ba0006oc25 | (1) | ICCBH2017
Kishnani Priya S.
, Rockman-Greenberg Cheryl
, Denker Andrew E.
, Moseley Scott
, Whyte Michael P.
Objective: To evaluate safety and efficacy after 5 years of treatment with asfotase alfa in adolescents and adults with hypophosphatasia (HPP) in a Phase 2, open-label, randomized, dose-ranging study (NCT01163149).Methods: Treatment with subcutaneous asfotase alfa 0.3 or 0.5 mg/kg per d was compared with no treatment (control) for 6 months in patients aged 1366 years. After 6 months, all patients (treatment and control groups) received active treat...