IP Library › Granted Patent US 9,034,890
Granted Patent B2
US 9,034,890 · App. 13/778,556 · Granted May 19, 2015

Combined acetylcholinesterase inhibitor and quaternary ammonium antimuscarinic therapy to alter progression of cognitive diseases

Inventor: Steven A. Rich (Canandaigua, NY)
A61K31/40A61K31/27A61K31/14A61K31/438A61K45/06A61K31/137A61K31/216
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Quick Facts
Patent No.
US 9,034,890
App. No.
13/778,556
Granted
May 19, 2015
Kind
B2
Abstract

A method administers quaternary ammonium anti-cholinergic muscarinic receptor antagonists in combination with acetyl-cholinesterase inhibitors to treat either cognitive impairment or acute delirium. This therapy results in a modification of a cognitive disorder or disease, namely a slow down in the disease progression. In one preferred embodiment, the disease is dementia with Lewy Bodies. New formulations for quaternary ammonium anti-cholinergic muscarinic receptor antagonists are also disclosed.

Claims (10)

1. A method for treating a cognitive disorder selected from the group consisting of Alzheimer's Disease, Dementia with Lewy Bodies, Parkinson's Disease, Fronto-temporal dementia, and Progressive Supranuclear Palsy comprising administering to a patient a therapeutic amount of glycopyrrolate and a therapeutic amount of rivastigmine.

2. The method of claim 1 , comprising administering a minimum of about 12 to 48 mg/day orally, or about 19 to 54 mg/day transdermally of rivastigmine to the patient.

3. The method of claim 1 , comprising administering from about 0.1 to about 0.8 mg/day parenterally, or about 3.0 to about 8.0 mg/day orally of glycopyrrolate to the patient.

4. The method of claim 1 , comprising administering a minimum of about 2-4 mg/day of glycopyrrolate and a minimum of about 12-24 mg/day of rivastigmine to the patient.

5. The method of claim 1 , comprising administering a minimum of about 12 mg/day orally or a minimum of about 9.5 mg/day transdermally of rivastigmine to the patient.

6. The method of claim 1 , comprising administering between about 24 and about 48 mg/day orally or administering between about 19 mg and 54 mg transdermally of rivastigmine to the patient.

7. The method of claim 1 , wherein an efficacious therapeutic amount of glycopyrrolate is administered to the patient either orally, intravenously or parenterally.

8. The method of claim 1 , wherein the therapeutic amount of rivastigmine is administered to the patient either orally or transdermally.

9. A method for treating Dementia with Lewy Bodies comprising administering to a patient a therapeutic amount of glycopyrrolate and a therapeutic amount of rivastigmine.

10. The method of claim 9 , comprising administering a minimum of about 2-4 mg/day of glycopyrrolate and a minimum of about 12-24 mg/day of rivastigmine to the patient.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 2, 2016
From: RICH, STEVEN A.
To: QAAM PHARMACEUTICALS, LLC
Reel/Frame 038787/0413 →
Continuity (4)
Continuation In Part 13325371 · Dec 14, 2011
Division 11935483 · Nov 6, 2007
Provisional Application 60865893 · Nov 15, 2006
Related Publication 20130172398A1 · Jul 4, 2013