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Clinical Trial Summary

This study is a randomized, open-label, fasting, single dose, crossover study to investigate the pharmacokinetic profiles and safety of high-dose CKD-385 in healthy volunteers under fasting conditions.


Clinical Trial Description

To 16 healthy subjects, following treatments are administered dosing in each period and wash-out period is a minimum of 7 days.

Reference drug: D744 Test drug: CKD-385 64 mg formulation I Pharmacokinetic blood samples are collected up to 48 hrs. The pharmacokinetic characteristics and safety are assessed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04083872
Study type Interventional
Source Chong Kun Dang Pharmaceutical
Contact
Status Completed
Phase Phase 1
Start date September 6, 2019
Completion date November 1, 2019

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