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Comparison · NCT02032823-9b419860

Olaparib vs Placebo: Invasive Disease Free Survival (IDFS)

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. Olaparib vs Placebo: Invasive Disease Free Survival (IDFS). Trial comparisons, record NCT02032823-9b419860. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02032823-9b419860

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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 10.1150.09610.137wilson
Risk in group 20.1950.170.221wilson
Risk difference, group 1 minus group 2-0.0794-0.112-0.0465newcombe hybrid score
Risk ratio, group 1 over group 20.5920.4740.739log
Odds ratio, group 1 over group 20.5390.4150.699log
Number needed to treat, for one fewer participant with the outcome on Olaparib than on Placebo12.68.921.5from the risk difference interval

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1OlaparibOlaparib tablets 300mg taken orally twice daily.106921OG000
Group 2PlaceboPlacebo tablets taken orally twice daily.178915OG001

Outcome

Type
PRIMARY
Title
Invasive Disease Free Survival (IDFS)
Description
An IDFS event is defined as the first occurrence of loco-regional or distant recurrence or new cancer or death from any cause.
Time frame
From date of randomisation to data cut off: 27 March 2020 (approximately 5 years 11 months)
Population
Full Analysis Set (FAS)

Source ClinicalTrials.gov

Trial

Title
Olaparib as Adjuvant Treatment in Patients With Germline BRCA Mutated High Risk HER2 Negative Primary Breast Cancer
NCT number
NCT02032823
Phases
PHASE3
Conditions
Breast Cancer
Interventions
Olaparib, Placebo
Lead sponsor
AstraZeneca
Results first posted
2021-12-08

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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