Clinical Trial Details
| Trial ID: | L2526 |
| Source ID: | NCT05274880 |
| Associated Drug: | Ckd-393 |
| Title: | Study to Evaluate the Food Effect on Pharmacokinetics Profile and Safety of CKD-393 |
| Acronym: | |
| Status: | COMPLETED |
| Study Results: | NO |
| Results: | |
| Conditions: | Type II Diabetes Mellitus |
| Interventions: | DRUG: CKD-393 |
| Outcome Measures: | Primary: AUCt of CKD-393, AUCt: Area under the curve from dosing to time, 0, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 5, 6, 7, 8, 10, 12, 24, 48 hours|Cmax of CKD-393, Cmax: Peak plasma drug concentration, 0, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 4, 5, 6, 7, 8, 10, 12, 24, 48 hours | |
| Sponsor/Collaborators: | Sponsor: Chong Kun Dang Pharmaceutical |
| Gender: | ALL |
| Age: | ADULT |
| Phases: | PHASE1 |
| Enrollment: | 28 |
| Study Type: | INTERVENTIONAL |
| Study Designs: | Allocation: RANDOMIZED|Intervention Model: CROSSOVER|Masking: NONE|Primary Purpose: TREATMENT |
| Start Date: | 2022-06-21 |
| Completion Date: | 2022-07-26 |
| Results First Posted: | |
| Last Update Posted: | 2022-11-30 |
| Locations: | Korea University Guro Hospital, Seoul, Korea, Republic of |
| URL: | https://clinicaltrials.gov/show/NCT05274880 |
| Drug ID | Drug Name | Type | DrugBank ID | Targets | Category | Latest Progress |
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