Viewing Study NCT00251940



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Last Modification Date: 2024-10-26 @ 9:20 AM
Study NCT ID: NCT00251940
Status: TERMINATED
Last Update Posted: 2008-03-17
First Post: 2005-11-09

Brief Title: GALLANT 7 Tesaglitazar Add-on to Sulphonylurea
Sponsor: AstraZeneca
Organization: AstraZeneca

Study Overview

Official Title: A 24-Week Randomised Double-Blind Parallel-Group Multi-Centre Placebo-Controlled Study to Evaluate the Efficacy Safety and Tolerability of Tesaglitazar Therapy When Added to the Therapy of Patients With Type 2 Diabetes Poorly Controlled on Sulphonylurea Alone
Status: TERMINATED
Status Verified Date: 2008-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: The development program has been terminated
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This is a 24-week randomized double-blind parallel-group multi-center placebo-controlled study of tesaglitazar 05 mg and 1 mg given as add-on therapy to sulphonylurea in patients with type 2 diabetes not adequately controlled on optimized sulphonylurea treatment and on dietlifestyle advice during the titration and run-in period The study comprises a 2-week enrollment period 6 week placebo metformin titration period 2-week single-blind run-in period followed by a 24-week double blind treatment period and a 3-week follow-up period
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 2004-001144-71 None None None