drugset / Trial / NCT01665144

Exploring the Efficacy and Safety of Siponimod in Patients With Secondary Progressive Multiple Sclerosis (EXPAND)

NCT01665144 ↗

Phase 3 Completed 1651 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupDouble-blindTreatment

Summary

Evaluate the safety and efficacy of Siponimod (BAF312) versus placebo in a variable treatment duration in patients with secondary progressive multiple sclerosis (Core Part) followed by extended treatment with open-label BAF312 to obtain data on long-term safety, tolerability and efficacy (Extension Part).

Timeline

Start
2012-12-20
Primary completion
2016-04-29
Completion
2023-03-31

Outcome

Met primary endpoint

registry analysis (superiority test); Siponimod (BAF312) vs Placebo; p = 0.0134; Hazard Ratio (HR) 0.79 (95% CI 0.65 to 0.95); Cox proportional hazards model NCT01665144 ↗

release “The Phase III EXPAND study of BAF312 (siponimod) in secondary progressive multiple sclerosis (SPMS) met its primary endpoint” novartis.com ↗

release “Approval is based on the Phase III EXPAND trial, the largest controlled clinical study of SPMS patients, showing Mayzent significantly reduced the risk of disease progression” novartis.com ↗

release “Phase III EXPAND trial, the largest randomized clinical study in a broad range of SPMS patients, showing Mayzent significantly reduced the risk of disease progression” novartis.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject BAF312 Unknown 2 mg Oral