The case for approval of Fintepla (fenfluramine) to treat seizures associated with Dravet syndrome has been given a boost by the addition of new data.
New results presented at the Childhood Neurology Society Congress include data showing a long-term, clinically-meaningful reduction in convulsive seizure frequency in Dravet syndrome patients aged under six years, in an ongoing open-label extension study.
Further data was presented from a post-hoc analysis showing clinically-meaningful and profound reduction in the frequency of high-risk tonic-clonic seizures in Dravet syndrome patients treated in two previously completed Phase III clinical trials.
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