Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Clinical Trial
. 2021 Jan;30(1):105-115.
doi: 10.1007/s11136-020-02623-1. Epub 2020 Sep 15.

Changes in patient functioning and disability: results from a phase 3, double-blind, randomized, placebo-controlled clinical trial evaluating galcanezumab for chronic migraine prevention (REGAIN)

Affiliations
Clinical Trial

Changes in patient functioning and disability: results from a phase 3, double-blind, randomized, placebo-controlled clinical trial evaluating galcanezumab for chronic migraine prevention (REGAIN)

Janet Ford et al. Qual Life Res. 2021 Jan.

Abstract

Purpose: To evaluate secondary outcomes including changes in functioning and disability associated with galcanezumab, a humanized monoclonal antibody to calcitonin gene-related peptide, in patients with chronic migraine.

Methods: Patients randomly received galcanezumab (120 mg n = 278, 240 mg n = 277) or placebo (n = 558) during 3 months of double-blind treatment, followed by a 9-month open-label extension. The Migraine-Specific Quality-of-Life Questionnaire v2.1 (MSQv2.1) measured the impact of migraine on patient functioning. The Migraine Disability Assessment (MIDAS) quantified headache-related disability. Changes from baseline were analyzed with mixed model repeated measures or analysis of covariance.

Results: Total MSQ score at baseline was 44.88 ± 18.02 (mean ± SD), indicating significant functional impairment. At Month 3, least squares (LS) mean change ± SE in total MSQ for galcanezumab-treated patients were 20.51 ± 1.49 (120 mg) and 20.49 ± 1.49 (240 mg), both statistically significantly greater vs placebo-treated patients (14.55 ± 1.21; both P < 0.001). Total MIDAS score at baseline was 67.24 ± 57.31 (mean ± SD). At Month 3, LS mean change ± SE from baseline in total MIDAS for galcanezumab-treated patients was statistically significantly greater than placebo for 120 mg group (placebo: - 11.53 ± 3.38 vs 120 mg: - 20.27 ± 4.07; P < 0.05) but not for 240 mg group (- 17.02 ± 4.05). At Month 12, within-group mean changes from baseline for total MSQ (28.56 ± 1.19 previous placebo; 29.53 ± 1.51 previous 120 mg; 25.83 ± 1.49 previous 240 mg) and MIDAS scores (- 28.47 ± 2.95 previous placebo; - 31.47 ± 3.69 previous 120 mg; - 31.13 ± 3.62 previous 240 mg) were statistically significant (P < 0.001) for the open-label treatment population regardless of previous double-blind treatment assignment.

Conclusions: Galcanezumab-treated patients with chronic migraine reported statistically significant improvements in functioning and disability, representing a clinically significant change.

Trial registration: ClinicalTrials.gov registry: NCT02614261. Registered 25 November 2015.

Keywords: Calcitonin gene-related peptide; Chronic migraine; Disability; Galcanezumab; Patient-reported outcomes; Quality of life.

PubMed Disclaimer

Conflict of interest statement

The following authors are employees and minor stockholders of Eli Lilly and Company or Lilly USA, LLC: JF, HD, SW, DA, and RN. CT has consulted for Allergan S.p.A., electroCore, Inc., Eli Lilly and Company, Novartis AG, and Teva Neuroscience and is also a principal investigator or collaborator for randomized controlled trials sponsored by Alder BioPharmaceuticals Inc., Eli Lilly and Company, Novartis, and Teva Pharmaceutical Industries Ltd. EL has consulted for Allergan, Aralez, Eli Lilly and Company, Novartis AG, and Teva Neuroscience.

Figures

Fig. 1
Fig. 1
Least squares mean change from baseline ± standard error for Migraine-Specific Quality of Life total score
Fig. 2
Fig. 2
Least squares mean change from baseline ± standard error for Migraine-Specific Quality of Life Role Function Restrictive domain score
Fig. 3
Fig. 3
Least squares mean change from baseline ± standard error for MIDAS total score

References

    1. Aurora SK, Brin MF. Chronic migraine: An update on physiology, imaging, and mechanism of action of two available pharmacologic therapies. Headache. 2017;57:109–125. doi: 10.1111/head.12999. - DOI - PMC - PubMed
    1. Bigal ME, Serrano D, Buse D, Scher A, Stewart WF, Lipton RB. Acute migraine medications and evolution from episodic to chronic migraine: A longitudinal population-based study. Headache. 2008;48:1157–1168. doi: 10.1111/j.1526-4610.2008.01217.x. - DOI - PubMed
    1. Katsarava Z, Schneeweiss S, Kurth T, Kroener U, Fritsche G, Eikermann A, et al. Incidence and predictors for chronicity of headache in patients with episodic migraine. Neurology. 2004;62:788–790. doi: 10.1212/01.WNL.0000113747.18760.D2. - DOI - PubMed
    1. Schwedt TJ. Chronic migraine. BMJ. 2014;348:g1416. doi: 10.1136/bmj.g1416. - DOI - PubMed
    1. May A, Schulte LH. Chronic migraine: Risk factors, mechanisms and treatment. Nature Reviews Neurology. 2016;12:455–464. doi: 10.1038/nrneurol.2016.93. - DOI - PubMed

Publication types

Substances

Associated data