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TM) labeling supplement for removal of blood screening requirement

Monday, May 28, 2007

VANCOUVER, May 29 /PRNewswire-FirstCall/ -- QLT Inc. ( Nachrichten ) (NASDAQ: QLTI; TSX: QLT) announced today that QLT USA, Inc. submitted a labeling supplement (sNDA) for Aczone(TM) to the U.S. Food and Drug Administration (FDA) to request the removal of the gluceose-6-phosphate dehydrogenase (G6PD) screening and blood monitoring requirements from its current label.
From: www.finanznachrichten.de

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