Trial record 5 of 29 for:
Friedreich's Ataxia
Pilot Study of Varenicline (Chantix®) in the Treatment of Friedreich's Ataxia
This study has been terminated.
(The DSMB recommended that the study be stopped as a result of concerns regarding safety and intolerability and insufficient evidence of efficacy.)
Sponsor:
University of South Florida
Collaborators:
Friedreich's Ataxia Research Alliance
Pfizer
Information provided by (Responsible Party):
University of South Florida
ClinicalTrials.gov Identifier:
NCT00803868
First received: December 4, 2008
Last updated: July 23, 2012
Last verified: July 2012
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Purpose
The purpose of this study is to determine if varenicline is effective in treating symptoms of Friedreich's ataxia.
| Condition | Intervention | Phase |
|---|---|---|
|
Friedreich's Ataxia |
Drug: varenicline Drug: placebo |
Phase 2 Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor) Primary Purpose: Treatment |
| Official Title: | Pilot Study of Varenicline (Chantix®) in the Treatment of Friedreich's Ataxia |
Resource links provided by NLM:
Genetics Home Reference related topics:
ataxia neuropathy spectrum
childhood myocerebrohepatopathy spectrum
deoxyguanosine kinase deficiency
Friedreich ataxia
infantile-onset spinocerebellar ataxia
Marinesco-Sjögren syndrome
mitochondrial neurogastrointestinal encephalopathy disease
myoclonic epilepsy myopathy sensory ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 2
spinocerebellar ataxia type 3
spinocerebellar ataxia type 6
MedlinePlus related topics:
Friedreich's Ataxia
U.S. FDA Resources
Further study details as provided by University of South Florida:
Primary Outcome Measures:
- Friedreich Ataxia Rating Scale (FARS) [ Time Frame: 9 weeks ] [ Designated as safety issue: No ]
| Enrollment: | 28 |
| Study Start Date: | May 2009 |
| Study Completion Date: | May 2010 |
| Primary Completion Date: | May 2010 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: 1
Varenicline
|
Drug: varenicline
up to 1mg po bid for 9 weeks
|
|
Placebo Comparator: 2
Placebo
|
Drug: placebo
placebo matching study drug up to 1mg po bid
|
Eligibility| Ages Eligible for Study: | 18 Years to 80 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Outpatients with FA diagnosed by confirmed by genetic testing.
- Age 18 years to 80 years.
- Women who are not pregnant or breast feeding, and who do not intend to become pregnant. Women of child-bearing potential must use a reliable method of contraception and must provide a negative urine pregnancy test at entry into the study.
CBC, CMP, and diabetes lab results not indicative of clinically relevant abnormalities (results within the past 6 months prior to screening). These would include but are not limited to:
Electrolytes (Chloride, Sodium, Potassium) within laboratory defined normal limits.
Hemoglobin, white cell count, platelet count and fasting glucose within laboratory defined normal limits. Creatinine must be (≤1.5 mg/dl).
ALT (6-40 u/l) and AST (10-30 u/l) must be less than 2 times normal limit
- Stable doses of all medications for 30 days prior to study entry and for the duration of the study.
- Patient permission (informed consent).
- Ambulatory status: Half of the enrolled patients must be able to ambulate with or without assistance; half of the enrolled patients must be non-ambulatory.
Exclusion Criteria:
- Any unstable illness that in the investigator's opinion preclude participation in this study.
- Use of another investigational product within the past 28 days.
- Patients with a history of substance abuse.
- Presence of preexisting psychiatric illness (specifically schizophrenia, bipolar disorder, or history of suicide attempt).
- Presence of diabetes (as determined by fasting blood glucose labs within the past 6 months).
- Presence of clinically significant cardiac disease (as determined by the investigator based on EKG and echocardiogram results within the past 6 months). Specifically, patients with an ejection fraction <40% or a prolonged QT interval (>50% of cycle duration) will be excluded. If abnormalities are noted on the EKG or echocardiogram, the patient will be eligible IF they provide clearance from a cardiologist.
- Presence of current uncontrolled depression as measured by PHQ9 (criteria for depression include all of the following to be present: At least one of the first two questions on PHQ9 endorsed as positive (little pleasure, feeling depressed) indicating the symptom has been present more than half the time in the past two weeks; Question 10 about difficulty at work or home or getting along with others should be answered at least "somewhat difficult."; and the total score ≥ 10.
- Concurrent treatment with any MAOIs, Wellbutrin, or nicotine patches.
- Patients who currently smoke or have smoked within the past 12 months (Smoking will be defined as having smoked any substance even on a single occasion).
- Dementia or other psychiatric illness that prevents the patient from giving informed consent (MMSE less than 25).
- Legal incapacity or limited legal capacity.
- Presence of severe renal disease (creatinine >1.6) or hepatic disease (AST or ALT>2x times normal) (as evidenced by labs reported within the past 6 months).
- Abnormal WBC hemoglobin or platelet count (as evidenced by labs reported within the past 6 months).
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00803868
Locations
| United States, Florida | |
| University of South Florida | |
| Tampa, Florida, United States, 33612 | |
| United States, Pennsylvania | |
| The Children's Hospital of Philadelphia | |
| Philadelphia, Pennsylvania, United States, 19104 | |
Sponsors and Collaborators
University of South Florida
Friedreich's Ataxia Research Alliance
Pfizer
Investigators
| Principal Investigator: | Theresa Zesiewicz, M.D. | University of South Florida |
More Information
No publications provided
| Responsible Party: | University of South Florida |
| ClinicalTrials.gov Identifier: | NCT00803868 History of Changes |
| Other Study ID Numbers: | 6 |
| Study First Received: | December 4, 2008 |
| Last Updated: | July 23, 2012 |
| Health Authority: | United States: Food and Drug Administration |
Additional relevant MeSH terms:
|
Ataxia Friedreich Ataxia Dyskinesias Neurologic Manifestations Nervous System Diseases Signs and Symptoms Spinocerebellar Degenerations Cerebellar Diseases Brain Diseases Central Nervous System Diseases Spinal Cord Diseases Heredodegenerative Disorders, Nervous System |
Neurodegenerative Diseases Genetic Diseases, Inborn Mitochondrial Diseases Metabolic Diseases Varenicline Nicotinic Agonists Cholinergic Agonists Cholinergic Agents Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action Pharmacologic Actions Physiological Effects of Drugs |
ClinicalTrials.gov processed this record on May 21, 2013