IP Library Patent Application 11733642
Patent Application
App. No. 11/733,642

COMPOSITIONS AND METHODS OF USING R(+) PRAMIPEXOLE

Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US None
App. No.
11/733,642
Abstract

Pharmaceutical compositions of R(+) pramipexole and methods of using such compositions for the treatment or prevention of diseases associated with or related to mitochondrial dysfunction or increased oxidative stress are disclosed.

Claims (86)

1 . A method of treating age-related macular degeneration comprising administering a therapeutically effective amount of R(+) pramipexole.

2 . The method of claim 1 , wherein said therapeutically effective amount of R(+) pramipexole is administered in a pharmaceutical composition.

3 . The method of claim 2 , wherein said pharmaceutical composition has a chiral purity for the R(+) enantiomer of pramipexole of 80% or greater.

4 . The method of claim 2 , wherein said pharmaceutical composition has a chiral purity for the R(+) enantiomer of pramipexole of 90% or greater.

5 . The method of claim 2 , wherein said pharmaceutical composition has a chiral purity for the R(+) enantiomer of pramipexole of 95% or greater.

6 . The method of claim 2 , wherein said pharmaceutical composition has a chiral purity for the R(+) enantiomer of pramipexole of 99% or greater.

7 . The method of claim 1 , wherein said the therapeutically effective amount of R(+) pramipexole is from about 50 milligrams to about 5000 milligrams.

8 . The method of claim 1 , wherein the therapeutically effective amount of R(+) pramipexole is from about 100 milligrams to about 3000 milligrams.

9 . The method of claim 1 , wherein the therapeutically effective amount of R(+) pramipexole is from about 300 milligrams to about 1500 milligrams.

10 . The method of claim 1 , wherein the therapeutically effective amount of R(+) pramipexole is from about 500 milligrams to about 1000 milligrams.

11 . The method of claim 2 , wherein said pharmaceutical composition is suitable for oral administration.

12 . The method of claim 2 , wherein said pharmaceutical composition is a solid oral dosage form.

13 . The method of claim 2 , wherein said pharmaceutical composition is a tablet.

14 . The method of claim 2 , wherein said pharmaceutical composition is a capsule.

15 . The method of claim 2 , wherein said pharmaceutical composition is a suitable for ocular administration.

16 . The method of claim 2 , wherein said pharmaceutical composition further comprises S(−) pramipexole in an amount that does not provide significant dopamine agonist activity.

17 . The method of claim 2 , wherein said pharmaceutical composition consists essentially of R(+) pramipexole.

18 . The method of claim 2 , wherein said pharmaceutical compositions further comprises an agent useful in treating age-related macular degeneration.

19 . A method of treating of treating type II diabetes comprising administering a therapeutically effective amount of R(+) pramipexole.

20 . The method of claim 19 , wherein said therapeutically effective amount of R(+) pramipexole is administered in a pharmaceutical composition.

21 . The method of claim 20 , wherein said pharmaceutical composition has a chiral purity for the R(+) enantiomer of pramipexole of 80% or greater.

22 . The method of claim 20 , wherein said pharmaceutical composition has a chiral purity for the R(+) enantiomer of pramipexole of 90% or greater.

23 . The method of claim 20 , wherein said pharmaceutical composition has a chiral purity for the R(+) enantiomer of pramipexole of 95% or greater.

24 . The method of claim 20 , wherein said pharmaceutical composition has a chiral purity for the R(+) enantiomer of pramipexole of 99% or greater.

25 . The method of claim 19 , wherein said the therapeutically effective amount of R(+) pramipexole is from about 50 milligrams to about 5000 milligrams.

26 . The method of claim 19 , wherein the therapeutically effective amount of R(+) pramipexole is from about 100 milligrams to about 3000 milligrams.

27 . The method of claim 19 , wherein the therapeutically effective amount of R(+) pramipexole is from about 300 milligrams to about 1500 milligrams.

28 . The method of claim 19 , wherein the therapeutically effective amount of R(+) pramipexole is from about 500 milligrams to about 1000 milligrams.

29 . The method of claim 20 , wherein said pharmaceutical composition is suitable for oral administration.

30 . The method of claim 20 , wherein said pharmaceutical composition is a solid oral dosage form.

31 . The method of claim 20 , wherein said pharmaceutical composition is a tablet.

32 . The method of claim 20 , wherein said pharmaceutical composition is a capsule.

33 . The method of claim 20 , wherein said pharmaceutical composition further comprises S(−) pramipexole in an amount that does not provide significant dopamine agonist activity.

34 . The method of claim 20 , wherein said pharmaceutical composition consists essentially of R(+) pramipexole.

35 . The method of claim 20 , wherein said pharmaceutical composition further comprises an agent useful in treating type II diabetes.

36 . A method of treating of treating skin disorders comprising administering a therapeutically effective amount of R(+) pramipexole.

37 . The method of claim 36 , wherein said therapeutically effective amount of R(+) pramipexole is administered in a pharmaceutical composition.

38 . The method of claim 37 , wherein said pharmaceutical composition has a chiral purity of the R(+) enantiomer of pramipexole of 80% or greater.

39 . The method of claim 37 , wherein said pharmaceutical composition has a chiral purity for the R(+) enantiomer of pramipexole of 90% or greater.

40 . The method of claim 37 , wherein said pharmaceutical composition has a chiral purity for the R(+) enantiomer of pramipexole of 95% or grater.

41 . The method of claim 37 , wherein said pharmaceutical composition has a chiral purity for the R(+) enantiomer of pramipexole of 99% or greater.

42 . The method of claim 36 , wherein said the therapeutically effective amount of R(+) pramipexole is from about 50 milligrams to about 5000 milligrams.

43 . The method of claim 36 , wherein the therapeutically effective amount of R(+) pramipexole is from about 100 milligrams to about 3000 milligrams.

44 . The method of claim 36 , wherein the therapeutically effective amount of R(+) pramipexole is from about 300 millgrams to about 1500 milligrams.

45 . The method of claim 36 , wherein the therapeutically effective amount of R(+) pramipexole is from about 500 milligrams to about 1000 milligrams.

46 . The method of claim 37 , wherein said pharmaceutical composition is suitable for oral administration.

47 . The method of claim 37 , wherein said pharmaceutical composition is a solid oral dosage form.

48 . The method of claim 37 , wherein said pharmaceutical composition is a tablet.

49 . The method of claim 37 , wherein said pharmaceutical competition is a capsule.

50 . The method of claim 37 , wherein said pharmaceutical composition is suitable for topical administration.

51 . The method of claim 37 , wherein said pharmaceutical composition further comprises S(−) pramipexole in an amount that does not provide significant dopamine agonist activity.

52 . The method of claim 37 , wherein said pharmaceutical consists essentially of R(+) pramipexole.

53 . The method of claim 37 , wherein the pharmaceutical compositions further comprises an agent useful in treating skin disorders.

54 . A method of treating of treating cardiovascular disorders comprising administering a therapeutically effective amount of R(+) pramipexole.

55 . The method of claim 54 , wherein said therapeutically effective amount of R(+) pramipexole is administered in a pharmaceutical composition.

56 . The method of claim 55 , wherein said pharmaceutical composition has a chiral purity for the R(+) enantiomer of pramipexole of 80% or greater.

57 . The method of claim 55 , wherein said pharmaceutical composition has a chiral purity for the R(+) enantiomer of pramipexole of 90% or greater.

58 . The method of claim 55 , wherein said pharmaceutical composition has a chiral purity for the R(+) enantiomer of pramipexole of 95% or greater.

59 . The method of claim 55 , wherein said pharmaceutical composition has a chiral purity for the R(+) enantiomer of pramipexole of 99% or greater.

60 . The method of claim 54 , wherein said the therapeutically effective amount of R(+) pramipexole is from about 50 milligrams to about 5000 milligrams.

61 . The method of claim 54 , wherein the therapeutically effective amount of R(+) pramipexole is from about 100 milligrams to about 3000 milligrams.

62 . The method of claim 54 , wherein the therapeutically effective amount of R(+) pramipexole is from about 300 milligrams to about 1500 milligrams.

63 . The method of claim 54 , wherein the therapeutically effective amount of R(+) pramipexole is from about 500 milligrams to about 1000 milligrams.

64 . The method of claim 55 , wherein said pharmaceutical composition is suitable for oral administration.

65 . The method of claim 55 , wherein said pharmaceutical composition is a solid oral dosage form.

66 . The method of claim 55 , wherein said pharmaceutical composition is a tablet.

67 . The method of claim 55 , wherein said pharmaceutical composition is a capsule.

68 . The method of claim 55 , wherein said pharmaceutical composition further comprises S(−) pramipexole in an amount that does not provide significant dopamine agonist activity.

69 . The method of claim 55 , wherein said pharmaceutical composition consists essentially of R(+) pramipexole.

70 . The method of claim 55 , wherein the pharmaceutical compositions further comprises an agent useful in treating cardiovascular disorders.

71 . A method of treating of treating inflammatory disorders comprising administering a therapeutically effective amount of R(+) pramipexole.

72 . The method of claim 71 , wherein said therapeutically effective amount of R(+) pramipexole is administered in a pharmaceutical composition.

73 . The method of claim 72 , wherein said pharmaceutical composition has a chiral purity for the R(+) enantiomer of pramipexole of 80% or greater.

74 . The method of claim 72 , wherein said pharmaceutical composition has a chiral purity for the R(+) enantiomer of pramipexole of 90% or greater.

75 . The method of claim 72 , wherein said pharmaceutical composition has a chiral purity for the R(+) enantiomer of pramipexole of 95% or greater.

76 . The method of claim 72 , wherein said pharmaceutical composition has a chiral purity for the R(+) enantiomer of pramipexole of 99% or greater.

77 . The method of claim 71 , wherein said the therapeutically effective amount of R(+) pramipexole is from about 50 milligrams to about 5000 milligrams.

78 . The method of claim 71 , wherein the therapeutically effective amount of R(+) pramipexole is from about 100 milligrams to about 3000 milligrams.

79 . The method of claim 71 , wherein the therapeutically effective amount of R(+) pramipexole is from about 300 milligrams to about 1500 milligrams.

80 . The method of claim 71 , wherein the therapeutically effective amount of R(+) pramipexole is from about 500 milligrams to about 1000 milligrams.

81 . The method of claim 72 , wherein said pharmaceutical composition is suitable for oral administration.

82 . The method of claim 72 , wherein said pharmaceutical composition is a solid oral dosage form.

83 . The method of claim 72 , wherein said pharmaceutical composition is a tablet.

84 . The method of claim 72 , wherein said pharmaceutical composition further comprises S(−) pramipexole in an amount that does not provide significant dopamine agonist activity.

85 . The method of claim 72 , wherein said pharmaceutical composition consists essentially of R(+) pramipexole.

86 . The method of claim 72 , wherein the pharmaceutical compositions further comprises an agent useful in treating inflammatory disorders.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 27, 2014
From: KNOPP NEUROSCIENCES INC.
To: KNOPP BIOSCIENCES LLC
Reel/Frame 032551/0311 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 5, 2007
From: BOZIK, MICHAEL E.; HEBRANK, GREGORY T.; PETZINGER, THOMAS, JR.
To: KNOPP NEUROSCIENCES, INC.
Reel/Frame 019784/0503 →