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12-Week Study of DS-8500a in Subjects With Type 2 Diabetes Mellitus on Metformin PHASE2 The hypothesis of this Phase 2, 12-week study, is that DS-8500a will improv...
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JanUmet Before Insulin Lantus In Eastern Population Evaluation Program (JUBILEE) In Type 2 Diabetic Patients PHASE4 To evaluate the efficacy and safety of a new treatment regimen of metformin...
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Department of Medicine & Therapeutics, Prince of Wales Hospital, The Chinese University of Hong Kong
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Pharmacokinetic Characteristics of GLH1SM Extended Release Tablets in Healthy Volunteers PHASE1 Crossover study to compare the pharmacokinetic characteristics of GLH1SM su...
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Chonbuk National University Hospital
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Treatment of Diabetes in Patients With Systolic Heart Failure PHASE4 Investigator Initiated Study to study the effects of Canagliflozin 100 mill...
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Virginia Commonwealth University
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Efficacy and Safety of Ertugliflozin (MK-8835/PF-04971729) With Sitagliptin in the Treatment of Participants With Type 2 Diabetes Mellitus (T2DM) With Inadequate Glycemic Control on Diet and Exercise (MK-8835-017) PHASE3 This is a study to evaluate the efficacy and safety of ertugliflozin (MK-88...
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Sitagliptin in Type I Diabetic Patients NA The purpose of the study is to evaluate the effect of sitagliptin on overal...
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Study of Sitagliptin Treatment in Patients With Type 2 Diabetes During Ramadan (0431-263) PHASE4 This study will examine whether the incidence of hypoglycemia in patients f...
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Sitagliptin Versus Glipizide in Participants With Type 2 Diabetes Mellitus and Chronic Renal Insufficiency (MK-0431-063 AM1) PHASE3 The purpose of the study is to compare how sitagliptin and glipizide lower ...
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A Trial Comparing the Safety and Efficacy of Semaglutide Once Weekly Versus Sitagliptin Once Daily in Japanese Subjects With Type 2 Diabetes PHASE3 This trial is conducted in Japan. The purpose is to compare the safety of o...
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Novo Nordisk Investigational Site
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Phase 1 Bioequivalence Study of Dapagliflozin/Sitagliptin FDC vs Loose Combination of Single Components PHASE1 A Study to Assess the Bioequivalence of the fixed dose combination (FDC) of...
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