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NIH Tests Memory Drug

http://www.reutershealth.com/news/rhdn/199702/1997021203.html

     NEW YORK, Feb 12 (Reuters) -- Government researchers are about to
     begin testing a memory-boosting drug in people with Alzheimer's
     disease.

     As reported previously on Health eLine, earlier safety studies of
     the compound ampakine CX-516 showed it dramatically increased the
     scores on memory tests taken by healthy volunteers, ages 65 to
     73.

     Beginning this week, the compound moves into another testing
     arena. National Institute of Health (NIH) researchers will try to
     determine if it will improve memory and overall mental
     functioning of Alzheimer's disease patients.

     "We're about to launch a clinical trial on CX-516, an ampakine
     compound designed to alleviate the symptoms of Alzheimer's
     disease, says Dr. Thomas N. Chase, head of experimental
     therapeutics at the National Institute of Neurological Diseases
     and Stroke, Bethesda, Maryland.

     "We will try to assess efficacy (effectiveness) and safety, or
     tolerability, of the compound in the target population," he
     explains.

     "This is an approach toward neurotransmitter replacement in
     Alzheimer's disease," says Chase.

     He notes that such strategies work well in Parkinson's disease
     where the missing neurotransmitter, dopamine, is replaced by the
     compound levodopa. Neurotransmitters are chemicals that help
     transmit impulses from one brain cell (neuron) to another.

     "In Alzheimer's disease there are several neurotransmitters whose
     function is reduced because the neurons that make the transmitter
     and release it are degenerating," Chase explains.

     The researcher points out that one of these chemicals is
     acetylcholine, and that the two drugs now on the market attempt
     to prevent its breakdown, known as "chemical degradation."

     These drugs are Cognex (tacrine) and Aricept (donepezil
     hydrochloride). "The problem with those drugs is that they're not
     very effective," says Chase. "The effect size is relatively small
     and many patients do not gain enough benefit from the drugs to be
     really worth the effort."

     Chase explains that the use of ampakines involves yet another
     neurotransmitter which is characteristically defective or reduced
     in Alzheimer's disease -- glutamate.

     "Glutamate stimulates a number of different kinds of
     neurotransmitter receptors in the brain, and the ampakine we're
     studying mimics the effects of the defective or missing
     neurotransmitter, glutamate," Chase explains.

     The new study will begin with about 10 Alzheimer's patients. "It
     will take about three months with each patient," says Chase, "and
     we'll probably spend six months or a year doing the trial
     depending on our (subject) recruitment."

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