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Long-term safety, tolerability, and efficacy of fremanezumab in migraine: A randomized study

OBJECTIVE: To assess the long-term safety, tolerability, and efficacy of fremanezumab, a fully humanized monoclonal antibody approved for the preventive treatment of migraine. METHODS: A 52-week, multicenter, randomized, double-blind, parallel-group study evaluated fremanezumab monthly or quarterly...

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Autores principales: Goadsby, Peter J., Silberstein, Stephen D., Yeung, Paul P., Cohen, Joshua M., Ning, Xiaoping, Yang, Ronghua, Dodick, David W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7682830/
https://www.ncbi.nlm.nih.gov/pubmed/32913018
http://dx.doi.org/10.1212/WNL.0000000000010600
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author Goadsby, Peter J.
Silberstein, Stephen D.
Yeung, Paul P.
Cohen, Joshua M.
Ning, Xiaoping
Yang, Ronghua
Dodick, David W.
author_facet Goadsby, Peter J.
Silberstein, Stephen D.
Yeung, Paul P.
Cohen, Joshua M.
Ning, Xiaoping
Yang, Ronghua
Dodick, David W.
author_sort Goadsby, Peter J.
collection PubMed
description OBJECTIVE: To assess the long-term safety, tolerability, and efficacy of fremanezumab, a fully humanized monoclonal antibody approved for the preventive treatment of migraine. METHODS: A 52-week, multicenter, randomized, double-blind, parallel-group study evaluated fremanezumab monthly or quarterly in adults with chronic migraine (CM) or episodic migraine (EM). Safety and tolerability were assessed by adverse event (AE) monitoring (performed by the investigators), systematic local injection-site assessments (immediately and 1 hour after injection), laboratory/vitals assessments, and immunogenicity testing. Prespecified exploratory evaluations included change from baseline in the monthly number of migraine days, headache days of at least moderate severity, and days with any acute headache medication use. Change from baseline in headache-related disability (6-item Headache Impact Test scores) was also measured. RESULTS: Of 1,890 patients enrolled, 551 and 559 patients with CM received quarterly and monthly dosing; 394 and 386 patients with EM received quarterly or monthly, respectively. The most commonly reported AEs were injection-site reactions (induration 33%, pain 31%, and erythema 26%). Fremanezumab reduced monthly migraine days (CM quarterly −7.2 days, CM monthly −8.0 days, EM quarterly −5.2 days, EM monthly −5.1 days) and headache days of at least moderate severity (CM quarterly −6.4 days, CM monthly −6.8 days, EM quarterly −4.4, EM monthly −4.2 days) from baseline to 12 months. Reductions in any acute headache medication use and headache-related disability were also maintained over 12 months. CONCLUSIONS: Fremanezumab quarterly and fremanezumab monthly were well tolerated and demonstrated sustained improvements in monthly migraine days, headache days, and headache-related disability for up to 12 months in patients with migraine. CLINICALTRIALS.GOV: NCT02638103. CLASSIFICATION OF EVIDENCE: This study provides Class IV evidence that long-term fremanezumab treatment is safe, well tolerated, and effective at sustaining reductions in monthly migraine and headache days.
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spelling pubmed-76828302020-11-24 Long-term safety, tolerability, and efficacy of fremanezumab in migraine: A randomized study Goadsby, Peter J. Silberstein, Stephen D. Yeung, Paul P. Cohen, Joshua M. Ning, Xiaoping Yang, Ronghua Dodick, David W. Neurology Article OBJECTIVE: To assess the long-term safety, tolerability, and efficacy of fremanezumab, a fully humanized monoclonal antibody approved for the preventive treatment of migraine. METHODS: A 52-week, multicenter, randomized, double-blind, parallel-group study evaluated fremanezumab monthly or quarterly in adults with chronic migraine (CM) or episodic migraine (EM). Safety and tolerability were assessed by adverse event (AE) monitoring (performed by the investigators), systematic local injection-site assessments (immediately and 1 hour after injection), laboratory/vitals assessments, and immunogenicity testing. Prespecified exploratory evaluations included change from baseline in the monthly number of migraine days, headache days of at least moderate severity, and days with any acute headache medication use. Change from baseline in headache-related disability (6-item Headache Impact Test scores) was also measured. RESULTS: Of 1,890 patients enrolled, 551 and 559 patients with CM received quarterly and monthly dosing; 394 and 386 patients with EM received quarterly or monthly, respectively. The most commonly reported AEs were injection-site reactions (induration 33%, pain 31%, and erythema 26%). Fremanezumab reduced monthly migraine days (CM quarterly −7.2 days, CM monthly −8.0 days, EM quarterly −5.2 days, EM monthly −5.1 days) and headache days of at least moderate severity (CM quarterly −6.4 days, CM monthly −6.8 days, EM quarterly −4.4, EM monthly −4.2 days) from baseline to 12 months. Reductions in any acute headache medication use and headache-related disability were also maintained over 12 months. CONCLUSIONS: Fremanezumab quarterly and fremanezumab monthly were well tolerated and demonstrated sustained improvements in monthly migraine days, headache days, and headache-related disability for up to 12 months in patients with migraine. CLINICALTRIALS.GOV: NCT02638103. CLASSIFICATION OF EVIDENCE: This study provides Class IV evidence that long-term fremanezumab treatment is safe, well tolerated, and effective at sustaining reductions in monthly migraine and headache days. Lippincott Williams & Wilkins 2020-11-03 /pmc/articles/PMC7682830/ /pubmed/32913018 http://dx.doi.org/10.1212/WNL.0000000000010600 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
Goadsby, Peter J.
Silberstein, Stephen D.
Yeung, Paul P.
Cohen, Joshua M.
Ning, Xiaoping
Yang, Ronghua
Dodick, David W.
Long-term safety, tolerability, and efficacy of fremanezumab in migraine: A randomized study
title Long-term safety, tolerability, and efficacy of fremanezumab in migraine: A randomized study
title_full Long-term safety, tolerability, and efficacy of fremanezumab in migraine: A randomized study
title_fullStr Long-term safety, tolerability, and efficacy of fremanezumab in migraine: A randomized study
title_full_unstemmed Long-term safety, tolerability, and efficacy of fremanezumab in migraine: A randomized study
title_short Long-term safety, tolerability, and efficacy of fremanezumab in migraine: A randomized study
title_sort long-term safety, tolerability, and efficacy of fremanezumab in migraine: a randomized study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7682830/
https://www.ncbi.nlm.nih.gov/pubmed/32913018
http://dx.doi.org/10.1212/WNL.0000000000010600
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