ConductScience.org, home

Comparison · NCT01924533-9e3ad3ea

Olaparib 100 mg Tablets bd + Paclitaxel 80 mg/m^2 vs Placebo Tablets bd + Paclitaxel 80 mg/m^2: Progression-Free Survival (PFS)

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

Download JSON
Cite this record

ConductScience Library. Olaparib 100 mg Tablets bd + Paclitaxel 80 mg/m^2 vs Placebo Tablets bd + Paclitaxel 80 mg/m^2: Progression-Free Survival (PFS). Trial comparisons, record NCT01924533-9e3ad3ea. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01924533-9e3ad3ea

On this page

Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.1790.1370.23wilson
Risk in group 20.1110.07820.154wilson
Risk difference, group 1 minus group 20.0680.007660.128newcombe hybrid score
Risk ratio, group 1 over group 21.611.052.48log
Odds ratio, group 1 over group 21.751.062.88log
Number needed to treat, for one more participant with the outcome on Olaparib 100 mg Tablets bd + Paclitaxel 80 mg/m^2 than on Placebo Tablets bd + Paclitaxel 80 mg/m^214.77.79131from the risk difference interval

Groups2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Olaparib 100 mg Tablets bd + Paclitaxel 80 mg/m^2Olaparib 100 mg tablets bd + Paclitaxel 80 mg/m\^247263OG000
Group 2Placebo Tablets bd + Paclitaxel 80 mg/m^2Placebo tablets bd + Paclitaxel 80 mg/m\^229262OG001

Outcome

Type
SECONDARY
Title
Progression-Free Survival (PFS)
Description
Time from randomization until the date of objective radiological disease progression according to RECIST (v1.1) or death by any cause in the absence of progression. Objective progression is defined as at least a 20% increase in the sum of the diameters of the target lesions (compared to previous minimum sum) or an overall non-target lesion assessment of progression or a new lesion.
Time frame
Scans taken at baseline and then follow up assessments taken every 8 weeks up to Week 40 and then every 16 weeks until objective disease progression as defined by RECIST 1.1, assessed up to 3 years
Population
FAS analysis set population

Source ClinicalTrials.gov

Trial

Title
Efficacy and Safety Study of Olaparib in Combination With Paclitaxel to Treat Advanced Gastric Cancer.
NCT number
NCT01924533
Phases
PHASE3
Conditions
Gastric Cancer
Interventions
Olaparib, Paclitaxel, Placebo
Lead sponsor
AstraZeneca
Results first posted
2018-11-07

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.

For software

Read this comparison from software.

The record is JSON. No key.

GET https://conductscience.org/api/comparisons/v1/NCT01924533-9e3ad3ea