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Palivizumab vs Motavizumab: Incidence of RSV Hospitalization (Includes Deaths by RSV)

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 10.01880.01470.024wilsonClinicalTrials.gov
Risk in group 20.01380.01040.0184wilsonClinicalTrials.gov
Risk difference, group 1 minus group 20.00494-0.00120.0112newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 21.360.931.98logClinicalTrials.gov
Odds ratio, group 1 over group 21.360.9292logClinicalTrials.gov
Number needed to treat, for one more participant with the outcome on Palivizumab than on Motavizumab203from 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 doses623,306OG000ClinicalTrials.gov
Group 2MotavizumabMotavizumab, 15 mg/kg administered intramuscularly for 5 monthly doses463,329OG001ClinicalTrials.gov

Outcome 5

FieldValueSource
TypePRIMARYClinicalTrials.gov
TitleIncidence of RSV Hospitalization (Includes Deaths by RSV)ClinicalTrials.gov
Description
RSV hospitalization was defined as 1) a respiratory hospitalization with a positive RSV test (primary), 2) a new onset of lower respiratory symptoms in an already hospitalized child, with an objective measure of worsening respiratory status and positive RSV test (nosocomial), or 3) death demonstrated to have been caused by RSV (by autopsy or clinical history and virologic evidence).
ClinicalTrials.gov
Time frameDays 0 - 150ClinicalTrials.gov
PopulationThe Intent-to-Treat (ITT) Population included all patients randomized into the study.ClinicalTrials.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.