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to treat adults with relapsing forms of multiple sclerosis (MS

Janssen announces U.S. FDA approval of PONVORY

Janssen announces U.S. FDA approval of PONVORY

TITUSVILLE, N.J. —The Janssen Pharmaceutical Companies of Johnson & Johnson announced Friday that the U.S. Food and Drug Administration (FDA) approved PONVORY (ponesimod), a once-daily oral selective sphingosine-1-phosphate receptor 1 (S1P1) modulator, to treat adults with relapsing forms of multiple sclerosis (MS), to include clinically isolated syndrome, relapsing-remitting disease and active secondary progressive disease. PONVORY

PP_1170x120_10-25-21