Type 2 & other diabetes

Time‐in‐range derived from self‐measured blood glucose in people with type 2 diabetes advancing to iGlarLixi : A participant‐level pooled analysis of three phase 3 LixiLan randomized controlled trials

Diabetes Obes MetabPublished Pooled analysis of randomised controlled trials

Authors' conclusion

iGlarLixi achieved improvements in dTIR, with low dTBR values, providing further evidence to inform clinical outcomes with the use of iGlarLixi.

Study context

Population
People with T2D in LixiLan-L, LixiLan-O and LixiLan-Gpooled LixiLan trials
Participants
2,420 people
Comparison
iGlarLixi vs iGlar, Lixi or GLP-1 RA
  • iGlarLixin = 1,093
  • iGlarn = 836reference
  • Lixin = 234reference
  • GLP-1 RAn = 257reference
Outcome
Derived TIR (70-180 mg/dL) from seven-point SMBG profiles
Follow-up
Baseline to end of treatment
Methodological detailsparticipant-level pooled analysis, LixiLan-L, LixiLan-O and LixiLan-G trials
  • Participant-level pooled analysis
  • LixiLan-L, LixiLan-O and LixiLan-G trials

Pooled result

As reported in the abstract

Change in LS mean dTIR · baseline to EOT

iGlarLixi

25.7%

Least square (LS) mean

iGlar

15.8%

LS mean

Lixi

11.7%

LS mean

GLP-1 RA

16.2%

LS mean

Further pooled results

Derived time-in-range (dTIR) change by age subgroup (<65 years, n = 1690; ≥65 years, n = 713) · baseline to end of treatment (EOT)

Numerically greater improvements in LS mean dTIR with iGlarLixi vs iGlar, Lixi or GLP-1 RA in both age subgroups

Safety

Mean

OutcomeiGlarLixiiGlarLixiGLP-1 RA
Derived TBR (<70 mg/dL) · EOT0.71% (SD 3.4%)0.61% (SD 3.2%)0.08% (SD 1.0%)0.0% (SD 0.0%)

Original publication

Time‐in‐range derived from self‐measured blood glucose in people with type 2 diabetes advancing to iGlarLixi : A participant‐level pooled analysis of three phase 3 LixiLan randomized controlled trials. Diabetes Obes Metab. Published 8 September 2024. doi:10.1111/dom.15811

Composed by AI from the published abstract and checked against it. How Briefs are made →

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