glycogen storage disease type ii
Showing 1 - 22 of 22
Pompe Disease, Muscle Loss, Obesity Trial (Multi-ingredient supplement (PDT-MIS), Placebo (PLA))
Not yet recruiting
- Pompe Disease
- +7 more
- Multi-ingredient supplement (PDT-MIS)
- Placebo (PLA)
- (no location specified)
Nov 8, 2023
Glycogen Storage Disease Type II, Pompe Disease (Late-onset) Trial in Milan (Inspiratory Muscle Training (IMT), Inspiratory
Recruiting
- Glycogen Storage Disease Type II
- Pompe Disease (Late-onset)
- Inspiratory Muscle Training (IMT)
- Inspiratory Muscle Training (IMT) + Air Stacking
-
Milan, ItalyIRCCS S. Maria Nascente - Fondazione Don Carlo Gnocchi
Jul 11, 2023
Glycogen Storage Disease Type II Trial in Worldwide (Alglucosidase alfa GZ419829)
Recruiting
- Glycogen Storage Disease Type II
- Alglucosidase alfa GZ419829
-
Leuven, Belgium
- +8 more
Jan 17, 2023
Glycogen Storage Disease Type II, Pompe Disease Trial in Worldwide
Recruiting
- Glycogen Storage Disease Type II
- Pompe Disease
-
Birmingham, Alabama
- +274 more
Jan 12, 2023
Pompe Disease, Pompe Disease (Late-onset), Glycogen Storage Disease Type 2 Trial in Worldwide (SPK-3006)
Active, not recruiting
- Pompe Disease
- +6 more
- SPK-3006
-
Phoenix, Arizona
- +28 more
Jul 22, 2022
Glycogen Storage Disease Type II Trial in France (Avalglucosidase alfa (GZ402666))
Recruiting
- Glycogen Storage Disease Type II
- Avalglucosidase alfa (GZ402666)
-
Brest, France
- +9 more
Jul 22, 2022
Glycogen Storage Disease Type II Trial in Worldwide (avalglucosidase alfa)
Recruiting
- Glycogen Storage Disease Type II
- avalglucosidase alfa
-
Leuven, Belgium
- +7 more
Jul 13, 2022
Higher Dose of Alglucosidase Alpha for Pompe Disease
Not yet recruiting
- Glycogen Storage Disease Type II
- Alglucosidase Alfa
- (no location specified)
Aug 17, 2021
Pompe Disease, Glycogen Storage Disease Type II, Lysosomal Storage Diseases Trial in Gainesville (Diet and Exercise)
Completed
- Pompe Disease
- +2 more
- Diet and Exercise
-
Gainesville, FloridaUniversity of Florida Clinical Research Center
May 13, 2021
Biomarker for Glycogen Storage Diseases (BioGlycogen)
Active, not recruiting
- Fructose Metabolism, Inborn Errors
- +9 more
-
Rostock, Germany
- +3 more
May 12, 2021
Metabolism, Inborn Errors, Lipid Metabolism, Inborn Errors, Carbohydrate Metabolism, Inborn Errors Trial in Copenhagen (Sugar)
Unknown status
- Metabolism, Inborn Errors
- +22 more
- Sugar
-
Copenhagen, DenmarkNeuromuscular Research Unit, 3342
Oct 15, 2019
Glycogen Storage Disease Type II Trial in Durham (RMT therapy using modified RMT device, Sham-RMT therapy using modified RMT
Completed
- Glycogen Storage Disease Type II
- RMT therapy using modified RMT device
- Sham-RMT therapy using modified RMT device
-
Durham, North CarolinaDuke University Medical Center
Jul 29, 2019
Motor Development, Motor Function and Electrophysiologic
Unknown status
- Glycogen Storage Disease Type II
- observation study
-
Taipei, TaiwanTaipei Veteran General Hospital : Taipei City, Taiwan 11217, R.O
May 2, 2016
Glycogen Storage Disease Type II Trial in New York (High Protein and Exercise Therapy along-with Nocturnal Enteral Feeding)
Withdrawn
- Glycogen Storage Disease Type II
- High Protein and Exercise Therapy along-with Nocturnal Enteral Feeding
-
New York, New YorkColumbia University Medical Center
Apr 9, 2015
Pompe Disease, Glycogen Storage Disease Type II, Acid Maltase Deficiency Disease Trial in Durham (recombinant human acid
Completed
- Pompe Disease
- +3 more
- recombinant human acid alpha-glucosidase (rhGAA)
-
Durham, North CarolinaDuke University Medical Center
Nov 12, 2014
Pompe Disease, Glycogen Storage Disease Type II Trial in Louisville, Durham (Alglucosidase Alfa, Methotrexate, Rituximab)
Completed
- Pompe Disease
- Glycogen Storage Disease Type II
- Alglucosidase Alfa
- +2 more
-
Louisville, Kentucky
- +1 more
Apr 9, 2014
Pompe Disease Infantile-Onset, Glycogen Storage Disease Type II Trial in France, South Africa, United States (Myozyme)
Completed
- Pompe Disease Infantile-Onset
- Glycogen Storage Disease Type II
- Myozyme
-
Oakland, California
- +7 more
Feb 4, 2014
Glycogen Storage Disease Type II, Pompe Disease, Acid Maltase Deficiency Disease Trial in New Brunswick (Alglucosidase alfa)
Completed
- Glycogen Storage Disease Type II
- +3 more
- Alglucosidase alfa
-
New Brunswick, New JerseySaint Peter's University Hospital
Feb 4, 2014
Glycogen Storage Disease Type II, Pompe Disease, Acid Maltase Deficiency Disease Trial in Worldwide (Myozyme)
Completed
- Glycogen Storage Disease Type II
- +3 more
- Myozyme
-
Gainesville, Florida
- +5 more
Feb 4, 2014
Glycogen Storage Disease Type II Trial in Worldwide (Myozyme)
Completed
- Glycogen Storage Disease Type II
- Myozyme
-
Gainesville, Florida
- +7 more
Feb 4, 2014
Effects of Pharmacological Chaperones in Cells From Pompe
Completed
- Pompe Disease
- Glycogen Storage Disease Type II
- Observation
-
Gainesville, Florida
- +3 more
Jun 4, 2008
Genetic and Family Studies of Inherited Muscle Diseases
Completed
- Dermatomyositis
- +4 more
-
Bethesda, MarylandNational Institute of Arthritis and Musculoskeletal and Skin Dis
Mar 4, 2008