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Potential for treatment benefit of small molecule CGRP receptor antagonist plus monoclonal antibody in migraine therapy
OBJECTIVE: To 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. METHODS: Case reports are presented of 2 patients participati...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7526667/ https://www.ncbi.nlm.nih.gov/pubmed/31932515 http://dx.doi.org/10.1212/WNL.0000000000008944 |
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author | Mullin, Kathleen Kudrow, David Croop, Robert Lovegren, Meghan Conway, Charles M. Coric, Vladimir Lipton, Richard B. |
author_facet | Mullin, Kathleen Kudrow, David Croop, Robert Lovegren, Meghan Conway, Charles M. Coric, Vladimir Lipton, Richard B. |
author_sort | Mullin, Kathleen |
collection | PubMed |
description | OBJECTIVE: To 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. METHODS: Case 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. RESULTS: Patients 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. CONCLUSIONS: Rimegepant 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. CLINICALTRIALS.GOV IDENTIFIER: NCT03266588. CLASSIFICATION OF EVIDENCE: This study provides Class IV evidence that for patients with migraine using erenumab, rimegepant is effective for acute treatment. |
format | Online Article Text |
id | pubmed-7526667 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-75266672020-10-14 Potential for treatment benefit of small molecule CGRP receptor antagonist plus monoclonal antibody in migraine therapy Mullin, Kathleen Kudrow, David Croop, Robert Lovegren, Meghan Conway, Charles M. Coric, Vladimir Lipton, Richard B. Neurology Article OBJECTIVE: To 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. METHODS: Case 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. RESULTS: Patients 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. CONCLUSIONS: Rimegepant 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. CLINICALTRIALS.GOV IDENTIFIER: NCT03266588. CLASSIFICATION OF EVIDENCE: This study provides Class IV evidence that for patients with migraine using erenumab, rimegepant is effective for acute treatment. Lippincott Williams & Wilkins 2020-05-19 /pmc/articles/PMC7526667/ /pubmed/31932515 http://dx.doi.org/10.1212/WNL.0000000000008944 Text en Copyright © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Article Mullin, Kathleen Kudrow, David Croop, Robert Lovegren, Meghan Conway, Charles M. Coric, Vladimir Lipton, Richard B. Potential for treatment benefit of small molecule CGRP receptor antagonist plus monoclonal antibody in migraine therapy |
title | Potential for treatment benefit of small molecule CGRP receptor antagonist plus monoclonal antibody in migraine therapy |
title_full | Potential for treatment benefit of small molecule CGRP receptor antagonist plus monoclonal antibody in migraine therapy |
title_fullStr | Potential for treatment benefit of small molecule CGRP receptor antagonist plus monoclonal antibody in migraine therapy |
title_full_unstemmed | Potential for treatment benefit of small molecule CGRP receptor antagonist plus monoclonal antibody in migraine therapy |
title_short | Potential for treatment benefit of small molecule CGRP receptor antagonist plus monoclonal antibody in migraine therapy |
title_sort | potential for treatment benefit of small molecule cgrp receptor antagonist plus monoclonal antibody in migraine therapy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7526667/ https://www.ncbi.nlm.nih.gov/pubmed/31932515 http://dx.doi.org/10.1212/WNL.0000000000008944 |
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