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Huntington Disease clinical trials

View clinical trials related to Huntington Disease.

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NCT ID: NCT01411150 Completed - Clinical trials for Huntington's Disease

Premanifest Huntington's Disease: Creatine Safety & Tolerability Extension Study

Pre-CREST-X
Start date: May 2009
Phase: Phase 2
Study type: Interventional

The purpose of this clinical trial is to extend the Pre-Crest study (Protocol # (NCT00592995) to further assess the long-term safety and tolerability of up to 30 grams daily creatine in individuals at-risk for Huntington's Disease (HD) and to assess whether biomarkers responsive to creatine in symptomatic individuals are informative in premanifest individuals over a longer duration.

NCT ID: NCT01359774 Completed - Huntington Disease Clinical Trials

31P-MRS and Huntington Disease

PRO-MH
Start date: April 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to identify and quantify a brain energy deficit in Huntington patients, using 31P-RMN spectroscopy.

NCT ID: NCT01357681 Completed - Huntington Disease Clinical Trials

Effects of EGCG (Epigallocatechin Gallate) in Huntington's Disease (ETON-Study)

ETON
Start date: September 2011
Phase: Phase 2
Study type: Interventional

Huntington's disease (HD) is an inherited autosomal dominant, progressive neurodegenerative disease. Clinically, HD is characterized by a triad of movement disorders, cognitive impairments and psychiatric disturbances. These symptoms represent a tremendous burden for patients and caregivers. HD is a fatal disorder with neither cure, nor evidence-based standard therapy available. The green tea polyphenon (2)-epigallocatechin-3-gallate (EGCG) was shown to have beneficial effects in cell and animal models of HD. The aim of this study is to evaluate the efficacy and tolerability of EGCG in HD. The investigators hypothesize that Sunphenon EGCG administered at a maximal daily dose of 1200 mg compared to placebo during a period of 12 months improves cognition in patients with HD. As primary outcome measure, the change of cognitive functions (as measured by the Unified Huntington's Disease Rating Scale (UHDRS)-Cognition composite score of Stroop test, Verbal fluency & Symbol Digit Modalities Test) after 12 months in comparison to Baseline was defined. The investigators further expect a positive influence of EGCG on other clinical manifestations of HD, measurable effects of EGCG on HD biomarkers and good safety and tolerability of EGCG in HD patients.

NCT ID: NCT01339130 Completed - Stroke Clinical Trials

Assessment of Social-emotional Functioning in Neurological Diseases

Emotion
Start date: June 2009
Phase: N/A
Study type: Interventional

Empathy, defined as the ability to understand others emotions, is a fundamental concept in social interactions. It is a psychological phenomenon involving various separable components : (i) the ability to feel and imagine the emotions, (ii) the ability to adopt the perspective of other people. Several neurological diseases with behavioral disorders may lead to impaired processing of social and/or emotional informations. These pathologies are likely to induce a lack of empathy that may result from impairments at different levels. The objective is simply to study how others' emotions are understood and how this allows for regulation of personal behavior. This study is being carried out among patients seen for various health problems and who can make behavior changes. This study could help to understand some neurological diseases and thereby to identify them earlier and/or to better differentiate them.

NCT ID: NCT01306929 Completed - Huntington Disease Clinical Trials

Open-label Extension Study of Pridopidine (ACR16) in the Symptomatic Treatment of Huntington Disease

OPEN-HART
Start date: March 24, 2011
Phase: Phase 2
Study type: Interventional

Huntington disease (HD) is a hereditary neurodegenerative disorder causing impairment in movement, behavioral dysfunction and dementia. The movement disorder is mainly characterized by chorea (involuntary movements) and a progressive loss of voluntary movement causing a substantial functional impairment over time. The study will assess the long-term safety of pridopidine and the treatment effects during long-term, open-label treatment.

NCT ID: NCT01290861 Completed - Clinical trials for Huntington's Disease

Cognitive Assessment Battery (CAB) Beta Study

CAB
Start date: February 2011
Phase: N/A
Study type: Observational

The overall objective of this study is to identify a 60 minute cognitive battery, for subsequent use in clinical trials, that detects cognitive deficits in early HD and late pre-manifest HD compared to controls, and that has a potential to show drug induced improvements.

NCT ID: NCT01085266 Terminated - Huntington Disease Clinical Trials

An Extension of the HORIZON Protocol Evaluating the Safety of Dimebon (Latrepirdine) in Subjects With Huntington Disease

HORIZON PLUS
Start date: February 2010
Phase: Phase 3
Study type: Interventional

An open-label extension study of the HORIZON protocol evaluating the safety of dimebon (latrepirdine)in subjects with Huntington disease.

NCT ID: NCT01019473 Terminated - Clinical trials for Huntington's Disease

Efficacy, Safety and Tolerability of AFQ056 in Patients With Huntington's Disease in Reducing Chorea

Start date: November 2009
Phase: Phase 2
Study type: Interventional

This study will assess the efficacy, safety and tolerability of AFQ056 when added to optimize standard therapy in patients that have Huntington's disease in reducing chorea.

NCT ID: NCT00990613 Completed - Alzheimer's Disease Clinical Trials

A Study Evaluating The Absorption Of Dimebon Into The Body From A Dimebon Solution Applied To The Skin

Start date: October 2009
Phase: Phase 1
Study type: Interventional

To estimate the absorption, safety, and tolerability of a dimebon transdermal solution relative to the dimebon immediate release oral formulation.

NCT ID: NCT00988624 Completed - Alzheimer's Disease Clinical Trials

A Study In Healthy Volunteers To Estimate The Pharmacokinetics Of Four Modified-Release Formulations Of Dimebon (Latrepirdine)

Start date: October 2009
Phase: Phase 1
Study type: Interventional

This study will evaluate four different modified release formulation to estimate the amount of dimebon available to the body relative to the current dimebon formulation that is given three times a day. The results of this study will help inform and guide further formulation development efforts with the ultimate goal of reducing dose frequency to once-a-day or twice-a-day.