Trial record 3 of 50 for:
"Glycogen storage disease type 2"
A Study of rhGAA in Patients With Late-Onset Pompe Disease
This study has been completed.
Sponsor:
Genzyme
Information provided by:
Genzyme
ClinicalTrials.gov Identifier:
NCT00250939
First received: November 8, 2005
Last updated: July 7, 2009
Last verified: April 2007
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Purpose
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 overall objective is to evaluate the safety, pharmacokinetics (PK) and efficacy of Myozyme treatment.
| Condition | Intervention | Phase |
|---|---|---|
|
Pompe Disease (Late-Onset) Glycogen Storage Disease Type II (GSD-II) Acid Maltase Deficiency Disease Glycogenosis 2 |
Biological: Myozyme |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Non-Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Single-Center, Open-Label Study of Safety, Pharmacokinetics and Efficacy of rhGAA in Patients With Late-Onset Pompe Disease |
Resource links provided by NLM:
Genetics Home Reference related topics:
glycogen storage disease type IX
Pompe disease
Schindler disease
succinic semialdehyde dehydrogenase deficiency
Drug Information available for:
Alglucosidase Alfa
U.S. FDA Resources
Further study details as provided by Genzyme:
Primary Outcome Measures:
- safety and PK profile rhGAA [ Time Frame: 74 weeks ] [ Designated as safety issue: No ]
- FVC [ Time Frame: 74 weeks ] [ Designated as safety issue: No ]
- MMT [ Time Frame: 74 weeks ] [ Designated as safety issue: No ]
- Effect of treatment on muscle function [ Time Frame: 74 weeks ] [ Designated as safety issue: No ]
| Enrollment: | 5 |
| Study Start Date: | February 2005 |
| Study Completion Date: | November 2006 |
| Primary Completion Date: | July 2006 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Experimental: 1 |
Biological: Myozyme
20 mg/kg qow
Other Name: alglucosidase alfa
|
Eligibility| Ages Eligible for Study: | 5 Years to 18 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- patient's legally authorized guardian(s) must provide signed, informed consent prior to performing any study-related procedures; patient's signature required if patient understands informed consent
- patient must have a diagnosis of Pompe disease based on deficient endogenous GAA activity or GAA gene mutations
- patient must have demonstrable muscle weakness
- patient must be greater than or equal to five years of age and younger than eighteen years of age
- patient must be able to provide 3 reproducible FVC tests in sitting position during screening
- patient must perform muscle function testing
- patient must ambulate 10 meters (assistive devices permitted)
- patient and legal guardian must comply with the clinical protocol
Exclusion Criteria:
- patient requires the use of invasive ventilatory support
- patient requires the use of noninvasive ventilatory support while awake and in an upright position
- patient has received enzyme replacement therapy with GAA from any source
- patient has used an investigational product within 30 days prior to study enrollment, or is currently enrolled in another clinical or observational study
- patient has a medical condition, serious intercurrent illness, or other extenuating circumstance that, may significantly interfere with study compliance, including all prescribed evaluations and follow-up activities
- Female patients pregnant, lactating or unwilling to practice birth control methods during study
- Male patients unwilling to use barrier contraceptives during study
Contacts and Locations
More Information
No publications provided
| Responsible Party: | Medical Monitor, Genzyme Corporation |
| ClinicalTrials.gov Identifier: | NCT00250939 History of Changes |
| Other Study ID Numbers: | AGLU02804 |
| Study First Received: | November 8, 2005 |
| Last Updated: | July 7, 2009 |
| Health Authority: | European Union: European Medicines Agency |
Keywords provided by Genzyme:
|
Glycogen Storage Disease Type II GSD-II Pompe Disease |
Additional relevant MeSH terms:
|
Glycogen Storage Disease Type II Deficiency Diseases Glycogen Storage Disease Metabolic Diseases Malnutrition Nutrition Disorders Lysosomal Storage Diseases, Nervous System Brain Diseases, Metabolic, Inborn |
Brain Diseases, Metabolic Brain Diseases Central Nervous System Diseases Nervous System Diseases Metabolism, Inborn Errors Genetic Diseases, Inborn Carbohydrate Metabolism, Inborn Errors Lysosomal Storage Diseases |
ClinicalTrials.gov processed this record on May 22, 2013