Effectiveness and Safety of Treatment of Insulin Glargine in Type 2 Diabetes Mellitus Following Glucagon-like Peptide-1 (GLP-1) Failure

NCT ID: NCT01461577

Last Updated: 2013-01-30

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 89 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-11-30
• Study Completion Date: 2012-12-31

Brief Summary

Primary Objective:

• To assess the efficacy of insulin glargine as measured by changes of HbA1c levels from baseline in type 2 diabetes mellitus (T2DM) patients following GLP-1 failure.

Secondary Objective:

• To determine the change in glycemic control, safety, and treatment satisfaction in insulin glargine use in patients following GLP-1 failure.

Detailed Description

1-2 weeks screening period, 24 weeks treatment period, 1 week follow-up period

Conditions

Type 2 Diabetes Mellitus

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

insulin glargine

Insulin glargine will be administered once a day, in the morning, at initial dose of 4 units/day. Titration of insulin dose will be performed referred with the median fasting plasma glucose value for the last 3 consecutive days according to the titration algorithm

Group Type: EXPERIMENTAL

INSULIN GLARGINE HOE 901

Intervention Type: DRUG

Pharmaceutical form:solution Route of administration: subcutaneous

Interventions

INSULIN GLARGINE HOE 901

Pharmaceutical form:solution Route of administration: subcutaneous

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Patients of aged ≥30 and ≤75 years with type 2 diabetes mellitus (T2DM)
• Hemoglobin A1c (glycosylated hemoglobin; HbA1c) levels measured at screening ≥7.5%
• Continuous treatment with stable doses of GLP-1 analogue for >3 months prior to enrollment (for patients also using oral anti-hyperglycemic drugs [OADs], continuous treatment with stable doses of OADs for >3 months prior to enrollment)

Exclusion Criteria

• Inpatient with T2DM
• Diabetes other than T2DM (e.g. secondary to pancreatic disorders, drug or chemical agent intake)
• Fasting plasma glucose (FPG) levels <130mg/dL
• Body mass index (BMI) >28 kg/m2
• Patients using thiazolidinediones in the last 3 months prior to enrollment
• Use of any treatment for weight loss in the last 3 months prior to enrollment
• Treatment with systemic corticosteroids within the 3 months prior to enrollment
• Patients using non-selective ß-blockers
• Likelihood of requiring treatment during the study period with drugs not permitted by the clinical trial protocol
• Most recent ophthalmologic examination >6 months prior to enrollment
• Diabetic retinopathy with surgical treatment (last photocoagulation or vitrectomy) in the 3 months before enrollment or which may require surgical treatment
• Proliferative diabetic retinopathy or any other unstable rapidly progressive retinopathy
• Impaired renal function defined as, but not limited to, serum creatinine ≥1.3 mg/dL [males] or ≥1.2 mg/dL [females] or presence of macroproteinuria (>1 g/day)
• Active liver disease including hepatic cirrhosis, hepatic failure, and hepatitis or alanine transaminase (ALT) or aspartate aminotransferase (AST) >2 times upper limit or total bilirubin >1.5 times upper limit of normal (except in case of Gilbert's syndrome) at enrollment
• Have any condition (including known substance or alcohol abuse or psychiatric disorder) that precludes the patient from following and completing the study protocol
• Any medical condition that may have an influence on HbA1c rate
• Currently undergoing therapy for malignancy which may affect the study evaluation
• Use of any investigational product and/or device within the 2 months prior to enrollment
• History of ketoacidosis or hyperosmolar hyperglycemic state during the previous 12 months prior to enrollment
• History of stroke, myocardial infarction, angina pectoris, coronary artery bypass graft or percutaneous transluminal coronary angioplasty within the previous 12 months prior to enrollment
• History of congestive heart failure
• History of hypoglycemia unawareness or unexplained hypoglycemia during the previous 12 months prior to enrollment
• Hemoglobinopathy or hemolytic anemia, transfusion of blood or plasma products within 3 months prior to enrollment
• Known hypersensitivity / intolerance to insulin glargine or any of its excipients
• History of pancreatitis
• Pregnant or breast-feeding women (women of childbearing potential must have a negative pregnancy test at study entry and a medically approved contraception method)
• Shift workers or those who regularly work a night-time shift

The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

• Minimum Eligible Age: 30 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Sanofi

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Clinical Sciences & Operations

Role: STUDY_DIRECTOR

Sanofi

Locations

Administrative office

Tokyo, , Japan

Countries

Japan

Other Identifiers

U1111-1118-8753

Identifier Type: OTHER

Identifier Source: secondary_id

LANTU_L_05477

Identifier Type: -

Identifier Source: org_study_id