Randomized Comparison of Initiating the Fixed-Ratio Combination of iGlarLixi or Biosimilar Insulin Glargine Together With Gliclazide in Participants of South Asian Origin With Type 2 Diabetes: VARIATION 2 SA Trial

Objectives: The objective of this study was to compare initiation of a fixed-ratio combination of insulin glargine and lixisenatide (iGlarLixi) vs insulin glargine U100 (iGlar) along with gliclazide, exclusively in people of South Asian origin with type 2 diabetes (T2D). Methods: The Variability of glucose Assessed in a Randomized trial comparing the Initiation of A Treatment approach with biosimilar basal Insulin analog Or a titratable iGlarLixi combinatioN in type 2 diabetes among South Asian participants (VARIATION 2 SA) trial (ClinicalTrials.gov identifier: NCT03819790) randomized insulin-naive adults with T2D having glycated hemoglobin (A1C) 7.1% to 11% to initiate either iGlarLixi or iGlar thorn gliclazide. Insulin doses were titrated similarly to a prebreakfast glucose target of 4.0 to 5.5 mmol/L. Average time in range (TIR) on a masked continuous glucose monitor (CGM), A1C, fasting plasma glucose (FPG) and weight were assessed at the end of the 12-week treatment period. Results: Mean baseline characteristics for the 104 randomized participants were similar between treatment groups, including the following: age, 59+11 years; diabetes duration, 13.7+7.3 years; and A1C, 8.5%+/- 1.2%. Coprimary outcomes of average TIRs within 24- and 12-h (6 AM to 6 PM) periods at the end of trial were 70.5%+/- 16.8% and 72.9%+/- 17.6% for iGlarLixi, whereas these TIRs were 65.6%+/- 21.6% and 67.3%+/- 20.7% for the iGlar thorn gliclazide regimen, respectively, with no significant differences between groups (p=0.35 for 24-h TIR and p=0.14 for 12-h TIR). No significant difference in secondary outcomes was observed between treatment groups. Self-reported hypoglycemic events throughout the trial period and CGM-reported hypoglycemia (<4 and <3 mmol/L) were similar between randomized treatments. Conclusions: Initiation of iGlarLixi resulted in similar TIR, A1C, FPG, weight and hypoglycemia compared with the more affordable option of starting iGlar thorn gliclazide in adults of South Asian origin with T2D. (C) 2022 Canadian Diabetes Association.

Automated summary

This study compared the effects of iGlarLixi and iGlar combined with gliclazide on South Asian patients with type 2 diabetes. The results showed that there were no significant differences between the two treatment approaches in terms of glucose control, A1C levels, fasting plasma glucose, weight, and hypoglycemia occurrence.