Viewing Study NCT00046462



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Last Modification Date: 2024-10-26 @ 9:07 AM
Study NCT ID: NCT00046462
Status: COMPLETED
Last Update Posted: 2011-01-11
First Post: 2002-09-30

Brief Title: Determine Whether Glycemic Control is Different Between Lantus a 3rd Oral Agent When Failure With Other Treatment
Sponsor: Sanofi
Organization: Sanofi

Study Overview

Official Title: Substituting LantusInsulin GlarginerDNAoriginInj for a Thiazolidinedione vs a 3rd Oral Agent as add-on Therapy in Patients Failing a Thiazolidinedione Sulfonylurea or Metformin Combination
Status: COMPLETED
Status Verified Date: 2011-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purposes of the study is to determine whether blood sugar control is different between Lantus and a third oral anti-diabetic agent when added to patients who fail a thiazolidinedione and sulfonylurea or metformin combination
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