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Clinical Trial Details

Trial ID: L2252
Source ID: NCT02354222
Associated Drug: Canagliflozin
Title: Confirmatory Study of MT-2412 in Japanese Patients With Type 2 Diabetes (Add-on Study of Teneligliptin)
Acronym:
Status: COMPLETED
Study Results: YES
Results: https://ClinicalTrials.gov/show/NCT02354222/results
Conditions: Type 2 Diabetes Mellitus
Interventions: DRUG: Canagliflozin|DRUG: Teneligliptin|DRUG: Placebo
Outcome Measures: Primary: Change From Baseline in Percentage of Glycated Hemoglobin (HbA1c), The change from baseline in percentage of HbA1c (the concentration of glucose bound to hemoglobin as a percent of the absolute maximum that can be bound) collected at Week 24., Baseline, 24 Weeks | Secondary: Change From Baseline in Fasting Plasma Glucose Level, The change from baseline in fasting plasma glucose level collected at Week 24., Baseline, 24 Weeks|Percentage Change in Body Weight From Baseline, The percentage change from baseline in body weight collected at Week 24., Baseline, 24 Weeks|Change From Baseline in the AUC(0-2h) for Postprandial Plasma Glucose (PPG), The change from Baseline in AUC(0-2h) for Postprandial Plasma Glucose collected at Week 24., 0, 0.5, 1 and 2 hour postprandial, at Baseline and 24 Weeks|Change From Baseline in 2-hour Postprandial Plasma Glucose Level, The change from baseline in 2-hour postprandial plasma glucose level collected at Week 24., 2 Hours Postprandial, at Baseline and 24 Weeks
Sponsor/Collaborators: Sponsor: Mitsubishi Tanabe Pharma Corporation
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE3
Enrollment: 154
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: QUADRUPLE (PARTICIPANT, CARE_PROVIDER, INVESTIGATOR, OUTCOMES_ASSESSOR)|Primary Purpose: TREATMENT
Start Date: 2015-01
Completion Date: 2016-02
Results First Posted: 2018-08-16
Last Update Posted: 2018-11-01
Locations: Reserch site, Kanto, Japan|Reserch site, Kinki, Japan|Reserch site, Tohoku, Japan
URL: https://clinicaltrials.gov/show/NCT02354222