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Comparison · NCT03828539-8666501b

Erenumab vs Topiramate: Number of Patients With at Least 50% Reduction From Baseline in Monthly Migraine Days (MMD) Over the Last Three Months (Month 4, 5, and 6)

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. Erenumab vs Topiramate: Number of Patients With at Least 50% Reduction From Baseline in Monthly Migraine Days (MMD) Over the Last Three Months (Month 4, 5, and 6). Trial comparisons, record NCT03828539-8666501b. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03828539-8666501b

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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 10.5540.5040.603wilson
Risk in group 20.3120.2680.36wilson
Risk difference, group 1 minus group 20.2420.1730.308newcombe hybrid score
Risk ratio, group 1 over group 21.781.52.11log
Odds ratio, group 1 over group 22.742.043.68log
Number needed to treat, for one more participant with the outcome on Erenumab than on Topiramate4.133.255.77from the risk difference interval

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 Erenumab215388OG000
Group 2TopiramateTopiramate in the highest tolerated dose (50 - 100 mg/day)121388OG001

Outcome

Type
SECONDARY
Title
Number of Patients With at Least 50% Reduction From Baseline in Monthly Migraine Days (MMD) Over the Last Three Months (Month 4, 5, and 6)
Description
The secondary objective of this study was to evaluate the effect of erenumab compared to topiramate on the proportion of patients with at least 50% reduction from baseline in MMDs. The Baseline period was defined as the period between Week -4 and the day prior to first dose. This was analyzed by logistic regression over the last 3 months (months 4, 5, and 6) of treatment. All the subjects' data collected regarding 50% response in MMD was used in the analysis regardless of whether subjects discontinue study treatment or not. Subjects with missing response information on this endpoint were imputed as non-response (non-responder imputation).
Time frame
Baseline, Last three months (month 4, 5, and 6)
Population
Full Analysis Set (FAS)

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.

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