Methods for the treatment of CNS-related conditions
The invention provides methods for administering extended release memantine in combination with immediate release donepezil to a subject. Memantine in an extended release form containing 22.5 to 30 mg memantine or a pharmaceutically acceptable salt thereof in combination with donepezil is administered to a patient suffering from a neurological condition, such as Alzheimer's disease, Parkinson's disease or dementia. The extended release form of memantine achieves particular pharmacokinetic criteria such as change in plasma concentration of memantine over time and ratio of maximum memantine plasma concentration to mean memantine plasma concentration.
1. A method of treating a patient with a neurological condition selected from the group consisting of Alzheimer's disease, dementia, Parkinson's disease, and neuropathic pain, comprising orally administering to a human subject in need thereof:
(a) 22.5 mg to 30 mg memantine or a pharmaceutically acceptable salt thereof provided in a sustained release dosage form, wherein said sustained release memantine provides a change in mean plasma concentration of memantine as a function of time (dC/dT) that is: (1) less than about 50% of the dC/dT provided by the same quantity of an immediate release form of memantine, determined in a time period between 0-Tmax of the immediate release form of memantine; and (2) 2.1 ng/ml/hr or less, determined in a time period of 0 to 4 hours; wherein dC/dT is measured in a single dose human PK study; and
(b) a therapeutically effective amount of immediate release donepezil.
2. The method of claim 1 , wherein the dC/dT of 2.1 ng/mL/hr or less is determined in a time period of 2 to 4 hours.
3. The method of claim 1 , wherein the sustained release oral dosage form comprises 25 mg to 30 mg memantine or a pharmaceutically acceptable salt thereof.
4. The method of claim 3 , wherein the dC/dT of 2.1 ng/mL/hr or less is determined in a time period of 2 to 4 hours.
5. The method of claim 1 , wherein the sustained release oral dosage form comprises 28 mg memantine or a pharmaceutically acceptable salt thereof.
6. The method of claim 5 , wherein the dC/dT of 2.1 ng/mL/hr or less is determined in a time period of 2 to 4 hours.
7. A method of treating a patient with a neurological condition selected from the group consisting of Alzheimer's disease, dementia, Parkinson's disease, and neuropathic pain, comprising orally administering to a human subject in need thereof:
(a) 22.5 mg to 30 mg memantine or a pharmaceutically acceptable salt thereof provided in a sustained release dosage form, wherein said sustained release memantine provides a change in mean plasma concentration of memantine as a function of time (dC/dT) that is: (1) less than about 50% of the dC/dT provided by the same quantity of an immediate release form of memantine, determined in a time period between 0 hours and 6 hours of administration of memantine; and (2) 2.1 ng/ml/hr or less, determined in a time period of 0 to 4 hours; wherein dC/dT is measured in a single dose human PK study; and
(b) a therapeutically effective amount of immediate release donepezil.
8. The method of claim 7 , wherein the dC/dT of 2.1 ng/mL/hr or less is determined in a time period of 2 to 4 hours.
9. The method of claim 7 , wherein the sustained release oral dosage form comprises 25 mg to 30 mg memantine or a pharmaceutically acceptable salt thereof.
10. The method of claim 9 , wherein the dC/dT of 2.1 ng/mL/hr or less is determined in a time period of 2 to 4 hours.
11. The method of claim 7 , wherein the sustained release oral dosage form comprises 28 mg memantine or a pharmaceutically acceptable salt thereof.
12. The method of claim 11 , wherein the dC/dT of 2.1 ng/mL/hr or less is determined in a time period of 2 to 4 hours.