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Abstract Details

Eptinezumab Meaningfully Improves Quality of Life (QoL) in Patients with Episodic or Chronic Migraine Within 1 Month After Treatment
Headache
P2 - Poster Session 2 (5:30 PM-6:30 PM)
13-007
To evaluate changes in QoL after treatment with intravenous infusions of eptinezumab in patients with episodic migraine (EM) or chronic migraine (CM).

The Short-Form Health Survey (SF-36) is a robust measure of general health, with a score of ~50 representing the normative population. Eptinezumab, a selective and potent anti-CGRP monoclonal antibody, demonstrated significant reductions in monthly migraine days (primary efficacy endpoint) in patients with EM (NCT02559895) or CM (NCT02974153).

Adults with EM (N=888) or CM (N=1072) were randomized to eptinezumab 100mg, 300mg, or placebo (or 30mg in EM trial). QoL was evaluated descriptively using the SF-36 v2.0, administered at baseline, Week (Wk) 4, and Wk12. Patients in this analysis were stratified by baseline SF-36 scores (<35, 35-39, 40-44, 45-49, ≥50).

In patients with baseline SF-36 of <35, mean Mental Component Summary (MCS) score increased by 13.9 (300mg), 12.4 (100mg), and 7.2 (placebo), and mean Physical Component Summary (PCS) score increased by 11.0, 8.2, and 4.6 points, respectively, from baseline. In patients with baseline SF-36 of 35-39, mean MCS increased by 6.7 (300mg), 5.6 (100mg), and 4.5 (placebo), and mean PCS score increased by 7.8, 6.9, and 6.5 points, respectively, from baseline. In patients with baseline SF-36 of 40-44, mean MCS increased by 5.0 (300mg), 4.2 (100mg), and 4.3 (placebo), and mean PCS increased by 5.3, 4.7, and 3.2 points, respectively, from baseline. As expected, minimal improvement was observed in patients with normative population scores at baseline. Improvements were maintained or further improved for eptinezumab-treated patients through Wk12.

In migraine patients with diminished QoL, eptinezumab demonstrated rapid clinically meaningful improvements in SF-36 scores within the first month after the first infusion, with changes maintained or further improved through 3 months. Patients with worse QoL at baseline experienced greater improvements throughout the infusion period.

 

Authors/Disclosures
Egilius L. Spierings, MD, PhD (MEDVADIS RESEARCH)
PRESENTER
Dr. Spierings has received personal compensation in the range of $10,000-$49,999 for serving as a Consultant for Manistee. Dr. Spierings has received personal compensation in the range of $10,000-$49,999 for serving on a Speakers Bureau for Lundbeck. Dr. Spierings has received personal compensation in the range of $10,000-$49,999 for serving on a Speakers Bureau for Lilly. Dr. Spierings has received personal compensation in the range of $10,000-$49,999 for serving on a Speakers Bureau for Abbvie.
No disclosure on file
Roger Cady, MD (RK Consulting, LLC) Dr. Cady has received personal compensation for serving as an employee of Lundbeck. Dr. Cady has stock in Alder Biopharmaceutical.
No disclosure on file
Eric Kassel, PharmD No disclosure on file
David M. Biondi, DO, FAAN Dr. Biondi has received personal compensation for serving as an employee of Cohen Veterans Bioscience, Inc. Dr. Biondi has received personal compensation for serving as an employee of Alder Biopharmaceuticals, Inc. Dr. Biondi has received stock or an ownership interest from Johnson & Johnson . The institution of Dr. Biondi has received research support from US Department of Defense .
No disclosure on file