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Comparison · NCT02643862-sae

Xolair 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. Xolair vs Placebo: serious adverse events. Trial comparisons, record NCT02643862-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02643862-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 1000.0964wilson
Risk in group 200.00000000000000002780.242wilson
Risk difference, group 1 minus group 20-0.2420.0964newcombe hybrid score
Risk ratio, group 1 over group 2loga group has no participants with the outcome
Odds ratio, group 1 over group 2loga cell of the two-by-two table is zero
Number needed to harmfrom the risk difference intervalthe two groups' risks are equal

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1XolairPts will be randomized to receive xolair at a 3 active:1 placebo ratio~Xolair: Xolair is a monoclonal antibody approved by the FDA for asthma and chronic urticaria036EG000
Group 2PlaceboThis is a placebo that looks similar to Xolair and is given as a subcutaneous shot, just like Xolair~Xolair: Xolair is a monoclonal antibody approved by the FDA for asthma and chronic urticaria012EG001

Harm

What it counts
Total, serious adverse events
Time frame
AEs were collected over the entire course of the active study

Source ClinicalTrials.gov

Trial

Title
Study Using Xolair in Rush Multi Oral Immunotherapy in Multi Food Allergic Patients
NCT number
NCT02643862
Phases
PHASE1, PHASE2
Conditions
Food Allergy
Interventions
Xolair, Placebo
Lead sponsor
Stanford University
Results first posted
2017-10-25

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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