Xcopri FDA approval a milestone for Korea

22 November 2019

The US Food and Drug Administration (FDA) has approved SK Life Science’s Xcopri (cenobamate tablets) as a treatment for partial-onset seizures in adults.

With this approval, the company, which is part of SK Biopharmaceuticals and the wider SK Group conglomerate, becomes the first Korean firm to independently bring a compound from discovery to approval in the USA.

Xcopri, an anti-epileptic drug, is expected to be available in the USA in the second quarter of 2020, following scheduling review by the US Drug Enforcement Administration.

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