Thursday, 7 June 2012

Food And Drug Administration-Restless Legs Syndrome-Glaxosmithkline-Xenoport-Gsk

U.S. approves GSK, Xenoport drug for new use
Food And Drug Administration-Hospitalizations-Healthday News-Cosmetics
A GlaxoSmithKline logo is seen outside one of its buildings in west London

LONDON (Reuters) - GlaxoSmithKline and XenoPort have received approval from the U.S. Food and Drug Administration to sell Horizant to treat post-herpetic neuralgia, the companies said on Thursday. The medicine is already approved as a treatment for restless legs syndrome. XenoPort will receive a milestone payment of $10 million from GSK following first sales of the drug in its new use. (Reporting by Ben Hirschler; editing by Kate Kelland) read more..

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