LivingGLP1
Descriptive only

Medullary thyroid carcinoma

Overweight or obesity without diabetes (adults)

longest follow-upRecorded harmsDoses of a drug pooledHazard ratio (from event counts)
5
Randomized trials
5
Treatments
1,515
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 5 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.
EFPE_SCLIRA_SCMAZD_SCPLACEBOTIRZ_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 26 to 76 weeks
  • NoteOutcome assessment, definition: mixed: deaths 1, not stated 4
  • NoteData handling, input conversions: arms_combined 3
Comparability items per trial
Trialfundingtime weeksanalysis setdefinitioninstrumentadjudicatedproportion methodintercurrent events (discontinuation)intercurrent events (rescue)blindingstart yearEligibility
SURMOUNT-3industry76safetynot statednot statednot statednot statednot statednot stateddouble_blind2021age 18 or older; BMI 30 or more, or 27 or more with comorbidity; no diabetes; at least 5 percent loss in lead in
NCT02075281industry26safetynot statednot statednot statednot statednot statednot stateddouble_blind2014age 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
NCT04904913industry36safetynot statednot statednot statednot statednot statednot stateddouble_blind2021Chinese adults 18 to 75; BMI 28 or more, or 24 or more with comorbidity or hyperphagia; no diabetes, HbA1c below 6.5
NCT05623839industry27safetynot statednot statednot statednot statednot statednot stateddouble_blind2022age 18 to 70; BMI 27 to 50; HbA1c below 6.5 percent; no diabetes
NCT01557166industry34safetydeathsnot statednot statednot statednot statednot stateddouble_blind2012age 18 to 64; BMI 30 or more; AHI 15 or more; no diabetes; unable or unwilling to use CPAP

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
NCT02075281A1PLACEBO26arm, events0 / 60R0011218:Results
NCT02075281A2+A3+A4+A5EFPE_SC26arm, events0 / 237arms_combinedR0011218:Results
NCT04904913A1+A2+A3MAZD_SC36arm, events0 / 186arms_combinedR0016107:Results
NCT04904913A4PLACEBO36arm, events0 / 62R0016107:Results
NCT05623839A1PLACEBO27arm, events0 / 8R0013210:Supplement Table S2
NCT05623839A2+A3MAZD_SC27arm, events0 / 24arms_combinedR0013210:Supplement Table S2
SURMOUNT-3A1TIRZ_SC76arm, events0 / 287R0007405:Results
SURMOUNT-3A2PLACEBO76arm, events0 / 292R0007405:Results
NCT01557166A1LIRA_SC34arm, events0 / 180R0026203:Results
NCT01557166A2PLACEBO34arm, events0 / 179R0026203:Results

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