A phase 3 study demonstrates superiority over teriflunomide.
Ponesimod, a selective sphingosine-1-phosphate (S1P) receptor 1 modulator, was approved by the FDA on March 18, 2021, for use in patients with relapsing multiple sclerosis (MS). In this industry-sponsored, international, randomized, double-blind, phase 3 study, researchers evaluated 20 mg daily of ponesimod versus 14 mg daily of teriflunomide (both oral) for 108 weeks in 1133 patients with active relapsing MS.
Annualized relapse rate was reduced by 30.5% and combined unique active lesions were reduced by 56% with ponesimod compared with teriflunomide. Confirmed disability worsening was similar between the two treatment arms. Brain volume loss and no evidence of disease activity favored ponesimod. The most common adverse events were elevated …
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)