IP Library Granted Patent US 10,835,532
Granted Patent B2
US 10,835,532 · App. 14/056,616 · Granted Nov 17, 2020

Muscarinic agonists as cognitive enhancers

Inventors: William S. Messer, Jr. (Toledo, OH); Michael E. Ragozzino (Chicago, IL)
Assignees: The University of Toledo; The Board of Trustees of the University of Illinois
A61K31/506
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Quick Facts
Patent No.
US 10,835,532
App. No.
14/056,616
Granted
Nov 17, 2020
Kind
B2
Abstract

Methods of treating a mental condition by administering to a subject in need thereof an effective amount of compound CDD-102A, [5-(3-ethyl-1,2,4-oxadiazol-5-yl)-1,4,5,6-tetrahydropyrimidine] are described.

Claims (12)

1. A method of decreasing regressive errors while enhancing behavioral flexibility in a human subject in need thereof, comprising:

administering to a subject in need thereof an effective amount of 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 to selectively activate M 1 muscarinic receptors in the subject without substantially producing M 2 , M 3 , M 4 and/or M 5 muscarinic receptor subtype activity in the subject;

wherein the compound is administered in a daily dosage ranging from about 0.01 mg/kg to about 0.3 mg/kg of body weight;

wherein the subject has autism spectrum disorders (ASD), does not have attention deficit hyperactivity disorder (ADHD) and does not have a cholinergic deficit, but does exhibit regressive errors;

wherein the subject is treated for regressive errors not associated with cholinergic deficits, but where cognitive function or behavioral flexibility is impaired;

wherein the regressive errors have already developed and the subject is protected against worsening of the regressive errors;

and,

decreasing regressive errors by enhancing behavioral flexibility and increasing the ability to initially inhibit a previously relevant strategy and to maintain a new, relevant strategy once selected.

2. The method according to claim 1 , wherein the compound is administered in a dosage unit as a solid formulation; in a dosage unit as a tablet or capsule formulation.

3. The method according to claim 1 , wherein the compound is administered orally or by injection.

4. The method according to claim 1 , wherein the subject is evaluated before, during and/or after administration of the compound to determine efficacy of the treatment.

5. The method according to claim 1 , including obtaining systemic measurements of the levels of the compound at various time points after administration of the compound.

Assignments (3)
CONFIRMATORY LICENSE Recorded Mar 5, 2014
From: UNIVERSITY OF TOLEDO
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 032387/0697 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 18, 2013
From: MESSER, WILLAM S., JR
To: THE UNIVERSITY OF TOLEDO
Reel/Frame 031433/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 18, 2013
From: RAGOZZINO, MICHAEL E.
To: THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS
Reel/Frame 031433/0004 →
Continuity (3)
Division 12992709
Provisional Application 61053415 · May 15, 2008
Related Publication 20140045863A1 · Feb 13, 2014