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Comparison · NCT02610140-deaths

Anetumab Ravtansine (BAY94-9343) vs Vinorelbine: 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. Anetumab Ravtansine (BAY94-9343) vs Vinorelbine: deaths from any cause. Trial comparisons, record NCT02610140-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02610140-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 10.7730.7030.831wilson
Risk in group 20.7640.6540.847wilson
Risk difference, group 1 minus group 20.00912-0.09970.133newcombe hybrid score
Risk ratio, group 1 over group 21.010.8681.18log
Odds ratio, group 1 over group 21.050.5462.03log
Number needed to harm, for one more death from any cause on Anetumab Ravtansine (BAY94-9343) than on Vinorelbine110from 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 1Anetumab Ravtansine (BAY94-9343)Test drug: 6.5 mg/kg every 3 weeks; Intravenous (IV) infusion over 1 hour126163EG000
Group 2VinorelbineActive comparator: 30 mg/m\^2 once weekly5572EG001

Harm

What it counts
Total, all-cause mortality
Time frame
Up to approx. 55 months (data cut-off: 02-Jul-2019) - Time from randomization until 30 days after last treatment (general AEs), or further until death from any cause (selected AEs).

Source ClinicalTrials.gov

Trial

Title
Phase II Anetumab Ravtansine as 2nd Line Treatment for Malignant Pleural Mesothelioma (MPM)
NCT number
NCT02610140
Phases
PHASE2
Conditions
Mesothelioma
Interventions
Anetumab ravtansine (BAY94-9343), Vinorelbine
Lead sponsor
Bayer
Results first posted
2020-07-17

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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