Viewing Study NCT01264692



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Last Modification Date: 2024-10-26 @ 10:29 AM
Study NCT ID: NCT01264692
Status: COMPLETED
Last Update Posted: 2018-09-27
First Post: 2010-12-20

Brief Title: Essential Hypertension
Sponsor: Idorsia Pharmaceuticals Ltd
Organization: Idorsia Pharmaceuticals Ltd

Study Overview

Official Title: 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
Status: COMPLETED
Status Verified Date: 2018-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: REDUCE-1
Brief Summary: 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
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None