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Comparison · NCT02230670-sae

IDN-6556 (Baseline-Month 3) vs Placebo (Baseline-Month 3): 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. IDN-6556 (Baseline-Month 3) vs Placebo (Baseline-Month 3): serious adverse events. Trial comparisons, record NCT02230670-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02230670-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 10.1360.0640.267wilson
Risk in group 20.1190.05190.25wilson
Risk difference, group 1 minus group 20.0173-0.1320.164newcombe hybrid score
Risk ratio, group 1 over group 21.150.3783.47log
Odds ratio, group 1 over group 21.170.3284.16log
Number needed to harm, for one more participant with a serious adverse event on IDN-6556 (Baseline-Month 3) than on Placebo (Baseline-Month 3)57.8from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1IDN-6556 (Baseline-Month 3)25 mg BID of IDN-6556 (Baseline-Month 3).644EG000
Group 2Placebo (Baseline-Month 3)Placebo BID (Baseline-Month 3)542EG001

Harm

What it counts
Total, serious adverse events
Time frame
Adverse events were collected in a blinded fashion from baseline to Month 3. Double-blind adverse events are presented here

Source ClinicalTrials.gov

Trial

Title
A Study of IDN-6556 in Subjects With Liver Cirrhosis
NCT number
NCT02230670
Phases
PHASE2
Conditions
Liver Cirrhosis, Hepatic Cirrhosis
Interventions
IDN-6556, Placebo
Lead sponsor
Conatus Pharmaceuticals Inc.
Results first posted
2017-07-05

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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