LivingGLP1
Descriptive only

HbA1c change

Type 2 diabetes (adults); background therapy: basal insulin with or without non insulin drugs

weeks 36 to 64 (target week 52)Treatment policyEach dose separatelyMean differenceSeparate part 2 of a disconnected network
1
Randomized trials
2
Treatments
396
Participants
2
Trial arms

In plain language

No network meta-analysis was fitted here. The protocol requires at least two trials forming a connected network; this outcome has 1 trial. The trial data below are shown as reported.

Network of trials

Each circle is a treatment; each line joins treatments that were randomized against each other in at least one trial.
LIRA_SC_3p0MG_QDPLACEBO
Node area shows participants; line width shows trials comparing two treatments directly. Blue: GLP-1 receptor agonist containing treatments; grey: comparators. Hover over or tab to a node or line for details.

Baseline characteristics of the trials

The baseline value of each effect modifier or prognostic factor that applies here, per trial: mean or percent over arms, weighted by the number randomized. A note under a value names a stand in (a median for a mean, 100 minus the male share, Asian subgroup rows, an all Asian site list); "not reported" means no source of the trial prints it.
Baseline effect modifiers and prognostic factors per trial
TrialBaseline HbA1c (percent)
effect modifier, prognostic factor; 1 of 1
Background glucose lowering therapy (stratum S0 to S4)
effect modifier, prognostic factor; 1 of 1
Diabetes duration (years)
effect modifier, prognostic factor; 1 of 1
Asian ancestry or region (percent Asian)
effect modifier, prognostic factor; 1 of 1
Age (years)
prognostic factor; 1 of 1
Treatment duration (weeks)
effect modifier; 1 of 1
SCALE™ Insulin
S000159
7.95S212.1256.7556

Comparability of the trials

Checked across designs (the set of treatments each trial compares) for eligibility, outcome definition and assessment, and the baseline factors above. Flags point to possible intransitivity; notes describe variation that is not tied to design.

No comparability concerns were found.

Comparability items per trial
Trialtime weeksanalysis setdefinitioninstrumentadjudicatedproportion methodintercurrent events (discontinuation)intercurrent events (rescue)blindingfundingstart yearEligibility
SCALE™ Insulin56full_analysisnot statednot statednot statednot statednot statednot stateddouble_blindindustry2017age 18 or older; BMI 27 or higher; HbA1c 6.0 to 10 percent; basal insulin plus up to 2 oral drugs

Trial data

What each trial contributes. Arm rows give the arm value with its standard error, or events over participants; contrast rows give the mean difference on the analysis scale against the trial's first row. Flags mark converted, combined or approximated inputs.
Trial data entering this analysis
TrialArmTreatmentWeekDataValueSEEvents / NFlagsSource
SCALE™ InsulinA1LIRA_SC_3p0MG_QD56arm, change-1.1000.085198registry:outcomes
SCALE™ InsulinA2PLACEBO56arm, change-0.5000.085198registry:outcomes

Rerun this analysis yourself

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