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A Randomized, Double-blind, Multi-center, Multi-factorial, Phase 2 Trial to Evaluate the Efficacy and Safety of S-Amlodipine/Telmisartan Combined or Alone and Select Better Dose of CKD-828 in Patients With Essential Hypertension
The aim of this trial is to determine the best dose combination of S-Amlodipine and Telmisartan as compared to monotherapy by assessing the blood pressure lowering effects of a once daily regimen of various combinations of S-Amlodipine and Telmisartan, compared to their monotherapy components and placebo, in patients with stage I or II essential hypertension(a mean seated cuff diastolic blood pressure \>=95 and \<=115 mmHg).
Details
| Lead sponsor | Chong Kun Dang Pharmaceutical |
|---|---|
| Phase | Phase 2 |
| Status | COMPLETED |
| Enrolment | 430 |
| Start date | 2010-07 |
| Completion | 2011-03 |
Conditions
- Hypertension
Interventions
- S-Amlodipine, Telmisartan
- S-Amlodipine
- Telmisartan
- Placebo
Primary outcomes
- Mean Sitting Diastolic Blood Pressure(MSDBP) — After 8 weeks of treatment
Countries
South Korea