Safety and Efficacy of Fenofibrate as a Treatment for Huntington's Disease



Status:Active, not recruiting
Conditions:Neurology
Therapuetic Areas:Neurology
Healthy:No
Age Range:18 - Any
Updated:3/8/2019
Start Date:April 27, 2017
End Date:December 31, 2019

Use our guide to learn which trials are right for you!

A Phase IIa, Randomized, Double-blind, Placebo-controlled Study of the Safety and Efficacy of Fenofibrate as a Treatment for Huntington's Disease

The purpose of this research study is to study the safety and efficacy of fenofibrate, an
FDA-approved drug for high cholesterol and/or elevated triglyerides (fats), as a treatment
for Huntington's disease (HD). Subjects who meet the entry criteria will be randomized (3:1)
to either 145mg of fenofibrate or placebo.


Inclusion Criteria:

- An adult of either sex, ages 25-85 inclusive,

- Have proficiency with written and spoken English and corrected vision or hearing to
complete the cognitive testing,

- Are able to give informed consent,

- Have good overall health status with no known problems anticipated over the course of
the trial,

- Have a diagnosis of HD supported by positive gene test within the past 6 months.

Exclusion Criteria:

- Other major neurological disease [e.g., multiple sclerosis, parkinson's disease,
cortical stroke, etc]

- Clinically significant hepatic or renal disease,

- Current or recent (< 1 month) use of dopamine blocking agents such as tetrabenazine,
anticonvulsants, neuroleptics, HAART, antiemetics, and antipsychotics for any reason,

- Current use of Warfarin (Coumadin). Enrollment in another investigational drug study
within the prior three months.
We found this trial at
1
site
Irvine, California 92697
949-824-5011
Principal Investigator: Neal Hermanowicz, MD
Phone: 949-824-8116
University of California, Irvine Since 1965, the University of California, Irvine has combined the strengths...
?
mi
from
Irvine, CA
Click here to add this to my saved trials