Atlas Trials

Glycogen Storage Disease Type II

29 clinical trials · Condition

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RecordFirmDate
Avalglucosidase Alfa French Post-trial Access for Participants With Pompe Disease (PTA Avalglucosidase) (NCT05164055)Genzyme, a Sanofi Company2022-07-11
Clinical Study for Treatment-naïve IOPD Babies to Evaluate Efficacy and Safety of ERT With Avalglucosidase Alfa (NCT04910776)Sanofi2021-09-01
Higher Dose of Alglucosidase Alpha for Pompe Disease (NCT05017402)Taipei Veterans General Hospital, Taiwan2021-09-01
A Gene Transfer Study for Late-Onset Pompe Disease (RESOLUTE) (NCT04093349)Spark Therapeutics, Inc.2020-10-01
Evaluate Efficacy and Safety in Chinese Patients With Infantile-Onset Pompe Disease With One Year Alglucosidase Alfa Treatment (NCT03687333)Genzyme, a Sanofi Company2018-12-04
Biomarker for Glycogen Storage Diseases (BioGlycogen) (NCT02385162)CENTOGENE GmbH Rostock2018-08-20
Respiratory Muscle Training in L-Onset Pompe Disease (LOPD) (NCT02801539)Duke University2017-02-02
Effect of Motor Development, Motor Function and Electrophysiologic Findings of IOPD Under ERT (NCT02761421)Taipei Veterans General Hospital, Taiwan2016-01-01
Fat and Sugar Metabolism During Exercise in Patients With Metabolic Myopathy (NCT02635269)Rigshospitalet, Denmark2016-01-01
High Protein and Exercise Therapy Plus Nocturnal Enteral Feeding in Juvenile-onset Pompe Disease (NCT01656590)Columbia University2012-10-01
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)Genzyme, a Sanofi Company2009-10-01
A Study to Evaluate the Effects of Pharmacological Chaperones in Cells From Patients With Pompe Disease (NCT00515398)Amicus Therapeutics2007-08-01
Expanded Access Use of Myozyme (Alglucosidase Alfa) in Patients With Late-onset Pompe Disease (NCT00074932)Genzyme, a Sanofi Company2004-11-01
Pompe Disease Registry Protocol (NCT00231400)Genzyme, a Sanofi Company2004-09-15
A Prospective, Observational Study in Patients With Late-Onset Pompe Disease (NCT00077662)Genzyme, a Sanofi Company2004-03-01
Expanded Access Use of Myozyme (Alglucosidase Alfa) in Patients With Infantile-onset Pompe Disease (NCT00074919)Genzyme, a Sanofi Company2003-12-01
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 (NCT00763932)Genzyme, a Sanofi Company2003-04-01
A Study of the Safety and Efficacy of rhGAA in Patients With Infantile-onset Pompe Disease (NCT00059280)Genzyme, a Sanofi Company2003-04-01
rhGAA in Patients With Infantile-onset Glycogen Storage Disease-II (Pompe Disease) (NCT00053573)Genzyme, a Sanofi Company2003-02-01
A Study of the Safety and Pharmacokinetics of rhGAA in Siblings With Glycogen Storage Disease Type II (NCT00051935)Genzyme, a Sanofi Company2003-01-01
Safety and Efficacy of Recombinant Human Acid Alpha-Glucosidase in the Treatment of Classical Infantile Pompe Disease (NCT00025896)Genzyme, a Sanofi Company2001-05-01
Genetic and Family Studies of Inherited Muscle Diseases (NCT00001331)National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)1993-05-01

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