Trial record 5 of 50 for:
"Glycogen storage disease type 2"
Safety and Effectiveness Study of rhGAA in Patients With Advanced Late-Onset Pompe Disease Receiving Respiratory Support
This study has been completed.
Sponsor:
Genzyme
Information provided by:
Genzyme
ClinicalTrials.gov Identifier:
NCT00268944
First received: December 22, 2005
Last updated: July 7, 2009
Last verified: April 2007
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
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 and efficacy of rhGAA in patients with advanced Late-onset Pompe disease.
| Condition | Intervention | Phase |
|---|---|---|
|
Pompe Disease (Late-Onset) Glycogen Storage Disease Type II (GSD-II) Acid Maltase Deficiency Disease Glycogenosis 2 |
Biological: Myozyme |
Phase 3 |
| 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: | Prospective, Open-Label, Single-Arm, Exploratory Study of the Effect and Safety of rhGAA in Patients With Advanced Late-Onset Pompe Disease Who Are Receiving Respiratory Support |
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:
- Treatment effect on muscle strength and functional status. [ Time Frame: six months and one year ] [ Designated as safety issue: No ]
- Treatment effect on pulmonary function and/or ventilation conditions. [ Time Frame: six months and one year ] [ Designated as safety issue: No ]
- Treatment effect on cardiomyopathy noted at inclusion [ Time Frame: six months and one year ] [ Designated as safety issue: No ]
- Treatment effect on fatigue. [ Time Frame: six months and one year ] [ Designated as safety issue: No ]
- Treatment effect on quality of life. [ Time Frame: six months and one year ] [ Designated as safety issue: No ]
- Treatment effect on muscular atrophy. [ Time Frame: six months and one year ] [ Designated as safety issue: No ]
- Overall patient satisfaction with treatment (visual analog scale). [ Time Frame: six months and one year ] [ Designated as safety issue: No ]
- Pharmacodynamics assessment. [ Time Frame: six months and one year ] [ Designated as safety issue: No ]
| Enrollment: | 5 |
| Study Start Date: | December 2005 |
| Study Completion Date: | June 2007 |
| Primary Completion Date: | March 2007 (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: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- male or female aged greater than or equal to 18 years
- patient's legally authorized guardian(s) must provide signed, informed consent prior to initiation of study; patient's signature required if patient understands informed consent
- patient must have a documented deficit in acid alpha-glucosidase (GAA) activity , corresponding to the diagnosis of Pompe disease confirmed by documented genotyping
- patient presents with advanced documented symptoms of the disease defined as follows: patient is in a wheel chair and presents diaphragmatic dysfunction and requires invasive ventilation or non invasive ventilation (12 or more hours daily)
Exclusion Criteria:
- patient has received enzyme replacement therapy with GAA from any source
- patient has taken an experimental drug in the 30 days prior to study enrollment, or is currently included in another study involving clinical evaluations; If this is the case, inclusion of the patient in the present study will be subject to prior agreement by Genzyme
- major congenital anomaly
- clinically important organic disease (except for symptoms related to Pompe disease) or any other medical condition, serious intercurrent illness, or other extenuating circumstance that, in the physician's opinion should preclude the patient's participation in the study or may reduce survival
- pregnancy and breastfeeding (women of childbearing age must use a medically accepted method of contraception throughout the entire duration of the trial. Male patients must use a medically accepted birth control method throughout the entire duration of the study)
Contacts and Locations
More Information
No publications provided
| Responsible Party: | Medical Monitor, Genzyme Corporation |
| ClinicalTrials.gov Identifier: | NCT00268944 History of Changes |
| Other Study ID Numbers: | AGLU03105 |
| Study First Received: | December 22, 2005 |
| Last Updated: | July 7, 2009 |
| Health Authority: | France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis) |
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 23, 2013