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Ocrevus reduced disability progression in diverse MS patients and outperformed other treatments in real-world data, with new drug fenebrutinib showing strong results.
Roche presented new data at the 2025 ECTRIMS Congress showing OCREVUS (ocrelizumab) effectively reduces disability progression in diverse MS patients, including those with advanced primary progressive MS, pregnant or breastfeeding women, and children.
It demonstrated sustained relapse and lesion suppression over two years, with safety comparable to intravenous dosing.
Real-world data from three large registries found ocrelizumab more effective than several other MS therapies at reducing relapses, particularly in patients with active disease or prior treatment failure.
Additionally, phase II results for the experimental BTK inhibitor fenebrutinib showed near-complete suppression of disease activity through 96 weeks.
These findings reinforce ocrelizumab’s role as a key treatment for multiple MS types and highlight ongoing progress in managing the disease.
Ocrevus redujo la progresión de la discapacidad en diversos pacientes con EM y superó a otros tratamientos en datos del mundo real, con el nuevo medicamento fenebrutinib mostrando fuertes resultados.