Abstract
We aimed to compare the efficacy and safety of lobeglitazone and pioglitazone as add-ons to metformin in patients with type 2 diabetes. Patients who were inadequately controlled by metformin were randomized and treated once daily with either lobeglitazone (0.5mg, n=128) or pioglitazone (15mg, n=125) for 24weeks, with a 28-week extension trial of lobeglitazone treatment in patients who consented. The primary endpoint was the change in glycated haemoglobin (HbA1c) concentration from baseline to week24. At week24, the mean change from baseline in HbA1c was -0.74% for the lobeglitazone group and -0.74% for the pioglitazone group, with a mean difference of 0.01% [95% confidence interval (CI) of difference, -0.16 to 0.18]. The effects of lobeglitazone on lipid variables and the adverse events associated with lobeglitazone were similar to those observed with pioglitazone. Lobeglitazone was not inferior to pioglitazone as an add-on to metformin in terms of their efficacy and safety.
| Original language | English |
|---|---|
| Pages (from-to) | 599-602 |
| Number of pages | 4 |
| Journal | Diabetes, Obesity and Metabolism |
| Volume | 17 |
| Issue number | 6 |
| DOIs | |
| Publication status | Published - 2015 Jun 1 |
| Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2015 The Authors.
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Antidiabetic drug
- Clinical trial
- Phase III study
- Randomised trial
- Thiazolidinediones
ASJC Scopus subject areas
- Internal Medicine
- Endocrinology, Diabetes and Metabolism
- Endocrinology
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