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Comparison · NCT01227928-sae

Pazopanib 800 Milligrams vs Placebo: 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. Pazopanib 800 Milligrams vs Placebo: serious adverse events. Trial comparisons, record NCT01227928-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01227928-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 10.09720.04790.187wilson
Risk in group 20.05560.02180.134wilson
Risk difference, group 1 minus group 20.0417-0.05130.138newcombe hybrid score
Risk ratio, group 1 over group 21.750.5355.72log
Odds ratio, group 1 over group 21.830.5126.55log
Number needed to harm, for one more participant with a serious adverse event on Pazopanib 800 Milligrams than on Placebo24from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Pazopanib 800 MilligramsParticipants received pazopanib 800 milligrams administered orally once daily for up to 24 months.772EG001
Group 2PlaceboParticipants received matching placebo administered orally once daily for up to 24 months.472EG000

Harm

What it counts
Total, serious adverse events
Time frame

Source ClinicalTrials.gov

Trial

Title
Efficacy and Safety of Pazopanib Monotherapy After First-line Chemotherapy in Ovarian, Fallopian Tube, or Primary Peritoneal Cancer in Asian Women
NCT number
NCT01227928
Phases
PHASE2
Conditions
Neoplasms, Ovarian
Interventions
Pazopanib, Placebo comparator
Lead sponsor
GlaxoSmithKline
Results first posted
2013-06-04

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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