International audienceBackground and ObjectivesPompe disease is a rare, progressive neuromuscular disorder caused by deficiency of lysosomal acid α-glucosidase (GAA) and subsequent glycogen accumulation. Avalglucosidase alfa, a recombinant human GAA enzyme replacement therapy designed for increased cellular uptake and glycogen clearance, has been studied for long-term efficacy and safety in patients with late-onset Pompe disease (LOPD). Here, we report up to 6.5 years' experience with avalglucosidase alfa during the NEO1 and NEO-EXT studies.Methods: NEO1 participants with LOPD, either treatment naive (Naive Group) or receiving alglucosidase alfa for ≥9 months (Switch Group), received avalglucosidase alfa (5, 10, or 20 mg/kg every other week...
Background: Pompe disease is caused by a deficiency of acid alpha- glucosidase (GAA). Severe GAA def...
Background: Pompe’s disease is caused by a deficiency of acid alpha-glucosidase (GAA). Severe GAA de...
Glycogen storage disease type 2, Pompe disease, is a progressive muscle disorder with a wide range o...
International audienceBackground and ObjectivesPompe disease is a rare, progressive neuromuscular di...
Background: Pompe disease is a rare, progressive neuromuscular disorder caused by deficiency of acid...
Background: Pompe disease is a rare disorder characterised by progressive loss of muscle and respira...
This multicenter/multinational, open-label, ascending-dose study (NCT01898364) evaluated safety, tol...
Pompe disease (PD) is a glycogen storage disorder caused by deficient activity of acid alpha-glucosi...
Introduction: Pompe disease is an inherited, progressive neuromuscular disorder caused by deficiency...
BackgroundLate-onset Pompe disease is a rare genetic neuromuscular disorder caused by lysosomal acid...
Abstract Background Late-onset Pompe disease is a rare genetic neuromuscular disorder caused by lyso...
Purpose: Pompe disease results from lysosomal acid alpha-glucosidase (GAA) deficiency and its associ...
PURPOSE: Mini-COMET (NCT03019406; Sanofi) is a phase 2, open-label, ascending-dose, 3-cohort study, ...
AbstractEmerging phenotypes in long-term survivors with Pompe disease on standard enzyme replacement...
Altres ajuts: Projekt DEAL; Sanofi Genzyme.Background: Pompe disease is one of the few neuromuscular...
Background: Pompe disease is caused by a deficiency of acid alpha- glucosidase (GAA). Severe GAA def...
Background: Pompe’s disease is caused by a deficiency of acid alpha-glucosidase (GAA). Severe GAA de...
Glycogen storage disease type 2, Pompe disease, is a progressive muscle disorder with a wide range o...
International audienceBackground and ObjectivesPompe disease is a rare, progressive neuromuscular di...
Background: Pompe disease is a rare, progressive neuromuscular disorder caused by deficiency of acid...
Background: Pompe disease is a rare disorder characterised by progressive loss of muscle and respira...
This multicenter/multinational, open-label, ascending-dose study (NCT01898364) evaluated safety, tol...
Pompe disease (PD) is a glycogen storage disorder caused by deficient activity of acid alpha-glucosi...
Introduction: Pompe disease is an inherited, progressive neuromuscular disorder caused by deficiency...
BackgroundLate-onset Pompe disease is a rare genetic neuromuscular disorder caused by lysosomal acid...
Abstract Background Late-onset Pompe disease is a rare genetic neuromuscular disorder caused by lyso...
Purpose: Pompe disease results from lysosomal acid alpha-glucosidase (GAA) deficiency and its associ...
PURPOSE: Mini-COMET (NCT03019406; Sanofi) is a phase 2, open-label, ascending-dose, 3-cohort study, ...
AbstractEmerging phenotypes in long-term survivors with Pompe disease on standard enzyme replacement...
Altres ajuts: Projekt DEAL; Sanofi Genzyme.Background: Pompe disease is one of the few neuromuscular...
Background: Pompe disease is caused by a deficiency of acid alpha- glucosidase (GAA). Severe GAA def...
Background: Pompe’s disease is caused by a deficiency of acid alpha-glucosidase (GAA). Severe GAA de...
Glycogen storage disease type 2, Pompe disease, is a progressive muscle disorder with a wide range o...