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UnknownNCT04035538

A Clinical Study to Compare the Safety and Pharmacokinetics of CKD-320 and D012

A Randomized, Open-label, Single-dose, Replicate-crossover Study to Compare the Safety and Pharmacokinetics of CKD-320 and D012 in Healthy Subjects

Status
Unknown
Phase
Phase 1
Study type
Interventional
Enrollment
42 (estimated)
Sponsor
Chong Kun Dang Pharmaceutical · Industry
Sex
All
Age
19 Years
Healthy volunteers
Accepted

Summary

A clinical study to compare the safety and pharmacokinetics of CKD-320 and D012

Detailed description

A randomized, open-label, single-dose, replicate-crossover study to compare the safety and pharmacokinetics of CKD-320 and D012 in healthy subjects

Conditions

Interventions

TypeNameDescription
DRUGCKD-320, D012R: D012 1tablet, QD, PO T: CKD-320 2tablets, QD, PO

Timeline

Start date
2019-08-01
Primary completion
2019-11-01
Completion
2019-12-01
First posted
2019-07-29
Last updated
2019-07-29

Source: ClinicalTrials.gov record NCT04035538. Inclusion in this directory is not an endorsement.

A Clinical Study to Compare the Safety and Pharmacokinetics of CKD-320 and D012 (NCT04035538) · Clinical Trials Directory