drugset / Trial / NCT00701129

An Exploratory Study of the Safety and Efficacy of Prophylactic Immunomodulatory Treatment in Myozyme-naive Cross-Reacting Immunologic Material (CRIM[-]) Patients With Infantile-Onset Pompe Disease

NCT00701129

Phase 4 Completed 4 enrolled Genzyme, a Sanofi Company
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study was to evaluate the efficacy, clinical benefits and safety of a prophylactic immunomodulatory regimen given prior to first treatment with alglucosidase alfa (Myozyme®) in patients with infantile-onset Pompe disease. The objectives were to assess the efficacy of a prophylactic immunomodulatory regimen given prior to first treatment with alglucosidase alfa, as assessed by anti-recombinant human acid alpha-glucosidase (anti-rhGAA) antibody titers, and antibodies that inhibit the activity and/or uptake of alglucosidase alfa; to evaluate the clinical benefit as measured by overall survival, ventilator-free survival, left ventricular mass index (LVMI), gross motor function and development, disability index and the incidence of adverse events (AEs), serious adverse events (SAEs), and clinical laboratory abnormalities.

Timeline

Start
2009-10
Primary completion
2013-03
Completion
2013-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Methotrexate Small molecule 0.4 mg/kg Subcutaneous
Subject Rituximab Monoclonal antibody 12.5 mg/kg Intravenous
Subject Rituximab Monoclonal antibody 375 mg/m2 Intravenous
Subject alglucosidase alfa Protein / enzyme biologic 20 mg/kg Intravenous