Safety and Efficacy of Fingolimod in Pediatric Patients With Multiple Sclerosis
Phase 3
Active, not recruiting
NCT01892722
| Condition | Multiple Sclerosis |
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| Phase | Phase 3 |
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| Sponsor | Novartis Pharmaceuticals |
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| Status | Active, not recruiting |
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| Enrollment | 240 participants |
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| Interventions | Interferon beta-1a, Fingolimod, Placebo capsule, Placebo i.m. injection |
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| Start date | Jul 26, 2013 |
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| Completion date | Jul 14, 2017 |
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| Results posted | Sep 19, 2018 |
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Summary
To evaluate the safety and efficacy of fingolimod vs. interferon beta-1a i.m. in pediatric patients with multiple sclerosis (MS)
Frequency of Relapses in Patients Treated for up to 24 Months
24 months · Confirmed relapse per year
| Fingolimod | 0.122 Confirmed relapse per year |
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| Interferon Beta-1a | 0.675 Confirmed relapse per year |
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Open in BENITIONS
View on ClinicalTrials.gov
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