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Glycogen Storage Disease clinical trials

View clinical trials related to Glycogen Storage Disease.

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NCT ID: NCT00947960 Completed - Clinical trials for Glycogen Storage Disease Type IV

Triheptanoin Treatment Trial for Patients With Adult Polyglucosan Body Disease

Start date: June 2009
Phase: Phase 2
Study type: Interventional

The purpose of the study is to determine if triheptanoin is an effective treatment for the symptoms of Adult Polyglucosan Body Disease.

NCT ID: NCT00765414 Completed - Clinical trials for Pompe Disease Late-Onset

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.

Start date: April 2003
Phase: Phase 2
Study type: Interventional

This extension study was to monitor the long-term safety and efficacy of rhGAA treatment in a single patient with infantile-onset Pompe disease who were previously treated with rhGAA in a Genzyme study.

NCT ID: NCT00763932 Completed - Clinical trials for Glycogen Storage Disease Type II

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

Start date: April 2003
Phase: Phase 2
Study type: Interventional

This extension study was to monitor the long-term safety and efficacy of rhGAA treatment in patients with infantile-onset Pompe disease who were previously treated with rhGAA derived from the Synpac cell line

NCT ID: NCT00731081 Completed - Clinical trials for Pompe Disease (Late-Onset)

Study About the Evolution of Severe Late Onset Pompe Disease Patient With Pulmonary Dysfunction and Receiving Myozyme®

Start date: March 2007
Phase: N/A
Study type: Observational

To describe severe late onset patients with pompe disease receiving Myozyme®

NCT ID: NCT00701129 Completed - Pompe Disease Clinical Trials

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

Start date: October 2009
Phase: Phase 4
Study type: Interventional

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.

NCT ID: NCT00566878 Completed - Pompe Disease Clinical Trials

Pompe Lactation Sub-Registry

Start date: March 31, 2012
Phase:
Study type: Observational

The objective is to determine if alglucosidase alfa is present in breast milk from mothers with Pompe Disease being treated with alglucosidase alfa and to measure breast milk production and composition in women with Pompe Disease who receive alglucosidase alfa.

NCT ID: NCT00515398 Completed - Pompe Disease Clinical Trials

A Study to Evaluate the Effects of Pharmacological Chaperones in Cells From Patients With Pompe Disease

Start date: August 2007
Phase: N/A
Study type: Observational

The purpose of this study is to see how molecules called pharmacological chaperones affect the cells of patients with Pompe disease. The study will last 1 or 2 visits which will include a blood collection, urine collection, and two skin biopsies. Information will also be collected from the medical records about disease history and diagnosis. Patients will not receive any study medication.

NCT ID: NCT00486889 Completed - Pompe Disease Clinical Trials

Growth and Development Study of Alglucosidase Alfa

Start date: August 26, 2008
Phase: Phase 4
Study type: Interventional

Pompe disease (also known as glycogen storage disease Type II) is a rare autosomal recessive metabolic muscle disease caused by the deficiency of acid α glucosidase (GAA), an enzyme that degrades lysosomal glycogen. As opposed to the exclusively cytoplasmic accumulation of glycogen that occurs in other glycogen storage disorders, Pompe disease is characterized by organelle bound (lysosomal) and extra-lysosomal accumulation of glycogen in many body tissues, ultimately leading to multisystemic pathology. The overall objective of this study was to evaluate the long-term growth and development of participants with infantile-onset Pompe disease with alglucosidase alfa before 1 year of age. Participants were to be followed for a 10-year period.

NCT ID: NCT00483379 Completed - Pompe Disease Clinical Trials

High Dose or High Dose Frequency Study of Alglucosidase Alfa

Start date: May 2007
Phase: Phase 4
Study type: Interventional

Pompe disease (also known as glycogen storage disease Type II) is caused by a deficiency of a critical enzyme in the body called acid alpha-glucosidase (GAA). Normally, GAA is used by the body's cells to break down glycogen (a stored form of sugar) within specialized structures called lysosomes. In patients with Pompe disease, an excessive amount of glycogen accumulates and is stored in various tissues, especially heart and skeletal muscle, which prevents their normal function. The objective of this exploratory study is to evaluate the safety and efficacy of alternative dosing regimens of alglucosidase alfa in patients with Pompe disease who have not demonstrated an optimal response to the standard dosing regimen of 20 mg/kg every other week after a minimum of 6 months treatment immediately prior to study entry.

NCT ID: NCT00455195 Completed - Clinical trials for Pompe Disease (Late-Onset)

Late-Onset Treatment Study Extension Protocol

Start date: March 2007
Phase: Phase 4
Study type: Interventional

Pompe disease (also known as glycogen storage disease Type II) is caused by a deficiency of a critical enzyme in the body called acid alpha-glucosidase (GAA). Normally, GAA is used by the body's cells to break down glycogen (a stored form of sugar) within specialized structures called lysosomes. In patients with Pompe disease, an excessive amount of glycogen accumulates and is stored in various tissues, especially heart and skeletal muscle, which prevents their normal function. The objective of this extension study is to assess the long-term safety and efficacy of alglucosidase alfa treatment in patients with Late-Onset Pompe Disease who were previously treated under the placebo-controlled, double-blind study AGLU02704 (NCT00158600).