Pharmaceutical Compositions for Reducing Amyloid Deposition, Amyloid Neurotoxicity, and Microgliosis
First Claim
1. A pharmaceutical composition comprising a non-racemic mixture of (−
- ) and (+) enantiomers of nilvadipine or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, wherein said non-racemic mixture is from greater than 50% up to about 89% by weight (−
) enantiomer.
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Accused Products
Abstract
The present invention provides methods for reducing Aβ deposition, Aβ neurotoxicity and microgliosis in an animal or human afflicted with a cerebral amyloidogenic disease, such as Alzheimer'"'"'s disease (AD), by administering therapeutically effective amounts of the (R)-enantiomer of the dihydropyridine compound nilvadipine, also known as (−)-nilvadipine, to the animal or human, or by administering a non-racemic enantiomeric mixture of the dihydropyridine compound nilvadipine, to the animal or human. Further provided are methods for reducing the risk of Aβ deposition, Aβ neurotoxicity and microgliosis in animals or humans suffering from traumatic brain injury by administering (−)-nilvadipine, or non-racemic mixture of nilvadipine enantiomers, after the traumatic brain injury and continuing treatment for a prescribed period of time thereafter.
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Citations
12 Claims
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1. A pharmaceutical composition comprising a non-racemic mixture of (−
- ) and (+) enantiomers of nilvadipine or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, wherein said non-racemic mixture is from greater than 50% up to about 89% by weight (−
) enantiomer. - View Dependent Claims (2, 3, 4, 5, 6, 7, 8, 9, 10)
- ) and (+) enantiomers of nilvadipine or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, wherein said non-racemic mixture is from greater than 50% up to about 89% by weight (−
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11. A method of making a medicament comprising combining a non-racemic mixture of (−
- ) and (+) enantiomers of nilvadipine or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, wherein said non-racemic mixture is from greater than 50% up to about 89% by weight (−
) enantiomer.
- ) and (+) enantiomers of nilvadipine or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, wherein said non-racemic mixture is from greater than 50% up to about 89% by weight (−
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12. A method of treating Alzheimer'"'"'s Disease comprising administering to a patient in need thereof a pharmaceutical composition comprising a non-racemic mixture of (−
- ) and (+) enantiomers of nilvadipine or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, wherein said non-racemic mixture is from greater than 50% up to about 89% by weight (−
) enantiomer.
- ) and (+) enantiomers of nilvadipine or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, wherein said non-racemic mixture is from greater than 50% up to about 89% by weight (−
Specification