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Comparison · NCT02087306-sae

Pediatric vs Adult: 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. Pediatric vs Adult: serious adverse events. Trial comparisons, record NCT02087306-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02087306-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 10.7150.6330.786wilson
Risk in group 20.8170.7120.89wilson
Risk difference, group 1 minus group 2-0.102-0.2120.0253newcombe hybrid score
Risk ratio, group 1 over group 20.8760.751.02log
Odds ratio, group 1 over group 20.5630.2761.15log
Number needed to treat, for one fewer participant with a serious adverse event on Pediatric than on Adult9.85from the risk difference intervalthe interval includes no difference

Groups2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1PediatricSubjects aged 2 months to \<18 years.93130EG000
Group 2AdultSubjects aged ≥18 years5871EG001

Harm

What it counts
Total, serious adverse events
Time frame
Adverse events that started on or after the first dose of BCV up to 7 days after the last dose of BCV (through 13 weeks) are reported.

Source ClinicalTrials.gov

Trial

Title
Study to Assess the Safety and Efficacy of Brincidofovir in Treatment of Early Versus Late Adenovirus Infection
NCT number
NCT02087306
Phases
PHASE3
Conditions
Adenovirus Infection
Interventions
Brincidofovir
Lead sponsor
Jazz Pharmaceuticals
Results first posted
2021-08-13

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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