Use of pridopidine to improve cognitive function and for treating Alzheimer's disease
This invention provides a method of improving cognitive function in a subject comprising periodically administering to the subject an amount of pridopidine or a pharmaceutically acceptable salt thereof effective to improve a cognitive function in the subject. The invention also provides a method of treating a subject afflicted with Alzheimer's disease, comprising periodically administering to the subject a pharmaceutical composition comprising an amount of pridopidine or a pharmaceutically acceptable salt thereof effective to treat the subject.
1. A method of improving short term memory, working memory or long term memory in a human subject diagnosed to be in need of memory improvement comprising periodically administering to the subject between 22.5 mg/day-31.5 mg/day of pridopidine or a pharmaceutically acceptable salt thereof effective to improve memory in the subject, wherein the short term memory, working memory and long term memory is improved by S1R modulation.
2. The method of claim 1 , wherein memory is short term memory or working memory.
3. The method of claim 1 , wherein the subject is prone to or predisposed to have a memory deficit.
4. The method of claim 3 , wherein the memory deficit is a short-term memory deficit or memory loss.
5. The method of claim 4 , wherein the memory deficit is memory loss caused by one or more of age-related changes in memory, mild cognitive impairment dementia or depression.
6. The method of claim 1 wherein the amount of pridopidine or a pharmaceutically acceptable salt thereof is administered to the subject once daily.
7. The method of claim 1 , wherein the amount of pridopidine or a pharmaceutically acceptable salt thereof is administered to the subject more often than once daily.
8. The method of claim 1 , wherein the periodic administration continues for at least 3 days.
9. The method of claim 1 , wherein the pharmaceutically acceptable salt of pridopidine is pridopidine hydrochloride.
10. The method of claim 4 , wherein the memory loss is due to epilepsy, an anxiety disorder or Huntington's disease.
11. The method of claim 1 , comprising periodically administering to the subject an amount of pridopidine or a pharmaceutically acceptable salt thereof effective to reduce the toxic effect of p amyloid 1-42 in the subject.
12. The method of claim 1 , comprising periodically administering to the subject an amount of pridopidine or a pharmaceutically acceptable salt thereof effective to reduce neurotoxicity in the subject.