Therapeutic agents and uses thereof

Patent metadata

Field	Value
Publication number	US-2023348586-A1
Application number	US-202118026696-A
Country	US
Kind code	A1
Filing date	Sep 21, 2021
Priority date	Sep 21, 2020
Publication date	Nov 2, 2023
Grant date	—

Abstract

The present disclosure relates generally to therapeutic agents and related uses thereof, including, agents for reducing leptin in a patient or subject and methods of treatment thereof. The therapeutic agents can comprise (without limitation), an antibody or specific binding fragment thereof, a leptin antagonist, a leptin targeting antisense oligonucleotide, a leptin targeting small interfering RNA (siRNA), a leptin targeting short hairpin RNA (shRNA), and/or a gene editing composition directed to at least one target sequence of a leptin polynucleotide. The therapeutic agents can be used in various methods of treatment, including (without limitation), treating liver fibrosis, cancer, inducing or maintaining weight loss, reducing or preventing weight gain, and increasing insulin sensitivity, among others.

First claim

1 . A method of treating liver disease, liver fibrosis, liver cirrhosis, maintaining weight loss, treating cancer, treating colorectal cancer, treating acute lymphoblastic leukemia, treating cardiovascular disease or one or more symptoms of cardiovascular disease, reducing fasting glycemia, improving glucose tolerance, reducing an amount of GLP-1 agonist delivered to a subject, increasing insulin sensitivity within 24 or fewer hours, reducing inflammation and fibrosis in COVID-19 infections, inducing breast cancer regression, enhancing effectiveness of PD-1 checkpoint inhibitors, providing metabolic improvements for ciliopathy or Bardet-Biedel Syndrome, providing metabolic improvements for polycystic ovary syndrome (PCOS), and combinations thereof, comprising administering a therapeutic agent for lowering circulating leptin to a subject in need thereof,
wherein the therapeutic agent is an antibody or specific binding fragment thereof, a leptin antagonist, a leptin targeting antisense oligonucleotide, a leptin targeting small interfering RNA (siRNA), a leptin targeting short hairpin RNA (shRNA), or a gene editing composition directed to at least one target sequence of a leptin polynucleotide.

2 . The method of claim 1 , wherein the antibody is hLept-1, hLept-2, hLept-3, hLept-4, hLept-5, or hLept-6, and wherein the specific binding fragment is obtained from hLept-1, hLept-2, hLept-3, hLept-4, hLept-5, or hLept-6.

3 . The method of claim 1 , wherein the antibody or specific binding fragment has a variable heavy chain (V H ) CDR1 sequence as set forth in SEQ ID NOs: 1, 2, 3, 4 or 5; a V H CDR2 sequence as set forth in SEQ ID NOs: 6, 7, 8, 9 or 10; a V H CDR3 sequence as set forth in SEQ ID NOs: 11, 12, 13, 14 or 15; a variable light chain (V L ) CDR1 sequence as set forth in SEQ ID NOs: 16, 17, 18, 19 or 20; a V L CDR2 sequence as set forth in SEQ ID NOs: 21, 22, 23, 24 or 25; and a V L CDR3 sequence as set forth in SEQ ID NOs: 26, 27, 28, 29 or 30.

4 . The method of claim 1 , wherein the gene editing composition comprises at least one polynucleotide encoding an RNA-guided DNA endonuclease protein or an RNA-guided DNA endonuclease protein, and at least one guide RNA (gRNA) having a spacer sequence complementary to a leptin polynucleotide sequence.

5 . The method of claim 1 , wherein the leptin antagonist is a leptin mutein.

6 . The method of claim 5 , wherein the leptin mutein is LanI (L39A/D40A/F41A mutant), Lan2 (L39A/D40A/F41A/I42A mutant), or SHLA (D23L/L39 A/D40A/F41A mutant.

7 . The method of claim 1 , wherein an amount of circulating leptin is lowered by 30 to 90% in the subject.

8 . A method of inducing weight loss in a patient in need thereof comprising administering a treatment regimen comprising a therapeutic agent for lowering circulating leptin and a GLP-1 agonist to a subject in need thereof, wherein the GLP-1 agonist is liraglutide, exenatide, albiglutide, dulaglutide, lixisenatide, or semaglutide, and
wherein the therapeutic agent is an antibody or specific binding fragment thereof, a leptin antagonist, a leptin targeting antisense oligonucleotide, a leptin targeting small interfering RNA (siRNA), a leptin targeting short hairpin RNA (shRNA), or a gene editing composition directed to at least one target sequence of a leptin polynucleotide.

9 . The method of claim 8 , further comprising removing the GLP-1 agonist from the treatment regimen after a desired weight level is achieved.

10 . The method of claim 8 , wherein the antibody is hLept-1, hLept-2, hLept-3, hLept-4, hLept-5, or hLept-6, and wherein the specific binding fragment is obtained from hLept-1, hLept-2, hLept-3, hLept-4, hLept-5, or hLept-6.

11 . The method of claim 8 , wherein the antibody or specific binding fragment has a variable heavy chain (V H ) CDR1 sequence as set forth in SEQ ID NOs: 1, 2, 3, 4 or 5; a V H CDR2 sequence as set forth in SEQ ID NOs: 6, 7, 8, 9 or 10; a V H CDR3 sequence as set forth in SEQ ID NOs: 11, 12, 13, 14 or 15; a variable light chain (V L ) CDR1 sequence as set forth in SEQ ID NOs: 16, 17, 18, 19 or 20; a V L CDR2 sequence as set forth in SEQ ID NOs: 21, 22, 23, 24 or 25; and a V L CDR3 sequence as set forth in SEQ ID NOs: 26, 27, 28, 29 or 30.

12 . The method of claim 8 , wherein the gene editing composition comprises at least one polynucleotide encoding an RNA-guided DNA endonuclease protein or an RNA-guided DNA endonuclease protein, and at least one guide RNA (gRNA) having a spacer sequence complementary to a leptin polynucleotide sequence.

13 . The method of claim 8 , wherein the leptin antagonist is a leptin mutein.

14 . The method of claim 13 , wherein the leptin mutein is LanI (L39A/D40A/F41A mutant), Lan2 (L39A/D40A/F41A/I42A mutant), or SHLA (D23L/L39 A/D40A/F41A mutant.

15 . A method of reducing weight gain resulting from administration of an anti-psychotic medication comprising administering an anti-psychotic medication and a therapeutic agent for lowering circulating leptin to a subject in need thereof,
wherein the therapeutic agent is an antibody or specific binding fragment thereof, a leptin antagonist, a leptin targeting antisense oligonucleotide, a leptin targeting small interfering RNA (siRNA), a leptin targeting short hairpin RNA (shRNA), or a gene editing composition directed to at least one target sequence of a leptin polynucleotide.

16 . The method of claim 15 , wherein the antibody is hLept-1, hLept-2, hLept-3, hLept-4, hLept-5, or hLept-6, and wherein the specific binding fragment is obtained from hLept-1, hLept-2, hLept-3, hLept-4, hLept-5, or hLept-6.

17 . The method of claim 15 , wherein the antibody or specific binding fragment has a variable heavy chain (V H ) CDR1 sequence as set forth in SEQ ID NOs: 1, 2, 3, 4 or 5; a V H CDR2 sequence as set forth in SEQ ID NOs: 6, 7, 8, 9 or 10; a V H CDR3 sequence as set forth in SEQ ID NOs: 11, 12, 13, 14 or 15; a variable light chain (V L ) CDR1 sequence as set forth in SEQ ID NOs: 16, 17, 18, 19 or 20; a V L CDR2 sequence as set forth in SEQ ID NOs: 21, 22, 23, 24 or 25; and a V L CDR3 sequence as set forth in SEQ ID NOs: 26, 27, 28, 29 or 30.

18 . The method of claim 15 , wherein the gene editing composition comprises at least one polynucleotide encoding an RNA-guided DNA endonuclease protein or an RNA-guided DNA endonuclease protein, and at least one guide RNA (gRNA) having a spacer sequence complementary to a leptin polynucleotide sequence.

19 . The method of claim 15 , wherein the leptin antagonist is a leptin mutein.

20 . The method of claim 19 , wherein the leptin mutein is LanI (L39A/D40A/F41A mutant), Lan2 (L39A/D40A/F41A/I42A mutant), or SHLA (D23L/L39 A/D40A/F41A mutant.

Assignees

• Univ Texas

Inventors

• Scherer Phillipp E
• Zhao Shangang
• An Zhiqiang
• Zhang Ningyan

Classifications

• A61K38/26

  Glucagons · CPC title

• C07K14/605

  Glucagons · CPC title

• A61P9/00

  Drugs for disorders of the cardiovascular system · CPC title

• A61P3/04

  Anorexiants; Antiobesity agents · CPC title

• A61K38/2264

  Obesity-gene products, e.g. leptin · CPC title