any condition possibly affecting absorption (eg, gastrectomy, malabsorption syndromes, abdominal surgery other than appendectomy, cholecystectomy or hysterectomy).
Use of unacceptable medications (see Appendix A)
A positive urine drug screen.
History of regular alcohol consumption exceeding 7 drinks/week for females or 14 drinks/week for men (1 drink = 5 ounces (150 mL) of wine or 12 ounces (360 mL) of beer or 1.5 ounces (45 mL) of hard liquor) within 6 months of Screening.
Treatment with an investigational drug within 30 days or 5 half-lives preceding the first dose of study medication.
12 lead ECG demonstrating QTc >450 msec at Screening for males, 470 msec for females. If QTc exceeds 450/470 msec, the ECG should be repeated two more times and the average of the three QTc values should be used to determine the subject's eligibility. An ECG with evidence for possible old myocardial infarction will need to have prior ECGs to document stability of finding.
Supine blood pressure >=140 mm Hg (systolic) or 90 mm Hg (diastolic), on a single measurement. If elevated, confirm by a single repeat, following at least 10 minutes of rest.
Screening serum alanine transaminase (ALT) or serum aspartate transaminase (AST) greater than 2X the upper limit of the laboratory reference range.
Elevated fasting triglycerides at screening (>500 mg/dL), confirmed by a single repeat if deemed necessary.
Pregnant or nursing females; inability to use effective contraception.
Blood donation of approximately 1 pint (500 mL) within 56 days prior to dosing.
Participation in a clinical biomedical research study within prior two months may be excluded, depending on study type and details.
History of sensitivity to heparin or heparin-induced thrombocytopenia, if utilized by the site for blood draws.
Unwilling or unable to comply with directions and procedures described in this protocol.
Subject is the Investigator or a sub-Investigator, research assistant, pharmacist, study coordinator, other staff, or a relative of study personnel directly involved with the conduct of the study.
Other severe acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or investigational product administration or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the subject inappropriate for entry into this study.