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
| Type | Name | Description |
|---|---|---|
| DRUG | CKD-828 | Drug: Telmisartan 40mg + S-Amlodipine 5mg(FDC) Tablet, Oral, Once Daily |
| DRUG | Combination Therapy | Drug: 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.