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Clinical Trial Details

Trial ID: L3271
Source ID: NCT02375139
Associated Drug: Da-1229_01
Title: A Clinical Trial to Investigate Safety/Tolerability and Pharmacokinetics of DA-1229_01(Evogliptin/Metformin XR 2.5/500 mg x 2 Tablets) Compared to Co-administration of Evogliptin 5 mg and Metformin XR 1000 mg in Healthy Male Volunteers
Acronym:
Status: COMPLETED
Study Results: NO
Results:
Conditions: Type 2 Diabetes Mellitus
Interventions: DRUG: DA-1229_01|DRUG: E+M
Outcome Measures: Primary: Area Under Curve(AUC)last of Evogliptin and Metformin, 1d(15d) pre-dose, 1,2,3,4,5,6,7,8,10,12,15,24,36,48,60,72h post-dose|Maximum of concentration (Cmax) of Evogliptin and Metformin, 1d(15d) pre-dose, 1,2,3,4,5,6,7,8,10,12,15,24,36,48,60,72h post-dose | Secondary: Time of maximum concentration(Tmax) of Evogliptin and Metformin, 1d(15d) pre-dose, 1,2,3,4,5,6,7,8,10,12,15,24,36,48,60,72h post-dose|Terminal half-life(t1/2) of Evogliptin and Metformin, 1d(15d) pre-dose, 1,2,3,4,5,6,7,8,10,12,15,24,36,48,60,72h post-dose|Apparent Clearance(CL/F) of Evogliptin and Metformin, 1d(15d) pre-dose, 1,2,3,4,5,6,7,8,10,12,15,24,36,48,60,72h post-dose|Area Under Curve(AUC)inf of Evogliptin and Metformin, AUCinf = AUC last + Clast/λz, 1d(15d) pre-dose, 1,2,3,4,5,6,7,8,10,12,15,24,36,48,60,72h post-dose
Sponsor/Collaborators: Sponsor: Dong-A ST Co., Ltd.
Gender: MALE
Age: ADULT
Phases: PHASE1
Enrollment: 36
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: CROSSOVER|Masking: NONE|Primary Purpose: TREATMENT
Start Date: 2015-04
Completion Date: 2015-06
Results First Posted:
Last Update Posted: 2015-07-22
Locations: Clinical Trial Center, Seoul National University Hospital, Seoul, 110-744, Korea, Republic of
URL: https://clinicaltrials.gov/show/NCT02375139