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Comparison · NCT02586155-59a8daa2

High-Intensity Statin Therapy+RVX000222 vs High-Intensity Statin Therapy+Placebo: Incidence of All-cause Mortality

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. High-Intensity Statin Therapy+RVX000222 vs High-Intensity Statin Therapy+Placebo: Incidence of All-cause Mortality. Trial comparisons, record NCT02586155-59a8daa2. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02586155-59a8daa2

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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 10.05030.03940.0641wilson
Risk in group 20.05970.04760.0745wilson
Risk difference, group 1 minus group 2-0.00932-0.02770.00897newcombe hybrid score
Risk ratio, group 1 over group 20.8440.6061.18log
Odds ratio, group 1 over group 20.8350.5881.19log
Number needed to treat, for one fewer participant with the outcome on High-Intensity Statin Therapy+RVX000222 than on High-Intensity Statin Therapy+Placebo107from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1High-Intensity Statin Therapy+RVX000222Daily dose 100 mg capsule b.i.d. with high-intensity statin therapy (atorvastatin or rosuvastatin)~Apabetalone: 100 mg capsule~Atorvastatin: High-Intensity Statin~Rosuvastatin: High-Intensity Statin611,212OG000
Group 2High-Intensity Statin Therapy+Placebo
Placebo (for RVX000222 100 mg capsule) b.i.d. with high-intensity statin therapy (atorvastatin or rosuvastatin)~Placebo: Capsule manufactured to mimic RVX000222 100 mg capsule~Atorvastatin: High-Intensity Statin~Rosuvastatin: High-Intensity Statin
721,207OG001

Outcome

Type
SECONDARY
Title
Incidence of All-cause Mortality
Description
Time frame
120 weeks
Population

Source ClinicalTrials.gov

Trial

Title
Effect of RVX000222 on Time to Major Adverse Cardiovascular Events in High-Risk T2DM Subjects With CAD
NCT number
NCT02586155
Phases
PHASE3
Conditions
Diabetes Mellitus, Type 2, Coronary Artery Disease
Interventions
Apabetalone, Placebo, Atorvastatin, Rosuvastatin
Lead sponsor
Resverlogix Corp
Results first posted
2021-08-20

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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