Trials / Completed
CompletedNCT01246193
CKD-828(80/2.5mg) Pharmacokinetic Study
Open Label, Randomized, Single-dose, Crossover Study to Evaluate the Pharmacokinetic Characteristics of Telmisatan 80mg and S-Amlodipine 2.5mg as a Fixed Dose Combination Tablet Compared With Combination Therapy in Healthy Volunteers
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 65 (actual)
- Sponsor
- Chong Kun Dang Pharmaceutical · Industry
- Sex
- All
- 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(FDC) | Drug: Telmisartan 80mg + S-Amlodipine 2.5mg(FDC) Tablet, Oral, Once Daily |
| DRUG | Combination Therapy | Drug: Telmisatan 80mg Tablet, Oral, Once Daily Drug: S-Amlodipine 2.5mg Tablet, Oral, Once Daily |
Timeline
- Start date
- 2010-11-01
- Primary completion
- 2010-12-01
- Completion
- 2010-12-01
- First posted
- 2010-11-23
- Last updated
- 2011-01-19
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT01246193. Inclusion in this directory is not an endorsement.