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New antipsychotic could help in Alzheimer’s

New treatments for dementia in a decade - Featured Image

 

A new kind of antipsychotic has been found to relieve terrifying and disturbing symptoms suffered by millions of people with Alzheimer’s disease worldwide.

Research has found that pimavanserin significantly improves psychosis symptoms in people with the condition, without the devastating side-effects of currently-used antipsychotics.

Scientists also found that the drug had an even greater benefit in those with the most severe psychotic symptoms.

Up to half of the 45 million people worldwide who are living with Alzheimer’s disease will experience psychotic episodes, a figure that is even higher in some other forms of dementia. Psychosis is linked to a faster deterioration in dementia.

Currently there is no approved safe and effective treatment for these distressing symptoms.

In people with dementia, widely-used antipsychotics lead to sedation, falls and can double the speed at which brain function deteriorates.

Despite all of these negative effects, they have very little benefit in improving psychosis in people with dementia.

The scientists said that pimavanserin works differently to other antipsychotics, by blocking a very specific nerve receptor in the brain.

Professor Clive Ballard, from the University of Exeter Medical School, who led the research, said: “Psychosis is a particularly terrifying symptom of Alzheimer’s disease.

“People may experience paranoia, or see, hear or smell things that are not there. It’s distressing both for those experiencing the delusions and for their carers.

“We urgently need to do better by them, and our encouraging results provides hope. We’re delighted that our results have led to a larger phase three clinical trial which is now ongoing.”

The findings are the result of a double-blind, placebo-controlled exploratory trial designed to evaluate the efficacy and safety of pimavanserin in 181 patients with Alzheimer’s disease psychosis, with 90 of them given pimavanserin and 90 of them on a placebo.

The research, published in the journal Lancet Neurology, can be accessed here.

 

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