Valeant Pharma (VRX) Announces Brodalumab FDA Advisory Committee Meeting On July 19
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Valeant To Participate In FDA Advisory Committee Meeting On July 19
June 9, 2016 5:40 PM EDTCommittee to Review Valeant's BLA 761032 Brodalumab Subcutaneous Injection For Treatment of Adult Patients with Moderate to Severe Plaque Psoriasis
LAVAL, Quebec, June 9, 2016 /PRNewswire/ -- Valeant Pharmaceuticals International, Inc. (NYSE: VRX and TSX: VRX) ("Valeant" or the "Company") today announced that it has received notification from the U.S. Food and Drug Administration (FDA) that the Dermatologic and Ophthalmic Drugs Advisory Committee will review Valeant's New Drug Application (NDA) for brodalumab on July 19, 2016.
On January 25, 2016, Valeant announced that the FDA had accepted for review the Biologics License... More
