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Comparison · NCT01716715-sae

Cabozantinib vs Paclitaxel: serious adverse events

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. Cabozantinib vs Paclitaxel: serious adverse events. Trial comparisons, record NCT01716715-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01716715-sae

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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 10.4550.330.585wilson
Risk in group 20.160.08340.285wilson
Risk difference, group 1 minus group 20.2950.1180.446newcombe hybrid score
Risk ratio, group 1 over group 22.841.415.71log
Odds ratio, group 1 over group 24.381.7411log
Number needed to harm, for one more participant with a serious adverse event on Cabozantinib than on Paclitaxel3.42.248.46from 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 1CabozantinibCabozantinib 60 mg oral daily continously2555EG000
Group 2PaclitaxelPaclitaxel 80mg/m2 administered weekly on days 1, 8 and 15850EG001

Harm

What it counts
Total, serious adverse events
Time frame
During study treatment through 30 days after treatment ends, an average of 2.5 years.

Source ClinicalTrials.gov

Trial

Title
Cabozantinib or Paclitaxel in Treating Patients With Persistent or Recurrent Epithelial Ovarian, Fallopian Tube, or Primary Peritoneal Cavity Cancer
NCT number
NCT01716715
Phases
PHASE2
Conditions
Recurrent Fallopian Tube Carcinoma, Recurrent Ovarian Carcinoma, Recurrent Primary Peritoneal Carcinoma
Interventions
Cabozantinib S-malate, Laboratory Biomarker Analysis, Paclitaxel
Lead sponsor
National Cancer Institute (NCI)
Results first posted
2020-03-10

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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