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Clinical Trial Details

Trial ID: L6705
Source ID: NCT05113693
Associated Drug: Ckd-393
Title: Study to Evaluate the Pharmacokinetic Profiles and Safety of CKD-393
Acronym:
Status: COMPLETED
Study Results: NO
Results:
Conditions: Type 2 Diabetes
Interventions: DRUG: CKD-393|DRUG: CKD-501, D759, H053
Outcome Measures: Primary: AUCt of CKD-501, D759, H053, AUCt: Area under the concentration-time curve from time zero to time, Pre-dose(0 hour), 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 24, 48 hour|Cmax of CKD-501, D759, H053, Cmax: Maximum plasma concentration of the drug, Pre-dose(0 hour), 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 24, 48 hour |
Sponsor/Collaborators: Sponsor: Chong Kun Dang Pharmaceutical
Gender: ALL
Age: ADULT
Phases: PHASE1
Enrollment: 33
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: CROSSOVER|Masking: NONE|Primary Purpose: TREATMENT
Start Date: 2021-11-25
Completion Date: 2021-12-10
Results First Posted:
Last Update Posted: 2023-06-09
Locations: Chonbuk National University Hospital, Jeonju, Korea, Republic of
URL: https://clinicaltrials.gov/show/NCT05113693