The Cancer Letter

Inside information on cancer research and drug development

Drugs & Targets

FDA reassigns BLA goal date for subcutaneous Opdivo

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FDA has reassigned the previously announced Prescription Drug User Fee Act goal date of Bristol Myers Squibb’s Biologics License Application for the subcutaneous formulation of Opdivo (nivolumab) co-formulated with Halozyme’s proprietary recombinant human hyaluronidase (rHuPH20). 

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