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BioWorld - Wednesday, April 15, 2026
Home » epilepsy

Articles Tagged with ''epilepsy''

Neurocrine, Xenon in deal for $50M up front, up to $1.7B in milestones

Dec. 2, 2019
By Lee Landenberger
In its second large deal of the calendar year, Neurocrine Biosciences Inc. acquired the rights to Xenon Pharmaceutical Inc.’s selective sodium channel inhibitor for treating epileptic encephalopathy. Xenon receives $30 million up front, $20 million in equity and up to $1.7 billion in potential development, regulatory and commercial milestone payments.
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Green traffic light

FDA green-lights SK’s Xcopri in epileptic seizures; gate for Arvelle with EMA

Nov. 26, 2019
By Randy Osborne
On its PDUFA date Thursday, the FDA cleared Xcopri (cenobamate) tablets from South Korea’s SK Biopharmaceuticals Co. Ltd. to treat partial-onset seizures in adults. The drug’s mechanism of action is not fully understood, but it's believed to work through two separate mechanisms: enhancing inhibitory currents through positive modulation of GABA-A receptors and decreasing excitatory currents by inhibiting the persistent sodium current. 
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FDA green-lights SK’s Xcopri in epileptic seizures; gate for Arvelle with EMA

Nov. 22, 2019
By Randy Osborne
On its PDUFA date Thursday, the FDA cleared Xcopri (cenobamate) tablets from South Korea’s SK Biopharmaceuticals Co. Ltd. to treat partial-onset seizures in adults. The drug’s mechanism of action is not fully understood, but it's believed to work through two separate mechanisms: enhancing inhibitory currents through positive modulation of GABA-A receptors and decreasing excitatory currents by inhibiting the persistent sodium current. 
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Swiss startup Arvelle preps for FDA decision on epilepsy drug

Nov. 4, 2019
By Nuala Moran

LONDON – The Swiss headquarter operations of Arvelle Therapeutics GmbH are taking shape as the company awaits the outcome later this month of the FDA's deliberations on its in-licensed asset, cenobamate, and prepares to apply for EMA approval for the novel epilepsy treatment in the first half of 2020.


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Doc.ai software apps

Doc.ai study looks to optimize drug treatment for epilepsy patients

Oct. 18, 2019
By Meg Bryant
Palo Alto, Calif.-based startup Doc.ai is training its sights on the $9.5 billion global epilepsy market, with the aim of using artificial intelligence to help patients find the best medication to control their seizures. To that end, the company is teaming up with the Stanford University School of Medicine and the Stanford Epilepsy Center on a digital health trial to develop a predictive treatment model that will identify the right treatment at the right time for individuals living with epilepsy.
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Pipeline is expanding to meet the need for epilepsy treatments

Sep. 30, 2019
By Peter Winter
According to the U.S. Epilepsy Foundation, one in 26 people in the country will develop epilepsy at some point in their lives and the condition is the fourth most common neurological disease that affects people of all ages. That is why the current anti-epilepsy drug therapy market is large and estimated to be worth more than $8.5 billion currently, rising to in excess of $9.5 billion in five years. 
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