4.3 Article

Long-term efficacy and safety of siponimod in patients with secondary progressive multiple sclerosis: Analysis of EXPAND core and extension data up to >5 years

期刊

MULTIPLE SCLEROSIS JOURNAL
卷 28, 期 10, 页码 1591-1605

出版社

SAGE PUBLICATIONS LTD
DOI: 10.1177/13524585221083194

关键词

Confirmed disability progression; confirmed cognitive worsening; cortical gray matter; secondary progressive multiple sclerosis; siponimod; S1P modulator

资金

  1. Novartis Pharma AG, Basel, Switzerland

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This study evaluated the long-term efficacy and safety of siponimod in the treatment of SPMS. The results showed that continuous use of siponimod reduced the risk of disability progression and worsening in cognitive processing speed, and sustained efficacy was observed in relapse rate, brain atrophy, and inflammatory disease activity. No new safety signals were identified over the long term.
Background: Siponimod significantly reduced the risk of confirmed disability progression (CDP), worsening in cognitive processing speed (CPS), relapses, and magnetic resonance imaging (MRI) measures of brain atrophy and inflammation versus placebo in secondary progressive multiple sclerosis (SPMS) patients in the Phase 3 EXPAND study. Objective: The aim of this study was to assess long-term efficacy and safety of siponimod 2 mg/day from the EXPAND study including the extension part, up to > 5 years. Methods: In the open-label extension part, participants receiving placebo during the core part were switched to siponimod (placebo-siponimod group) and those on siponimod continued the same treatment (continuous siponimod group). Results: Continuous siponimod reduced the risk of 6-month CDP by 22% (hazard ratio (HR) (95% confidence interval (CI)): 0.78 (0.66-0.92) p = 0.0026) and 6-month confirmed worsening in CPS by 23% (HR (95% CI): 0.77 (0.65-0.92) p = 0.0047) versus the placebo-siponimod group. Sustained efficacy on annualized relapse rate, total and regional brain atrophy, and inflammatory disease activity was also observed. No new, unexpected safety signals for siponimod were identified over the long term. Conclusion: The sustained efficacy and consistent long-term safety profile of siponimod up to > 5 years support its clinical utility for long-term treatment of SPMS. Benefits in the continuous siponimod versus placebo-siponimod group highlight the significance of earlier treatment initiation.

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