IP Library Patent Application 12992709
Patent Application
App. No. 12/992,709

Muscarinic Agonists as Cognitive Enhancers

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Quick Facts
Patent No.
US None
App. No.
12/992,709
Abstract

A method of treating a mental condition in a subject in need thereof, comprising: administering to a subject in need thereof an effective amount of compound CDD-102A.

Claims (88)

1 . A composition comprising an effective amount of a CDD-0102 [5-(3-ethyl-1,2,4-oxadiazol-5-yl)-1,4,5,6-tetrahydropyrimidine] compound, or a pharmaceutically acceptable salt or hydrate thereof sufficient to enhance behavioral flexibility by enhancing one or more of executive functioning, reasoning, problem solving, and learning functioning in a subject in need thereof.

2 . (canceled)

3 . (canceled)

4 . The composition according to claim 1 , wherein the behavioral flexibility function includes one or more of: perseveration errors, regressive errors and never-reinforced errors.

5 . The composition according to claim 1 , wherein the administration of the compound gives rise to efficacious treatment without substantially interfering with M 2 , M 3 , M 4 and M 5 receptor activity in the subject.

6 . (canceled)

7 . (canceled)

8 . (canceled)

9 . The pharmaceutical composition according to claim 1 , formulated to be administered to a subject in need thereof in a dosage ranging from about 0.001 mg/kg to about 10 mg/kg body weight.

10 . The pharmaceutical composition according to claim 1 , formulated to be administered to a subject in need thereof in a dosage ranging from about 0.01 to about 10 mg/kg of body weight.

11 . The pharmaceutical composition according to claim 1 , formulated to be administered to a subject in need thereof in a dosage ranging from about 0.01 mg/kg to about 0.1 mg/kg of body weight.

12 . The pharmaceutical composition according to claim 1 , formulated to be administered to a subject in need thereof in a daily dosage.

13 . The pharmaceutical composition according to claim 1 , formulated to be administered to a subject in need thereof in a regimen of 1 to 4 times per day.

14 . (canceled)

15 . (canceled)

16 . (canceled)

17 . (canceled)

18 . (canceled)

19 . (canceled)

20 . (canceled)

21 . (canceled)

22 . (canceled)

23 . (canceled)

24 . (canceled)

25 . (canceled)

26 . (canceled)

27 . (canceled)

28 . (canceled)

29 . (canceled)

30 . (canceled)

31 . A method of improving and/or modulating a loss of behavioral flexibility in a subject in need thereof, comprising:

administering to a subject in need thereof an effective amount of CDD-102A [5-(3-ethyl-1,2,4-oxadiazol-5-yl)-1,4,5,6-tetrahydropyrimidine] compound or a pharmaceutically acceptable salt or hydrate thereof,

sufficient to enhance behavioral flexibility by enhancing one or more of: executive function, reasoning and problem solving, a memory function, a learning function.

32 . The method according to claim 31 , wherein the behavioral flexibility function includes one or more of: perseveration errors, regressive errors and never-reinforced errors.

33 . The method according to claim 31 , wherein the administration of the compound gives rise to efficacious treatment without substantially interfering with M 2 , M 3 , M 4 and/or M 5 subtype receptor activity in the subject.

34 . The method according to claim 31 , wherein the mental condition is at least partially due to decreased M 1 receptor activity.

35 . The method according to claim 31 , wherein the subject has a mental condition selected from the group consisting of one or more of: neurodegenerative diseases, Alzheimer's disease, Parkinson's disease, schizophrenia, age-related cognitive decline, and attention-deficit disorder.

36 . (canceled)

37 . (canceled)

38 . (canceled)

39 . (canceled)

40 . (canceled)

41 . (canceled)

42 . (canceled)

43 . (canceled)

44 . (canceled)

45 . The method according to claim 31 , wherein the subject is a human.

46 . (canceled)

47 . (canceled)

48 . (canceled)

49 . (canceled)

50 . Use of CDD-102A [5-(3-ethyl-1,2,4-oxadiazol-5-yl)-1,4,5,6-tetrahydropyrimidine] compound or a pharmaceutically acceptable salt or hydrate thereof, or a composition comprising CDD-102A [5-(3-ethyl-1,2,4-oxadiazol-5-yl)-1,4,5,6-tetrahydropyrimidine] compound or a pharmaceutically acceptable salt or hydrate thereof in the manufacture of a medicament for use in improving and/or ameliorating a loss of behavioral flexibility in a subject in need thereof.

51 . (canceled)

52 . (canceled)

53 . (canceled)

54 . Use of CDD-102A compound or a pharmaceutically acceptable salt or hydrate thereof, or a composition comprising CDD-102A compound or a pharmaceutically acceptable salt or hydrate thereof, in the manufacture of a medicament for treating a mental condition affecting behavioral flexibility in a subject.

55 . (canceled)

56 . Use according to claim 54 ,

wherein the mental condition is selected from the group consisting of one or more of: neurodegenerative diseases, Alzheimer's disease, Parkinson's disease, schizophrenia, age-related cognitive decline, and attention-deficit disorder.

57 . (canceled)

58 . (canceled)

59 . (canceled)

60 . (canceled)

61 . (canceled)

62 . (canceled)

63 . (canceled)

64 . (canceled)

65 . (canceled)

66 . (canceled)

67 . (canceled)

68 . (canceled)

69 . (canceled)

70 . (canceled)

71 . (canceled)

72 . (canceled)

73 . Use according to claim 54 ,

wherein the use includes preventing the development of the condition, and/or whereby the condition has already developed and the subject is protected against worsening of the condition.

74 . Use according to claim 54 ,

wherein the disease or condition results from defective or malfunctioning M 1 receptors in the subject.

75 . Use according to claim 54 ,

wherein the treatment disease or condition results from suppressed M 1 receptor transmission in the subject.

76 . Use according to claim 54 ,

for use in selectively activating M 1 muscarinic receptor, without substantially interfering with M 2 , M 3 , M 4 and M 5 receptor activity.

77 . (canceled)

78 . (canceled)

79 . (canceled)

80 . (canceled)

81 . Use according to claim 54 , wherein the subject is a human.

Assignments (3)
CONFIRMATORY LICENSE Recorded Dec 9, 2011
From: UNIVERSITY OF TOLEDO
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 027358/0071 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 24, 2011
From: MESSER, WILLIAM S., JR.
To: THE UNIVERSITY OF TOLEDO
Reel/Frame 025682/0669 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 24, 2011
From: RAGOZZINO, MICHAEL E.
To: THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS
Reel/Frame 025682/0684 →