Viewing Study NCT00229684



Ignite Creation Date: 2024-05-05 @ 12:02 PM
Last Modification Date: 2024-10-26 @ 9:19 AM
Study NCT ID: NCT00229684
Status: TERMINATED
Last Update Posted: 2011-08-30
First Post: 2005-09-28

Brief Title: ARMOR Analyzing Renal Mechanisms of Creatinine Excretion in Patients On tesaglitazaR
Sponsor: AstraZeneca
Organization: AstraZeneca

Study Overview

Official Title: A 24-week Randomised Parallel-Group Multi-Centre Open-Label Study of the Renal Effects of Tesaglitazar in Patients With Type 2 Diabetes Mellitus
Status: TERMINATED
Status Verified Date: 2011-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: The development program has been terminated
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This is a prospective 24-week randomized parallel-group multi-center active-controlled pioglitazone 45 mg open-label study designed to assess the effects of tesaglitazar 2 mg per day on components of renal excretion of creatinine in type 2 diabetics The study comprises a 2-week enrollment period followed by a 24-week double blind treatment period and an 8-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