Safety and Tolerability Study of Phenylbutyrate in Huntington's Disease (PHEND-HD)
Information source: University of Rochester
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Huntington's Disease
Intervention: sodium phenylbutyrate (Drug)
Phase: Phase 2
Status: Completed
Sponsored by: University of Rochester Official(s) and/or principal investigator(s): Steven M. Hersch, MD, PhD, Principal Investigator, Affiliation: Co-Chair, Huntington Study Group, Massachusetts General Hospital Karl Kieburtz, MD, MPH, Principal Investigator, Affiliation: Director, Clinical Trials Coordination Center, University of Rochester
Summary
The purpose of this study is to evaluate the safety, tolerability and clinical impact of
15-grams daily of sodium phenylbutyrate (phenylbutyrate) in Huntington's disease and to lay
the groundwork for possible subsequent trials designed to specifically address its ability
to slow or halt the progression of the disease.
Clinical Details
Official title: Phenylbutyrate Development for Huntington's Disease (PHEND-HD): A Multi-Center, Double-Blind, Placebo-Controlled Study With Open-Label Follow-Up to Determine the Safety and Tolerability of Phenylbutyrate in Subjects With Huntington's Disease
Study design: Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment
Primary outcome: Proportion of subjects able to complete treatment (Week 16)
Secondary outcome: Secondary safety and tolerability outcomes at Weeks 1, 4, 5, 10, 16, & 20 include:adverse events, changes in vital signs, and clinical lab assessments. Secondary clinical measures at Weeks 4, 10, 16, and 20 include components of the UHDRS: total motor, Stroop, independence, & total functional capacity. Secondary biological indicators of treatment affects at Weeks 4, 10, 16, & 20 include: markers of neuroprotection (e.g. NAA) via MRS, histone acetylation (levels in WBC; fetal hemoglobin levels in blood), depletion of glutamine, gene expression analyses, and biochemical analyses for pharmacokinetics.
Detailed description:
Huntington's disease (HD) is an autosomal dominant disorder resulting in selective loss of
neurons in the striatum—an area of the brain that controls movement, balance, and
walking—and other areas of the brain. The disease is characterized by progressive motor and
cognitive decline. There is no cure or even plausible treatment to offset the fatal course
of the disease. Therefore, any treatment that ameliorates the disease would be of enormous
importance.
The purpose of this double-blind, placebo-controlled study—with open-label follow-up—is to
determine the safety and tolerability of 15-grams daily of oral phenylbutyrate in people
with HD. The study will enroll 60 individuals. Eligible participants will be initially
randomized to receive either phenylbutyrate or the matching placebo for 4 weeks.
After the placebo-controlled phase, all participants will enter the open-label phase to
receive phenylbutyrate for 12 weeks. Participants will be followed for one month off
phenylbutyrate.
This combination of a short-term double-blind, placebo-controlled phase followed by a longer
open-label phase will favor the primary goals of detecting toxicity and intolerability while
facilitating recruitment and maximizing number of subjects on study drug.
Eligibility
Minimum age: 18 Years.
Maximum age: N/A.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Subjects with clinical diagnosis of HD and family history of HD or a CAG repeat
expansion greater than or equal to 37
- Subjects in stage I or II of illness (TFC greater than or equal to 7)
- Subjects must be ambulatory and not requiring skilled nursing care
- Age of 18 years or older
- Women of childbearing potential (i. e., those not postmenopausal or surgically
sterile) must confirm to the best of their knowledge that they are not pregnant or
plan to get pregnant
- Women of childbearing potential must have negative pregnancy test, be non-lactating
and use adequate contraception methods, such as oral birth control pills plus a
barrier method (i. e. condoms, diaphragm) or IUD during their participation in the
study
- Subjects currently taking psychotropic medications (including antidepressants and
neuroleptics) must be on stable dosages for at least 4 weeks prior to baseline visit
and should be maintained on constant dosage throughout the study
- Subjects must be capable of providing informed consent and complying with trial
procedures
- Subjects must be able to take oral medication, a person willing and able to serve as
an informant and provide information about the daily dosing of study medication
Exclusion Criteria:
- Exposure to phenylbutyrate, valproic acid, probenecid, known HDAC inhibitors or other
transcriptionally active compounds within 3 months (90 days) prior to the baseline
visit
- History of known sensitivity or intolerability to phenylbutyrate, sodium butyrate or
sodium acetate
- Existence of a known malignancy that might require treatment during the course of
this study
- Exposure to any investigational drug within 30 days of the baseline visit
- Subjects with underlying hematologic, hepatic or renal disease; screening white blood
cell (WBC) count less than 3,800/mm3, screening creatinine greater than 2. 0 or
alanine aminotransferase (ALT) greater than 2 times the upper limit of normal
- Clinical evidence of unstable medical illness in the investigator's judgment
- Clinical illness that requires use of warfarin (Coumadin)
- Unstable psychiatric illness defined as psychosis (hallucinations or delusions)
untreated major depression or plan for suicide within 90 days of the baseline visit
- Current or history of substance (alcohol or drug) abuse within 1 year of the baseline
visit
- Pregnant women or women who are currently breast-feeding
- History of heart failure or other conditions that might be exacerbated by sodium
loading
Locations and Contacts
University of Alabama, Birmingham, Alabama, United States
University of California—San Diego, San Diego, California, United States
University of Iowa Hospital and Clinics, Iowa City, Iowa, United States
University of Kansas Medical Center, Kansas City, Kansas, United States
Johns Hopkins University, Baltimore, Maryland, United States
Massachusetts General Hospital, Boston, Massachusetts, United States
Columbia University, New York, New York, United States
University of Rochester, Rochester, New York, United States
Additional Information
Starting date: August 2005
Last updated: August 14, 2012
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