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Comparison · NCT02959983-sae

Eluxadoline 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. Eluxadoline vs Placebo: serious adverse events. Trial comparisons, record NCT02959983-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02959983-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 10.005850.001030.0324wilson
Risk in group 20.01730.005910.0497wilson
Risk difference, group 1 minus group 2-0.0115-0.04420.0174newcombe hybrid score
Risk ratio, group 1 over group 20.3370.03543.21log
Odds ratio, group 1 over group 20.3330.03433.24log
Number needed to treat, for one fewer participant with a serious adverse event on Eluxadoline than on Placebo87from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1EluxadolineEluxadoline 100 mg oral tablets twice daily (BID) with food for 12 weeks.1171EG000
Group 2PlaceboPlacebo matching eluxadoline oral tablets BID with food for 12 weeks.3173EG001

Harm

What it counts
Total, serious adverse events
Time frame
Up to 12 weeks

Source ClinicalTrials.gov

Trial

Title
Efficacy of Eluxadoline in the Treatment of Irritable Bowel Syndrome With Diarrhea in Patients With Inadequate Control of Symptoms With Prior Loperamide Use
NCT number
NCT02959983
Phases
PHASE4
Conditions
Irritable Bowel Syndrome With Diarrhea
Interventions
Eluxadoline, Placebo
Lead sponsor
Allergan
Results first posted
2019-02-15

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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