Related Experiment Videos
Glycemic control with Humalog Mix25 in type 2 diabetes inadequately controlled with glyburide
Roach1, E Koledova, S Metcalfe
1Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana, USA. paroach@iupui.edu
Clinical Therapeutics
|December 1, 2001
Summary
Humalog Mix25 (Mix25) improved glycemic control and treatment satisfaction in type 2 diabetes patients compared to glyburide (GB). Mix25 showed better HbA1c reduction but a higher hypoglycemia rate.
Area of Science:
- Endocrinology
- Metabolic Diseases
- Pharmacology
Background:
- Humalog Mix25 (Mix25) is an insulin mixture comprising 25% insulin lispro and 75% neutral protamine lispro.
- Type 2 diabetes management often requires optimizing glycemic control in patients inadequately managed with oral agents.
Purpose of the Study:
- To compare the efficacy of Mix25 against maximum-dose glyburide (GB) in improving glycemic control.
- To assess treatment satisfaction and hypoglycemia rates in patients with type 2 diabetes inadequately controlled with GB.
Main Methods:
- A 4-month randomized, parallel, open-label study.
- Patients received either Mix25 twice daily or maximum-dose glyburide (15 mg daily).
- Glycemic control was measured by HbA1c, blood glucose profiles, and hypoglycemia incidence.
Main Results:
- Mix25 significantly reduced HbA1c compared to glyburide (8.5% vs 9.4%, P=0.001).
- Greater reductions in all blood glucose measurements were observed with Mix25.
- Patients reported higher satisfaction with Mix25, despite a significantly higher rate of hypoglycemia (0.30 vs 0.05 events/patient/30 days).
Conclusions:
- Twice-daily Mix25 injections offer improved glycemic control and treatment satisfaction versus maximum-dose glyburide in type 2 diabetes.
- The enhanced efficacy of Mix25 is associated with a predictable increase in hypoglycemia.
- The study provides real-world comparative data, though a double-blind trial in treatment-naive patients might yield different outcomes.