Evidence map›Paper›PMID 34521260›Full record

Trial reportCephalalgia : an international journal of headache2022

Time course of efficacy of atogepant for the preventive treatment of migraine: Results from the randomized, double-blind ADVANCE trial.

Todd J Schwedt, Richard B Lipton, Jessica Ailani, Stephen D Silberstein, Cristina Tassorelli, Hua Guo, Kaifeng Lu, Brett Dabruzzo, Rosa Miceli, Lawrence Severt and 2 more

Registry-linked trialOpen access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Cephalalgia : an international journal of headache, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06414044 (STudio Osservazionale Sull'Efficacia, Sicurezza e tollerabilità di Atogepant in Pazienti Real Life Affetti da Emicrania in Italia), which is not on this map. Cited by 34 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 5 pooled it
7.5field-weighted citation impact, top 2% of its field
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.

NCT06414044 active not recruitingnot on this mapstarted 2024, after this paper: background citation

STudio Osservazionale Sull'Efficacia, Sicurezza e tollerabilità di Atogepant in Pazienti Real Life Affetti da Emicrania in Italia (Studio STAR)

TypeobservationalSponsorUniversity of FlorenceRan2024 to 2026Enrolled500ConditionsMigraine, Migraine With Aura, Migraine Without Aura, Chronic MigraineArmsAtogepant 60 mg
3 · Its place in the literature

Who cites it

34 citing papers in PubMed, 5 syntheses or guidelines pooled it, 58 citations in OpenAlex.

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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

12 authors at 6 institutions in 2 countries.

Todd J SchwedtDepartment of Neurology, Mayo Clinic, Phoenix, AZ, USA.
Richard B LiptonAlbert Einstein College of Medicine, Bronx, NY, USA.
Jessica AilaniMedStar Georgetown University Hospital, Washington, DC, USA.
Stephen D SilbersteinDepartment of Neurology, Thomas Jefferson University, Philadelphia, PA, USA.ORCID 0000-0001-9467-5567
Cristina TassorelliIRCCS Mondino Foundation, Headache Science Center, Pavia, Italy.ORCID 0000-0003-1513-2113
Hua GuoNeuroscience Development, AbbVie, Madison, NJ, USA.
Kaifeng LuNeuroscience Development, AbbVie, Madison, NJ, USA.
Brett DabruzzoNeuroscience Development, AbbVie, Madison, NJ, USA.
Rosa MiceliNeuroscience Development, AbbVie, Madison, NJ, USA.
Lawrence SevertNeuroscience Development, AbbVie, Madison, NJ, USA.
Michelle FinneganNeuroscience Development, AbbVie, Madison, NJ, USA.
Joel M TrugmanNeuroscience Development, AbbVie, Madison, NJ, USA.
AbbVie (United States) · USAlbert Einstein College of Medicine · USGeorgetown University · USMayo Clinic Hospital · USThomas Jefferson University · USUniversity of Pavia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAtogepant is an oral, small-molecule, calcitonin gene-related peptide receptor antagonist for the preventive treatment of migraine.

methodsIn the double-blind, phase 3 ADVANCE trial, participants with 4-14 migraine days/month were randomized to atogepant 10 mg, 30 mg, 60 mg, or placebo once daily for 12 weeks. We evaluated the time course of efficacy of atogepant for the preventive treatment of migraine. Analyses included change from baseline in mean monthly migraine days during each of the three 4-week treatment periods, change in weekly migraine days during weeks 1-4, and proportion of participants with a migraine on each day during the first week.

resultsWe analyzed 873 participants (n = 214 atogepant 10 mg, n = 223 atogepant 30 mg, n = 222 atogepant 60 mg, n = 214 placebo). For weeks 1-4, mean change from baseline in mean monthly migraine days ranged from -3.1 to -3.9 across atogepant doses vs -1.6 for placebo (

conclusionAtogepant demonstrated treatment benefits as early as the first full day after treatment initiation, and sustained efficacy across each 4-week interval during the 12-week treatment period.

Indexed as

Migraine DisordersAnalgesicsDouble-Blind MethodHumansPiperidinesPyridinesPyrrolesSpiro CompoundsTreatment OutcomeAnalgesicsatogepantPiperidinesPyridinesPyrrolesSpiro CompoundsAtogepantcalcitonin gene–related peptideefficacytime course

Identifiers

PMID34521260
PMCPMC8739573
OpenAlexW3198972203

What OpenQuestion holds

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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.