MedPath

LANTUSTITR: Insulin Glargine in Type 2 Diabetes Mellitus

Phase 4
Terminated
Conditions
Diabetes Mellitus, Type 2
Registration Number
NCT00349986
Lead Sponsor
Sanofi
Brief Summary

The rationale of the study is to determine:

* the first dose and the titration of basal insulin

* the exact daily time administration of basal insulin in poorly controlled type II diabetic patients.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
4
Inclusion Criteria
  • Type 2 Diabetes Mellitus
  • Insufficient combined oral antidiabetic treatment (biguanide + sulfonylurea)
  • BMI >25 kg/m2 , <30 kg/m2
  • HbA1c value >7.0%, <9.0% within one month
Read More
Exclusion Criteria
  • Type 1 Diabetes Mellitus
  • Known malignancy
  • Drug or alcohol abuse
  • Severe liver disease
  • Renal failure (se Creatinine > 150 micro mol/l)

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

Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
HgbA1c measurement
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Sanofi-Aventis

🇭🇺

Budapest, Hungary

© Copyright 2025. All Rights Reserved by MedPath