Evidence map›Paper›PMID 32887548›Full record

ArticleThe journal of headache and pain2020

Improvements across a range of patient-reported domains with fremanezumab treatment: results from a patient survey study.

Dawn C Buse, Sanjay K Gandhi, Joshua M Cohen, Verena Ramirez-Campos, Blaine Cloud, Ronghua Yang, Robert P Cowan

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in The journal of headache and pain, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02638103 (A Multicenter, Randomized, Double-Blind, Parallel-Group Study Evaluating the Long-Term Safety, Tolerability, and Efficacy of Subcutaneous Administration of Fremanezumab), which is not on this map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 16% 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.

NCT02638103 phase3completednot on this map

A Multicenter, Randomized, Double-Blind, Parallel-Group Study Evaluating the Long-Term Safety, Tolerability, and Efficacy of Subcutaneous Administration of Fremanezumab (TEV-48125) for the Preventive Treatment of Migraine

TypeinterventionalSponsorTeva Branded Pharmaceutical Products R&D, Inc.Ran2016 to 2018Enrolled1,890ConditionsMigraineArmsFremanezumab, Placebo
3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. The first interim analysis of Italian patients enrolled in the real-world, Pan-European, prospective, observational, phase 4 PEARL study of fremanezumab effectiveness.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024
    Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Migraine Management in Medically Complex Patients: a Narrative Review.Current neurology and neuroscience reports · 2024
    Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
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

7 authors at 3 institutions in 1 country.

Dawn C BuseAlbert Einstein College of Medicine, Bronx, NY, 10461, USA. dbuse@montefiore.org.ORCID http://orcid.org/0000-0002-1223-1215
Sanjay K GandhiTeva Branded Pharmaceutical Products R&D, Inc., West Chester, PA, USA.
Joshua M CohenTeva Branded Pharmaceutical Products R&D, Inc., West Chester, PA, USA.
Verena Ramirez-CamposTeva Branded Pharmaceutical Products R&D, Inc., West Chester, PA, USA.
Blaine CloudClinical SCORE, Chadds Ford, PA, USA.
Ronghua YangTeva Branded Pharmaceutical Products R&D, Inc., West Chester, PA, USA.
Robert P CowanStanford University, Stanford, CA, USA.
Teva Pharmaceuticals (United States) · USAlbert Einstein College of Medicine · USStanford University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe long-term safety and efficacy of fremanezumab were evaluated in a 52-week extension study (NCT02638103). Patient satisfaction with fremanezumab, dosing preferences, and patient-reported outcomes were assessed in a subpopulation who completed the extension study and consented to a follow-up questionnaire.

methodsIn the extension study (N = 1842), adults with migraine were randomized to quarterly or monthly fremanezumab. After completing active treatment, patients answered a survey evaluating patient satisfaction, treatment and dosing preferences, and changes in patient-reported outcomes.

resultsOf the 557 patients who could have been contacted upon completing the extension study, 302 consented and 253 completed the survey. The mean (standard deviation) satisfaction rating for fremanezumab was 6.1 (1.4; 1 = "extremely dissatisfied" to 7 = "extremely satisfied"). Most patients (175 [69.2%]) preferred quarterly over monthly fremanezumab dosing. Among patients taking antiepileptics (most common class of prior preventive medication; n = 130), 91.5% preferred fremanezumab. Patients reported improvements in anxiety (74 [67.9%]), sleep quality (143 [56.5%]), and quality of time spent with others (210 [83.0%]) with fremanezumab.

conclusionIn this study, treatment satisfaction with fremanezumab was high, most patients preferred quarterly fremanezumab dosing, and fremanezumab was generally preferred to prior preventive medications.

trial registrationClinicalTrials.gov NCT02638103 (HALO LTS), registered December 22, 2015.

Indexed as

Surveys and QuestionnairesAdultAntibodies, MonoclonalFemaleHumansInjections, SubcutaneousMaleMiddle AgedMigraine DisordersPatient Reported Outcome MeasuresPatient SatisfactionAntibodies, MonoclonalfremanezumabAnxietyMigrainePreventionSatisfactionSleepTreatment preference

Identifiers

PMID32887548
PMCPMC7487845
OpenAlexW3083285006

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.