Composition and method for treating neurological disease
View Patent ↗A method of administering amantadine is provided. The method comprises orally administering to a subject a pharmaceutical composition comprising amantadine, or a pharmaceutically acceptable salt thereof, and one or more excipients, wherein at least one of the excipients modifies release of the amantadine. A dose of the composition provides a mean change in amantadine plasma concentration as a function of time (dC/dT) that is less than 40% of the change in amantadine plasma concentration provided by a dose of the same quantity of an immediate release form of amantadine. The change in plasma concentration over time (dC/dT) is measured in a single dose human pharmacokinetic study in a defined time period of 0 to 4 hours after administration. The amantadine, or pharmaceutically acceptable salt thereof, is administered once daily at a dose of 300 to 500 mg per day.
1. A dosage form suitable for once-daily oral administration to a human subject consisting of
(i) 50 mg to 500 mg of a drug selected from the group consisting of amantadine and pharmaceutically acceptable salts thereof, and (ii) at least one excipient, wherein at least 50% of the drug in the dosage form is in an extended release form, and wherein the dosage form provides a mean change in amantadine plasma concentration as a function of time (dC/dT) that is less than 40% of the dC/dT provided by the same quantity of the drug in an immediate release form, wherein the dC/dT values are measured in a single dose human pharmacokinetic study over the time period between 0 and 4 hours after administration.
2. A dosage form suitable for once-daily oral administration to a human subject consisting of
(i) 50 mg to 500 mg of a drug selected from the group consisting of amantadine and pharmaceutically acceptable salts thereof, and (ii) at least one excipient, wherein at least 50% of the drug in the dosage form is in an extended release form, and wherein the dosage form provides a mean change in amantadine plasma concentration as a function of time (dC/dT) that is less than 40% of the dC/dT provided by the same quantity of the drug in an immediate release form, wherein the dC/dT values are measured in a single dose human pharmacokinetic study over the time period between administration and Tmax of the immediate release form.
3. A dosage form suitable for once-daily oral administration to a human subject consisting of
(i) 50 mg to 500 mg of a drug selected from the group consisting of amantadine and pharmaceutically acceptable salts thereof, and (ii) at least one excipient, wherein at least 50% of the drug in the dosage form is in an extended release form, and wherein the dosage form provides a mean change in amantadine plasma concentration as a function of time (dC/dT) that is less than 40% of the dC/dT provided by the same quantity of the drug in an immediate release form, wherein the dC/dT of the dosage form is measured in a single dose human pharmacokinetic study over the time period between 2 hours and 4 hours after administration and the dC/dT provided by the same quantity of the drug in an immediate release form is measured in a single dose human pharmacokinetic study over the time period between administration and Tmax of the immediate release form.
4. The dosage form of any of claims 1 - 3 , comprising an osmotic device, which utilizes an osmotic driving force to provide extended release of amantadine.
5. The dosage form of any of claims 1 - 3 , wherein the amount of drug is 100 to 500 mg.
6. The dosage form of any of claims 1 - 3 , wherein the amount of drug is 200 to 500 mg.
7. The dosage form of any of claims 1 - 3 , wherein at least 75% of the drug in the dosage form is in an extended release form.
8. The dosage form of any of claims 1 - 3 , wherein at least 90% of the drug in the dosage form is in an extended release form.
9. The dosage form of any of claims 1 - 3 , wherein the dosage form provides a shift in amantadine Tmax of 2 hours to 16 hours relative to an immediate release form of amantadine, wherein the Tmax is measured in a single dose human pharmacokinetic study.
10. The dosage form of any of claims 1 - 3 , wherein the extent of drug bioavailability is maintained.
11. The dosage form of any of claims 1 - 3 , any of, wherein the dosage form additionally comprises the drug in an immediate release form.