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Galcanezumab in chronic migraine: The randomized, double-blind, placebo-controlled REGAIN study
OBJECTIVE: To evaluate the efficacy and safety of galcanezumab, a humanized monoclonal antibody that selectively binds to calcitonin gene-related peptide, in the preventive treatment of chronic migraine. METHODS: A phase 3, randomized, double-blind, placebo-controlled study of LY2951742 in patients...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329331/ https://www.ncbi.nlm.nih.gov/pubmed/30446596 http://dx.doi.org/10.1212/WNL.0000000000006640 |
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author | Detke, Holland C. Goadsby, Peter J. Wang, Shufang Friedman, Deborah I. Selzler, Katherine J. Aurora, Sheena K. |
author_facet | Detke, Holland C. Goadsby, Peter J. Wang, Shufang Friedman, Deborah I. Selzler, Katherine J. Aurora, Sheena K. |
author_sort | Detke, Holland C. |
collection | PubMed |
description | OBJECTIVE: To evaluate the efficacy and safety of galcanezumab, a humanized monoclonal antibody that selectively binds to calcitonin gene-related peptide, in the preventive treatment of chronic migraine. METHODS: A phase 3, randomized, double-blind, placebo-controlled study of LY2951742 in patients with chronic migraine (Evaluation of Galcanezumab in the Prevention of Chronic Migraine [REGAIN]) was a phase 3 study with a 3-month double-blind, placebo-controlled treatment phase and a 9-month open-label extension. Eligible patients 18 to 65 years of age with chronic migraine were randomized 2:1:1 to monthly subcutaneous injections of placebo (n = 558), galcanezumab 120 mg (with a 240-mg loading dose, n = 278), or galcanezumab 240 mg (n = 277). The primary endpoint was the overall mean change from baseline in the number of monthly migraine headache days (MHDs) during the 3-month double-blind treatment phase. RESULTS: Mean number of monthly MHDs at baseline was 19.4 for the total sample. Both galcanezumab dose groups demonstrated greater overall mean reduction in the number of monthly MHDs compared to placebo (placebo −2.7, galcanezumab 120 mg −4.8, galcanezumab 240 mg −4.6) (p < 0.001 for each dose compared to placebo). There were no clinically meaningful differences between galcanezumab doses and placebo on any safety or tolerability outcome except for a higher incidence of treatment-emergent injection-site reaction (p < 0.01), injection-site erythema (p < 0.001), injection-site pruritus (p < 0.01), and sinusitis (p < 0.05) in the galcanezumab 240-mg group relative to placebo. CONCLUSIONS: Both doses of galcanezumab were superior to placebo in reducing the number of monthly MHDs. Galcanezumab appears efficacious, safe, and well tolerated for the preventive treatment of chronic migraine. CLINICALTRIALS.GOV IDENTIFIER: NCT02614261. CLASSIFICATION OF EVIDENCE: This interventional study provides Class I evidence that galcanezumab is superior to placebo in the reduction of the number of monthly MHDs. |
format | Online Article Text |
id | pubmed-6329331 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-63293312019-01-18 Galcanezumab in chronic migraine: The randomized, double-blind, placebo-controlled REGAIN study Detke, Holland C. Goadsby, Peter J. Wang, Shufang Friedman, Deborah I. Selzler, Katherine J. Aurora, Sheena K. Neurology Article OBJECTIVE: To evaluate the efficacy and safety of galcanezumab, a humanized monoclonal antibody that selectively binds to calcitonin gene-related peptide, in the preventive treatment of chronic migraine. METHODS: A phase 3, randomized, double-blind, placebo-controlled study of LY2951742 in patients with chronic migraine (Evaluation of Galcanezumab in the Prevention of Chronic Migraine [REGAIN]) was a phase 3 study with a 3-month double-blind, placebo-controlled treatment phase and a 9-month open-label extension. Eligible patients 18 to 65 years of age with chronic migraine were randomized 2:1:1 to monthly subcutaneous injections of placebo (n = 558), galcanezumab 120 mg (with a 240-mg loading dose, n = 278), or galcanezumab 240 mg (n = 277). The primary endpoint was the overall mean change from baseline in the number of monthly migraine headache days (MHDs) during the 3-month double-blind treatment phase. RESULTS: Mean number of monthly MHDs at baseline was 19.4 for the total sample. Both galcanezumab dose groups demonstrated greater overall mean reduction in the number of monthly MHDs compared to placebo (placebo −2.7, galcanezumab 120 mg −4.8, galcanezumab 240 mg −4.6) (p < 0.001 for each dose compared to placebo). There were no clinically meaningful differences between galcanezumab doses and placebo on any safety or tolerability outcome except for a higher incidence of treatment-emergent injection-site reaction (p < 0.01), injection-site erythema (p < 0.001), injection-site pruritus (p < 0.01), and sinusitis (p < 0.05) in the galcanezumab 240-mg group relative to placebo. CONCLUSIONS: Both doses of galcanezumab were superior to placebo in reducing the number of monthly MHDs. Galcanezumab appears efficacious, safe, and well tolerated for the preventive treatment of chronic migraine. CLINICALTRIALS.GOV IDENTIFIER: NCT02614261. CLASSIFICATION OF EVIDENCE: This interventional study provides Class I evidence that galcanezumab is superior to placebo in the reduction of the number of monthly MHDs. Lippincott Williams & Wilkins 2018-12-11 /pmc/articles/PMC6329331/ /pubmed/30446596 http://dx.doi.org/10.1212/WNL.0000000000006640 Text en Copyright © 2018 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 Detke, Holland C. Goadsby, Peter J. Wang, Shufang Friedman, Deborah I. Selzler, Katherine J. Aurora, Sheena K. Galcanezumab in chronic migraine: The randomized, double-blind, placebo-controlled REGAIN study |
title | Galcanezumab in chronic migraine: The randomized, double-blind, placebo-controlled REGAIN study |
title_full | Galcanezumab in chronic migraine: The randomized, double-blind, placebo-controlled REGAIN study |
title_fullStr | Galcanezumab in chronic migraine: The randomized, double-blind, placebo-controlled REGAIN study |
title_full_unstemmed | Galcanezumab in chronic migraine: The randomized, double-blind, placebo-controlled REGAIN study |
title_short | Galcanezumab in chronic migraine: The randomized, double-blind, placebo-controlled REGAIN study |
title_sort | galcanezumab in chronic migraine: the randomized, double-blind, placebo-controlled regain study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329331/ https://www.ncbi.nlm.nih.gov/pubmed/30446596 http://dx.doi.org/10.1212/WNL.0000000000006640 |
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