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Study · Non-randomized trial · n = 234 · 2024

2 results

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.

Haluzík M, Al-Sofiani ME, Cheng AYY, Lauand F, Melas-Melt L, Rosenstock J

Diabetes, obesity & metabolism8 Sept 2024Cited by 2 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: CC BY-NC. Results still quote short attributed sentences.

Results from this study2

2 results from studies that gave the peptide. 2 results from people.

  1. 01HumanNon-randomized trialEfficacy outcome

    In people with type 2 diabetes receiving lixisenatide alone, derived time-in-range improved by 11.7% from baseline to treatment end.

    In plain wordsIn people with diabetes receiving lixisenatide alone, time in glucose range increased from baseline.

    Outcome
    IncreaseDerived time-in-range change with lixisenatide alone
    Study

    n = 234

    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    Dose not stated

    Measurements

    dTIR improvement
    11.7%
    Lixi

    Source sentences

    Summary
    Numerically greater improvements in least square (LS) means dTIR were seen from baseline to end of treatment (EOT) with iGlarLixi (25.7%) versus iGlar (15.8%), Lixi (11.7%) or GLP-1 RA (16.2%).
    3 context sentences
    Summary · context
    To evaluate the efficacy of a fixed-ratio combination of insulin glargine 100 U/mL plus lixisenatide (iGlarLixi) in people with type 2 diabetes (T2D) using derived time-in-range (dTIR).
    Summary · context
    Participant-level data from LixiLan-L, LixiLan-O and LixiLan-G were pooled and dTIR (70-180 mg/dL), derived time-above-range (> 180 mg/dL) and derived time-below-range (dTBR; < 70 mg/dL) were calculated from participant seven-point self-monitored blood glucose profiles.
    Summary · context
    This pooled analysis included data from 2420 participants receiving iGlarLixi (n = 1093), iGlar (n = 836), Lixi (n = 234) or a glucagon-like peptide-1 receptor agonist (GLP-1 RA) (n = 257).
  2. 02HumanNon-randomized trialEfficacy outcome

    In people with diabetes receiving lixisenatide alone, end-of-treatment dTBR was 0.08% ± 1.0%.

    In plain wordsIn people with diabetes receiving lixisenatide alone, time below glucose range averaged 0.08% at treatment end.

    Outcome
    Not applicableDerived time-below-range with lixisenatide alone
    Study

    n = 234

    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    Dose not stated

    Measurements

    Mean derived time-below-range at end of treatment
    0.08%
    Lixi arm
    Standard deviation of derived time-below-range at end of treatment
    1%
    Lixi arm

    Source sentences

    Summary
    At EOT, the mean (standard deviation) dTBR was 0.71% ± 3.4%, 0.61% ± 3.2%, 0.08% ± 1.0% and 0.0% ± 0.0% for iGlarLixi, iGlar, Lixi and GLP-1 RA, respectively.
    3 context sentences
    Summary · context
    To evaluate the efficacy of a fixed-ratio combination of insulin glargine 100 U/mL plus lixisenatide (iGlarLixi) in people with type 2 diabetes (T2D) using derived time-in-range (dTIR).
    Summary · context
    Participant-level data from LixiLan-L, LixiLan-O and LixiLan-G were pooled and dTIR (70-180 mg/dL), derived time-above-range (> 180 mg/dL) and derived time-below-range (dTBR; < 70 mg/dL) were calculated from participant seven-point self-monitored blood glucose profiles.
    Summary · context
    This pooled analysis included data from 2420 participants receiving iGlarLixi (n = 1093), iGlar (n = 836), Lixi (n = 234) or a glucagon-like peptide-1 receptor agonist (GLP-1 RA) (n = 257).

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    28 Oct 2026, 02:03 UTC

    Study results updated

  2. Version 1

    27 Oct 2026, 16:36 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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