Viewing Study NCT00449605



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Last Modification Date: 2024-10-26 @ 9:31 AM
Study NCT ID: NCT00449605
Status: TERMINATED
Last Update Posted: 2016-05-16
First Post: 2007-03-19

Brief Title: A Glycemic Control Evaluation of Glimepiride Versus Rimonabant on Top of Metformin in Type 2 Diabetes
Sponsor: Sanofi
Organization: Sanofi

Study Overview

Official Title: A Randomized Double-Blind Parallel-Group Multicenter Multinational Study to Assess Glycemic Control With Rimonabant in Comparison With Glimepiride Over 1 Year in OverweightObese Type2 Diabetic Patients Not Adequately Controlled With Metformin
Status: TERMINATED
Status Verified Date: 2016-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Company decision taken in light of demands by certain national health authorities
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: ALLEGRO
Brief Summary: The primary objective is to demonstrate after 52 weeks of treatment the non-inferiority of rimonabant 20 mg once daily od versus glimepiride od in reducing glycosylated haemoglobin HbA1c in overweightobese patients with type 2 diabetes not adequately controlled with metformin at a stable dose 1500 mgday for at least 3 months

The main secondary objectives are to assess the effect of rimonabant in comparison with glimepiride on body weight and HDL-Cholesterol and the long-term safety and tolerability of rimonabant in comparison with glimepiride
Detailed Description: The total duration per patient will be approximately 65 weeks including a 52-week double-blind treatment period

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
2006-005385-39 EUDRACT_NUMBER None None