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
| Type | Name | Description |
|---|---|---|
| DRUG | CKD-828 | Telmisartan 80mg /S-Amlodipine 5mg(FDC) Tablet, Oral, Once Daily |
| DRUG | Telmisartan | \- Telmisartan 80mg tablet, Oral, Once Daily (Combination Therapy with S-amlodipine) |
| DRUG | S-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.