ConductScience.org, home

Comparison · NCT03828539-sae

Erenumab vs Topiramate: serious adverse events

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

Download JSON
Cite this record

ConductScience Library. Erenumab vs Topiramate: serious adverse events. Trial comparisons, record NCT03828539-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03828539-sae

On this page

Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.02580.01410.0468wilson
Risk in group 20.0490.03160.0752wilson
Risk difference, group 1 minus group 2-0.0232-0.05190.00408newcombe hybrid score
Risk ratio, group 1 over group 20.5260.2481.12log
Odds ratio, group 1 over group 20.5140.2361.12log
Number needed to treat, for one fewer participant with a serious adverse event on Erenumab than on Topiramate43.1from 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 1Erenumab70 mg and 140 mg Erenumab10388EG000
Group 2TopiramateTopiramate in the highest tolerated dose (50 - 100 mg/day)19388EG001

Harm

What it counts
Total, serious adverse events
Time frame
Adverse events were collected from first dose of study treatment until 8 weeks after the last Investigational Medicinal product (IMP) injection, assessed up to approximately 33 weeks (treatment duration ranged from 4.0 to 25.1 weeks).

Source ClinicalTrials.gov

Trial

Title
Head-to-head Study of Erenumab Against Topiramate in Patients With Episodic and Chronic Migraine
NCT number
NCT03828539
Phases
PHASE4
Conditions
Migraine
Interventions
Erenumab, Topiramate, Erenumab matching placebo, Topiramate matching placebo
Lead sponsor
Novartis Pharmaceuticals
Results first posted
2021-08-09

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.

For software

Read this comparison from software.

The record is JSON. No key.

GET https://conductscience.org/api/comparisons/v1/NCT03828539-sae