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

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

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Veröffentlicht in:Neurology 2020-11, Vol.95 (18), p.e2487-e2499
Hauptverfasser: Goadsby, Peter J., Silberstein, Stephen D., Yeung, Paul P., Cohen, Joshua M., Ning, Xiaoping, Yang, Ronghua, Dodick, David W.
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container_end_page e2499
container_issue 18
container_start_page e2487
container_title Neurology
container_volume 95
creator Goadsby, Peter J.
Silberstein, Stephen D.
Yeung, Paul P.
Cohen, Joshua M.
Ning, Xiaoping
Yang, Ronghua
Dodick, David W.
description OBJECTIVETo assess the long-term safety, tolerability, and efficacy of fremanezumab, a fully humanized monoclonal antibody approved for the preventive treatment of migraine. METHODSA 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. RESULTSOf 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. CONCLUSIONSFremanezumab 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.GOVNCT02638103. CLASSIFICATION OF EVIDENCEThis 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.
doi_str_mv 10.1212/WNL.0000000000010600
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METHODSA 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. RESULTSOf 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. CONCLUSIONSFremanezumab 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.GOVNCT02638103. CLASSIFICATION OF EVIDENCEThis 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.</description><identifier>ISSN: 0028-3878</identifier><identifier>EISSN: 1526-632X</identifier><identifier>DOI: 10.1212/WNL.0000000000010600</identifier><identifier>PMID: 32913018</identifier><language>eng</language><publisher>United States: American Academy of Neurology</publisher><subject>Adolescent ; Adult ; Aged ; Antibodies, Monoclonal - adverse effects ; Antibodies, Monoclonal - therapeutic use ; Antibodies, Monoclonal, Humanized - adverse effects ; Antibodies, Monoclonal, Humanized - therapeutic use ; Double-Blind Method ; Female ; Humans ; Male ; Middle Aged ; Migraine Disorders - drug therapy ; Time Factors ; Treatment Outcome ; Young Adult</subject><ispartof>Neurology, 2020-11, Vol.95 (18), p.e2487-e2499</ispartof><rights>American Academy of Neurology</rights><rights>2020 American Academy of Neurology</rights><rights>Copyright © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology.</rights><rights>Copyright © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. 2020 American Academy of Neurology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4050-dcc268c766c6bffacdcf75506296598d1e29b69baf4afd552fe1bd118d1f1f323</cites><orcidid>0000-0002-9486-6790 ; 0000-0003-3260-5904</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32913018$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Goadsby, Peter J.</creatorcontrib><creatorcontrib>Silberstein, Stephen D.</creatorcontrib><creatorcontrib>Yeung, Paul P.</creatorcontrib><creatorcontrib>Cohen, Joshua M.</creatorcontrib><creatorcontrib>Ning, Xiaoping</creatorcontrib><creatorcontrib>Yang, Ronghua</creatorcontrib><creatorcontrib>Dodick, David W.</creatorcontrib><title>Long-term safety, tolerability, and efficacy of fremanezumab in migraine: A randomized study</title><title>Neurology</title><addtitle>Neurology</addtitle><description>OBJECTIVETo assess the long-term safety, tolerability, and efficacy of fremanezumab, a fully humanized monoclonal antibody approved for the preventive treatment of migraine. METHODSA 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. RESULTSOf 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. CONCLUSIONSFremanezumab 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.GOVNCT02638103. CLASSIFICATION OF EVIDENCEThis 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.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Antibodies, Monoclonal - adverse effects</subject><subject>Antibodies, Monoclonal - therapeutic use</subject><subject>Antibodies, Monoclonal, Humanized - adverse effects</subject><subject>Antibodies, Monoclonal, Humanized - therapeutic use</subject><subject>Double-Blind Method</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Migraine Disorders - drug therapy</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>Young Adult</subject><issn>0028-3878</issn><issn>1526-632X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkF1P2zAUhi3ENEq3f4CQfwCBc-zEcbhAQhUMpGq7GWIXkyzHH60hH8hJqcKvX6pu3eCC-cayz_O-R3oIOUI4RYbs7P7r_BT-HgQBsEcmmDGRCM5-7JMJAJMJl7k8IIdd9zBCGcuLj-SAswI5oJyQn_O2WSS9izXttHf9cEL7tnJRl6EKm5duLHXeB6PNQFtPfXS1btzLqtYlDQ2twyLq0LhzeknjCLd1eHGWdv3KDp_IB6-rzn3-fU_J3fXV99lNMv_25XZ2OU9MChkk1hgmpMmFMKL0XhtrfJ5lIFghskJadKwoRVFqn2pvs4x5h6VFHCcePWd8Si62vU-rsnbWuKaPulJPMdQ6DqrVQb2eNGGpFu2zyoVkksNYkG4LTGy7Ljq_yyKojW012lZvbY-x43_37kJ_9I6A3ALrthodd4_Vau2iWjpd9cv_dafvRDecQEwTBgwQgUOy-cr5LymIniA</recordid><startdate>20201103</startdate><enddate>20201103</enddate><creator>Goadsby, Peter J.</creator><creator>Silberstein, Stephen D.</creator><creator>Yeung, Paul P.</creator><creator>Cohen, Joshua M.</creator><creator>Ning, Xiaoping</creator><creator>Yang, Ronghua</creator><creator>Dodick, David W.</creator><general>American Academy of Neurology</general><general>Lippincott Williams &amp; Wilkins</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-9486-6790</orcidid><orcidid>https://orcid.org/0000-0003-3260-5904</orcidid></search><sort><creationdate>20201103</creationdate><title>Long-term safety, tolerability, and efficacy of fremanezumab in migraine: A randomized study</title><author>Goadsby, Peter J. ; Silberstein, Stephen D. ; Yeung, Paul P. ; Cohen, Joshua M. ; Ning, Xiaoping ; Yang, Ronghua ; Dodick, David W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4050-dcc268c766c6bffacdcf75506296598d1e29b69baf4afd552fe1bd118d1f1f323</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Antibodies, Monoclonal - adverse effects</topic><topic>Antibodies, Monoclonal - therapeutic use</topic><topic>Antibodies, Monoclonal, Humanized - adverse effects</topic><topic>Antibodies, Monoclonal, Humanized - therapeutic use</topic><topic>Double-Blind Method</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Migraine Disorders - drug therapy</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Goadsby, Peter J.</creatorcontrib><creatorcontrib>Silberstein, Stephen D.</creatorcontrib><creatorcontrib>Yeung, Paul P.</creatorcontrib><creatorcontrib>Cohen, Joshua M.</creatorcontrib><creatorcontrib>Ning, Xiaoping</creatorcontrib><creatorcontrib>Yang, Ronghua</creatorcontrib><creatorcontrib>Dodick, David W.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Goadsby, Peter J.</au><au>Silberstein, Stephen D.</au><au>Yeung, Paul P.</au><au>Cohen, Joshua M.</au><au>Ning, Xiaoping</au><au>Yang, Ronghua</au><au>Dodick, David W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long-term safety, tolerability, and efficacy of fremanezumab in migraine: A randomized study</atitle><jtitle>Neurology</jtitle><addtitle>Neurology</addtitle><date>2020-11-03</date><risdate>2020</risdate><volume>95</volume><issue>18</issue><spage>e2487</spage><epage>e2499</epage><pages>e2487-e2499</pages><issn>0028-3878</issn><eissn>1526-632X</eissn><abstract>OBJECTIVETo assess the long-term safety, tolerability, and efficacy of fremanezumab, a fully humanized monoclonal antibody approved for the preventive treatment of migraine. METHODSA 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. RESULTSOf 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. CONCLUSIONSFremanezumab 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.GOVNCT02638103. CLASSIFICATION OF EVIDENCEThis 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.</abstract><cop>United States</cop><pub>American Academy of Neurology</pub><pmid>32913018</pmid><doi>10.1212/WNL.0000000000010600</doi><orcidid>https://orcid.org/0000-0002-9486-6790</orcidid><orcidid>https://orcid.org/0000-0003-3260-5904</orcidid><oa>free_for_read</oa></addata></record>
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subjects Adolescent
Adult
Aged
Antibodies, Monoclonal - adverse effects
Antibodies, Monoclonal - therapeutic use
Antibodies, Monoclonal, Humanized - adverse effects
Antibodies, Monoclonal, Humanized - therapeutic use
Double-Blind Method
Female
Humans
Male
Middle Aged
Migraine Disorders - drug therapy
Time Factors
Treatment Outcome
Young Adult
title Long-term safety, tolerability, and efficacy of fremanezumab in migraine: A randomized study
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