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Chugai Pharmaceutical Co., Ltd. and F. Hoffmann–La Roche Ltd. announced today that FDA has accepted the complete response resubmission that Roche made to the U.S. Food and Drug Administration for the Biologics License Application (BLA) for Actemra the humanized anti–human IL–6 (interleukin–6) receptor monoclonal antibody, following the receipt of the Complete Response Letter in September 2008.


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