A double-blind, randomized, placebo-controlled phase 2 trial evaluating the selective dihydroorotate dehydrogenase inhibitor vidofludimus calcium in relapsing-remitting multiple sclerosis.

Robert J Fox, Heinz Wiendl, Christian Wolf, Nicola De Stefano, Johann Sellner, Viktoriia Gryb, Konrad Rejdak, Plamen Stoyanov Bozhinov, Nataliya Tomakh, Iryna Skrypchenko, Andreas R Muehler

Journal: Annals of clinical and translational neurology 2022;9(7):977-987

PMID: 35698927

Abstract

OBJECTIVE

Inhibition of dihydroorotate dehydrogenase suppresses magnetic resonance imaging brain lesions and disease activity in multiple sclerosis but has limiting tolerability. We assessed the safety and efficacy of vidofludimus calcium, a novel, selective dihydroorotate dehydrogenase inhibitor, in patients with relapsing-remitting multiple sclerosis.

METHODS

This double-blind, 24 weeks, placebo-controlled, phase 2 trial (EMPhASIS) enrolled patients 18-55 years with relapsing-remitting multiple sclerosis. Eligible patients were randomly assigned (1:1:1) to once-daily vidofludimus calcium (30 mg or 45 mg) or placebo. The primary endpoint was the cumulative number of combined unique active lesions to week 24 between vidofludimus calcium 45 mg and placebo (clinicalTrials.gov number NCT03846219; EudraCT 2018-001896-19).

RESULTS

After 24 weeks, the mean cumulative number of combined unique active lesions was 6.4 (95% CI: 2.8-13.9) with placebo compared to 2.4 (95% CI: 1.1-4.9) with vidofludimus calcium 45 mg (rate ratio 0.38, 95% CI: 0.22-0.64; p = 0.0002); the rate ratio between vidofludimus calcium 30 mg and placebo was 0.30 (95% CI: 0.17-0.53; p < 0.0001). Treatment-emergent adverse events occurred in 30 (44%) of patients assigned placebo and 60 (43%) of patients assigned vidofludimus calcium. Serious adverse events occurred in one (1%) assigned placebo and two (1%) assigned vidofludimus calcium. No increased incidence of infectious, hepatic, or renal treatment-emergent adverse events or serious adverse events was observed.

INTERPRETATION

Treatment with vidofludimus calcium led to a reduction in new magnetic resonance imaging lesions in patients with relapsing-remitting multiple sclerosis and was well tolerated with a favorable safety profile. Assessment in longer, larger trials is justified.

© 2022 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association.

Address: Mellen Center for Multiple Sclerosis, Cleveland Clinic, Cleveland, Ohio, USA.; Department of Neurology with Institute of Translational Neurology, University of Münster, Münster, Germany.; Lycalis sprl, Brussels, Belgium.; Department of Medicine, Surgery and Neuroscience, University of Siena, Siena, Italy.; Department of Neurology, Landesklinikum Mistelbach-Gänserndorf, 2130, Mistelbach, Austria.; Regional Clinical Hospital Department of Vascular Neurology, Ivano-Frankivsk, Ukraine.; Medical University of Lublin, Department of Neurology, Jaczewskiego 8, 20-954, Lublin, Poland.; Medical University of Pleven, 1 Saint Kliment Ohridski Street, 5800, Pleven, Bulgaria.; LLC "INET-09" 32, Zhabotinskogo Leonida Street, Zaporozhye, Ukraine.; Kharkiv Regional Clinical Hospital Department of Neurology, Kharkiv, Ukraine.; Immunic AG, Lochhamer Schlage 21, 82166, Gräfelfing, Germany.
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