Viewing Study NCT00263965



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Study NCT ID: NCT00263965
Status: TERMINATED
Last Update Posted: 2008-03-17
First Post: 2005-12-09

Brief Title: ARAMIS Actions of tesaglitazaR on fAt Metabolism and Insulin Sensitivity
Sponsor: AstraZeneca
Organization: AstraZeneca

Study Overview

Official Title: A 16-Week Randomized Double-Blind Parallel-Group Multicenter Placebo- and Active- Metformin Controlled Study to Evaluate the Effect on Whole Body Insulin Sensitivity of Tesaglitazar Therapy When Administered to Patients With Type 2 Diabetes
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 16-week randomized double-blind parallel-group multi-center placebo- and active- metformin 15 g controlled study of tesaglitazar 1 mg in patients with type 2 diabetes After a 1-week enrollment period a 3 week placebo single blind run in period and 1-week placebo single-blind baseline measurement period the patients will be given the investigational product for 16 weeks in a double blind fashion Metformin will be titrated up during the first 3 weeks of the double-blind period The total study duration including enrollment run-in randomized treatment and follow-up is 29 weeks
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 2004-000350-24 None None None