Fatal cases of acute liver failure reported in patients treated with Zolgensma (onasemnogene abeparvovec) were raised this week at the European Medicines Agency’s (EMA) Pharmacovigilance Risk Assessment Committee (PRAC).
The committee discussed a direct healthcare professional communication (DHPC) containing information on Zolgensma, Novartis’ (NOVN: VX) gene therapy indicated for the treatment of spinal muscular atrophy (SMA).
This DHPC informs healthcare professionals of the fatal cases of liver failure and the updated recommendations for monitoring liver function, assessing suspected liver injury after infusion and further advice regarding tapering the corticosteroid treatment.
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