IP Library Granted Patent US 9,937,140
Granted Patent B2
US 9,937,140 · App. 14/212,939 · Granted Apr 10, 2018

Branched chain amino acids: formulations and methods of treatment

Inventors: Evan Dale Abel (Coralville, IA); Christian Michael Riehle (Offenburg, DE)
Assignee: University of Utah Research Foundation
A61K31/198A61K9/0019A61K9/19
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Quick Facts
Patent No.
US 9,937,140
App. No.
14/212,939
Granted
Apr 10, 2018
Kind
B2
Abstract

The present disclosure includes a formulation of branched chain amino acids and arginine for treatment of diseases for which the pathological mechanism includes autophagy. The formulation includes defined ratios of the branched chain amino acids Isoleucine, Leucine, and Valine along with Arginine. These disease indications include congestive heart failure, myocardial infarction, and ischemia reperfusion injury. Diseases of other organs that involve autophagy are also disclosed. Additionally, methods of using the disclosed formulation to treat these disease indications are provided. The disclosure also describes a kit that includes a lyophilized form of the formulation, a solvent for reconstitution, and instructions directing reconstitution.

Claims (16)

1. A formulation comprising:

a medically useful amount of L-isoleucine, L-leucine, L-valine, and L-arginine wherein the relative ratio of L-isoleucine:L-leucine:L-valine, by mass, is 1:2(±0.2):1.2(±0.2),

wherein the medically useful amount of L-isoleucine, L-leucine, L-valine, and L-arginine is dissolved in an aqueous solvent to form a solution; and

wherein the osmolarity of the solution is below 325 mosm.

2. The formulation of claim 1 , wherein the relative ratio, by mass, of L-isoleucine:L-leucine:L-valine:L-arginine is about 1:2(±0.2):1.2(±0.2):1(±0.2).

3. The formulation of claim 1 , wherein L-isoleucine is present in a concentration of 6 g/L (±0.3 g/L), L-leucine is present in a concentration of 12 g/L (±0.3 g/L), L-valine is present in a concentration of 7.2 g/L (±0.3 g/L), and L-arginine is present in a concentration of 6.04 g/L (±0.3 g/L).

4. The formulation of claim 1 , wherein the pH of the formulation is buffered to a physiologically tolerable pH.

5. The formulation of claim 4 , wherein the pH of the formulation is about 7.4.

6. The formulation of claim 4 , wherein the formulation is buffered with a phosphate buffer.

7. The formulation of claim 1 , wherein the formulation is sterile and pyrogen-free.

8. A kit comprising:

(a) a lyophilized formulation comprising a medically useful amount of L-isoleucine, L-leucine, L-valine, and L-arginine, wherein the relative ratio of L-isoleucine:L-leucine:L-valine, by mass, is 1:2(±0.2):1.2(±0.2);

(b) a vial or ampoule of a sterile aqueous solution; and

(c) instructions for combining the lyophilized formulation with the sterile aqueous solution to form a solution having an osmolarity below 325 mosm.

9. The kit of claim 8 , further comprising an injection device for administration.

10. The formulation of claim 1 , wherein L-isoleucine, L-leucine, L-valine, and L-arginine are the only amino acids in the solution.

Assignments (3)
CONFIRMATORY LICENSE Recorded Mar 17, 2015
From: UNIVERSITY OF UTAH
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 035209/0018 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 15, 2014
From: ABEL, EVAN DALE; RIEHLE, CHRISTIAN MICHAEL
To: THE UNIVERSITY OF UTAH
Reel/Frame 032680/0014 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 15, 2014
From: THE UNIVERSITY OF UTAH
To: THE UNIVERSITY OF UTAH RESEARCH FOUNDATION
Reel/Frame 032680/0127 →
Continuity (2)
Provisional Application 61784939 · Mar 14, 2013
Related Publication 20150126604A1 · May 7, 2015