IP Library Granted Patent US 10,596,230
Granted Patent B2
US 10,596,230 · App. 16/000,300 · Granted Mar 24, 2020

Methods of increasing nutrient absorption in the intestine using therapeutic agents comprising GLP-2 and elastin-like peptides

Inventor: Ashutosh Chilkoti (Durham, NC)
Assignee: DUKE UNIVERSITY
A61K38/28A61K38/16A61K38/2278A61K38/26A61K38/4846A61K45/06A61K47/6435A61K47/65C07K14/575C07K14/605C07K14/78C07K19/00C07K2319/31
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Quick Facts
Patent No.
US 10,596,230
App. No.
16/000,300
Granted
Mar 24, 2020
Kind
B2
Abstract

The present invention provides therapeutic agents and compositions comprising elastin-like peptides (ELPs) and therapeutic proteins. In some embodiments, the therapeutic protein is a GLP-1 receptor agonist, insulin, or Factor VII/VIIa, including functional analogs. The present invention further provides encoding polynucleotides, as well as methods of making and using the therapeutic agents. The therapeutic agents have improvements in relation to their use as therapeutics, including, inter alia, one or more of half-life, clearance and/or persistence in the body, solubility, and bioavailability.

Claims (10)

1. A method of increasing nutrient absorption in the intestine in a patient in need thereof comprising administering to the subject a therapeutic composition comprising a GLP-2 peptide in a fusion with an elastin-like peptide (ELP) comprising at least 90 repeating units of VPGXG (SEQ ID NO: 3) and a pharmaceutically acceptable carrier or excipient, and wherein the fusion protein exhibits an increased half-life in serum compared to an unfused GLP-2 peptide.

2. The method of claim 1 , wherein each X is independently selected from alanine, glycine, and valine residues.

3. The method of claim 1 , wherein the elastin-like peptide comprises at least 120 repeating units of VPGXG (SEQ ID NO: 3), wherein X is Val, Ala, or Gly at a ratio of 5:2:3.

4. The method of claim 1 , wherein the elastin-like peptide comprises at least 144 repeating units of VPGXG (SEQ ID NO: 3).

5. The method of claim 1 , wherein the GLP-2 peptide is positioned at the N-terminal end of the ELP component.

6. The method of claim 1 , wherein the composition is formulated for parenteral administration.

7. The method of claim 1 , wherein the composition is formulated for subcutaneous administration.

8. The method of claim 1 wherein the composition is formulated for systemic delivery.

9. A method of stimulating epithelial cell proliferation in the intestine in a patient in need thereof comprising administering to the subject a therapeutic composition comprising a GLP-2 peptide in a fusion with an elastin-like peptide (ELP) comprising 120 repeating units of VPGXG (SEQ ID NO: 3) wherein X is Val, Ala, or Gly at a ratio of 5:2:3 and a pharmaceutically acceptable carrier or excipient, and wherein the fusion protein exhibits an increased half-life in serum compared to an unfused GLP-2 peptide.

10. A method of stimulating epithelial cell proliferation in the intestine in a patient in need thereof comprising administering to the subject a therapeutic composition comprising a GLP-2 peptide in a fusion with an elastin-like peptide (ELP) comprising 144 repeating units of VPGXG (SEQ ID NO: 3) and a pharmaceutically acceptable carrier or excipient, and wherein the fusion protein exhibits an increased half-life in serum compared to an unfused GLP-2 peptide.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 15, 2018
From: CHILKOTI, ASHUTOSH
To: DUKE UNIVERSITY
Reel/Frame 046097/0328 →
Continuity (7)
Continuation 15816018 · Nov 17, 2017
Continuation 14822512 · Aug 10, 2015
Continuation 13524812 · Jun 15, 2012
Continuation 13445979 · Apr 13, 2012
Continuation 12493912 · Jun 29, 2009
Provisional Application 61076221 · Jun 27, 2008
Related Publication 20190091297A1 · Mar 28, 2019