Progress for Patients With Pediatric MS, Fingolimod's Risk-Benefit Profile: Brenda Banwell, MD
The chief of neurology and codirector of the neuroscience Center at the Children's Hospital of Philadelphia spoke about her presentation at ECTRIMS 2022 on the treatment of pediatric MS. [WATCH TIME: 5 minutes]
WATCH TIME: 5 minutes
“Given that pediatric MS is a highly inflammatory disease, with high relapse rates and a lot of T2 lesion burden, the imperative to get these highly effective therapies to our patients is extremely high and urgent.”
At the
Banwell also gave an oral presentation on fingolimod’s superior efficacy on relapses and MRI outcomes over interferon (IFN) beta-1a in POMS from the core phase (CP) of PARADIGMS trial (NCT01892722), which was was a double-blind, active-controlled, randomized trial of patients with PedMS that included 215 individuals treated up to 2 years followed by a 5-year, open-label expansion phase (EP) (n = 171). The dosage of fingolimod was at 0.5 mg/d or 0.25 mg/d according to the patients’ body weight (patients more than 40 kg received 0.5 mg/d dose).
Adjusted annualized relapse rate (ARR) was 0.11 (95% CI, 0.08, 0.16) for the continuous fingolimod group in CP+EP and 0.34 (95% CI, 0.25, 0.47) in the switch group. The most frequently reported adverse events (more than 20%) were nasopharyngitis (43.5%), headache (34.1%), leukopenia (25.3%), and upper respiratory tract infection (21.2%).
In a recent interview with NeurologyLive®, Banwell, chief of neurology, codirector of the neuroscience Center, The Children's Hospital of Philadelphia, professor of neurology and Pediatrics, the University of Pennsylvania, discussed her presentation from ECTRIMS 2022. Additionally, she gave an overview of the takeaway points on POMS from a clinician's perspective.
REFERENCES
1. Deiva K, Banwell B, Gärtner J. Long-term efficacy and safety of fingolimod in paediatric multiple sclerosis patients: analysis of PARADIGMS study up to 6 years of treatment. Presented at: 2022 ECTRIMS Congress; October 26-28; Amsterdam, Netherlands. Oral Presentation 69
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