Study achieved key objectives for safety, efficacy and pharmacokinetics
After completion of the study, all patients enrolled in an extension study
pegunigalsidase alfa (PRX-102) provided coverage to patients for the entire 4-week period in treated patients
No new patients developed treatment-induced anti-drug antibodies following switch to PRX-102
Third clinical study to demonstrate positive outcome in support of PRX-102, with data from PB-102-F01 and F02 Phase I/II clinical trials and BRIDGE studies previously announced
PR Newswire
CARMIEL, Israel, Feb. 23, 2021
