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| Sponsor: | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) |
|---|---|
| Collaborator: |
Food and Drug Administration (FDA) |
| Information provided by: | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) |
| ClinicalTrials.gov Identifier: | NCT00545597 |
Purpose
Study of the use of Lorenzo's oil in adults with adrenomyeloneuropathy, the adult form of Lorenzo's oil.
| Condition | Intervention | Phase |
|---|---|---|
|
Adrenomyeloneuropathy Adrenoleukodystrophy |
Drug: Lorenzo's oil |
Phase III |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double Blind (Subject, Investigator), Placebo Control, Parallel Assignment, Efficacy Study |
| Official Title: | A Phase III Trial of Lorenzo's Oil in Adrenomyeloneuropathy |
| Estimated Enrollment: | 240 |
| Study Start Date: | March 2005 |
| Estimated Study Completion Date: | June 2012 |
This is a double-masked placebo controlled study of glyceryl trioleate-glyceryl trierucate (Lorenzo's Oil (LO)) therapy in adrenomyeloneuropathy (AMN), the adult form of X-linked adrenoleukodystrophy (X-ALD). AMN is a slowly progressive distal axonopathy that involves the long tracts of the spinal cord and differs from the rapidly progressive inflammatory cerebral forms that most commonly affect boys and adolescents. All forms of X-ALD are associated with the abnormal accumulation of very long chain fatty acids (VLCFA) in plasma and tissues. The oral administration of LO normalizes plasma VLCFA levels within 4 weeks. While previous therapeutic trials of LO therapy in patients with the cerebral forms of X-ALD have been disappointing, recent studies suggest that it is beneficial in two types of X-ALD: 1) as a preventive of neurological involvement in asymptomatic boys; and 2) in AMN, where it appears to slow the rate of progression. None of the previous studies have been controlled, and we are now conducting the first placebo-controlled trial.
The 4-year study will include 120 men with AMN who do not have evidence of cerebral involvement, and 120 women who are heterozygous for X-ALD and have an AMN-like syndrome. The rate of progression will be compared in the LO and placebo groups using the Kurtzke EDSS score as the primary outcome and a variety of secondary outcomes.
Adrenomyeloneuropathy affects about 1 in 40,000 men and 1 in 30,000 women. It is a progressive disorder that leads to inability to walk and other severe deficits. This study will provide definitive information whether Lorenzo's Oil therapy can slow progression.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Contact: Gerald V Raymond, M.D. | 443-923-2750 | raymond@kennedykrieger.org |
| Contact: Kim Hollandsworth, RN, BSN | 443-923-2772 | hollandsworth@kennedykrieger.org |
| United States, Maryland | |
| Kennedy Krieger Institute | Recruiting |
| Baltimore, Maryland, United States, 21205 | |
| Principal Investigator: Gerald V Raymond, M.D. | |
| Principal Investigator: | Gerald V Raymond, M.D. | Hugo W. Moser Research Institute at Kennedy Krieger, Inc. |
More Information
| Study ID Numbers: | R01 HD39276, R01FD003030 |
| Study First Received: | October 16, 2007 |
| Last Updated: | October 16, 2007 |
| ClinicalTrials.gov Identifier: | NCT00545597 History of Changes |
| Health Authority: | United States: Food and Drug Administration |
|
adrenoleukodystrophy adrenomyeloneuropathy |
|
Adrenal Insufficiency Autoimmune Diseases Metabolic Diseases Immune System Diseases Demyelinating Diseases Nervous System Diseases Endocrine System Diseases Adrenal Gland Diseases Central Nervous System Diseases Brain Diseases Hereditary Central Nervous System Demyelinating Diseases Mental Retardation |
Metabolism, Inborn Errors Heredodegenerative Disorders, Nervous System Genetic Diseases, Inborn Peroxisomal Disorders Adrenoleukodystrophy Genetic Diseases, X-Linked Addison Disease Neurologic Manifestations Brain Diseases, Metabolic, Inborn Mental Retardation, X-Linked Neurobehavioral Manifestations Brain Diseases, Metabolic |