Combination therapies for the treatment of alzheimer's disease and related disorders
The present invention relates to combination therapies for treating Alzheimer's disease or an amyloidosis-associated pathological condition comprising co-administering a therapeutically effective amount of a first compound, and a therapeutically effective amount of a second compound. In certain embodiments, the first compound or the second compound inhibits AB peptide polymerization; is an anti-inflammatory; improves cognitive function, mood, or social behavior; is associated with Tau or alpha-synuclein; or regulates amyloid peptide washout.
1. A method of treating a disease or condition in a subject in need thereof comprising co-administering a first amount of a first compound and a second amount of a second compound, wherein the disease or condition is Alzheimer's disease, dementia, an amyloidosis-associated condition, or a head injury; the first compound is cromolyn or a pharmaceutically acceptable salt thereof; the first amount is about 16 mg/day or about 20 mg/day; the second compound is a cholinesterase inhibitor; and the first amount of the first compound and the second amount of the second compound, taken together, are therapeutically effective.
2. The method of claim 1 , wherein the cholinesterase inhibitor is selected from the group consisting of donepezil, riastigmine and galantamine.
3. The method of claim 1 , wherein the disease or condition is Alzheimer's disease.
4. The method of claim 1 , wherein the first compound is formulated as a dry powder.
5. The method of claim 1 , wherein the subject is a human subject.
6. The method of claim 1 , wherein the first compound is a pharmaceutically acceptable salt of cromolyn.
7. The method of claim 1 , wherein the first compound is a pharmaceutically acceptable salt of cromolyn.
8. The method of claim 1 , wherein the first compound is cromolyn sodium.
9. A method of slowing the progression of a disease or condition in a subject in need thereof comprising co-administering a first amount of a first compound and a second amount of a second compound, wherein the disease or condition is Alzheimer's disease, dementia, an amyloidosis-associated condition, or a head injury; the first compound is cromolyn or a pharmaceutically acceptable salt thereof; the first amount is about 16 mg/day or about 20 mg/day; the second compound is a cholinesterase inhibitor; and the first amount of the first compound and the second amount of the second compound, taken together, are therapeutically effective.
10. The method of claim 9 , wherein the cholinesterase inhibitor is selected from the group consisting of donepezil, riastigmine and galantamine.
11. The method of claim 9 , wherein the disease or condition is Alzheimer's disease.
12. The method of claim 9 , wherein the first compound is formulated as a dry powder.
13. The method of claim 9 , wherein the subject is a human subject.
14. The method of claim 9 , wherein the first compound is cromolyn sodium.