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Comparison · NCT01968213-deaths

Rucaparib 600 mg Tablets vs Placebo Tablets: 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. Rucaparib 600 mg Tablets vs Placebo Tablets: deaths from any cause. Trial comparisons, record NCT01968213-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01968213-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 10.02420.01280.0453wilson
Risk in group 20.01060.002910.0378wilson
Risk difference, group 1 minus group 20.0136-0.01590.0361newcombe hybrid score
Risk ratio, group 1 over group 22.290.49910.5log
Odds ratio, group 1 over group 22.320.49610.8log
Number needed to harm, for one more death from any cause on Rucaparib 600 mg Tablets than on Placebo Tablets73.5from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Rucaparib 600 mg TabletsTaken orally twice daily (continuous 28 day treatment cycles)9372EG000
Group 2Placebo TabletsTaken orally twice daily (continuous 28 day treatment cycles)2189EG001

Harm

What it counts
Total, all-cause mortality
Time frame
Adverse events were reported from the date of first dose of study drug and until 28 days after last dose of study drug, approximately 8.2 years.

Source ClinicalTrials.gov

Trial

Title
Phase 3 Study of Rucaparib as Switch Maintenance After Platinum in Relapsed High Grade Serous or Endometrioid Ovarian Cancer (ARIEL3)
NCT number
NCT01968213
Phases
PHASE3
Conditions
Ovarian Cancer, Fallopian Tube Cancer, Peritoneal Cancer
Interventions
Rucaparib, Placebo
Lead sponsor
pharmaand GmbH
Results first posted
2018-08-03

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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