FDA Dermatology and Ophthalmology Drugs Advisory Committee to review Lux Biosciences' Luveniq NDA

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FDA Dermatology and Ophthalmology Drugs Advisory Committee to review Lux Biosciences' Luveniq NDA

news-medical.net

Lux Biosciences, Inc. today announced that the Dermatology and Ophthalmology Drugs Advisory Committee of the U.S. Food and Drug Administration (FDA) is scheduled to review its New Drug Application (NDA) for Luveniq" (oral voclosporin) for the treatment of non-infectious uveitis involving the intermediate or posterior segments of the eye on June 28, 2010.

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Tags: Dermatology, Eye, Drug, FDA, Ophthalmology

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FDA Advisory Committee To Review Lux Biosciences' Uveitis Candidate Luveniq™

medicalnewstoday.com — “Lux Biosciences, Inc. today announced that the Dermatology and Ophthalmology Drugs Advisory Committee of the U.S. Food and Drug Administration (FDA) is scheduled to review its New Drug ApplicationView full resource at medicalnewstoday.com

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