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A Multi-center, Double-blind, Randomized, Placebo- and Active-controlled, Parallel-group, Proof-of-concept Study to Evaluate the Efficacy, Safety, and Tolerability of 10 mg of ACT-280778 in Patients With Mild to Moderate Essential Hypertension (REDUCE-1)
The purpose of this study is to demonstrate the antihypertensive efficacy of once daily oral administration of ACT 280778 on DBP compared to placebo after 28 days.
Details
| Lead sponsor | Idorsia Pharmaceuticals Ltd. |
|---|---|
| Phase | Phase 2 |
| Status | COMPLETED |
| Enrolment | 196 |
| Start date | 2011-02 |
| Completion | 2012-02 |
Conditions
- Essential Hypertension
Interventions
- ACT-280778
- Placebo
- Amlodipine
Primary outcomes
- Change in mean(c) trough(d) SiDBP — Baseline to day 28
Change from baseline(b) to Day 28 (± 2 days) of Period 2 (Visit 7)in mean(c) trough(d) SiDBP.
Countries
Israel, Serbia