Safety and Efficacy of YH14617 in Diabetes Mellitus
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government.
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The objective of this study is to assess the safety, efficacy and pharmacokinetic of YH14617 after once weekly or biweekly injection in patients with type 2 Diabetes Mellitus to investigate the optimal recommended dosage. Study period is 20 weeks including 12 weeks of treatment period and 8weeks of follow-up period without treatment.
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Ages Eligible for Study:
20 Years to 75 Years (Adult, Senior)
Sexes Eligible for Study:
Accepts Healthy Volunteers:
Have signed a written informed consent voluntary, prior to the any procedure
Volunteers of aged between 20 years to 75 years
Have been diagnosed with type 2 diabetes at least 3 months prior to study
Have a body mass index (BMI) of > 23kg/m2 and have a history of stable body weight during 3 months prior to the first administration (not varying by > 5% in weight)
Have been treated with stable dose regimen of Metformin > 1500mg/day or maximum tolerant dose for at least 3 months prior to the first administration
Have an HbA1c between 7% and 10% inclusive
Have been treated with insulin, sulfonylurea, thiazolidinedione class hypoglycemic drugs, exenatide or other GLP-1 receptor agonist, DPP4-inhibitor, glucocorticoid and drugs that promote weight loss within 3 months prior to the first administration
Have acute disease, other untreated disease or diabetic complications that needs additional treatment
Have severe renal disorder(serum creatinine concentration > 1.5 times of normal upper limit) or liver disorder(liver enzyme > 2 times of normal upper limit)
Have blood pressure > 160/100mmHg
Have been hospitalized due to cardiac disorder(angina, cardiac infarction, heart failure and etc.) within 1 year prior to the first administration
Have history of critical disease within 1 year prior to the first administration
Have untreated malignant tumor or have history of significant malignant tumor within 5 years prior to the first administration
Have fasting plasma glucose(FPG) > 250mg/dl or have random glucose level > 350mg/dl
Have more than 1 history of severe hypoglycemia that needed others help within 3 months prior to the first administration
Have a known allergy or hypersensitivity to drugs
Pregnant women, nursing mothers or subject who does not agree to assigned contraception in the study
Participated in any other clinical trials within 30 days prior to the first administration
Subject who is judged to be ineligible by principal investigator or sub-investigator according to various reasons other than above