Presented interim FRONTIER4 data evaluate the long-term safety and efficacy of investigational denecimig across once-weekly, once-every-two-weeks, and once-monthly dosing in hemophilia A participants of all ages and disease severities1,2Denecimig is an investigational subcutaneous FVIIIa-mimetic antibody under review with the US Food and Drug Administration (FDA)1Separate phase 3 explorer10 data observed that concizumab reduced annualized bleeding rate compared to on-demand treatment in children with hemophilia A or B, with inhibitors3

Presented interim FRONTIER4 data evaluate the long-term safety and efficacy of investigational denecimig across once-weekly, once-every-two-weeks, and once-monthly dosing in hemophilia A participants of all ages and disease severities1,2Denecimig is an investigational subcutaneous FVIIIa-mimetic antibody under review with the US Food and Drug Administration (FDA)1Separate phase 3 explorer10 data observed that concizumab reduced annualized bleeding rate compared to on-demand treatment in children with hemophilia A or B, with inhibitors3