Last reviewed · How we verify

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)

NCT01264692 Phase 2 COMPLETED

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 sponsorIdorsia Pharmaceuticals Ltd.
PhasePhase 2
StatusCOMPLETED
Enrolment196
Start date2011-02
Completion2012-02

Conditions

Interventions

Primary outcomes

Countries

Israel, Serbia