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Palivizumab vs Motavizumab: serious adverse events

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

Measures 6

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

MeasureValue95% interval, lower95% interval, upperMethodNoteSource
Risk in group 10.1530.1420.166wilsonClinicalTrials.gov
Risk in group 20.1460.1350.159wilsonClinicalTrials.gov
Risk difference, group 1 minus group 20.00712-0.01010.0243newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 21.050.9351.18logClinicalTrials.gov
Odds ratio, group 1 over group 21.060.9241.21logClinicalTrials.gov
Number needed to harm, for one more participant with a serious adverse event on Palivizumab than on Motavizumab140from the risk difference intervalthe interval includes no differenceClinicalTrials.gov

Groups 2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1PalivizumabPalivizumab, 15 mg/kg administered intramuscularly for 5 monthly doses5063,298EG000ClinicalTrials.gov
Group 2MotavizumabMotavizumab, 15 mg/kg administered intramuscularly for 5 monthly doses4853,315EG001ClinicalTrials.gov

Harm 2

FieldValueSource
What it countsTotal, serious adverse eventsClinicalTrials.gov
Time frameDay 0 - Day 150ClinicalTrials.gov

Trial 8

FieldValueSource
TitleStudy of MEDI-524 (Motavizumab) for the Prophylaxis of Serious Respiratory Syncytial Virus (RSV) Disease in High-Risk ChildrenClinicalTrials.gov
NCT numberNCT00129766ClinicalTrials.gov
PhasesPHASE3ClinicalTrials.gov
ConditionsRespiratory Syncytial Virus InfectionsClinicalTrials.gov
Interventionsmotavizumab (MEDI-524), palivizumabClinicalTrials.gov
Lead sponsorMedImmune LLCClinicalTrials.gov
Results first posted2013-08-28ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT00129766?tab=resultsClinicalTrials.gov

Source 4

FieldValueSource
Releasetrial-comparisons-2026-03-23-0.1.0ClinicalTrials.gov
Release manifest SHA-256f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57ClinicalTrials.gov
AACT copy2026-03-23ClinicalTrials.gov
Tables readoutcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquetClinicalTrials.gov

The same record as JSON

Release trial-comparisons-2026-03-23-0.1.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.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.

ClinicalTrials.gov: none 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.