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Comparison · NCT02988115-sae

Bempedoic Acid 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. Bempedoic Acid vs Placebo: serious adverse events. Trial comparisons, record NCT02988115-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02988115-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 10.05980.0360.0979wilson
Risk in group 20.0360.01410.089wilson
Risk difference, group 1 minus group 20.0238-0.03430.0677newcombe hybrid score
Risk ratio, group 1 over group 21.660.5594.93log
Odds ratio, group 1 over group 21.70.5475.3log
Number needed to harm, for one more participant with a serious adverse event on Bempedoic Acid than on Placebo42from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Bempedoic AcidParticipants received bempedoic acid 180 milligram (mg) tablet taken orally once a day.14234EG000
Group 2PlaceboParticipants received matching oral placebo once a day.4111EG001

Harm

What it counts
Total, serious adverse events
Time frame
Up to 24 weeks plus 30 days

Source ClinicalTrials.gov

Trial

Title
Evaluation of the Efficacy and Safety of Bempedoic Acid (ETC-1002) in Patients With Hyperlipidemia and Statin Intolerant
NCT number
NCT02988115
Phases
PHASE3
Conditions
Hypercholesterolemia, Atherosclerotic Cardiovascular Disease, Statin Adverse Reaction
Interventions
bempedoic acid, placebo
Lead sponsor
Esperion Therapeutics, Inc.
Results first posted
2020-04-03

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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