Evidence map›Paper›PMID 41834318›Full record

Trial reportEuropean journal of neurology2026

Long-Term Improvements Following Initial Migraine Response in Eptinezumab-Treated Participants With Migraine for Whom 2-4 Prior Preventive Treatments Have Failed.

Jessica Ailani, Messoud Ashina, Susanne F Awad, Xin Ying Lee, Line Pickering Boserup, Seema Soni-Brahmbhatt, Bjørn Sperling, Richard B Lipton

Registry-linked trialAbstract readClinical Trial, Phase IIIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in European journal of neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04418765 (Interventional, Randomized, Double-blind, Parallel-group, Placebo-controlled Study With an Extension Period to Evaluate the Efficacy and Safety of Eptinezumab for the Prevention of Migraine in Patients With Unsuccessful Prior Preventive Treatments), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04418765 phase3completednot on this map

Interventional, Randomized, Double-blind, Parallel-group, Placebo-controlled Study With an Extension Period to Evaluate the Efficacy and Safety of Eptinezumab for the Prevention of Migraine in Patients With Unsuccessful Prior Preventive Treatments

TypeinterventionalSponsorH. Lundbeck A/SRan2020 to 2022Enrolled892ConditionsMigraineArmsEptinezumab, Placebo
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Jessica AilaniDepartment of Neurology, Georgetown University Hospital, Washington, DC, USA.ORCID https://orcid.org/0000-0001-8106-4927
Messoud AshinaDepartment of Neurology, Danish Headache Center, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.ORCID https://orcid.org/0000-0003-0951-5804
Susanne F AwadH. Lundbeck A/S, Copenhagen, Denmark.ORCID https://orcid.org/0000-0002-5060-7404
Xin Ying LeeH. Lundbeck A/S, Copenhagen, Denmark.ORCID https://orcid.org/0000-0002-1102-3756
Line Pickering BoserupH. Lundbeck A/S, Copenhagen, Denmark.ORCID https://orcid.org/0000-0002-3062-8881
Seema Soni-BrahmbhattLundbeck LLC, Deerfield, Illinois, USA.ORCID https://orcid.org/0000-0002-4714-6010
Bjørn SperlingH. Lundbeck A/S, Copenhagen, Denmark.
Richard B LiptonDepartment of Neurology and the Montefiore Headache Center, Albert Einstein College of Medicine, Bronx, New York, USA.ORCID https://orcid.org/0000-0003-2652-2897

Funding

H. Lundbeck A/S
6 · The paper itself

Abstract

backgroundIn the DELIVER trial, eptinezumab administration was associated with sustained reductions in headache frequency and migraine-related impact in participants for whom previous preventive treatments have failed. This post hoc analysis evaluated long-term maintenance of initial ≥ 50% and ≥ 75% migraine response.

methodsDELIVER was a 24-week, randomized, double-blind, placebo-controlled trial with a 48-week dose-blinded extension. For participants with initial ≥ 50% or ≥ 75% reduction in monthly migraine days-defined as response following their first dose (Weeks 1-12) or first and second dose (Weeks 1-24)-maintenance of ≥ 50% or ≥ 75% migraine response was assessed for each subsequent 12-week dosing interval. Proportions of severe migraine attacks, 6-Item Headache Impact Test (HIT-6) total score, migraine-specific Work Productivity and Activity Impairment (WPAI:M) presenteeism subscore, and Patient Global Impression of Change (PGIC) categories were also evaluated in Weeks 1-12 responders.

resultsOf participants with ≥ 50% migraine response over Weeks 1-12, 61.0% (69/113, 100 mg) and 73.8% (93/126, 300 mg) maintained response over the entire 72-week treatment period; ≥ 50% responders (Weeks 1-24) and ≥ 75% responders (Weeks 1-12 and 1-24) showed similar trends. Weeks 1-12 responders (≥ 50% and ≥ 75%) experienced sustained reductions in migraine severity, HIT-6 total score, and presenteeism subscore, with most reporting improvements per the PGIC.

conclusionsFor both eptinezumab doses, ≥ 50% or ≥ 75% migraine response over Weeks 1-12 or 1-24 was maintained for the entire 72-week treatment period for many participants. An initial response within the first two doses of eptinezumab can indicate long-term improvements.

trial registrationClinicalTrials.gov (Identifier: NCT04418765; URL: https://clinicaltrials.gov/study/NCT04418765); EudraCT (Identifier: 2019-004497-25; URL: https://www.clinicaltrialsregister.eu/ctr-search/search?query=2019-004497-25).

Indexed as

Antibodies, Monoclonal, HumanizedMigraine DisordersAdultDouble-Blind MethodFemaleHumansMaleMiddle AgedTreatment OutcomeAntibodies, Monoclonal, Humanizedeptinezumabcalcitonin gene‐related peptideefficacyeptinezumabmigrainetreatment failures

Identifiers

PMID41834318
PMCPMC13093837

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Registered trials

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.