Clinical Trials Directory

Trials / Completed

CompletedNCT01340131

CKD-828 (40/5mg) Pharmacokinetic Study

Open Label, Randomized, Single-dose, Crossover Study to Evaluate the Pharmacokinetic Characteristics of Telmisatan 40mg and S-Amlodipine 5mg as a Fixed Dose Combination Tablet Compared With Combination Therapy in Healthy Volunteers

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

Summary

The purpose of this study is to evaluate the pharmacokinetic characteristics of CKD-828 (Fixed Dose Combination Tablet; Telmisartan and S-Amlodipine) in healthy volunteer.

Conditions

Interventions

TypeNameDescription
DRUGCKD-828Drug: Telmisartan 40mg + S-Amlodipine 5mg(FDC) Tablet, Oral, Once Daily
DRUGCombination TherapyDrug: Telmisartan 40mg Tablet, Oral, Once Daily Drug: S-amlodipine 5mg Tablet, Oral, Once Daily

Timeline

Start date
2011-01-01
Primary completion
2011-03-01
Completion
2011-04-01
First posted
2011-04-22
Last updated
2011-04-28

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01340131. Inclusion in this directory is not an endorsement.