IP Library Granted Patent US 10,307,441
Granted Patent B2
US 10,307,441 · App. 14/847,966 · Granted Jun 4, 2019

Pharmaceutical formulations of nitrite and uses thereof

Inventors: Christopher Kevil (Shreveport, LA); Anthony Giordano (Shreveport, LA); Douglas R Flanagan (Iowa City, IA); Panayiotis P Constantinides (Gurnee, IL)
Assignee: Board of Supervisors of Louisiana State University and Agricultural and Mechanical College
A61K33/00A61K9/0053A61K9/2068A61K9/2866A61K9/5042
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Quick Facts
Patent No.
US 10,307,441
App. No.
14/847,966
Granted
Jun 4, 2019
Kind
B2
Abstract

The present invention relates to pharmaceutical compositions of nitrites such as inorganic nitrites, or any pharmaceutically acceptable salts, solvates, or prodrugs thereof, and the medical use of these compositions. The pharmaceutical compositions, which can be formulated for oral administration, can provide immediate release or extended release of the nitrite ion (NO 2 − ). The pharmaceutical compositions of the invention are useful, for example, for the treatment of chronic tissue ischemia.

Claims (7)

1. A method for treating peripheral neuropathy in a human, the method comprising orally administering two times per day for at least three days a solid, sustained release pharmaceutical composition comprising about 40 mg of sodium nitrite, or a pharmaceutically acceptable salt thereof, and a binding agent, wherein the pharmaceutical composition is coated with an enteric coating.

2. The method of claim 1 , wherein the sodium nitrite is not substantially released in the stomach of the human.

3. The method of claim 1 , wherein the sustained release pharmaceutical composition is administered for at least seven days.

4. The method of claim 1 , wherein the sustained release pharmaceutical composition is administered for at least ten days.

5. The method of claim 1 , wherein the binding agent is sucrose, glucose, sorbitol, acacia, alginic acid, sodium alginate, gelatin, starch, pregelatinized starch, microcrystalline cellulose, magnesium aluminum silicate, carboxymethylcellulose sodium, methylcellulose, hydroxypropyl methylcellulose, ethylcellulose, polyvinylpyrrolidone, or polyethlene glycol.

6. The method of claim 5 , wherein the binding agent is hydroxypropyl methylcellulose, microcrystalline cellulose, or polyvinyl pyrrolidone.

7. The method of claim 1 , wherein the enteric coating comprises a polymer selected from cellulose acetate phthalate, hydroxypropylmethylcellulose acetate succinate, methacrylate acid copolymers, cellulose acetate trimellitate, polyvinyl acetate phthalate, hydroxyethylcellulose phthalate, and hydroxypropyl methylcellulose phthalate.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 24, 2018
From: THERAVASC, INC.
To: BOARD OF SUPERVISORS OF LOUISIANA STATE UNIVERSITY AND AGRICULTURAL AND MECHANICAL COLLEGE
Reel/Frame 046950/0959 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 20, 2015
From: KEVIL, CHRISTOPHER; GIORDANO, ANTHONY; FLANAGAN, DOUGLAS R.; CONSTANTINIDES, PANAYIOTIS P.
To: THERAVASC, LLC
Reel/Frame 036834/0057 →
Continuity (3)
Division 12904791 · Oct 14, 2010
Provisional Application 61251483 · Oct 14, 2009
Related Publication 20160067279A1 · Mar 10, 2016