Sécurité et efficacité de l'omarigliptine chez les jeunes adultes atteints de diabète de type 2 et présentant un contrôle glycémique inadéquat

Date de début de l'étude : 3 mai 2013

Inclusion Criteria: Has type 2 diabetes mellitus Currently not on an antihyperglycemic agent (AHA) for at least the past 12 weeks and has not been treated with omarigliptin at any time prior to study participation Participant is one of the following: Male Female who is not of reproductive potential Female of reproductive potential who agrees to remain abstinent from heterosexual activity or use (or have her partner use) 2 acceptable methods of contraception to prevent pregnancy during the study and for 21 days after the last dose of study drug Exclusion Criteria: History of type 1 diabetes mellitus or a history of ketoacidosis History of hypersensitivity to dipeptidyl-peptidase-4 (DPP-4) inhibitor Currently participating in or has participated in a clinical trial in the past 12 weeks Is on a weight loss program and not in the maintenance phase; has been on a weight loss medication in the past 6 months; or has undergone bariatric surgery within 12 months prior to study participation Has undergone a surgical procedure within 4 weeks of study participation or has planned major surgery during the study Is on or likely to require treatment for ≥14 consecutive days or repeated courses of pharmacologic doses of corticosteroids Is currently being treated for hyperthyroidism or is on thyroid replacement therapy and has not been on a stable dose for at least 6 weeks Is expecting to undergo hormonal therapy in preparation to donate eggs during the study, including 21 days following the last dose of study drug History of active liver disease (other than non-alcoholic hepatic steatosis) including chronic active hepatitis B or C, primary biliary cirrhosis, or symptomatic gallbladder disease Has human immunodeficiency virus (HIV) Has had new or worsening coronary heart disease or congestive heart failure within the past 3 months, or has any of the following disorders within the past 3 months: Acute coronary syndrome Coronary artery intervention Stroke or transient ischemic neurological disorder Has poorly controlled hypertension History of malignancy ≤5 years prior to study participation, except for basal cell or squamous cell skin cancer or in situ cervical cancer Has a hematological disorder (such as aplastic anemia, myeloproliferative or myelodysplastic syndromes, thrombocytopenia) Has a positive urine pregnancy test Pregnant or breastfeeding, or is expecting to conceive during the study, including 21 days following the last dose of study drug User of recreational or illicit drugs or has had a recent history of drug abuse. Routinely consumes >2 alcoholic drinks per day or >14 alcoholic drinks per week, or engages in binge drinking. Has donated blood products or has had a phlebotomy (>300 mL) within 8 weeks of study participation, or intends to donate blood products during the study or has received, or is anticipated to receive, blood products within 12 weeks of study participation or during the study Has a clinically significant electrocardiogram abnormality