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Glycogen Storage Disease Type II - 32 Studies Found
Estado | Estudiar |
Withdrawn |
Nombre del estudio: High Protein and Exercise Therapy Plus Nocturnal Enteral Feeding in Juvenile-onset Pompe Disease Condición: Glycogen Storage Disease Type II Fecha: 2012-08-01 Intervenciones: Other: High Protein and Exercise Therapy along-with Nocturnal Enteral Feeding |
Completed |
Nombre del estudio: A Prospective, Observational Study in Patients With Late-Onset Pompe Disease Condición: Glycogen Storage Disease Type II Fecha: 2004-02-10 |
Completed |
Nombre del estudio: A Study of the Safety and Efficacy of rhGAA in Patients With Infantile-onset Pompe Disease Condición: Glycogen Storage Disease Type II Fecha: 2003-04-22 Intervenciones: Biological: Myozyme 20 mg/kg qow or 40mg/kg qow Othe |
Completed |
Nombre del estudio: Extension Study of Patients With Infantile-Onset Pompe Disease Who Were Previously Enrolled in Protocol AGLU01602 Condición: Glycogen Storage Disease Type II Fecha: 2005-08-01 Intervenciones: Biological: Myozyme 20 mg/kg qow or 40 mg/kg qow Oth |
Recruiting |
Nombre del estudio: Respiratory Muscle Training in L-Onset Pompe Disease (LOPD) Condición: Glycogen Storage Disease Type II Fecha: 2016-06-13 Intervenciones:
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Recruiting |
Nombre del estudio: Pompe Disease Registry Condición:
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Completed |
Nombre del estudio: Expanded Access Use of Myozyme (Alglucosidase Alfa) in Patients With Late-onset Pompe Disease Condición:
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Approved for marketing |
Nombre del estudio: Expanded Access Use of Myozyme (Alglucosidase Alfa) in Patients With Infantile-onset Pompe Disease Condición:
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Completed |
Nombre del estudio: Extension Study of Long-term Safety and Efficacy of Myozyme in Patients With Pompe Disease Who Were Previously Enrolled in Genzyme Sponsored Enzyme Replacement Therapy (ERT) Studies Condición:
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Completed |
Nombre del estudio: Extension Study of Long-term Safety and Efficacy of Myozyme for a Single Patient With Pompe Disease Who Were Previously Enrolled in Genzyme Sponsored ERT Studies. Condición:
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