Long-term tolerability and nonvascular safety of erenumab, a novel calcitonin gene-related peptide receptor antagonist for prevention of migraine: A pooled analysis of four placebo-controlled trials with long-term extensions. (December 2019)
- Record Type:
- Journal Article
- Title:
- Long-term tolerability and nonvascular safety of erenumab, a novel calcitonin gene-related peptide receptor antagonist for prevention of migraine: A pooled analysis of four placebo-controlled trials with long-term extensions. (December 2019)
- Main Title:
- Long-term tolerability and nonvascular safety of erenumab, a novel calcitonin gene-related peptide receptor antagonist for prevention of migraine: A pooled analysis of four placebo-controlled trials with long-term extensions
- Authors:
- Ashina, Messoud
Kudrow, David
Reuter, Uwe
Dolezil, David
Silberstein, Stephen
Tepper, Stewart J
Xue, Fei
Picard, Hernan
Zhang, Feng
Wang, Andrea
Zhou, Yanchen
Hong, Frank
Klatt, Jan
Mikol, Daniel D - Abstract:
- Background: Efficacy and safety of erenumab have been evaluated in a comprehensive clinical development program resulting in approval for migraine prevention in over 40 countries to date. Methods: This integrated safety analysis included four double-blind randomized trials and their extensions (up to three-plus years). Safety endpoints included exposure-adjusted patient incidences of adverse events, serious adverse events, and anti-erenumab antibodies. Results: In all, 2375 of the patients randomized across the four studies received at least one dose of erenumab (70 mg or 140 mg), with cumulative exposure of 2641.2 patient-years. Exposure-adjusted adverse event rates during the double-blind treatment phase were similar to placebo, with the exception of injection-site reactions (17.1 vs. 10.8 per 100 patient-years), constipation (7.0 vs. 3.8 per 100 patient-years), and muscle spasm (2.3 vs. 1.2 per 100 patient-years). During the long-term extensions, adverse events reported were similar to those observed during the double-blind treatment phase, and rates of injection site reactions, constipation, and muscle spasm were reported at lower rates than in the double-blind treatment phase. There were two deaths reported, both confounded by pre-existing conditions. Conclusions: This pooled safety analysis revealed a favorable and stable adverse event profile over time for erenumab with more than three years of exposure. Trial registration: ClinicalTrials.gov NCT01952574, NCT02483585,Background: Efficacy and safety of erenumab have been evaluated in a comprehensive clinical development program resulting in approval for migraine prevention in over 40 countries to date. Methods: This integrated safety analysis included four double-blind randomized trials and their extensions (up to three-plus years). Safety endpoints included exposure-adjusted patient incidences of adverse events, serious adverse events, and anti-erenumab antibodies. Results: In all, 2375 of the patients randomized across the four studies received at least one dose of erenumab (70 mg or 140 mg), with cumulative exposure of 2641.2 patient-years. Exposure-adjusted adverse event rates during the double-blind treatment phase were similar to placebo, with the exception of injection-site reactions (17.1 vs. 10.8 per 100 patient-years), constipation (7.0 vs. 3.8 per 100 patient-years), and muscle spasm (2.3 vs. 1.2 per 100 patient-years). During the long-term extensions, adverse events reported were similar to those observed during the double-blind treatment phase, and rates of injection site reactions, constipation, and muscle spasm were reported at lower rates than in the double-blind treatment phase. There were two deaths reported, both confounded by pre-existing conditions. Conclusions: This pooled safety analysis revealed a favorable and stable adverse event profile over time for erenumab with more than three years of exposure. Trial registration: ClinicalTrials.gov NCT01952574, NCT02483585, NCT02456740, NCT02066415, and NCT02174861. … (more)
- Is Part Of:
- Cephalalgia. Volume 39:Number 14(2019)
- Journal:
- Cephalalgia
- Issue:
- Volume 39:Number 14(2019)
- Issue Display:
- Volume 39, Issue 14 (2019)
- Year:
- 2019
- Volume:
- 39
- Issue:
- 14
- Issue Sort Value:
- 2019-0039-0014-0000
- Page Start:
- 1798
- Page End:
- 1808
- Publication Date:
- 2019-12
- Subjects:
- Erenumab -- safety -- migraine
Headache -- Periodicals
616.8491 - Journal URLs:
- http://cep.sagepub.com/ ↗
http://firstsearch.oclc.org/journal=0333-1024;screen=info;ECOIP ↗
http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=cha ↗
http://www.uk.sagepub.com/home.nav ↗ - DOI:
- 10.1177/0333102419888222 ↗
- Languages:
- English
- ISSNs:
- 0333-1024
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3113.691000
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