This B-cell depleting therapy reduced worsening disability by 24%.
Effective treatments for primary progressive multiple sclerosis (PPMS) have remained a major unmet need. A phase II study of rituximab in PPMS was overall negative, but subgroup analyses suggested possible benefit in younger and less disabled patients. Similar to rituximab, the investigational drug ocrelizumab depletes B cells via binding by CD20. For this multicenter, randomized, double-blind, placebo-controlled, manufacturer-sponsored phase 3 study, investigators recruited 732 patients with PPMS (age range, 18–55; Expanded Disability Status Scale score 3.0– 6.5 [i.e., mild disability through walker dependent]; disease duration <15 years) who met diagnostic criteria plus the presence of abnormal cerebrospinal fluid. Ocrelizumab or placebo …
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)