Compositions and methods for treating synucleinopathies
The present invention describes the use of a 5HT3-antagonist, in combination with a 6-propylamino-4,5,6,7-tetrahydro-1,3-benzothiazole-2-amine, to reduce adverse effects and to facilitate the neuroprotective treatment of a patient suffering from a synucleinopathic disorder to enable a therapeutically effective 6-propylamino-4,5,6,7-tetrahydro-1,3-benzothiazole-2-amine daily dose without the dose-limiting adverse effects caused by pramipexole when administered alone.
1. A pharmaceutical composition in dosage unit form which comprises
(a) a 5HT3-antagonist, in an amount per unit form of from 1 μg to 300 mg; and
(b) a 6-propylamino-4,5,6,7-tetrahydro-1,3-benzothiazole-2-amine selected from the group consisting of the racemate or a pharmaceutically acceptable salt thereof, in an amount per unit form equivalent to from 0.75 mg to 90 mg of pramipexole dihydrochloride monohydrate; pramipexole or a pharmaceutically acceptable salt thereof, in an amount per unit form equivalent to from 0.375 mg to 45 mg of pramipexole dihydrochloride monohydrate; and an (R)/(S)-mixture, in an amount per unit form of from 50 mg to 3000 mg, inclusive of an (S)-enantiomer or a pharmaceutically acceptable salt thereof in amount per unit form equivalent to from 0.375 mg to 45 mg of pramipexole dihydrochloride monohydrate,
in admixture with a pharmaceutical carrier or vehicle.
2. The composition of claim 1 , wherein said 6-propylamino-4,5,6,7-tetrahydro-1,3-benzothiazole-2-amine is pramipexole or a pharmaceutically acceptable salt thereof, in an amount per unit form equivalent to from more than 4.5 mg to 42 mg of pramipexole dihydrochloride monohydrate.
3. The composition of claim 1 , wherein said 6-propylamino-4,5,6,7-tetrahydro-1,3-benzothiazole-2-amine is pramipexole or a pharmaceutically acceptable salt thereof, in an amount per unit form equivalent to from more than 6 mg to 42 mg of pramipexole dihydrochloride monohydrate.
4. The composition of claim 1 , wherein said 6-propylamino-4,5,6,7-tetrahydro-1,3-benzothiazole-2-amine is pramipexole or a pharmaceutically acceptable salt thereof, in an amount per unit form equivalent to from 6.5 mg to 42 mg of pramipexole dihydrochloride monohydrate.
5. The composition of claim 1 , wherein said 5HT3-antagonist is ondansetron hydrochloride dihydrate, in an amount per unit for equivalent to from 2 mg to 32 mg of ondansetron base, and said 6-propylamino-4,5,6,7-tetrahydro-1,3-benzothiazole-2-amine is pramipexole or a pharmaceutically acceptable salt thereof, in an amount per unit form equivalent to from 0.375 mg to 42 mg of pramipexole dihydrochloride monohydrate.
6. The composition of claim 1 , wherein said 6-propylamino-4,5,6,7-tetrahydro-1,3-benzothiazole-2-amine is pramipexole or a pharmaceutically acceptable salt thereof, in an amount per IR-unit form equivalent to from more than 6 mg to 22.5 mg of pramipexole dihydrochloride monohydrate.
7. The composition of claim 1 , wherein said 6-propylamino-4,5,6,7-tetrahydro-1,3-benzothiazole-2-amine is pramipexole or a pharmaceutically acceptable salt thereof, in an amount per ER-unit form equivalent to from more than 6 mg to 45 mg of pramipexole dihydrochloride monohydrate.
8. The composition of claim 1 , wherein said 5HT3-antagonist is selected from the group consisting of alosetron and pharmaceutically acceptable salts and solvates thereof, azasetron and pharmaceutically acceptable salts and solvates thereof, bemesetron and pharmaceutically acceptable salts and solvates thereof, cilansetron and pharmaceutically acceptable salts and solvates thereof, dolasetron and pharmaceutically acceptable salts and solvates thereof, fabesetron and pharmaceutically acceptable salts and solvates thereof, granisetron and pharmaceutically acceptable salts and solvates thereof, itasetron and pharmaceutically acceptable salts and solvates thereof, lerisetron and pharmaceutically acceptable salts and solvates thereof, lurosetron and pharmaceutically acceptable salts and solvates thereof, ondansetron and pharmaceutically acceptable salts and solvates thereof, palonosetron and pharmaceutically acceptable salts and solvates thereof, ramosetron and pharmaceutically acceptable salts and solvates thereof, ricasetron and pharmaceutically acceptable salts and solvates thereof, tropisetron and pharmaceutically acceptable salts and solvates thereof, and zatosetron and pharmaceutically acceptable salts and solvates thereof.
9. The composition of claim 5 , wherein said 6-propylamino-4,5,6,7-tetrahydro-1,3-benzothiazole-2-amine is pramipexole or a pharmaceutically acceptable salt thereof, in an amount per unit form equivalent to from more than 4.5 mg to 42 mg of pramipexole dihydrochloride monohydrate.
10. The composition of claim 5 , wherein said 6-propylamino-4,5,6,7-tetrahydro-1,3-benzothiazole-2-amine is pramipexole or a pharmaceutically acceptable salt thereof, in an amount per unit form equivalent to from more than 6.0 mg to 42 mg of pramipexole dihydrochloride monohydrate.
11. The composition of claim 5 , wherein said 6-propylamino-4,5,6,7-tetrahydro-1,3-benzothiazole-2-amine is pramipexole or a pharmaceutically acceptable salt thereof, in an amount per unit form equivalent to from 6.5 mg to 42 mg of pramipexole dihydrochloride monohydrate.