FDA Approves Subcutaneous Formulation Of ORENCIA (Abatacept) For Adults With Moderate To Severe Rheumatoid Arthritis
Bristol-Myers Squibb Company announced today that the U.S. Food and Drug Administration (FDA) has approved a subcutaneous (SC) formulation of ORENCIA® (abatacept) for the treatment of adults with moderate to severe rheumatoid arthritis (RA)...
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