Roche receives USFDA approval for Ocrevus Zunovo for treatment of progressive multiple sclerosis
This approval is backed by a decade of proven safety and efficacy data of Ocrevus® IV, with over 350,000 people treated globally
This approval is backed by a decade of proven safety and efficacy data of Ocrevus® IV, with over 350,000 people treated globally
New safety data show a consistent benefit-risk profile across all Ocrevus clinical trials
Fenebrutinib targets cells in the immune system known as B cells and microglia
US FDA and EMA accepted filings based on the data from OCARINA II, with EU approval anticipated mid-2024 and U.S. approval anticipated September 2024
Several late-stage pipeline products have the potential to address some of these unmet needs
Additional data across neurological disorders, including Alzheimer’s disease, help advance the scientific understanding of these conditions and the potential impact of early treatment
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