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Clinical Study to Evaluate the Pharmacokinetic Profiles and Safety of CKD-386 in Healthy Volunteers Under Fasting Conditions

Hypertension and Dyslipidemia Clinical Trial

Official title:
A Phase I Clinical Trial to Evaluate the Tolerability and the Pharmacokinetics of CKD-386 With Co-administration of D013, D326, and D337 in Healthy Adult Volunteers

Clinical Trial Summary

This study is a randomized, open-label, single dose, crossover study to evaluate the pharmacokinetic profiles and safety of CKD-386 in healthy volunteers under fasting conditions.

Clinical Trial Description

To 30 healthy subjects, following treatments are administered dosing in each period and wash-out period is a minimum of 14 days Pharmacokinetic blood samples are collected up to 72hrs. The pharmacokinetic characteristics and safety are assessed. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05552495
Study type Interventional
Source Chong Kun Dang Pharmaceutical
Contact
Status Completed
Phase Phase 1
Start date September 23, 2022
Completion date December 12, 2022
View Details
See also
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Completed NCT04587206 - A Clinical Trial to Evaluate the Pharmacokinetics and Tolerability of CKD-348 Phase 1
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Completed NCT04883658 - A Clinical Trial to Evaluate the Tolerability and Pharmacokinetics of CKD-348(2) Phase 1
Completed NCT05698043 - A Clinical Trial to Evaluate the Tolerability and Pharmacokinetics of CKD-386(5) 80/20/10mg Phase 1
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Completed NCT04673864 - A Clinical Trial to Evaluate the Tolerability and Pharmacokinetics of CKD-386 Phase 1
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