Pridopidine for treating drug induced dyskinesias
The invention provides a method of treating a subject afflicted with a drug-induced movement disorder including levodopa-induced dyskinesia comprising periodically administering to the subject in need thereof an amount of pridopidine effective to treat the subject. The invention further provides a method of treating a subject at risk of developing a drug-induced movement disorder, including levodopa-induced dyskinesia. The invention also provides pharmaceutical compositions suitable for carrying out these methods and packages containing such pharmaceutical compositions.
1. A method of treating levodopa-induced dyskinesia (LID) in a subject in need thereof, comprising administering to the subject an amount of pridopidine or pharmaceutically acceptable salt thereof, effective to treat the subject, wherein the amount of between 150-400 mg/day.
2. The method of claim 1 , wherein the subject is afflicted with Parkinson's disease.
3. The method of claim 1 , wherein the subject is afflicted with parkinsonism other than Parkinson's disease.
4. The method of claim 1 , wherein the subject is concurrently being treated with levodopa.
5. The method of claim 4 wherein pridopidine and the levodopa are administered simultaneously.
6. The method of claim 5 wherein pridopidine and the levodopa are co-formulated.
7. The method of claim 4 , wherein the pridopidine and the levodopa are administered sequentially and in separate pharmaceutical formulations.
8. The method of claim 1 , wherein the amount of pridopidine is effective to alleviate or reduce a symptom associated with the levodopa treatment.
9. The method of claim 8 , wherein the symptom is abnormal movements, myoclonic jerks, irregular movements of extremities, gait, facial grimacing, ataxia, inability to sustain motor act, hand movement or balance, choreiform peak dose dyskinesia, or dystonic peak dose dyskinesia.
10. The method of claim 8 , wherein the symptom is bad quality on-time evoked by levodopa.
11. The method of claim 8 , wherein the administration of pridopidine improves the symptom of the levodopa induced dyskinesia by at least 8%, by at least 20%, by at least 30% or by at least 50% as measured by MDS-UPDRS or UDysRS.
12. The method of claim 1 , wherein the pridopidine is administered via oral administration.
13. The method of claim 1 , wherein pridopidine is administered once or twice daily.
14. The method of claim 1 , wherein the pridopidine is administered in the form of a pridopidine salt.
15. The method of claim 14 , wherein the pridopidine salt is pridopidine hydrochloride.
16. The method of claim 1 , wherein the pridopidine is administered at a daily dose of 200 mg given in the form of pridopidine HCl.
17. The method of claim 1 , wherein the pridopidine is administered in equal doses, twice daily, thrice daily or four times daily.
18. The method of claim 1 , wherein the AUC 0-24 achieved is about 25,000 h*ng/ml to about 60,000 h*ng/ml.
19. The method of claim 1 , further delaying the onset of LID or reduce the risk of developing LID.
20. The method of claim 1 , wherein the subject is receiving levodopa for treatment of Parkinson's disease.