New to the Huntington's Disease Lighthouse?
 Welcome to the HDlighthouse!
 Getting started.
 
Home \ Research \ Drugs and Supplements \ Updates
A pilot study of the clinical efficacy and safety of memantine for Huntington's disease.

HD Lighthouse Contributing Editor's Comment: Memantine is a glutamate receptor regulator marketed under the trade name Namenda. It was FDA approved for treatment for moderate to severe Alzheimer's after a Phase III clinical trial showed that it slowed functional and cognitive decline.

The mechanism by which memantine is thought to work in Alzheimer's and proposed to work in Huntington's Disease is by reducing excitotoxicity. The idea behind excitotoxicity is that the overstimulation of N-methyl-d-aspartate (NMDA)-type glutamate receptors causes a variety of problems including excessive calcium in the associated ion channels and eventually leads to cell death. Researchers know that this is a problem in stroke and brain injury, and have reason to believe that it also occurs in chronic neurological diseases. Memantine reduces the excessive stimulation of the NMDA glutamate receptors without blocking them altogether. See: HDL: More on Memantine

The Lighthouse previously reported on a two year pilot study which suggested that memantine might slow disease progression in Huntington's. 27 patients were followed for two years and showed no disease progression as one would expect based on past studies. See: HDL: Glutamate Blockers in the Lab and in the Clinic

As referenced below, Baylor researchers report on the results of a small, open label study with twelve patients, three of whom dropped out during the study. Patients were followed for three months, too short a time to see if the drug might slow disease progression. However, chorea improved significantly, which is a promising finding. They recommend larger clinical trials.

Johns Hopkins is conducting a clinical trial of memantine to see if it will improve memory and thinking in HD patients. More details and contact information may be found at: John Hopkins: Memantine Study

-- Marsha L. Miller, Ph.D.
Posted to the HDL: 04 Dec 2006



William G. Ondo, M.D.

A Pilot Study of the Clinical Efficacy and Safety of Memantine for Huntington's Disease.

W. Ondo, N. Mejia, and C. Hunter

Excerpt from this letter to the editor: "In our small pilot trial, 20 mg daily dose of memantine significantly improved motor symptoms, powered by improved chorea, but failed to improve patient's cognitive behavioral, functional, or independence ratings. Most patients tolerated memantine without side effects. The absence of cognitive improvement may result from the small power or intrinsic differences in the dementia of Alzheimer's and HD."
# # #

Source: Parkinsonism and Related Disorders 2006 Oct 12; [Epub ahead of print]

print this
printer friendly
version

 

Read the HDAC/HDLighthouse Forum. Post your comments
   
Related Topics
Research focusing on the formation of aggregates caused by HD
 
Research related to the role Brain Derived Neurotrophic Factor has on the pathology of HD in the brain
 
Research related HD and it's general affect on the brain
 
Learn more about the clinical trial process, trials that have been conducted and those that are underway.
 
Research focusing on gene therapy.
 
Research focusing on gene transcription.
 
General research related to HD
 
Research studying the genetics of Huntington's Disease
 
Research studying the Immune System and it's effect on the progression of HD
 
Research studying the brain tissue and research related to stem cells
 
Recent Updates
17 Aug 2008
FDA approves tetrabenazine
The FDA approves the first drug specifically for Huntington
 
19 Jul 2008
The FDA approves a Phase IIB clinical trial for ACR16
Neurosearch will begin recruiting for the trial later this year.
 
7 Jul 2008
Encouraging results from the Phase II Dimebon trial
Dimebon was found to be safe and well tolerated and there are indications of effectiveness.
 
24 Mar 2008
Approved drugs found to induce autophagy
UK researchers have found promising drugs which induce autophagy, an alternate way to clear away the HD protein.
 
5 Jan 2008
Zoloft raises BDNF, helps the HD mice
Sertaline (Zoloft) improves symptoms, reduces brain atrophy, and prolongs survival in the R6/2 mice.
 
1 Jan 2008
Screening Yields a Promising Compound
High throughput screening has identified a compound which inhibits protein aggregation. Part 1 of 3.
 
1 Jan 2008
C2-8 Suppresses Neurodegeneration in Drosophilia
C2-8 moves another step on the research pipeline with success in a fruitfly model of HD. Part 2 of 3.
 
1 Jan 2008
C2-8 Slows Progression in HD Mice
R6/2 mice given C2-8 experience delayed progression of motor symptoms and reduced cell death. Part 3 of 3
 
4 Dec 2007
Buck Institute and Neurobiological Technologies, Inc. Partner to Develop Treatment for HD
Following promising results in mouse models, researchers at Buck Institute and NTI will work on developing FGF-2 as a drug for HD patients.
 
19 Nov 2007
Miraxion results look promising
One more Phase III clinical trial is needed to support a New Drug Application.
 

All Updates for Drugs and Supplements
Disclaimer & Privacy Policy | Welcome | Site Feedback Marsha@HDLighthouse.org