IP Library Granted Patent US 9,796,673
Granted Patent B2
US 9,796,673 · App. 14/975,248 · Granted Oct 24, 2017

L-tartrate salt of pridopidine

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Quick Facts
Patent No.
US 9,796,673
App. No.
14/975,248
Granted
Oct 24, 2017
Kind
B2
Abstract

The subject invention provides pridopidine L-tartrate, compositions and a process for manufacture thereof.

Claims (21)

1. Pridopidine L-tartrate, characterized by a XRPD pattern with reflections corresponding to the d-spacing values 8.5±0.1, 4.8±0.1, 4.3±0.1, and 3.7±0.1, wherein the pridopidine L-tartrate is in crystalline form A1.

2. The pridopidine L-tartrate of claim 1 , which is pridopidine mono L-tartrate.

3. The pridopidine L-tartrate of claim 1 characterized by a XRPD pattern with reflections corresponding to the d-spacing values 8.5±0.1, 6.2±0.1, 5.7±0.1, 4.8±0.1, 4.5±0.1, 4.3±0.1, 4.1±0.1, 3.9±0.1, 3.8±0.1, 3.7±0.1, and 3.2±0.1, wherein the pridopidine L-tartrate is in crystalline form A1.

4. The pridopidine L-tartrate of claim 1 which is isolated.

5. A composition comprising the pridopidine L-tartrate of claim 1 , and a carrier.

6. A composition comprising the pridopidine L-tartrate of claim 1 , wherein the composition is free of L-tartaric acid.

7. A composition comprising the pridopidine L-tartrate of claim 1 , wherein the composition has less than 5% L-tartaric acid by weight.

8. The composition of claim 5 , further comprising pridopidine base.

9. The composition of claim 8 , wherein the pridopidine base is present in an amount of less than 5% based on total pridopidine content of the composition.

10. The composition of claim 5 , which is free of pridopidine base.

11. The composition of claim 5 , wherein the composition has less than 5% pridopidine base by weight.

12. The composition of claim 5 , wherein the composition is a pharmaceutical composition and the carrier is a pharmaceutically acceptable carrier.

13. The pharmaceutical composition of claim 12 , which is in tablet form.

14. The pharmaceutical composition of claim 13 , wherein the tablet unit form comprises between 22.5-315 mg pridopidine or between 90-315 mg pridopidine.

15. The pharmaceutical composition of claim 13 , wherein the tablet unit form comprises about 22.5 mg, about 45 mg, about 67.5 mg, about 90 mg, about 100 mg, about 112.5 mg, about 125 mg, about 135 mg, about 150 mg, about 180 mg, about 200 mg, about 250 mg, or about 315 mg pridopidine.

16. The pharmaceutical composition of claim 13 , wherein the tablet unit form is prepared for once daily administration.

17. The pharmaceutical composition of claim 13 , wherein the tablet unit form is prepared for more than once daily administration.

18. A process for manufacture of the pridopidine L-tartrate of claim 1 comprising:

a) combining L-tartaric acid with pridopidine free base to form a mixture

b) obtaining pridopidine L-tartrate from the mixture.

19. A method of treating a human subject afflicted with Huntington's disease comprising administering to the human subject an amount of the pridopidine L-tartrate of claim 1 effective to treat the human subject.

Assignments (3)
CHANGE OF NAME Recorded Jul 23, 2019
From: PRILENIA THERAPEUTICS DEVELOPMENT LTD.
To: PRILENIA NEUROTHERAPEUTICS LTD.
Reel/Frame 049827/0527 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 10, 2018
From: TEVA PHARMACEUTICALS INTERNATIONAL GMBH
To: PRILENIA THERAPEUTICS DEVELOPMENT LTD.
Reel/Frame 047716/0148 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 20, 2016
From: WU, RAEANN; HALTIWANGER, RALPH CURTIS; BIERLMAIER, STEPHEN; YAZDANIAN, MEHRAN
To: TEVA PHARMACEUTICALS INTERNATIONAL GMBH
Reel/Frame 037535/0504 →