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UCB Receives Complete Response Letter from U.S. FDA Regarding NeuproŽ (Rotigotine)

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Old 04-29-2010, 09:58 AM #1
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Default UCB Receives Complete Response Letter from U.S. FDA Regarding NeuproŽ (Rotigotine)
UCB Receives Complete Response Letter from U.S. FDA Regarding NeuproŽ (Rotigotine)

23-Apr-2010 18:00 pm CET | Brussels (Belgium)
  • FDA recommends reformulation of NeuproŽ in the U.S.
  • In Europe and other countries, NeuproŽ is not impacted by this recommendation
  • UCB has already made progress in reformulation and remains committed to bringing NeuproŽ to U.S. patients suffering from Parkinson's disease and Restless Leg Syndrome

Full press release content: http://www.ucb.com/media-room/newsdetail/?det=1407441
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