LivingGLP1
Descriptive only

Death by suicide

Overweight or obesity without diabetes (adults)

longest follow-upRecorded harmsDoses of a drug pooledHazard ratio (from event counts)
17
Randomized trials
15
Treatments
6,155
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 17 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.
BOFANG_SCDAPIGL_SCEFPE_SCEXENER_SCHRS7535_POLIFESTYLELIRA_SCLOTI_POPLACEBORETA_SCSEMA_SCSITAGLIPTINSTANDARD_CARETIRZ_SCVCT220_PO
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 14 to 76 weeks
  • NoteOutcome assessment, analysis set: mixed: randomized 3, randomized;safety 1, safety 13
  • NoteOutcome assessment, definition: mixed: C-SSRS post baseline category 1, deaths 1, not stated 15
  • NoteOutcome assessment, intercurrent events (discontinuation): mixed: not stated 16, while_on_treatment 1
  • NoteOutcome assessment, intercurrent events (rescue): mixed: not stated 16, treatment_policy 1
  • NoteRisk of bias, blinding: mixed: double_blind 15, open_label 1, single_blind 1
  • NoteRisk of bias, funding: mixed: industry 16, mixed 1
  • NoteData handling, input conversions: arms_combined 7, printed_denominator 2
Comparability items per trial
Trialtime weeksanalysis setdefinitioninstrumentadjudicatedproportion methodintercurrent events (discontinuation)intercurrent events (rescue)blindingfundingstart yearEligibility
NCT0408133722randomized;safetynot statednot statednot statednot statednot statednot stateddouble_blindindustry2020age 18 to 60; BMI 30 to 45; no diabetes; at least one metabolic impairment
SURMOUNT-572safetynot statednot statednot statednot statednot statednot statedopen_labelindustry2023adults; BMI 30 or more, or 27 with complication; no diabetes
STEP 175safetynot statednot statednot statednot statedwhile_on_treatmenttreatment_policydouble_blindindustry2018adults; BMI 30 or more, or 27 or more with a weight related condition; no diabetes; HbA1c below 6.5 percent
NCT0557997728safetyC-SSRS post baseline categorynot statednot statednot statednot statednot stateddouble_blindindustry2022age 18 to 75; T2D cohort on metformin, HbA1c 7.0 to 10.0, BMI 23 or more; obesity cohort BMI 30 or more without diabetes
NCT0207528126randomizednot statednot statednot statednot statednot statednot stateddouble_blindindustry2014age 18 to 64 years; BMI 30 to 42, or 27 to 30 with comorbidity; FPG below 7 mmol/L; HbA1c 6.5 percent or less; no diabetes
Dapalost24safetynot statednot statednot statednot statednot statednot stateddouble_blindindustry2014age 18 to 70; BMI 30 to 45 kg/m2; no diabetes
STABLE Wt Loss60randomizednot statednot statednot statednot statednot statednot stateddouble_blindindustry2022age 18 to 70; BMI 30 or more, or 27 or more with comorbidity; no diabetes; HbA1c 6.5 percent or less
NCT0310193014safetynot statednot statednot statednot statednot statednot stateddouble_blindmixed2017age 18 to 65; BMI >=30 kg/m2; prediabetes by ADA criteria; no diabetes
NCT0488176052safetynot statednot statednot statednot statednot statednot stateddouble_blindindustry202118 to 75 years; BMI 30 or more, or 27 to less than 30 with weight related complication; no type 2 diabetes
TOGETHER-PsA36safetynot statednot statednot statednot statednot statednot statedsingle_blindindustry2024age 18 to 80; active psoriatic arthritis; BMI 30 or more, or 27 to 30 with a weight related comorbidity
DREAM16randomizednot statednot statednot statednot statednot statednot stateddouble_blindindustry2023age 18 to 75; BMI 30 or more; no diabetes, HbA1c below 48 mmol/mol
SURMOUNT-376safetynot statednot statednot statednot statednot statednot stateddouble_blindindustry2021age 18 or older; BMI 30 or more, or 27 or more with comorbidity; no diabetes; at least 5 percent loss in lead in
NCT0625094636safetynot statednot statednot statednot statednot statednot stateddouble_blindindustry2024age 18 to 65; BMI 28 to 40; no diabetes, HbA1c below 6.5 percent
NCT0155716634safetydeathsnot statednot statednot statednot statednot stateddouble_blindindustry2012age 18 to 64; BMI 30 or more; AHI 15 or more; no diabetes; unable or unwilling to use CPAP
NCT0656935518safetynot statednot statednot statednot statednot statednot stateddouble_blindindustry2023age 18 to 75; BMI 28 or more, or 24 to 28 with comorbidity; no diabetes
NCT0625656233safetynot statednot statednot statednot statednot statednot stateddouble_blindindustry2023age 18 to 75; BMI 24 to <28 kg/m2 with comorbidity or 28 or more (Chinese criteria); no diabetes
S00301752.14safetynot statednot statednot statednot statednot statednot stateddouble_blindindustry2019age 20 to 65; BMI above 35; 12 to 36 months after bariatric surgery with suboptimal stable weight loss or regain

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
NCT04081337A1PLACEBO22arm, events0 / 28R0004227:Supplement Table S1
NCT04081337A2TIRZ_SC22arm, events0 / 27registry:adverse_events
SURMOUNT-5A1TIRZ_SC72arm, events0 / 375registry:adverse_events
SURMOUNT-5A2SEMA_SC72arm, events0 / 376registry:adverse_events
STEP 1A1SEMA_SC75arm, events0 / 1,306R0023399:Table 3
STEP 1A2PLACEBO75arm, events0 / 655R0023399:Table 3
NCT05579977A10+A11+A12+A13+A9LOTI_PO28arm, events0 / 325arms_combinedregistry:outcomes
NCT05579977A8PLACEBO28arm, events0 / 64registry:outcomes
NCT02075281A1PLACEBO26arm, events0 / 60R0011218:Figure S2
NCT02075281A2+A3+A4+A5EFPE_SC26arm, events0 / 237arms_combinedR0011218:Figure S2
DapalostA1EXENER_SC24arm, events0 / 25R0025627:Table 3
DapalostA2PLACEBO24arm, events0 / 25R0025627:Table 3
STABLE Wt LossA1SEMA_SC60arm, events0 / 72R0013679:Table 4
STABLE Wt LossA2PLACEBO60arm, events0 / 48R0013679:Table 4
NCT03101930A1LIRA_SC14arm, events0 / 46registry:adverse_events
NCT03101930A2SITAGLIPTIN14arm, events0 / 23registry:adverse_events
NCT03101930A3LIFESTYLE14arm, events0 / 24registry:adverse_events
NCT04881760A1PLACEBO52arm, events0 / 70registry:adverse_events
NCT04881760A2+A3+A5+A6+A7RETA_SC52arm, events0 / 234arms_combinedregistry:adverse_events
TOGETHER-PsAA1STANDARD_CARE36arm, events0 / 132printed_denominatorR0018951:Table 3
TOGETHER-PsAA2TIRZ_SC36arm, events0 / 138printed_denominatorR0018951:Table 3
DREAMA1PLACEBO16arm, events0 / 18R0011013:Table 3
DREAMA2+A3DAPIGL_SC16arm, events0 / 36arms_combinedR0011013:Table 3
SURMOUNT-3A1TIRZ_SC76arm, events0 / 287R0007405:Results
SURMOUNT-3A2PLACEBO76arm, events0 / 292R0007405:Results
NCT06250946A1PLACEBO36arm, events0 / 46R0001289:Table 6
NCT06250946A2+A3+A4+A5HRS7535_PO36arm, events0 / 189arms_combinedR0001289:Table 6
NCT01557166A1LIRA_SC34arm, events0 / 180R0026203:Results
NCT01557166A2PLACEBO34arm, events0 / 179R0026203:Results
NCT06569355A1+A2+A3+A4VCT220_PO18arm, events0 / 189arms_combinedR0001121:Results
NCT06569355A5PLACEBO18arm, events0 / 61R0001121:Results
NCT06256562A1+A2+A3+A4+A5BOFANG_SC33arm, events0 / 274arms_combinedR0002409:Table 3
NCT06256562A6PLACEBO33arm, events0 / 66R0002409:Table 3
S003017A1LIRA_SC52.14arm, events0 / 24R0016758:Discussion
S003017A2PLACEBO52.14arm, events0 / 24R0016758:Discussion

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