Huntington Disease Clinical Trial
Official title:
Ursodiol in Huntington's Disease
The purpose of this study is to evaluate the safety of the drug ursodiol (ursodeoxycholic acid, UDCA) in people with Huntington's disease (HD) and to explore how the compound is processed by the body.
Huntington's disease is an inherited neurodegenerative disease that causes a movement
disorder, dementia, and psychiatric and behavioral disturbance in affected individuals.
Tauroursodeoxycholic acid (TUDCA) is a bile acid synthesized in the liver by the conjugation
of taurine to ursodeoxycholic acid (UDCA). It is thought to function as an anti-apoptotic
agent in HD, evidenced by studies in toxic cell models and both toxic and transgenic rodent
models of the disease.
Ursodiol is a commercially-available exogenous form of UDCA, the precursor of TUDCA.
Although the compound has an established dosing, safety, tolerability and efficacy profile
in patients with hepatobiliary disorders, gaps exist in the understanding of the
pharmacokinetics / pharmacodynamics of the compound, particularly in patients with normal
gastrointestinal function, and no human data exist for its therapeutic use in
neurodegenerative disorders. The specific aims of this study are:
1. To establish whether treatment with the drug ursodiol will result in measurable levels
of its bile acid metabolites in serum and CSF at standard oral doses; and whether a
dose-response can be detected using these measures.
2. To establish a preliminary safety and tolerability profile of the drug in subjects with
HD.
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Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
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