LivingGLP1
Descriptive only

Body weight change in kilograms (diabetes)

Type 2 diabetes (adults); background therapy: one or more non insulin glucose lowering drugs

weeks 64 to 130 (target week 104)Treatment policyEach dose separatelyMean difference
1
Randomized trials
2
Treatments
775
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.
SEMA_SC_FLEX_0p25-0p5-1p0_QWSTANDARD_CARE
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 BMI or body weight (kg/m2)
effect modifier, prognostic factor; 0 of 1
Sex (percent female)
effect modifier, prognostic factor; 1 of 1
Background glucose lowering therapy (stratum S0 to S4)
effect modifier, prognostic factor; 1 of 1
Asian ancestry or region (percent Asian)
effect modifier, prognostic factor; 0 of 1
Kidney function (eGFR) (mL/min/1.73 m2)
prognostic factor, effect modifier; 0 of 1
Treatment duration (weeks)
effect modifier; 1 of 1
Lifestyle co-intervention intensity (none standard intensive)
effect modifier, prognostic factor; 1 of 1
NCT03596450
S000545
not reported45.77S1not reportednot reported104.36not_reported

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.
  • FlagBaseline, Baseline BMI or body weight: not reported by 1 of 1 trials
  • FlagBaseline, Asian ancestry or region: not reported by 1 of 1 trials
  • FlagBaseline, Kidney function (eGFR): not reported by 1 of 1 trials
Comparability items per trial
Trialtime weeksanalysis setdefinitioninstrumentadjudicatedproportion methodintercurrent events (discontinuation)intercurrent events (rescue)blindingfundingstart yearEligibility
NCT03596450104.36completersnot statednot statednot statednot statedtreatment_policynot statedopen_labelindustry2018adults with type 2 diabetes on metformin, later up to 2 oral drugs, needing intensification

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
NCT03596450A1SEMA_SC_FLEX_0p25-0p5-1p0_QW104.36arm, change-5.0350.567389registry:outcomes
NCT03596450A2STANDARD_CARE104.36arm, change-3.0840.428386registry:outcomes

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