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Home » Aveo Receives CRL from FDA After Stopping RCC Program
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Aveo Receives CRL from FDA After Stopping RCC Program

June 11, 2013
By Peter Winter
After acknowledging in a conference call Friday that the FDA would not in all likelihood approve its lead product tivozanib for renal cell carcinoma (RCC), Aveo Pharmaceuticals Inc. said Monday it received a complete response letter (CRL) from the agency informing the biotech it will not approve in its present form the new drug application (NDA) for the product.
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