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Comparison · NCT04681170-sae

Age 5-10 Years vs Age 11-17 Years: 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. Age 5-10 Years vs Age 11-17 Years: serious adverse events. Trial comparisons, record NCT04681170-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04681170-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 10.20.08070.416wilson
Risk in group 20.3040.1560.509wilson
Risk difference, group 1 minus group 2-0.104-0.3410.158newcombe hybrid score
Risk ratio, group 1 over group 20.6570.2251.92log
Odds ratio, group 1 over group 20.5710.1392.34log
Number needed to treat, for one fewer participant with a serious adverse event on Age 5-10 Years than on Age 11-17 Years9.58from 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 1Age 5-10 YearsPatients aged 5-10 years.420EG000
Group 2Age 11-17 YearsPatients aged 11-17 years.723EG001

Harm

What it counts
Total, serious adverse events
Time frame
AEs were monitored throughout the study from the time of informed consent through Week 108.

Source ClinicalTrials.gov

Trial

Title
Efficacy and Safety of Lomitapide in Paediatric Patients With Homozygous Familial Hypercholesterolaemia (HoFH)
NCT number
NCT04681170
Phases
PHASE3
Conditions
Homozygous Familial Hypercholesterolaemia (HoFH)
Interventions
Lomitapide
Lead sponsor
Amryt Pharma
Results first posted
2025-08-27

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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