Ocrevus data to show sustained reduction in disability progression through 8 years for primary progressive multiple sclerosis (PPMS) and 7.5 years for relapsing MS (RMS)
Long-term safety analysis of all clinical trials will reinforce the consistently favorable benefit-risk profile of Ocrevus
Enspryng data to show efficacy and safety sustained over four years of treatment for people living with neuromyelitis optica spectrum disorder (NMOSD)
Study design for SAkuraBONSAI, a new study on disease activity and progression in Enspryng patients, who are treatment naïve or where prior rituximab (or biosimilar) treatment has failed, will be presented
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