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Comparison · NCT03597464-deaths

Voclosporin vs Placebo Oral Capsule: deaths from any cause

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. Voclosporin vs Placebo Oral Capsule: deaths from any cause. Trial comparisons, record NCT03597464-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03597464-deaths

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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 1000.0321wilson
Risk in group 20.030.01030.0845wilson
Risk difference, group 1 minus group 2-0.03-0.08450.00765newcombe hybrid score
Risk ratio, group 1 over group 2loga group has no participants with the outcome
Odds ratio, group 1 over group 2loga cell of the two-by-two table is zero
Number needed to treat, for one fewer death from any cause on Voclosporin than on Placebo Oral Capsule33.3from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1VoclosporinVoclosporin~Voclosporin: Calcineurin inhibitor, oral, 23.7 mg BID0116EG000
Group 2Placebo Oral CapsulePlacebo~Placebo Oral Capsule: Voclosporin placebo, oral, 3 capsules BID3100EG001

Harm

What it counts
Total, all-cause mortality
Time frame
Treatment-emergent adverse events (TEAEs) are events occurring from Month 12 of treatment (AURORA 2 baseline) up to 30 days after study treatment end in AURORA 2 (Month 37).

Source ClinicalTrials.gov

Trial

Title
Aurinia Renal Assessments 2: Aurinia Renal Response in Lupus With Voclosporin
NCT number
NCT03597464
Phases
PHASE3
Conditions
Lupus Nephritis
Interventions
Voclosporin, Placebo Oral Capsule
Lead sponsor
Aurinia Pharmaceuticals Inc.
Results first posted
2022-12-14

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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