Comparative efficacy and safety of Gla‐300 versus IDegAsp in insulin‐naïve people with type 2 diabetes mellitus uncontrolled on oral anti‐diabetics

Author:

Ritzel Robert1,Ghosh Sujoy2ORCID,Emral Rifat3ORCID,Malek Rachid4,Zeng Longyi5,Mabunay Maria Aileen6,Landgraf Wolfgang7ORCID,Guyot Patricia8,Serafini Paul9,Pushkarna Divya9ORCID,Malik Rayaz A.10ORCID

Affiliation:

1. Division of Endocrinology, Diabetes and Angiology München Klinik Schwabing Munich Germany

2. Department of Endocrinology Institute of Post Graduate Medical Education & Research Kolkata India

3. Faculty of Medicine, Department of Endocrinology and Metabolic Diseases Ankara University Ankara Turkey

4. Department of Internal Medicine Setif University Hospital Sétif Algeria

5. Department of Endocrinology and Metabolism The Third Affiliated Hospital‐Sun Yat‐sen University Guangzhou China

6. Sanofi, Global Medical Singapore Singapore

7. Sanofi, Global Medical Frankfurt Germany

8. Sanofi Chilly Mazarin France

9. Evidinno Outcomes Research Inc., Operations Vancouver British Columbia Canada

10. Department of Medicine Weill Cornell Medicine Doha Qatar

Abstract

AbstractAimTo compare the efficacy and safety of insulin glargine‐300 once daily (Gla‐300) with insulin degludec/aspart (IDegAsp) once daily in patients with type 2 diabetes (T2D) inadequately controlled on oral anti‐diabetic drugs (OADs).Materials and methodsA systematic literature review of randomized controlled trials was followed by an indirect treatment comparison of studies involving insulin naïve adults, inadequately controlled [glycated haemoglobin (HbA1c) ≥7.0%] on OADs, who received Gla‐300 or IDegAsp once daily. Outcomes of interest were change in HbA1c, blood glucose, weight and insulin dose, as well as incidence and event rate of hypoglycaemia and other adverse events.ResultsFour trials with broadly similar baseline patient characteristics were included in the meta‐analyses and indirect treatment comparison. At 24‐28 weeks, the indirect comparison of Gla‐300 to IDegAsp once daily estimated no statistically significant difference for change in HbA1c (%) from baseline [mean difference of 0.10% (95% CI: −0.20, 0.39; p = .52)]; a statistically significant mean difference of −1.31 kg (95% CI: −1.97, −0.65; p < .05) for change in body weight from baseline; statistically significant odds ratios of 0.62 (95% CI: 0.41, 0.93; p < .05) for incidence of any hypoglycaemia; and 0.47 (95% CI: 0.25, 0.87; p < .05) for incidence of anytime confirmed hypoglycaemia (plasma glucose <3.0‐3.1 mmol/L). No significant differences were observed for insulin dose and adverse events.ConclusionIn insulin‐naïve patients with T2D inadequately controlled on OADs, commencing Gla‐300 shows a comparable HbA1c reduction, but with significantly less weight gain and a lower incidence of any and confirmed hypoglycaemia compared with commencing IDegAsp.

Funder

Sanofi

Publisher

Wiley

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Internal Medicine

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