IP Library Granted Patent US 9,896,495
Granted Patent B2
US 9,896,495 · App. 14/517,497 · Granted Feb 20, 2018

Acylated glucagon analogues

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Quick Facts
Patent No.
US 9,896,495
App. No.
14/517,497
Granted
Feb 20, 2018
Kind
B2
Abstract

The invention provides materials and methods for the treatment of obesity and excess weight, diabetes, and other associated metabolic disorders. In particular, the invention provides novel acylated glucagon analog peptides effective in such methods. The peptides may mediate their effect by having increased selectivity for the GLP-1 receptor as compared to human glucagon.

Claims (62)

1. A compound having the formula:

R 1 —P 1 —P 2 —R 2

wherein

R 1 is H, C 1-4 alkyl, acetyl, formyl, benzoyl or trifluoroacetyl;

R 2 is OH or NH 2 ;

P 1 is a peptide having the sequence:

H-Aib-QGTFTSDYSKYLDE-K([17-carboxy-heptadecanoyl]-isoGlu)-AAKDFIEWLESA (SEQ ID NO: 45);

H-Ac4c-QGTFTSDYSKYLDE-K([17-carboxy-heptadecanoyl]-isoGlu-Peg3-Peg3)-RAKDFIEWLESA (SEQ ID NO: 46);

H-Ac4c-HGTFTSDYSKYLDE-K([17-carboxy-heptadecanoyl]-isoGlu-Peg3-Peg3)-RAKDFIEWLESA (SEQ ID NO: 47);

H-Ac4c-QGTFTSDYSKYLDE-K([17-carboxy-heptadecanoyl]-isoGlu)-AAKDFIEWLESA (SEQ ID NO: 48);

H-Ac4c-QGTFTSDYSKYLDE-K([17-carboxy-heptadecanoyl]-isoGlu)-RAKDFIEWLESA (SEQ ID NO: 49);

H-Aib-QGTFTSDYSKYLDERAAKDFI-K([17-carboxy-heptadecanoyl]-isoGlu-GSGSGG)-WLESA (SEQ ID NO: 50);

H-Ac4c-QGTFTSDYSKYLDERAAKDFI-K([17-carboxy-heptadecanoyl]-isoGlu-GSGSGG)-WLESA (SEQ ID NO: 51);

H-Ac4c-QGTFTSDYSKYLDERRAKDFI-K([17-carboxy-heptadecanoyl]-isoGlu-GSGSGG)-WLESA (SEQ ID NO: 52);

H-Ac4c-QGTFTSDYSKYLDERAAKDFIEWLE-K([17-carboxy-heptadecanoyl]-isoGlu-GSGSGG)-A (SEQ ID NO: 53); or

H-Ac4c-QGTFTSDYSKYLDERRAKDFIEWLE-K([17-carboxy-heptadecanoyl]-isoGlu-GSGSGG)-A (SEQ ID NO: 54);

and P 2 is absent;

or a pharmaceutically acceptable salt thereof.

2. A compound according to claim 1 which is selected from:

H—H-Aib-QGTFTSDYSKYLDE-K([17-carboxy-heptadecanoyl]-isoGlu)-AAKDFIEWLESA-NH 2 (SEQ ID NO: 55);

H—H-Ac4c-QGTFTSDYSKYLDE-K([17-carboxy-heptadecanoyl]-isoGlu-Peg3-Peg3)-RAKDFIEWLESA-NH 2 (SEQ ID NO: 56);

H—H-Ac4c-HGTFTSDYSKYLDE-K([17-carboxy-heptadecanoyl]-isoGlu-Peg3-Peg3)-RAKDFIEWLESA-NH 2 (SEQ ID NO: 57);

H—H-Ac4c-QGTFTSDYSKYLDE-K([17-carboxy-heptadecanoyl]-isoGlu)-AAKDFIEWLESA-NH 2 (SEQ ID NO: 58);

H—H-Ac4c-QGTFTSDYSKYLDE-K([17-carboxy-heptadecanoyl]-isoGlu)-RAKDFIEWLESA-NH 2 (SEQ ID NO: 59);

H—H-Aib-QGTFTSDYSKYLDERAAKDFI-K([17-carboxy-heptadecanoyl]-isoGlu-GSGSGG)-WLESA-NH 2 (SEQ ID NO: 60);

H—H-Ac4c-QGTFTSDYSKYLDERAAKDFI-K([17-carboxy-heptadecanoyl]-isoGlu-GSGSGG)-WLESA-NH 2 (SEQ ID NO: 61);

H—H-Ac4c-QGTFTSDYSKYLDERRAKDFI-K([17-carboxy-heptadecanoyl]-isoGlu-GSGSGG)-WLESA-NH 2 (SEQ ID NO: 62);

H—H-Ac4c-QGTFTSDYSKYLDERAAKDFIEWLE-K([17-carboxy-heptadecanoyl]-isoGlu-GSGSGG)-A-NH 2 (SEQ ID NO: 63); and

H—H-Ac4c-QGTFTSDYSKYLDERRAKDFIEWLE-K([17-carboxy-heptadecanoyl]-isoGlu-GSGSGG)-A-NH 2 (SEQ ID NO: 64).

3. A composition comprising a compound according to claim 1 in admixture with a carrier.

4. A composition according to claim 3 wherein the composition is a pharmaceutical composition, and the carrier is a pharmaceutically acceptable carrier.

5. A method of preventing weight gain or promoting weight loss in an individual in need thereof, said method comprising administering a compound according to claim 1 .

6. A method of lowering circulating LDL levels, and/or increasing HDL/LDL ratio in an individual in need thereof, said method comprising administering a compound according to claim 1 .

7. A method of treating a condition caused or characterised by excess body weight, said method comprising administering a compound according to claim 1 .

8. A method of preventing or treating obesity, morbid obesity, morbid obesity prior to surgery, obesity linked inflammation, obesity linked gallbladder disease, obesity induced sleep apnea, diabetes, metabolic syndrome, hypertension, atherogenic dyslipidimia, atherosclerois, arteriosclerosis, coronary heart disease, peripheral artery disease, stroke, or microvascular disease, said method comprising administering a compound according to claim 1 .

9. A method of preventing weight gain or promoting weight loss in an individual in need thereof; lowering circulating LDL levels, and/or increasing HDL/LDL ratio in an individual in need thereof; treating a condition caused or characterised by excess body weight; or preventing or treating obesity, morbid obesity, morbid obesity prior to surgery, obesity linked inflammation, obesity linked gallbladder disease, obesity induced sleep apnea, diabetes, metabolic syndrome, hypertension, atherogenic dyslipidimia, atherosclerois, arteriosclerosis, coronary heart disease, peripheral artery disease, stroke, or microvascular disease, said method comprising administering a compound according to claim 1 as part of a combination therapy together with an agent for treatment of diabetes, obesity, dyslipidemia or hypertension.

10. The method of claim 9 , wherein the agent for treatment of diabetes is selected from the group consisting of a biguanide, a sulfonylurea, a meglitinide or glinide, a DPP-IV inhibitor, an SGLT2 inhibitor, a glitazone, a different GLP-1 agonist, an insulin, and an insulin analogue.

11. The method of claim 9 , wherein the agent for treatment of obesity is selected from the group consisting of a glucagon-like peptide receptor 1 agonist, a peptide YY receptor agonist or analogue thereof, a cannabinoid receptor 1 antagonist, a lipase inhibitor, a melanocortin receptor 4 agonist, a melanin concentrating hormone receptor 1 antagonist, phentermine, a combination of norepinephrine/dopamine reuptake inhibitor and opioid receptor antagonist, a combination of bupropion and naltrexone, and a serotonergic agent.

12. The method of claim 9 , wherein the agent for treatment of hypertension is selected from the group consisting of an angiotensin-converting enzyme inhibitor, an angiotensin II receptor blocker, a diuretic, a beta-blocker, and a calcium channel blocker.

13. The method of claim 9 , wherein the agent for treatment of dyslipidaemia is selected from the group consisting of a statin, a fibrate, a niacin, and a cholesterol absorption inhibitor.

14. A therapeutic kit comprising a compound according to claim 1 optionally in admixture with a carrier.

15. A method of producing a compound according to claim 1 , the method comprising expressing a precursor peptide sequence from a nucleic acid construct that encodes the precursor peptide, recovering the expression product, and modifying the precursor peptide to yield a compound according to claim 1 .

16. A compound selected from:

H-H-Ac4c-QGTFTSDYSKYLDE-K([17-carboxy-heptadecanoyl]-isoGlu-Peg3-Peg3)-RAKDFIEWLESA-NH 2 (SEQ ID NO: 56);

H-H-Aib-QGTFTSDYSKYLDERAAKDFI-K([17-carboxy-heptadecanoyl]-isoGlu-GSGSGG)-WLESA-NH 2 (SEQ ID NO: 60);

H-H-Ac4c-QGTFTSDYSKYLDERAAKDFI-K([17-carboxy-heptadecanoyl]-isoGlu-GSGSGG)-WLESA-NH 2 (SEQ ID NO: 61 );

H-H-Ac4c-QGTFTSDYSKYLDERAAKDFIEWLE-K([17-carboxy-heptadecanoyl]-isoGlu-GSGSGG)-A-NH 2 (SEQ ID NO: 63); and

H-H-Ac4c-QGTFTSDYSKYLDERRAKDFIEWLE-K([17-carboxy-heptadecanoyl]-isoGlu-GSGSGG)-A-NH 2 (SEQ ID NO: 64);

or a pharmaceutically acceptable salt thereof.

17. A compound according to claim 16 , wherein the compound is:

H-H-Ac4c-QGTFTSDYSKYLDE-K([17-carboxy-heptadecanoyl]-isoGlu-Peg3-Peg3)-RAKDFIEWLESA-NH 2 (SEQ ID NO: 56)

or a pharmaceutically acceptable salt thereof.

18. A compound according to claim 16 , wherein the compound is:

H-H-Aib-QGTFTSDYSKYLDERAAKDFI-K([17-carboxy-heptadecanoyl]-isoGlu-GSGSGG)-WLESA-NH 2 (SEQ ID NO: 60)

or a pharmaceutically acceptable salt thereof.

19. A compound according to claim 16 , wherein the compound is:

H-H-Ac4c-QGTFTSDYSKYLDERAAKDFI-K([17-carboxy-heptadecanoyl]-isoGlu-GSGSGG)-WLESA-NH 2 (SEQ ID NO: 61)

or a pharmaceutically acceptable salt thereof.

20. A compound according to claim 16 , wherein the compound is: H-H-Ac4c-QGTFTSDYSKYLDERAAKDFIEWLE-K([17-carboxy-heptadecanoyl]-isoGlu-GSGSGG)-A-NH 2 (SEQ ID NO: 63)

or a pharmaceutically acceptable salt thereof.

21. A compound according to claim 16 , wherein the compound is: H-H-Ac4c-QGTFTSDYSKYLDERRAKDFIEWLE-K([17-carboxy-heptadecanoyl]-isoGlu-GSGSGG)-A-NH 2 (SEQ ID NO: 64)

or a pharmaceutically acceptable salt thereof.

Assignments (7)
RELEASE OF SECURITY INTEREST Recorded May 11, 2023
From: ZOOLANDER SA LLC
To: ZEALAND PHARMA A/S
Reel/Frame 063624/0547 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 31, 2015
From: RIST, WOLFGANG
To: BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG.
Reel/Frame 036228/0593 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 31, 2015
From: BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG.
To: BOEHRINGER INGELHEIM INTERNATIONAL GMBH
Reel/Frame 036228/0710 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 31, 2015
From: RIBER, DITTE; TOLBORG, JAKOB LIND
To: ZEALAND PHARMA A/S
Reel/Frame 036228/0320 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 31, 2015
From: BI RESEARCH ITALIA S.A.S. DI BI IT S.R.L
To: BOEHRINGER INGELHEIM INTERNATIONAL GMBH
Reel/Frame 036229/0628 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 31, 2015
From: BOEHRINGER INGELHEIM INTERNATIONAL GMBH
To: ZEALAND PHARMA A/S
Reel/Frame 036229/0821 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 31, 2015
From: HAMPRECHT, DIETER WOLFGANG
To: BI RESEARCH ITALIA S.A.S. DI BI IT S.R.L
Reel/Frame 036228/0901 →