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Trials / Completed

CompletedNCT02250833

CKD-828 (80/5mg) Pharmacokinetic Study

To Compare the Pharmacokinetics and Safety of CKD-828 80/5mg to Coadministration of Telmisartan 80mg and S-amlodipine 5mg in Healthy Male Volunteers

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
69 (actual)
Sponsor
Chong Kun Dang Pharmaceutical · Industry
Sex
Male
Age
19 Years – 55 Years
Healthy volunteers
Accepted

Summary

A randomized, open-label, single-dose, two-period, two-way, crossover study to compare the pharmacokinetics and safety CKD-828 (Fixed Dose Combination Tablet) to coadministration telmisartan and s-amlodipine in health volunteers.

Conditions

Interventions

TypeNameDescription
DRUGCKD-828Telmisartan 80mg /S-Amlodipine 5mg(FDC) Tablet, Oral, Once Daily
DRUGTelmisartan\- Telmisartan 80mg tablet, Oral, Once Daily (Combination Therapy with S-amlodipine)
DRUGS-amlodipine\- S-amlodipine 5mg tablet, Oral, Once Daily (combination Therapy with Telmisartan)

Timeline

Start date
2014-09-01
Primary completion
2014-12-01
Completion
2014-12-01
First posted
2014-09-26
Last updated
2015-04-10

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT02250833. Inclusion in this directory is not an endorsement.

CKD-828 (80/5mg) Pharmacokinetic Study (NCT02250833) · Clinical Trials Directory