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Comparison · NCT04657016-sae

Tirzepatide vs Placebo: serious adverse events

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Tirzepatide vs Placebo: serious adverse events. Trial comparisons, record NCT04657016-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04657016-sae

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.05920.03730.0928wilson
Risk in group 20.04790.02880.0789wilson
Risk difference, group 1 minus group 20.0113-0.02660.0499newcombe hybrid score
Risk ratio, group 1 over group 21.240.6212.46log
Odds ratio, group 1 over group 21.250.6042.59log
Number needed to harm, for one more participant with a serious adverse event on Tirzepatide than on Placebo88.6from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1TirzepatideParticipants received weekly doses of tirzepatide SC for 72 weeks, starting at 2.5 mg for 4 weeks. Subsequently, the dose was increased by 2.5 mg every 4 weeks up to the MTD of either 10 mg or 15 mg.17287EG001
Group 2PlaceboParticipants received matching placebo SC once weekly QW.14292EG000

Harm

What it counts
Total, serious adverse events
Time frame
Baseline up to week 76

Source ClinicalTrials.gov

Trial

Title
A Study of Tirzepatide (LY3298176) In Participants After A Lifestyle Weight Loss Program
NCT number
NCT04657016
Phases
PHASE3
Conditions
Obesity, Overweight
Interventions
Tirzepatide, Placebo
Lead sponsor
Eli Lilly and Company
Results first posted
2024-05-16

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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