Long-acting co-agonists of the glucagon and GLP-1 receptors

Patent metadata

Field	Value
Publication number	US-10793615-B2
Application number	US-201615759911-A
Country	US
Kind code	B2
Filing date	Oct 21, 2016
Priority date	Oct 27, 2015
Publication date	Oct 6, 2020
Grant date	Oct 6, 2020

Abstract

Long-acting co-agonists of the glucagon and GLP-1 receptors are described.

First claim

What is claimed:

1. A peptide comprising the formula

(SEQ ID NO: 50)

HX 2 QGTFTSX 9 X 10 SX 12 YX 14 DX 16 RAAX 20 X 21 X 22 VX 24 WLX 27 X 28 TX 30 -NH 2

wherein
X 2 is aminoisobutyric acid (aib), D-Ser or alpha-Methyl-L-Serine (alpha-MS);
X 9 is Asp or alpha-Methyl-L-Aspartic acid (alpha-MD);
X 10 is Lys conjugated to a fatty diacid, p-aminomethyl-L-phenylalanine (pAF) conjugated to a fatty diacid or Tyr-;
X 12 is Lys conjugated to a fatty diacid, pAF conjugated to a fatty diacid, Lys, or (1S,2S)-Fmoc-2-aminocyclopentane carboxylic acid (βc);
X 14 is Leu or alpha-L-Leucine (alpha-ML);
X 16 is aib, Ala, or Glu;
X 20 is Lys is conjugated to a fatty diacid, pAF conjugated to a fatty diacid or Gln;
X 21 is Lys conjugated to a fatty diacid, pAF conjugated to a fatty diacid, Asp, or alpha-MD;
X 22 is Phe or alpha-Methyl-L-phenylalanine (alpha-MF);
X 24 is Gln (1S,2S)-Fmoc-2-aminocyclopentane carboxylic acid (βc), Lys conjugated to a fatty diacid or pAF conjugated to a fatty diacid;
X 27 is L-Met sulphone or Leucine;
X 28 is Asp, alpha-MD, alpha-Methyl-L-Tryptophan (alpha-MW), Lys, Ala, Lys conjugated to a fatty diacid, or pAF conjugated to a fatty diacid; and
X 30 is Lys linked at the C-terminus to gamma-Glu when X 27 is Leu and X 28 is Ala, or absent;
with the proviso that for each peptide, only one of X 10 , x 12 , x 20 , X 21 , X 24 , or X 28 is conjugated to a fatty diacid.

2. The peptide of claim 1 , wherein the fatty diacid comprises a C14, C15, C16, C17, C18, C19, or C20 fatty diacid.

3. The peptide of claim 1 , wherein the peptide comprises the fatty diacid conjugated to the Lys or pAF via a gamma-Glu, gamma-Glu linker.

4. The peptide of claim 1 , wherein the peptide comprises the fatty diacid conjugated to Lys or pAF via a PEG 2 PEG 2 -gamma-Glu linker wherein PEG 2 is 8-amino-3,6-dioxaoctanoic acid.

5. The peptide of claim 1 , wherein the peptide comprises at X 10 the pAF conjugated to a fatty diacid or a Lys conjugated to a fatty diacid.

6. The peptide of claim 1 , wherein the peptide comprises at x 12 the pAF conjugated to a fatty diacid or a Lys conjugated to a fatty diacid.

7. The peptide of claim 1 , wherein the peptide comprises at x 20 the pAF conjugated to a fatty diacid or a Lys conjugated to a fatty diacid.

8. The peptide of claim 1 , wherein the peptide comprises at x 21 the pAF conjugated to a fatty diacid or a Lys conjugated to a fatty diacid.

9. The peptide of claim 1 , wherein the peptide comprises at x 24 the pAF conjugated to a fatty diacid or a Lys conjugated to a fatty diacid.

10. A composition comprising one or more peptides of claim 1 , or pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.

11. A composition comprising one or more peptides of claim 1 , or pharmaceutically acceptable salt thereof, an insulin or insulin analog, and a pharmaceutically acceptable carrier.

12. The composition of claim 11 , wherein the insulin analog comprises insulin detemir, insulin glargine, insulin glulisine, insulin degludec, or insulin lispro.

13. A method for treating a patient for a metabolic disease or disorder comprising administering to a patient in need thereof an effective amount of one or more of the peptides of claim 1 to treat the metabolic disease or disorder in the patient wherein, the metabolic disease or disorder comprises diabetes, nonalcoholic fatty liver disease (NAFLD), non-alcoholic steatohepatitis (NASH), or obesity.

14. The method of claim 13 , wherein the diabetes comprises Type I diabetes, Type II diabetes, or gestational diabetes.

15. A method for treating a metabolic disease or disorder in a patient comprising administering to the patient in need thereof an effective amount of one or more of the peptides of claim 1 and administering to the patient in need thereof an effective amount of a composition comprising an insulin or insulin analog to treat the metabolic disease or disorder in the patient, wherein the metabolic disease or disorder comprises diabetes, nonalcoholic fatty liver disease (NAFLD), non-alcoholic steatohepatitis (NASH), or obesity.

16. The method of claim 15 , wherein the insulin analog comprises insulin detemir, insulin glargine, insulin levemir, insulin glulisine, insulin degludec, or insulin lispro.

17. The method of claim 15 , wherein the diabetes comprises Type I diabetes, Type II diabetes, or gestational diabetes.

Assignees

• Merck Sharp & Dohme
• Palani Anandan
• Nargund Ravi
• Carrington Paul E
• Sawyer Tomi
• Deng Qiaolin
• Pessi Antonello
• Bianchi Elisabetta
• Orvieto Federica

Inventors

• Palani Anandan
• Nargund Ravi
• Carrington Paul E
• Sawyer Tomi
• Deng Qiaolin
• Pessi Antonello
• Bianchi Elisabetta
• Orvieto Federica

Classifications

• A61P3/04

  Anorexiants; Antiobesity agents · CPC title

• A61K38/00

  Medicinal preparations containing peptides (peptides containing beta-lactam rings A61K31/00; cyclic dipeptides not having in their molecule any other peptide link than those which form their ring, e.g. piperazine-2,5-diones, A61K31/00; ergot alkaloids of the cyclic peptide type A61K31/48; containing macromolecular compounds having statistically distributed amino acid units A61K31/74; medicinal preparations containing antigens or antibodies A61K39/00; medicinal preparations characterised by the non-active ingredients, e.g. peptides as drug carriers, A61K47/00) · CPC title

• A61P7/12

  Antidiuretics, e.g. drugs for diabetes insipidus (ADH A61P5/10) · CPC title

• A61K38/28 Primary

  Insulins · CPC title

• C07K14/605 Primary

  Glucagons · CPC title