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Comparison · NCT03126227-deaths

AR101 Powder Provided in Capsules vs Placebo Powder: deaths from any cause

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. AR101 Powder Provided in Capsules vs Placebo Powder: deaths from any cause. Trial comparisons, record NCT03126227-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03126227-deaths

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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 100.0000000000000000008670.0113wilson
Risk in group 20.005950.001050.0329wilson
Risk difference, group 1 minus group 2-0.00595-0.03290.00634newcombe 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 treat, for one fewer death from any cause on AR101 Powder Provided in Capsules than on Placebo Powder168from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1AR101 Powder Provided in CapsulesStudy product formulated to contain peanut protein at different dosage strengths for use as defined in the protocol~AR101: AR101 powder provided in capsules0337EG000
Group 2Placebo PowderPlacebo formulation in pull-apart capsules containing only excipients color-matched to AR101 study product.~Placebo: Placebo powder provided in capsules1168EG001

Harm

What it counts
Total, all-cause mortality
Time frame
Approximately 6 months

Source ClinicalTrials.gov

Trial

Title
Real-World AR101 Market-Supporting Experience Study in Peanut-Allergic Children (RAMSES)
NCT number
NCT03126227
Phases
PHASE3
Conditions
Peanut Allergy
Interventions
AR101, Placebo
Lead sponsor
Aimmune Therapeutics, Inc.
Results first posted
2021-11-02

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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