A greater proportion of amantadine recipients than placebo recipients had a clinically meaningful improvement in walking with treatment at 4 weeks in a phase-2 study.
Better treatments are needed for gait disorders in patients with multiple sclerosis (MS). Amantadine extended-release was studied in a randomized, double-blind, phase 2, multicenter, manufacturer-sponsored trial for those diagnosed with MS who were ambulatory. After a 1-week titration, 59 patients took the full 274 mg daily dose or placebo during weeks 2 through 4.
Improvements over baseline walking speed by the timed 25-foot walk (T25W) were 17% at week 2 and 25% at week 4 in the amantadine group, versus 8% at both weeks 2 and 4 in the placebo group. The proportion of responders (those with ≥20% improvement on the T25W, averaged over weeks 2 and 4) was 30% with amantadine and 17% with placebo. Five amantadine recipients discontinued due to …
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)