Changes in migraine interictal burden following treatment with galcanezumab: Results from a phase III randomized, placebo‐controlled study

Author:

Lipton Richard B.1,Buse Dawn C.1,Sandoe Claire H.2,Ford Janet H.3ORCID,Hand Austin L.4,Jedynak Jakub P.3,Port Martha D.3ORCID,Detke Holland C.3ORCID

Affiliation:

1. The Saul R. Korey Department of Neurology Albert Einstein College of Medicine of Yeshiva University Bronx New York USA

2. Department of Neurology Women's College Hospital Centre for Headache Toronto Ontario Canada

3. Lilly Corporate Center Eli Lilly and Company Indianapolis Indiana USA

4. Biostatistics IQVIA Durham North Carolina USA

Abstract

AbstractObjectiveTo evaluate changes in interictal burden with galcanezumab versus placebo in patients with episodic (EM) or chronic migraine (CM).BackgroundThe disruptive effects of migraine occur both during attacks (ictal period) and between attacks (interictal period), affecting work, school, family, and social life. Migraine clinical trials typically assess ictal burden endpoints, neglecting interictal burden.MethodsCONQUER was a 3‐month, double‐blind study that randomized adult patients with EM or CM who had experienced failure of two to four standard‐of‐care migraine preventive medication categories to receive monthly galcanezumab (n = 232) or placebo (n = 230), followed by 3 months of open‐label galcanezumab. The mean change in interictal burden, a secondary objective, was measured using the four‐item Migraine Interictal Burden Scale (MIBS‐4). The total score for MIBS‐4 can range from zero to 12, with scores ≥5 indicating severe interictal burden. Post hoc analyses evaluated shifts in MIBS‐4 severity categories and item‐level improvement.ResultsThe MIBS‐4 total score indicated severe interictal burden at baseline (mean [SD]: all patients, 5.5 [3.5]; EM, 5.0 [3.4]; CM, 6.2 [3.5]). Reductions in the MIBS‐4 score were significantly greater with galcanezumab versus placebo at Month 3 (mean [SE]: all patients −1.9 [0.2] vs. −0.8 [0.2], p < 0.0001; EM, −1.8 [0.3] vs. −1.1 [0.3], p = 0.033; CM, −1.8 [0.4] vs. −0.3 [0.4], p < 0.001), with further improvement at Month 6 after all patients had received galcanezumab (mean [SE]: all patients, −2.4 [0.2] vs. −2.0 [0.2]; EM, −2.3 [0.3] vs. −2.2 [0.3]; CM, −2.1 [0.4] vs. −1.5 [0.4]). The percentage of patients with severe interictal burden decreased substantially for the galcanezumab‐treated patients, from 59% (137/232) at baseline to 27% (58/217) at Month 6 (EM from 51% [70/137] to 23% [30/131]; CM from 71% [67/95] to 33% [28/86]).ConclusionIn addition to the known efficacy of galcanezumab in the ictal period, these findings suggest treatment with galcanezumab results in a significant reduction in interictal burden.

Funder

Eli Lilly and Company

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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