Clinical Trials Directory

Trials / Completed

CompletedNCT05452525

Pharmacokinetics and Safety/Tolerability Profile of CKD-379

A Randomized, Open-label, Single Dose, 3-period, 6-treatment, Crossover Study to Compare the Pharmacokinetics and Safety/Tolerability of CKD-379 and Coadministration of D759, D745 and D150 in Healthy Subjects

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
24 (actual)
Sponsor
Chong Kun Dang Pharmaceutical · Industry
Sex
All
Age
19 Years – 50 Years
Healthy volunteers
Accepted

Summary

A study to compare the pharmacokinetics and safety/tolerability between CKD-379 tablet and D759, D745, D150 combination

Detailed description

A randomized, open-label, single dose, 3-period, 6-treatment, crossover study to compare the pharmacokinetics and safety/tolerability of CKD-379 in healthy subjects under fed conditions

Conditions

Interventions

TypeNameDescription
DRUGCKD-379 I1 tablet administration under fed condition
DRUGCKD-379 II1 tablet administration under fed condition
DRUGD759+D745+D1503 tablet coadministration under fed condition

Timeline

Start date
2022-07-26
Primary completion
2022-08-27
Completion
2022-09-21
First posted
2022-07-11
Last updated
2022-10-18

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT05452525. Inclusion in this directory is not an endorsement.