ADVENTRX Pharmaceuticals to meet FDA to review its NDA for ANX-530 ADVENTRX Pharmaceuticals, Inc. today announced that it’ll meet up with the U.S sulbutiamine uk . Meals and Medication Administration in Washington D.C. Over the last week of April 2010 to examine the Company’s New Drug Software for ANX-530 and the FDA’s refusal-to-document letter. ADVENTRX experienced requested a face-to-face ending up in the FDA to understand its requirements and define the path to an effective filing of an ANX-530 NDA at the initial possible time. Culley, Chief Executive Officer of ADVENTRX. In December 2009 ADVENTRX submitted an NDA for ANX-530 to the FDA.
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