IP Library Granted Patent US 11,865,160
Granted Patent B2
US 11,865,160 · App. 17/317,631 · Granted Jan 9, 2024

Modified therapeutic agents, stapled peptide lipid conjugates, and compositions thereof

Inventors: Weijun Shen (San Diego, CA); Pengyu Yang (San Diego, CA); Huafei Zou (San Diego, CA); Peter G. Schultz (La Jolla, CA)
Assignee: THE SCRIPPS RESEARCH INSTITUTE
A61K38/22A61K9/0019A61K9/0021A61K38/2278A61K38/26A61K45/06A61K47/54A61K47/542A61K47/543A61K47/554A61K47/60A61K9/703
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Quick Facts
Patent No.
US 11,865,160
App. No.
17/317,631
Granted
Jan 9, 2024
Kind
B2
Abstract

Methods and compositions are provided for extending the half-life of a therapeutic agent. A modified therapeutic agent (mTA) comprises a therapeutic agent, a staple, and a half-life extending molecule. The mTAs disclosed herein may be used to treat a disease or a condition in a subject in need thereof.

Claims (11)

1. A composition comprising a peptide, a staple, and a half-life extending molecule comprising i) a lipid, ii) a polyglycol unit, or iii) a lipid and a polyglycol unit; wherein the peptide comprises a glucagon-like protein-1 receptor (GLP1R) agonist, a glucagon receptor (GCGR) agonist, a glucagon-like protein-2 receptor (GLP2) agonist, a glucose-dependent insulinotropic peptide receptor (GIPR) agonist, a GLP1R and GIPR dual agonist, a GLP1R and GCGR dual agonist, or a GLP1R, GCGR and GIPR tri-agonist; wherein a first amino acid and a second amino acid of the GLP1R agonist, the GCGR agonist, the GLP2 agonist, the GIPR agonist, the GLP1R and GIPR dual agonist, the GLP1R and GCGR dual agonist, or the GLPR1R, GCGR and GIPR tri-agonist, are connected via covalent attachment to the staple; and wherein the half-life extending molecule is covalently attached to the staple.

2. The composition of claim 1 , wherein the first amino acid and the second amino acid are each cysteine amino acids.

3. The composition of claim 1 , wherein the first amino acid is at position i in the GLP1R agonist, the GCGR agonist, the GLP2 agonist, the GIPR agonist, the GLP1R and GIPR dual agonist, the GLP1R and GCGR dual agonist, or the GLPR1R, GCGR and GIPR tri-agonist, and the second amino acid is at position i+7 in the GLP1R agonist, the GCGR agonist, the GLP2 agonist, the GIPR agonist, the GLP1R and GIPR dual agonist, the GLP1R and GCGR dual agonist, or the GLPR1R, GCGR and GIPR tri-agonist.

4. The composition of claim 1 , wherein the half-life extending molecule comprises the lipid or the lipid and the polyglycol unit, and the lipid comprises a sterol, a sterol derivative, a bile acid, a vitamin E derivative, a fatty di-acid, a fatty acid, a fatty amide, or a fatty alcohol, or a combination of two or more thereof.

5. The composition of claim 1 , comprising the lipid or the lipid and the polyglycol unit, wherein the lipid comprises a fatty acid having 5 to 30 carbons, or a fatty di-acid having 5 to 30 carbons.

6. The composition of claim 1 , wherein the half-life extending molecule comprises the polyglycol unit or the lipid and the polyglycol unit, wherein the polyglycol unit comprises i) a polyethylene glycol unit, ii) a polypropylene glycol unit or iii) a polybutylene glycol.

7. The composition of claim 1 , wherein the half-life extending molecule comprises the polyglycol unit or the lipid and polyglycol unit, wherein the polyglycol unit comprises

wherein m is 1 to 20.

8. The composition of claim 7 , wherein m is 2.

9. The composition of claim 7 , wherein m is 3.

10. The composition of claim 1 , wherein the half-life of the composition is longer than the half-life of the peptide alone.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 4, 2021
From: SHEN, WEIJUN; YANG, PENGYU; ZOU, HUAFEI; SCHULTZ, PETER G.
To: THE SCRIPPS RESEARCH INSTITUTE
Reel/Frame 057072/0797 →
Continuity (4)
Continuation 16000829 · Jun 5, 2018
Continuation 15104807
Provisional Application 61917816 · Dec 18, 2013
Related Publication 20220000981A1 · Jan 6, 2022
Cited By (3)
US 12,329,823 US 12,337,028 US 12,583,900