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Xenon expects to identify a Nav1.6 sodium channel inhibitor for the treatment of rare infantile epileptic encephalopathies development candidate in 2016

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Xenon's development of a Nav1.6 sodium channel inhibitor for the treatment of rare infantile epileptic encephalopathies – such as Dravet Syndrome and SCN8A (Nav1.6 gain-of-function) Epilepsy – continues to progress well. Xenon has identified potent, selective Nav1.6 inhibitors, and encouraging results from in vivo animal studies indicate that selective Nav1.6 inhibitors have demonstrated efficacy for seizures in a model of Nav1.6 gain-of-function SCN8A epilepsy, supporting the hypothesis that SCN8A epilepsies can be treated with potent, selective Nav1.6 inhibitors. Xenon expects to identify a development candidate in 2016 and file an investigational new drug (IND) application in the first half of 2017.
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Catalyst Date
Occurred on:
Mar 08, 2017
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Related Keywords Nav1.6 Sodium Channel Inhibitor, Rare Infantile Epileptic Encephalopathies, Ind, Scn8a Epilepsies