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Clinical Trial Details

Trial ID: L5737
Source ID: NCT04322032
Associated Drug: Reference Drug
Title: Clinical Study to Evaluate the Pharmacokinetic Profiles and Safety of CKD-389
Acronym:
Status: UNKNOWN
Study Results: NO
Results:
Conditions: Type 2 Diabetes
Interventions: DRUG: Reference drug|DRUG: Test drug
Outcome Measures: Primary: AUCt(Area Under Curve last), Area under the plasma concentration time curve of CKD-389/D759\&D308, from time zero up to the last measurable concentration., Each period: Pre-dose (0 hour), post-dose 0.17, 0.33, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 24, 48 h|Cmax, The maximum concentration observed of CKD-389/D759\&D308 over blood sampling time., Each period: Pre-dose (0 hour), post-dose 0.17, 0.33, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 24, 48 h |
Sponsor/Collaborators: Sponsor: Chong Kun Dang Pharmaceutical
Gender: ALL
Age: ADULT
Phases: PHASE1
Enrollment: 34
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: CROSSOVER|Masking: NONE|Primary Purpose: TREATMENT
Start Date: 2020-04-06
Completion Date: 2020-05-18
Results First Posted:
Last Update Posted: 2020-03-26
Locations: Chonbuk National University Hospital, Jeonju, Korea, Republic of
URL: https://clinicaltrials.gov/show/NCT04322032