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BMS’ ZEPOSIA Wins Approval for RMS

Oral medication offers RMS patients an initiation with no genetic test and no label-based first-dose observation required.

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By: Kristin Brooks

Managing Editor, Contract Pharma

Bristol-Myers Squibb Co. received approval from the U.S. FDA for ZEPOSIA (ozanimod) 0.92 mg for the treatment of adults with relapsing forms of multiple sclerosis (RMS), including clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease.   ZEPOSIA, an oral medication taken once daily, is the only approved sphingosine-1-phosphate (S1P) receptor modulator that offers RMS patients an initiation with no genetic test and no label-based first-dose observati...

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