drugset / Trial / NCT05113693

Study to Evaluate the Pharmacokinetic Profiles and Safety of CKD-393

NCT05113693

Phase 1 Completed 33 enrolled Chong Kun Dang Pharmaceutical
RandomizedCrossoverOpen-labelTreatment

Summary

Objective \- Evaluation of the pharmacokinetic properties and safety of CKD-393 0.25/50/750 mg oral administration in healthy adults under fed condition.

Timeline

Start
2021-11-25
Primary completion
2021-12-06
Completion
2021-12-10

Drugs

EvaluationDrugModalityDoseRoute
Subject CKD-393 Unknown 0.25 mg Oral
Subject CKD-393 Unknown 50 mg Oral
Subject CKD-393 Unknown 750 mg Oral
Subject D759 Unknown Oral
Subject H053 Unknown Oral
Subject Lobeglitazone Small molecule Oral