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FDA Accepts Biologics License Application for Subcutaneous Formulation of Nivolumab

The new administration method, which is co-formulated with rHuPH20, is usable in previous approved nivolumab indications for solid tumors in adult patients.

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Bristol-Myers Squibb (BMY) Announces FDA Accepts Supplemental Biologics License Application and European Medicines Agency Validates Application for Opdivo

Bristol-Myers Squibb (BMY) Announces FDA Accepts Supplemental Biologics License Application and European Medicines Agency Validates Application for Opdivo
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