Novartis Remibrutinib Meets Primary Endpoint in Late-Stage MS Studies

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Novartis announced positive top-line results from the late-stage REMODEL-1 and REMODEL-2 studies, showing that its oral BTK inhibitor remibrutinib significantly reduced annualized relapse rate compared to Aubagio in patients with relapsing multiple sclerosis. The identical phase III trials, which enrolled approximately 2,000 patients worldwide, also demonstrated favorable safety and clinically meaningful reductions in disability progression. Following the news, Novartis shares rose 6%, bringing year-to-date gains to 17%. The company plans to present full data at MSToronto2026 and pursue global regulatory approvals for remibrutinib in RMS. This comes as Novartis already markets remibrutinib as Rhapsido for chronic spontaneous urticaria, which generated $101 million in first-half 2026 sales.

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Remibrutinib meets primary endpoint in phase III MS studies, reducing relapse rate vs Aubagio.

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