Long-term safety and tolerability of eptinezumab in patients with chronic migraine: a 2-year, open-label, phase 3 trial

Abstract Background Eptinezumab, an anti-calcitonin gene-related peptide monoclonal antibody recently approved in the United States for preventive treatment of migraine in adults, was found to be well tolerated in double-blind, placebo-controlled studies in patients with episodic and chronic migrain...

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Main Authors: David Kudrow, Roger K. Cady, Brent Allan, Susan M. Pederson, Joe Hirman, Lahar R. Mehta, Barbara A. Schaeffler
Format: Article
Language:English
Published: BMC 2021-03-01
Series:BMC Neurology
Subjects:
Online Access:https://doi.org/10.1186/s12883-021-02123-w
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spelling doaj-7ae3b25ea70f489ca35e15e25c6fbe792021-03-21T12:25:01ZengBMCBMC Neurology1471-23772021-03-0121111210.1186/s12883-021-02123-wLong-term safety and tolerability of eptinezumab in patients with chronic migraine: a 2-year, open-label, phase 3 trialDavid Kudrow0Roger K. Cady1Brent Allan2Susan M. Pederson3Joe Hirman4Lahar R. Mehta5Barbara A. Schaeffler6California Medical Clinic for HeadacheLundbeck La Jolla Research CenterAlder BioPharmaceuticals, Inc. (CKA Lundbeck Seattle BioPharmaceuticals, Inc.)Lundbeck La Jolla Research CenterPacific Northwest Statistical ConsultingLundbeck La Jolla Research CenterLundbeck La Jolla Research CenterAbstract Background Eptinezumab, an anti-calcitonin gene-related peptide monoclonal antibody recently approved in the United States for preventive treatment of migraine in adults, was found to be well tolerated in double-blind, placebo-controlled studies in patients with episodic and chronic migraine. The objective of the PREVAIL study was to evaluate the long-term safety, immunogenicity, and impact on patient-reported outcomes of repeat doses of eptinezumab in patients with chronic migraine. Methods PREVAIL was an open-label, phase 3 trial comprising a 48-week treatment phase followed by a second 48-week treatment phase. Adults with chronic migraine received eptinezumab 300 mg by 30-min intravenous administration every 12 weeks for up to 8 doses. Patients were followed for 20 weeks after the final infusion (end-of-study visit at week 104). Results Overall, 128 adults (mean age, 41.5 years) with chronic migraine were included. During the 2 years, the most frequently reported treatment-emergent adverse events were nasopharyngitis (14.1%), upper respiratory tract infection (7.8%), sinusitis (7.8%), influenza (6.3%), bronchitis (5.5%), and migraine (5.5%). The rate of study-drug discontinuation due to adverse events was 6.3%, which included 3 patients with infusion-related hypersensitivity. The incidence of anti-eptinezumab antibodies peaked at week 24 and declined despite continued dosing, to nondetectable levels at week 104. Improvements in patient-reported outcomes were observed at first assessment (week 4) and generally sustained through week 104. Conclusion In adults with chronic migraine, eptinezumab 300 mg demonstrated a favorable safety profile, limited long-term immunogenicity, early and sustained reductions in migraine-related burden, and improvements in health-related quality of life over 2 years. Trial registration ClinicalTrials.gov (Identifier: NCT02985398 ).https://doi.org/10.1186/s12883-021-02123-wEptinezumabChronic migraineEffectivenessSafetyImmunogenicity
collection DOAJ
language English
format Article
sources DOAJ
author David Kudrow
Roger K. Cady
Brent Allan
Susan M. Pederson
Joe Hirman
Lahar R. Mehta
Barbara A. Schaeffler
spellingShingle David Kudrow
Roger K. Cady
Brent Allan
Susan M. Pederson
Joe Hirman
Lahar R. Mehta
Barbara A. Schaeffler
Long-term safety and tolerability of eptinezumab in patients with chronic migraine: a 2-year, open-label, phase 3 trial
BMC Neurology
Eptinezumab
Chronic migraine
Effectiveness
Safety
Immunogenicity
author_facet David Kudrow
Roger K. Cady
Brent Allan
Susan M. Pederson
Joe Hirman
Lahar R. Mehta
Barbara A. Schaeffler
author_sort David Kudrow
title Long-term safety and tolerability of eptinezumab in patients with chronic migraine: a 2-year, open-label, phase 3 trial
title_short Long-term safety and tolerability of eptinezumab in patients with chronic migraine: a 2-year, open-label, phase 3 trial
title_full Long-term safety and tolerability of eptinezumab in patients with chronic migraine: a 2-year, open-label, phase 3 trial
title_fullStr Long-term safety and tolerability of eptinezumab in patients with chronic migraine: a 2-year, open-label, phase 3 trial
title_full_unstemmed Long-term safety and tolerability of eptinezumab in patients with chronic migraine: a 2-year, open-label, phase 3 trial
title_sort long-term safety and tolerability of eptinezumab in patients with chronic migraine: a 2-year, open-label, phase 3 trial
publisher BMC
series BMC Neurology
issn 1471-2377
publishDate 2021-03-01
description Abstract Background Eptinezumab, an anti-calcitonin gene-related peptide monoclonal antibody recently approved in the United States for preventive treatment of migraine in adults, was found to be well tolerated in double-blind, placebo-controlled studies in patients with episodic and chronic migraine. The objective of the PREVAIL study was to evaluate the long-term safety, immunogenicity, and impact on patient-reported outcomes of repeat doses of eptinezumab in patients with chronic migraine. Methods PREVAIL was an open-label, phase 3 trial comprising a 48-week treatment phase followed by a second 48-week treatment phase. Adults with chronic migraine received eptinezumab 300 mg by 30-min intravenous administration every 12 weeks for up to 8 doses. Patients were followed for 20 weeks after the final infusion (end-of-study visit at week 104). Results Overall, 128 adults (mean age, 41.5 years) with chronic migraine were included. During the 2 years, the most frequently reported treatment-emergent adverse events were nasopharyngitis (14.1%), upper respiratory tract infection (7.8%), sinusitis (7.8%), influenza (6.3%), bronchitis (5.5%), and migraine (5.5%). The rate of study-drug discontinuation due to adverse events was 6.3%, which included 3 patients with infusion-related hypersensitivity. The incidence of anti-eptinezumab antibodies peaked at week 24 and declined despite continued dosing, to nondetectable levels at week 104. Improvements in patient-reported outcomes were observed at first assessment (week 4) and generally sustained through week 104. Conclusion In adults with chronic migraine, eptinezumab 300 mg demonstrated a favorable safety profile, limited long-term immunogenicity, early and sustained reductions in migraine-related burden, and improvements in health-related quality of life over 2 years. Trial registration ClinicalTrials.gov (Identifier: NCT02985398 ).
topic Eptinezumab
Chronic migraine
Effectiveness
Safety
Immunogenicity
url https://doi.org/10.1186/s12883-021-02123-w
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