Evidence map›Paper›PMID 31932515›Full record

ArticleNeurology2020

Potential for treatment benefit of small molecule CGRP receptor antagonist plus monoclonal antibody in migraine therapy.

Kathleen Mullin, David Kudrow, Robert Croop, Meghan Lovegren, Charles M Conway, Vladimir Coric, Richard B Lipton

Erratum issued Registry-linked trialOpen access · hybridAbstract readCase Reports
In one paragraph

Article in Neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT03266588 (A Multicenter, Open Label Long-Term Safety Study of BHV-3000 in the Acute Treatment of Migraine), which is not on this map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
7.9field-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.

NCT03266588 phase2 / phase3completednot on this map

A Multicenter, Open Label Long-Term Safety Study of BHV-3000 in the Acute Treatment of Migraine

TypeinterventionalSponsorPfizerRan2017 to 2019Enrolled3,019ConditionsMigraine, With or Without AuraArmsRimegepant
3 · Its place in the literature

Who cites it

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 82 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Trial
  7. Retrospective Review of Dual CGRP-Targeted Regimens for Acute and Preventive Treatment of Migraines in a Veteran Population.Federal practitioner : for the health care professionals of the VA, DoD, and PHS · 2026
    Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Update on gepants for the treatment of chronic migraine.Journal of the Chinese Medical Association : JCMA · 2024
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Observational
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Kathleen MullinFrom the New England Institute of Neurology and Headache (K.M.), Stamford, CT; California Medical Clinic for Headache (D.K.), Santa Monica; Biohaven Pharmaceuticals, Inc (R.C., M.L., C.M.C., V.C.), New Haven, CT; and Albert Einstein College of Medicine (R.B.L.), Bronx, NY. kate@neinh.com.
David KudrowFrom the New England Institute of Neurology and Headache (K.M.), Stamford, CT; California Medical Clinic for Headache (D.K.), Santa Monica; Biohaven Pharmaceuticals, Inc (R.C., M.L., C.M.C., V.C.), New Haven, CT; and Albert Einstein College of Medicine (R.B.L.), Bronx, NY.
Robert CroopFrom the New England Institute of Neurology and Headache (K.M.), Stamford, CT; California Medical Clinic for Headache (D.K.), Santa Monica; Biohaven Pharmaceuticals, Inc (R.C., M.L., C.M.C., V.C.), New Haven, CT; and Albert Einstein College of Medicine (R.B.L.), Bronx, NY.
Meghan LovegrenFrom the New England Institute of Neurology and Headache (K.M.), Stamford, CT; California Medical Clinic for Headache (D.K.), Santa Monica; Biohaven Pharmaceuticals, Inc (R.C., M.L., C.M.C., V.C.), New Haven, CT; and Albert Einstein College of Medicine (R.B.L.), Bronx, NY.
Charles M ConwayFrom the New England Institute of Neurology and Headache (K.M.), Stamford, CT; California Medical Clinic for Headache (D.K.), Santa Monica; Biohaven Pharmaceuticals, Inc (R.C., M.L., C.M.C., V.C.), New Haven, CT; and Albert Einstein College of Medicine (R.B.L.), Bronx, NY.
Vladimir CoricFrom the New England Institute of Neurology and Headache (K.M.), Stamford, CT; California Medical Clinic for Headache (D.K.), Santa Monica; Biohaven Pharmaceuticals, Inc (R.C., M.L., C.M.C., V.C.), New Haven, CT; and Albert Einstein College of Medicine (R.B.L.), Bronx, NY.
Richard B LiptonFrom the New England Institute of Neurology and Headache (K.M.), Stamford, CT; California Medical Clinic for Headache (D.K.), Santa Monica; Biohaven Pharmaceuticals, Inc (R.C., M.L., C.M.C., V.C.), New Haven, CT; and Albert Einstein College of Medicine (R.B.L.), Bronx, NY.
California Medical Clinic for Headache · USNew England Institute for Neurology and Headache · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo provide the first clinical report that 2 calcitonin gene-related peptide (CGRP) therapies, a small molecule CGRP receptor antagonist and an anti-CGRP receptor antibody, can be used concomitantly to treat refractory migraine.

methodsCase reports are presented of 2 patients participating in a long-term safety study of rimegepant 75 mg oral tablets for acute treatment (NCT03266588). After Food and Drug Administration approval of erenumab, both patients started subcutaneous erenumab monthly as allowed per protocol.

resultsPatients were women 44 and 36 years of age with ≥2 decades of self-reported suboptimal response to multiple migraine medications. Patient 1 used rimegepant for 6 months and then started erenumab 70 mg subcutaneous monthly. Despite a response to preventive treatment with erenumab, she experienced substantial relief treating 7 of 7 acute attacks with rimegepant and eliminated regular, frequent use of ibuprofen and a caffeinated analgesic. Patient 2 used rimegepant for 60 days before starting erenumab 140 mg subcutaneously monthly. While on erenumab, 9 of 9 attacks treated with rimegepant responded. She stopped near-daily use of injectable ketorolac and diphenhydramine. While using rimegepant alone or together with erenumab, patients reported no related adverse events.

conclusionsRimegepant 75 mg may be effective for acute treatment during concomitant erenumab preventive administration. The mechanism underlying the benefits of concomitant use of a small molecule CGRP receptor antagonist and an anti-CGRP receptor antibody is unknown and requires further study. CLINICALTRIALSGOV IDENTIFIER: NCT03266588. CLASSIFICATION OF EVIDENCE: This study provides Class IV evidence that for patients with migraine using erenumab, rimegepant is effective for acute treatment.

Indexed as

AdultAnalgesicsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedCalcitonin Gene-Related PeptideCalcitonin Gene-Related Peptide Receptor AntagonistsFemaleHumansMigraine DisordersReceptors, Calcitonin Gene-Related PeptideAnalgesicsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedCalcitonin Gene-Related PeptideCalcitonin Gene-Related Peptide Receptor AntagonistserenumabReceptors, Calcitonin Gene-Related Peptide

Identifiers

PMID31932515
PMCPMC7526667
OpenAlexW3000581217

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.