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Long‐term efficacy and safety during open‐label erenumab treatment in Japanese patients with episodic migraine
OBJECTIVE: To assess long‐term (up to 2 years) efficacy, tolerability, and safety of erenumab for the prevention of episodic migraine (EM) in Japanese patients. BACKGROUND: Previously published results from the double‐blind treatment phase (DBTP) of a phase 2 clinical study have demonstrated the eff...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8251924/ https://www.ncbi.nlm.nih.gov/pubmed/33764538 http://dx.doi.org/10.1111/head.14096 |
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author | Sakai, Fumihiko Takeshima, Takao Tatsuoka, Yoshihisa Hirata, Koichi Cheng, Sunfa Numachi, Yotaro Peng, Cheng Xue, Fei Mikol, Daniel D. |
author_facet | Sakai, Fumihiko Takeshima, Takao Tatsuoka, Yoshihisa Hirata, Koichi Cheng, Sunfa Numachi, Yotaro Peng, Cheng Xue, Fei Mikol, Daniel D. |
author_sort | Sakai, Fumihiko |
collection | PubMed |
description | OBJECTIVE: To assess long‐term (up to 2 years) efficacy, tolerability, and safety of erenumab for the prevention of episodic migraine (EM) in Japanese patients. BACKGROUND: Previously published results from the double‐blind treatment phase (DBTP) of a phase 2 clinical study have demonstrated the efficacy and safety of erenumab in Japanese patients with EM. METHODS: Patients completing the 24‐week placebo‐controlled DBTP could continue into the 76‐week open‐label treatment phase (OLTP), receiving erenumab 70 mg or 140 mg subcutaneously once monthly. The initial dose in the OLTP was erenumab 70 mg monthly, which was later changed to 140 mg. After study completion, the following were assessed: change from baseline in monthly migraine days (MMD), change from baseline in monthly acute migraine‐specific medication days (MSMD), percentage of patients achieving ≥50% and ≥75% reduction in MMD, change from baseline in the 6‐item Headache Impact Test (HIT‐6™) score, and safety (exposure‐adjusted patient‐incidence of adverse events [AEs], calculated as number of patients per 100 patient‐years). RESULTS: Of 475 patients enrolled in the DBTP, 459 (96.6%) continued in the OLTP. The mean (SD) MMD was 7.9 (2.3) at baseline with the overall change from baseline at week 100 of –2.9 (4.1) days. The monthly acute MSMD was 5.7 (2.8) at baseline with change from baseline at week 100 of −1.7 (3.7) days. The proportion of patients who achieved ≥50% and ≥75% reduction in MMD from baseline at week 100 was 177/398 (44.5%) and 94/398 (23.6%), respectively. The HIT‐6™ score was 58.4 (5.4) at baseline with a change of −6.4 (8.2) at week 100. The exposure‐adjusted patient‐incidence of AEs during the OLTP was 207.1/100 patient‐years for the combined erenumab group, similar to that observed for either erenumab (271.0/100 patient‐years) or placebo (257.3/100 patient‐years) during the DBTP, and no new safety signals were detected during the OLTP. CONCLUSION: Long‐term erenumab treatment in Japanese patients with EM demonstrated sustained efficacy for up to 2 years, with a safety profile similar to previous studies, supporting erenumab as a potential new therapy for EM prevention in Japan. |
format | Online Article Text |
id | pubmed-8251924 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82519242021-07-07 Long‐term efficacy and safety during open‐label erenumab treatment in Japanese patients with episodic migraine Sakai, Fumihiko Takeshima, Takao Tatsuoka, Yoshihisa Hirata, Koichi Cheng, Sunfa Numachi, Yotaro Peng, Cheng Xue, Fei Mikol, Daniel D. Headache Research Submissions OBJECTIVE: To assess long‐term (up to 2 years) efficacy, tolerability, and safety of erenumab for the prevention of episodic migraine (EM) in Japanese patients. BACKGROUND: Previously published results from the double‐blind treatment phase (DBTP) of a phase 2 clinical study have demonstrated the efficacy and safety of erenumab in Japanese patients with EM. METHODS: Patients completing the 24‐week placebo‐controlled DBTP could continue into the 76‐week open‐label treatment phase (OLTP), receiving erenumab 70 mg or 140 mg subcutaneously once monthly. The initial dose in the OLTP was erenumab 70 mg monthly, which was later changed to 140 mg. After study completion, the following were assessed: change from baseline in monthly migraine days (MMD), change from baseline in monthly acute migraine‐specific medication days (MSMD), percentage of patients achieving ≥50% and ≥75% reduction in MMD, change from baseline in the 6‐item Headache Impact Test (HIT‐6™) score, and safety (exposure‐adjusted patient‐incidence of adverse events [AEs], calculated as number of patients per 100 patient‐years). RESULTS: Of 475 patients enrolled in the DBTP, 459 (96.6%) continued in the OLTP. The mean (SD) MMD was 7.9 (2.3) at baseline with the overall change from baseline at week 100 of –2.9 (4.1) days. The monthly acute MSMD was 5.7 (2.8) at baseline with change from baseline at week 100 of −1.7 (3.7) days. The proportion of patients who achieved ≥50% and ≥75% reduction in MMD from baseline at week 100 was 177/398 (44.5%) and 94/398 (23.6%), respectively. The HIT‐6™ score was 58.4 (5.4) at baseline with a change of −6.4 (8.2) at week 100. The exposure‐adjusted patient‐incidence of AEs during the OLTP was 207.1/100 patient‐years for the combined erenumab group, similar to that observed for either erenumab (271.0/100 patient‐years) or placebo (257.3/100 patient‐years) during the DBTP, and no new safety signals were detected during the OLTP. CONCLUSION: Long‐term erenumab treatment in Japanese patients with EM demonstrated sustained efficacy for up to 2 years, with a safety profile similar to previous studies, supporting erenumab as a potential new therapy for EM prevention in Japan. John Wiley and Sons Inc. 2021-03-25 2021-04 /pmc/articles/PMC8251924/ /pubmed/33764538 http://dx.doi.org/10.1111/head.14096 Text en © 2021 The Authors. Headache: The Journal of Head and Face Pain published by Wiley Periodicals LLC on behalf of American Headache Society https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Submissions Sakai, Fumihiko Takeshima, Takao Tatsuoka, Yoshihisa Hirata, Koichi Cheng, Sunfa Numachi, Yotaro Peng, Cheng Xue, Fei Mikol, Daniel D. Long‐term efficacy and safety during open‐label erenumab treatment in Japanese patients with episodic migraine |
title | Long‐term efficacy and safety during open‐label erenumab treatment in Japanese patients with episodic migraine |
title_full | Long‐term efficacy and safety during open‐label erenumab treatment in Japanese patients with episodic migraine |
title_fullStr | Long‐term efficacy and safety during open‐label erenumab treatment in Japanese patients with episodic migraine |
title_full_unstemmed | Long‐term efficacy and safety during open‐label erenumab treatment in Japanese patients with episodic migraine |
title_short | Long‐term efficacy and safety during open‐label erenumab treatment in Japanese patients with episodic migraine |
title_sort | long‐term efficacy and safety during open‐label erenumab treatment in japanese patients with episodic migraine |
topic | Research Submissions |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8251924/ https://www.ncbi.nlm.nih.gov/pubmed/33764538 http://dx.doi.org/10.1111/head.14096 |
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