Both weekly and thrice-weekly dosing was effective for patients with a first demyelinating event.
To gain regulatory approval to label subcutaneous interferon beta-1a (IFN-β-1a) for use in clinically isolated syndrome, investigators compared the effects of two different dosages of the drug in a multicenter, industry-sponsored, randomized, double-blind, placebo-controlled trial. Participants were aged 18 to 50, had a recent first demyelinating event typical of multiple sclerosis (MS), and had baseline T2 magnetic resonance imaging (MRI) abnormalities suggestive of MS. Participants were randomized to placebo, weekly subcutaneous IFN-β-1a, or thrice-weekly subcutaneous IFN-β-1a. Upon conversion to clinically definite MS (by having a second clinical event or new MRI activity on quarterly scans), patients were switched to open-label, thrice-…
Reviewing Author
DisclosuresConsultant/Advisory BoardAlexion Pharmaceuticals; Amgen; Astoria; Biogen; Bristol Myers Squibb; Celltrion; Genentech; Hoffmann-La Roche; Genzyme; EMD Serono; Immpact-Bio; Immunic Therapeutics; Kyverna; Lundbeck; Novartis; Sandoz; TG Therapeutics
Grant/Research SupportNational Institutes of Health; National Multiple Sclerosis Society; U.S. Department of Defense
Leadership Positions in Professional SocietiesConsortium of Multiple Sclerosis Centers (Treasurer)
DisclosuresConsultant/Advisory BoardAlexion Pharmaceuticals; Amgen; Astoria; Biogen; Bristol Myers Squibb; Celltrion; Genentech; Hoffmann-La Roche; Genzyme; EMD Serono; Immpact-Bio; Immunic Therapeutics; Kyverna; Lundbeck; Novartis; Sandoz; TG Therapeutics
Grant/Research SupportNational Institutes of Health; National Multiple Sclerosis Society; U.S. Department of Defense
Leadership Positions in Professional SocietiesConsortium of Multiple Sclerosis Centers (Treasurer)