|
|
Home
Search
Study Topics
Glossary
|
 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||||||||||||||||||||||||||||||||
| Sponsored by: |
National Institute of Neurological Disorders and Stroke (NINDS) |
|---|---|
| Information provided by: | National Institutes of Health Clinical Center (CC) |
| ClinicalTrials.gov Identifier: | NCT00001416 |
Purpose
The purpose of this study is to examine how the skeleton responds to repeated doses of enzyme replacement therapy in patients with type I Gaucher's disease who have had their spleens removed.
Gaucher disease is a lysosomal storage disease resulting from glycocerebroside accumulation in macrophages due to a genetic deficiency of the enzyme glucocerebrosidase. It may occur in adults but occurs most severely in infants, in whom cerebroside also accumulates in neurons. Patients with Gaucher's disease experience enlargement of the liver and spleen and bone destruction. The condition is passed from generation to generation through autosomal recessive inheritance.
Type I is the most common form. It is a chronic non-neuronopathic form, meaning the disease does not affect nerve cells. The symptoms of type I can appear at any age.
In this study patients will be divided into three groups. Each group will receive different doses of enzyme replacement (Ceredase). In addition, two of the three groups will also receive doses of a form of vitamin D (calcitriol). Researchers believe the groups receiving vitamin D will have an improved response as compared to those patients only receiving enzyme replacement.
Patients in each group who respond to enzyme replacement with increases in bone density will be compared to the other treatment groups.
| Condition | Intervention | Phase |
|---|---|---|
|
Gaucher's Disease |
Drug: CEREDASE™ |
Phase II |
| Study Type: | Interventional |
| Study Design: | Treatment, Safety/Efficacy Study |
| Official Title: | Skeletal Responses to Macrophage-Targeted Glucocerebrosidase in Patients With Type 1 Gaucher's Disease |
| Estimated Enrollment: | 100 |
| Study Start Date: | December 1993 |
| Estimated Study Completion Date: | November 2000 |
The purpose of this study is to examine the response of the skeleton to repeated infusions of macrophage-targeted glucocerebrosidase (CEREDASE™ (Trademark) ) in splenectomized patients with type I Gaucher's disease. The magnitude and rate of development of the skeletal response will be monitored non-invasively. Theoretically, an enhanced response should occur in patients supplemented with pharmacologic doses of 1, 25-dihydroxyvitamin D3 (calcitriol), since calcium absorption and enzyme delivery to bone marrow macrophages should be increased in this setting. These issues will be addressed in a clinical trial that uses a modified factorial design. A total of 57 patients will be assigned to three treatment groups by block randomization.
Group 1: CEREDASE™ (Trademark) (60 IU/kg q2wks; 0-6 months)
CEREDASE™ (Trademark) (30 IU/kg q2wks; 7-24 months)
Group 2: Calcitriol (0.25-3.0 micrograms/day; 0-24 months)
CEREDASE™ (Trademark) (60 IU/kg q2wks; 7-12 months)
CEREDASE™ (Trademark) (30 IU/kg q2wks; 13-24 months)
Group 3: Calcitriol (0.25-3.0 micrograms/day; 0-24 months)
CEREDASE™ (Trademark) (60 IU/kg q2wks; 0-6 months)
CEREDASE™ (Trademark) (30 IU/kg q2wks; 7-24 months)
The number of patients responding to enzyme replacement with a significant decrease in hepatic volume and a significant increase in trabecular bone density of the lumbar spine will be compared between the treatment groups.
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Splenectomized Gaucher patients.
Aged 18-45 who have not received enzyme therapy for at least 1 year.
No patients with other illnesses (pulmonary, liver, kidney, bone, hematologic).
Contacts and Locations More Information
| Study ID Numbers: | 940050, 94-N-0050 |
| Study First Received: | November 3, 1999 |
| Last Updated: | March 3, 2008 |
| ClinicalTrials.gov Identifier: | NCT00001416 |
| Health Authority: | United States: Federal Government |
|
Bone Disease Calcitriol Enzyme Replacement Therapy Gaucher's Disease Vitamin D |
|
Lipid Metabolism, Inborn Errors Sphingolipidoses Metabolic Diseases Lysosomal Storage Diseases Ergocalciferols Sphingolipidosis Central Nervous System Diseases Brain Diseases Bone Diseases Calcitriol |
Lymphatic Diseases Metabolism, Inborn Errors Vitamin D Genetic Diseases, Inborn Brain Diseases, Metabolic, Inborn Lipidoses Metabolic disorder Gaucher Disease Lipid Metabolism Disorders Brain Diseases, Metabolic |
|
Reticuloendotheliosis Lysosomal Storage Diseases, Nervous System Nervous System Diseases |
