Viewing Study NCT00444834



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Last Modification Date: 2024-10-26 @ 9:31 AM
Study NCT ID: NCT00444834
Status: TERMINATED
Last Update Posted: 2016-08-29
First Post: 2007-03-07

Brief Title: A Study of Controlled-Release Carvedilol Compared to Immediate-Release Carvedilol in Patients With Primary Hypertension
Sponsor: Egalet Ltd
Organization: Egalet Ltd

Study Overview

Official Title: A Phase II Multi-center Multiple-dose Double-blind Randomized Crossover Study Comparing the Pharmacodynamic Effects of a Once-daily Controlled-Release Carvedilol CRC Egalet Formulation and an Immediate-Release Carvedilol IRC Formulation in Patients With Primary Hypertension
Status: TERMINATED
Status Verified Date: 2016-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: IMP supply
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to compare the efficacy of the Egalet controlled release formulation to an immediate release Carvedilol tablet
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
Secondary IDs
Secondary ID Type Domain Link
EudraCT no 2006-006534-17 None None None