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Comparison · NCT03597464-sae

Voclosporin vs Placebo Oral Capsule: 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. Voclosporin vs Placebo Oral Capsule: serious adverse events. Trial comparisons, record NCT03597464-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03597464-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 10.1810.1220.261wilson
Risk in group 20.230.1580.322wilson
Risk difference, group 1 minus group 2-0.049-0.1580.0583newcombe hybrid score
Risk ratio, group 1 over group 20.7870.4641.33log
Odds ratio, group 1 over group 20.740.3811.44log
Number needed to treat, for one fewer participant with a serious adverse event on Voclosporin than on Placebo Oral Capsule20.4from 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 BID21116EG000
Group 2Placebo Oral CapsulePlacebo~Placebo Oral Capsule: Voclosporin placebo, oral, 3 capsules BID23100EG001

Harm

What it counts
Total, serious adverse events
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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