Zogenix, Inc.
(NASDAQ: ZGNX), a global pharmaceutical company developing rare disease
therapies, today announced positive new data for its investigational
drug, FINTEPLA® (ZX008, fenfluramine), for the treatment of seizures
associated with Dravet syndrome. The data were presented in five
scientific posters, available here,
at the recent Childhood Neurology Society (CNS) Congress. The posters
include data showing long-term, clinically meaningful reduction in
convulsive seizure frequency in young Dravet syndrome patients (under 6
years of age) in an ongoing Open-Label Extension (OLE) study, as well as
data from a post-hoc analysis showing clinically meaningful and
profound reduction in the frequency of high-risk tonic-clonic
(grand-mal) seizures in Dravet syndrome patients treated in two
previously completed Phase 3 clinical trials. Other data include the
results of a Phase 1 study to assess the potential drug-drug interaction
of fenfluramine and cannabidiol (CBD).
“These data continue to demonstrate the significant clinical impact
Fintepla has shown in studies of Dravet syndrome patients,” said Bradley
Galer, M.D., Executive Vice President and Chief Medical Officer at
Zogenix. “These new results clearly show the impact this drug candidate
has had on some of the most vulnerable patients, those who are younger
than 6 years of age, as well as those suffering from generalized
tonic-clonic seizures, a recognized risk factor for sudden unexplained
death in epilepsy (SUDEP).”
https://www.biospace.com/article/releases/zogenix-announces-new-positive-data-for-its-investigational-drug-fintepla-in-dravet-syndrome/
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