Evidence map›Paper›PMID 39248147›Full record

ArticleHeadache2025

Changes in use of acute and preventive medications for migraine after erenumab initiation over 12 months: A United States retrospective cohort study.

Jasjit K Multani, Robert Urman, Andrew S Park, Karminder Gill, Fiston Vuvu, Kainan Sun, Leah B Patel, Karen M Stockl, Kevin Hawkins, Christopher Rhyne and 1 more

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Article in Headache, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Jasjit K MultaniIQVIA, Falls Church, Virginia, USA.
Robert UrmanAmgen Inc., Thousand Oaks, California, USA.
Andrew S ParkAmgen Inc., Thousand Oaks, California, USA.
Karminder GillAmgen Inc., Thousand Oaks, California, USA.
Fiston VuvuAmgen Inc., Thousand Oaks, California, USA.
Kainan SunIQVIA, Falls Church, Virginia, USA.
Leah B PatelAmgen Inc., Thousand Oaks, California, USA.
Karen M StocklIQVIA, Falls Church, Virginia, USA.
Kevin HawkinsIQVIA, Falls Church, Virginia, USA.
Christopher RhyneDiamond Headache Clinic, Chicago, Illinois, USA.
Mark E BensinkBenofit Consulting, Brisbane, Queensland, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo assess changes in real-world use of acute and preventive medications for migraine over a 12-month follow-up period in the United States following initiation of the anti-calcitonin gene-related peptide (CGRP) pathway monoclonal antibody (mAb) erenumab.

backgroundEarly assessments of real-world use of acute and preventive medications for migraine after initiation of erenumab have been limited to 6 months of follow-up.

methodsThis retrospective cohort study used data from the IQVIA open-source longitudinal prescription (LRx) and medical (Dx) claims databases. Adult patients with an initial claim (index date) for erenumab between May 2018 and April 2020 were identified.

resultsAmong 201,176 patients who met inclusion criteria, the mean (standard deviation [SD]) age was 47.5 (13.8) years and 85.6% (n = 172,153) were female. Most patients used one or more acute (88.4%; n = 177,795) and one or more traditional preventive (86.1%; n = 173,225) medications during the 12-month pre-index period. Adherence to erenumab (proportion of days covered [PDC] ≥0.80) was 40.2% (n = 80,927) with an overall mean (SD) PDC of 0.60 (0.34). Among all patients, 70.0% (n = 140,809) discontinued erenumab. After accounting for 24.7% (n = 49,720) of patients who restarted erenumab, discontinuation without reinitiation was observed in 45.3% (n = 91,089) of total patients. Switching to a different anti-CGRP pathway mAb was observed in 13.1% (n = 26,446) of total patients. Among 177,795 patients with pre-index use of one or more acute migraine medication class, 86.5% (n = 153,788) had post-index use of the same class, and 56.7% (87,134/153,788) of them discontinued one or more class of acute medication in the 12-month follow-up period. Similarly, among 173,225 patients with pre-index use of one or more traditional migraine preventive medication class, 67.7% (n = 117,274) had post-index use of the same class, and 46.7% (54,790/117,274) of them discontinued one or more class of traditional preventive medication in the 12-month follow-up period.

conclusionsIn this long-term study, we observed the discontinuation of both acute and preventive medications for migraine post-erenumab initiation.

Indexed as

Antibodies, Monoclonal, HumanizedCalcitonin Gene-Related Peptide Receptor AntagonistsMigraine DisordersAdultFemaleFollow-Up StudiesHumansMaleMiddle AgedRetrospective StudiesUnited StatesAntibodies, Monoclonal, HumanizedCalcitonin Gene-Related Peptide Receptor Antagonistserenumabadherenceerenumabmigrainepreventive treatmentreal‐world

Identifiers

PMID39248147
PMCPMC11726006

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.