drugset / Trial / NCT05526742

A Study to Evaluate the Relative Bioavailability of Formulations of CKD-510 and to Assess the Effect of Food on the CKD-510 Tablet Formulation in Healthy Subjects

NCT05526742 ↗

Phase 1 Completed 16 enrolled Chong Kun Dang Pharmaceutical
RandomizedCrossoverOpen-labelTreatment

Summary

The purpose of this study is to determine the relative bioavailability of CKD-510 tablet formulation compared with CKD-510 capsule formulation, and to characterize the effect of food on the CKD-510 tablet.

Timeline

Start
2022-08-24
Primary completion
2022-09-13
Completion
2022-09-13

Drugs

EvaluationDrugModalityDoseRoute
Subject CKD-510 Unknown — Oral

Indications

No indication recorded.