IP Library Granted Patent US 8,217,001
Granted Patent B2
US 8,217,001 · App. 12/202,197 · Granted Jul 10, 2012

Modification of feeding behavior

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Quick Facts
Patent No.
US 8,217,001
App. No.
12/202,197
Granted
Jul 10, 2012
Kind
B2
Abstract

Methods are disclosed for decreasing calorie intake, food intake, and appetite in a subject. The methods include peripherally administering a therapeutically effective amount of PYY or an agonist thereof to the subject, thereby decreasing the calorie intake of the subject.

Claims (38)

1. A method for decreasing calorie intake, food intake or appetite in a human subject in need thereof, comprising peripherally administering a therapeutically effective amount of PYY or an agonist thereof to the subject, wherein the PYY or agonist thereof is administered at a dose of 1 to 100 nmoles per 70 to 75 kg of body weight of said subject by subcutaneous, intravenous, intramuscular, or intraperitoneal administration.

2. The method of claim 1 , wherein the subject is overweight.

3. The method of claim 1 , wherein the subject is obese.

4. The method of claim 1 , wherein the subject is diabetic.

5. The method of claim 1 , wherein peripherally administering PYY or the agonist thereof comprises administering about 45 to about 135 pmol per kilogram body weight of the subject.

6. The method of claim 1 , wherein peripherally administering the therapeutically effective amount of PYY or the agonist thereof comprises administration of about 45 to about 135 pmol per kilogram of body weight at least 30 minutes prior to a meal.

7. The method of claim 1 , further comprising administering a therapeutically effective amount of amfepramone (diethylpropion), phentermine, mazindol, phenylpropanolamine, fenfluramine, dexfenfluramine, or fluoxetine.

8. The method of claim 1 , wherein the PYY or the agonist thereof is administered in an amount sufficient to decrease calorie intake for a period of at least 2 hours.

9. The method of claim 1 , wherein the PYY or the agonist thereof is PYY 3-36 .

10. The method of claim 9 , wherein the PYY 3-36 is administered by a subcutaneous route.

11. The method of claim 1 , wherein the PYY agonist comprises a molecule that specifically binds the Y2 receptor.

12. The method of claim 1 , wherein the PYY or agonist thereof is administered to the subject at least 30 minutes prior to a meal.

13. The method of claim 1 , wherein the PYY or agonist thereof is administered subcutaneously at a dose of 90 nmoles or less per 70 to 75 kg of body weight of said subject.

14. The method of claim 1 , wherein the PYY or agonist thereof is administered subcutaneously at a dose from 1 to 90 nmoles per 70 to 75 kg of body weight of said subject.

15. The method of claim 1 , wherein the PYY or agonist thereof is administered subcutaneously at a dose from 5 to 80 nmoles per 70 to 75 kg of body weight of said subject.

16. The method of claim 1 , wherein the PYY or agonist thereof comprises the amino acid sequence of SEQ ID NO:334, or a mutant thereof having up to 4 amino acid deletions, insertions or substitutions.

17. The method of claim 16 , wherein the PYY 3-36 is modified by amidation, glycosylation, acylation, sulfation, phosphorylation, cyclisation, lipidisation, pegylation or by fusion to another protein or polypeptide.

18. The method of claim 16 , further comprising administering an additional appetite suppressant to said subject.

19. The method of claim 1 , wherein the peripheral administration comprises administration in a sustained or controlled release preparation or from a pump or implantable drug infusion device.

20. A method for treating obesity in a human subject in need thereof, comprising peripherally administering a therapeutically effective amount of PYY or an agonist thereof to the subject, wherein the PYY or agonist thereof is administered at a dose of 1 to 100 nmoles per 70 to 75 kg of body weight of said subject by subcutaneous, intravenous, intramuscular, or intraperitoneal administration.

21. The method of claim 20 , wherein the subject is diabetic.

22. The method of claim 20 , wherein peripherally administering PYY or the agonist thereof comprises administering about 45 to about 135 pmol per kilogram body weight of the subject.

23. The method of claim 20 , wherein peripherally administering PYY or the agonist thereof comprises administering about 72 pmol per kilogram body weight of the subject.

24. The method of claim 20 , wherein peripherally administering the therapeutically effective amount of PYY or the agonist thereof comprises administering PYY or an agonist thereof to the subject in a multitude of doses, wherein each dose in the multitude of doses comprises administration of about 45 to about 135 pmol per kilogram of body weight at least 30 minutes prior to a meal.

25. The method of claim 20 , further comprising administering a therapeutically effective amount of amfepramone (diethylpropion), phentermine, mazindol, phenylpropanolamine, fenfluramine, dexfenfluramine, or fluoxetine.

26. The method of claim 20 , wherein the PYY or the agonist thereof is administered in an amount sufficient to decrease calorie intake for a period of at least 2 hours.

27. The method of claim 20 , wherein the PYY agonist comprises a molecule that specifically binds the Y2 receptor.

28. The method of claim 20 , wherein the PYY or the agonist thereof is PYY 3-36 .

29. The method of claim 28 wherein the PYY 3-36 is administered by a subcutaneous route.

30. The method of claim 20 , wherein the PYY or agonist thereof is administered to the subject at least 30 minutes prior to a meal.

31. The method of claim 20 , wherein the PYY or agonist thereof is administered subcutaneously at a dose of 90 nmoles or less per 70 to 75 kg of body weight of said subject.

32. The method of claim 20 , wherein the PYY or agonist thereof is administered subcutaneously at a dose from 1 to 90 nmoles per 70 to 75 kg of body weight of said subject.

33. The method of claim 20 , wherein the PYY or agonist thereof is administered subcutaneously at a dose from 5 to 80 nmoles per 70 to 75 kg of body weight of said subject.

34. The method of claim 20 , wherein the PYY or agonist thereof comprises the amino acid sequence of SEQ ID NO:334, or a mutant thereof having up to 4 amino acid deletions, insertions or substitutions.

35. The method of claim 34 , wherein the PYY 3-36 is modified by amidation, glycosylation, acylation, sulfation, phosphorylation, cyclisation, lipidisation, pegylation or by fusion to another protein or polypeptide.

36. The method of claim 34 , further comprising administering an additional appetite suppressant to said subject.

37. The method of claim 20 , wherein the peripheral administration comprises administration in a sustained or controlled release preparation or from a pump or implantable drug infusion device.

38. A method for decreasing calorie intake, food intake or appetite in a subject in need thereof, comprising peripherally administering a PYY or an agonist thereof to the subject at a dose of 1 to 100 nmoles per 70 to 75 kg of body weight of said subject by subcutaneous, intravenous, intramuscular, or intraperitoneal administration.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 24, 2012
From: COWLEY, MICHAEL; LOW, MALCOLM; BUTLER, ANDREW
To: OREGON HEALTH AND SCIENCE UNIVERSITY
Reel/Frame 028266/0337 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 14, 2012
From: CONE, ROGER
To: OREGON HEALTH AND SCIENCE UNIVERSITY
Reel/Frame 028205/0443 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 28, 2011
From: GHATEI, MOHAMMAD ALI; SMALL, CAROLINE JANE; BATTERHAM, RACHEL LOUISE; BLOOM, STEPHEN ROBERT
To: IMPERIAL INNOVATIONS LIMITED
Reel/Frame 026031/0924 →