IP Library Granted Patent US 8,173,596
Granted Patent B2
US 8,173,596 · App. 11/596,493 · Granted May 8, 2012

Prouroguanylin, and synthetic analogs or proteolytic cleavage products derived from it, as therapeutic and diagnostic agents for diseases involving salt and/or fluid homeostasis

Assignee: The University of North Carolina at Chapel Hill
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Quick Facts
Patent No.
US 8,173,596
App. No.
11/596,493
Granted
May 8, 2012
Kind
B2
Abstract

A method for treating a disorder characterized by salt retention, fluid retention, and combinations thereof. A method for determining the presence of or the progression of a disorder characterized by salt retention, fluid retention, salt loss, fluid loss, and combinations thereof. An immunoassay kit for detecting a level of prouroguanylin in a sample.

Claims (8)

1. A method for treating a disorder characterized by salt retention, fluid retention, and combinations thereof, in a patient in need thereof, the method comprising administering an effective amount of preprouroguanylin, prouroguanylin, or analog thereof, to the patient, thereby producing diuresis, natriuresis, or a combination thereof, wherein said analog comprises preprouroguanylin or prouroguanylin modified by the addition of a non-peptide moiety selected from the group consisting of a radiolabelling component, a fluorescent moiety, a fatty acid group, a carbohydrate, and a polymer.

2. The method of claim 1 , wherein the disorder is selected from the group consisting of kidney disease, heart disease, liver disease, hypertension, and combinations thereof.

3. The method of claim 1 , wherein the preprouroguanylin, prouroguanylin, or analog thereof, is administered by infusion.

4. The method of claim 1 , wherein the preprouroguanylin, prouroguanylin, or analog thereof, is selected from the group consisting of a synthetic, natural, and recombinant preprouroguanylin, prouroguanylin, or analog thereof.

5. The method of claim 1 , wherein the effective amount of preprouroguanylin, prouroguanylin, or analog thereof, is administered in combination with at least one other drug that has diuretic properties, natriuretic properties, or both diuretic and natriuretic properties.

6. The method of claim 5 , wherein the other drug is a diuretic.

7. The method of claim 6 , wherein the diuretic is selected from the group consisting of carbonic anhydrase inhibitors, thiazide-like diuretics, loop or high ceiling diuretics, and potassium-sparing diuretics.

8. The method of claim 6 , wherein the diuretic is selected from the group consisting of furosemide, bumetadine, torsemide, hydrochlorothiazide, triamterine, indapamide, ethocrinic acid, spironolactone, and metolazone.

Assignments (3)
CONFIRMATORY LICENSE Recorded Apr 5, 2017
From: THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL
To: NATIONAL INSTITUTES OF HEALTH-DIRECTOR DEITR
Reel/Frame 042166/0393 →
CONFIRMATORY LICENSE Recorded Feb 19, 2009
From: UNIVERSITY OF NORTH CAROLINA CHAPEL HIL
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 022283/0359 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 30, 2006
From: GOY, MICHAEL; MOSS, NICHOLAS G.; QIAN, XUN
To: NORTH CAROLINA AT CHAPEL HILL, THE UNIVERSITY OF
Reel/Frame 018583/0395 →
Continuity (2)
Provisional Application 60571172 · May 14, 2004
Related Publication 20080221022A1 · Sep 11, 2008