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Comparison · NCT02436668-deaths

Placebo (Plus Nab-paclitaxel and Gemcitabine) vs Ibrutinib (Plus Nab-paclitaxel and Gemcitabine): 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. Placebo (Plus Nab-paclitaxel and Gemcitabine) vs Ibrutinib (Plus Nab-paclitaxel and Gemcitabine): deaths from any cause. Trial comparisons, record NCT02436668-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02436668-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 10.8870.8370.923wilson
Risk in group 20.9090.8620.941wilson
Risk difference, group 1 minus group 2-0.0219-0.0810.0372newcombe hybrid score
Risk ratio, group 1 over group 20.9760.9151.04log
Odds ratio, group 1 over group 20.7870.4171.49log
Number needed to treat, for one fewer death from any cause on Placebo (Plus Nab-paclitaxel and Gemcitabine) than on Ibrutinib (Plus Nab-paclitaxel and Gemcitabine)45.7from the risk difference intervalthe interval includes no difference

Groups2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Placebo (Plus Nab-paclitaxel and Gemcitabine)
Placebo daily in combination with:~Nab-paclitaxel and gemcitabine~Nab-paclitaxel 125 mg/m2 and gemcitabine 1000 mg/m2 were administered on Days 1, 8, and 15 of each 28-day cycle, each as a 30- to 40-minute intravenous infusion
188212EG000
Group 2Ibrutinib (Plus Nab-paclitaxel and Gemcitabine)
Ibrutinib 560 mg (4 x 140 mg capsules) (or placebo) was administered orally once daily beginning on Day 1 of Cycle 1 of the treatment phase, with the first dose of ibrutinib given no more than 72 hours after randomization~Nab-paclitaxel 125 mg/m2 and gemcitabine 1000 mg/m2 were administered on Days 1, 8, and 15 of each 28-day cycle, each as a 30- to 40-minute intravenous infusion
189208EG001

Harm

What it counts
Total, all-cause mortality
Time frame
From first dose of study drug up to 30 days after the last dose of study drug

Source ClinicalTrials.gov

Trial

Title
Study of Ibrutinib vs Placebo, in Combination With Nab-paclitaxel and Gemcitabine, in the First Line Treatment of Patients With Metastatic Pancreatic Adenocarcinoma (RESOLVE)
NCT number
NCT02436668
Phases
PHASE3
Conditions
Metastatic Pancreatic Adenocarcinoma
Interventions
Ibrutinib, Gemcitabine, Nab-paclitaxel
Lead sponsor
Pharmacyclics LLC.
Results first posted
2020-11-16

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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