LivingGLP1
Descriptive only

Death by suicide

Metabolic dysfunction associated steatotic liver disease or steatohepatitis

longest follow-upRecorded harmsDoses of a drug pooledHazard ratio (from event counts)
3
Randomized trials
3
Treatments
581
Participants
0
Events

In plain language

No network meta-analysis was fitted here. The protocol requires at least two trials forming a connected network; this outcome has 3 trials. 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.
PLACEBOSEMA_SCTIRZ_SC
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.

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.
  • NoteOutcome assessment, time point: selected time points span 55 to 79 weeks
  • NoteOutcome assessment, definition: mixed: not stated 2, severe hypoglycemia per ADA classification 1
  • NoteData handling, input conversions: arms_combined 2
Comparability items per trial
Trialtime weeksanalysis setdefinitioninstrumentadjudicatedproportion methodintercurrent events (discontinuation)intercurrent events (rescue)blindingfundingstart yearEligibility
SYNERGY-NASH56safetynot statednot statednot statednot statednot statednot stateddouble_blindindustry2019age 18 to 80, BMI 27 to 50, biopsy MASH with NAS 4 or more and fibrosis F2 to F3, HbA1c up to 9.5 percent
NCT0297094279safetynot statednot statednot statednot statednot statednot stateddouble_blindindustry2016age 18 to 75; biopsy NASH F1 to F3; NAS 4 or more; BMI above 25; HbA1c 10 percent or less
NCT0398745155safetysevere hypoglycemia per ADA classificationnot statednot statednot statednot statednot stateddouble_blindindustry2019age 18 to 75; biopsy NASH with F4 compensated cirrhosis; NAS 3 or more; BMI 27 or more

Trial data

What each trial contributes. Arm rows give the arm value with its standard error, or events over participants; contrast rows give the hazard ratio (from event counts) on the analysis scale (log) against the trial's first row. Flags mark converted, combined or approximated inputs.
Trial data entering this analysis
TrialArmTreatmentWeekDataValueSEEvents / NFlagsSource
SYNERGY-NASHA1+A2+A3TIRZ_SC56arm, events0 / 142arms_combinedregistry:adverse_events
SYNERGY-NASHA4PLACEBO56arm, events0 / 48registry:adverse_events
NCT02970942A1+A2+A3SEMA_SC79arm, events0 / 240arms_combinedregistry:adverse_events
NCT02970942A4PLACEBO79arm, events0 / 80registry:adverse_events
NCT03987451A1SEMA_SC55arm, events0 / 47R0017043:Results
NCT03987451A2PLACEBO55arm, events0 / 24R0017043:Results

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