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US FDA endocrine/metabolic panel to review two orphan drugs in January
24 November 2009
Sue Sutter

sue.sutter@informa.com

The US FDA's endocrinologic and metabolic drugs panel will convene on January 12th to discuss Actelion's NDA for Zavesca (miglustat) for the treatment of progressive neurological manifestations in patients with Niemann-Pick type C (NP-C) disease.

On January 13th, the panel will consider...



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