Method and composition for the treatment of diabetes

• US 6,153,632 A
• Filed: 02/24/1997
• Issued: 11/28/2000
• Est. Priority Date: 02/24/1997
• Status: Expired due to Fees

• Current Assignee: Cheryl Anne Rieveley
• Original Assignee: Robert B. Rieveley
• Inventors: Rieveley, Robert B.
• Primary Examiner(s): Weddington, Kevin E.
• Application Number:
  US08/804,903
• Time in Patent Office: 1,373 Days
• Field of Search: 514/3, 514/369, 514/592, 514/866, 514/635
• US Class Current: 514/369
• CPC Class Codes: A61K 2300/00 Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
• CPC Class Codes: A61K 38/28 Insulins
• CPC Class Codes: A61K 45/06 Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca

Abstract

This invention is directed to a novel method and composition for the treatment of diabetes mellitus (Type I, Impaired Glucose Tolerance ["IGT"]and Type II). More specifically, this invention pertains to a novel method of treating diabetes mellitus by incorporating a therapeutic amount of one or more insulin sensitizers along with one or more of an orally ingested insulin, an injected insulin, a sulfonylurea, a biguanide or an alpha-glucosidase inhibitor for the treatment of diabetes mellitus.

Claims

1. A composition for the treatment of diabetes mellitus comprising:

(a) a therapeutic amount of an insulin sensitizer; and

(b) a therapeutic amount of an anti-diabetic agent.

2. A composition as claimed in claim 1, wherein the anti-diabetic agent is selected from the group consisting of:

an orally ingestible insulin;

an injectible insulin;

a sulfonylurea;

a biguanide; and

an alpha-glucosidase inhibitor.

3. A composition as claimed in claim 2, wherein the anti-diabetic agent is insulin.

4. A composition as claimed in claim 3, wherein the insulin is injectible insulin.

15. A composition as claimed in claim 1 wherein the insulin sensitizer is selected from the group consisting of BRL-49653, Pioglitazone HCL, Troglitazone, MC 555, ALRT 268, LGD 1069, Chromic Picolinate, V-411, Vanadyl Sulfate and Chromic Polynicotinate.

5. A composition for the treatment of diabetes mellitus in a mammal comprising:

(a) a therapeutically effective amount of an orally ingestible insulin which is formulated to withstand degradation by passage through the stomach and upper intestine of the mammal so that a therapeutically effective level of insulin reaches the bloodstream of the mammal; and

,

(b) a therapeutically effective amount of one or more of a orally ingestible insulin sensitizer which withstands degradation by the stomach contents and upper intestinal tract of the mammal and reaches the bloodstream of the mammal and thereby sensitizes the cells of the mammal to enhance insulin uptake and/or utilization of glucose by the cells of the mammal thus reducing the orally ingested insulin required for a therapeutic dose.

7. A composition as claimed in claim 5 including a pharmaceutically acceptable carrier.

9. A composition as claimed in claim 5 wherein the insulin is synthetic insulin.

11. A composition as claimed in claim 5 wherein the orally ingestible insulin is present in the composition in the range of about 1 mcg to 100 mg and the insulin sensitizer is present in the composition in the range of about 10 mcg to 10 mg.

13. Any composition as claimed in claim 5 wherein the insulin sensitizer is present in the composition in the range of about 10 mcg to 10 mg.

6. A composition for the treatment of diabetes mellitus comprising:

(a) a therapeutically effective amount of an injected insulin; and

,

(b) a therapeutically effective amount of one or more insulin sensitizers to sensitize the cells of the mammal so as to enhance insulin uptake and/or utilization of glucose by the cells of the mammal thus reducing the therapeutic dose required of injected insulin.

8. A composition as claimed in claim 6 including a pharmaceutically acceptable carrier.

10. A composition as claimed in claim 6 wherein the insulin is synthetic insulin.

12. A composition as claimed in claim 6 wherein the injected insulin is present in the composition in the range of about 1 mcg to 100 mg and the insulin sensitizer is present in the composition in the range of about 10 mcg to 10 mg.

14. A composition as claimed in claim 6 wherein the insulin sensitizer is present in the composition in the range of about 10 mcg to 10 mg.

16. A method for the treatment of diabetes mellitus comprising administering to a person afflicted with diabetes mellitus a therapeutic amount of an insulin sensitizer with a therapeutic amount of an anti-diabetic agent.

17. A method as claimed in claim 16 comprising an insulin sensitizer and an orally ingestible insulin.

18. A method as claimed in claim 16 comprising an insulin sensitizer and an injectible insulin.

19. A method as claimed in claim 16, wherein a pharmaceutical carrier is administered to the person with the therapeutically effective amount of the anti-diabetic agent.

20. A method as claimed in claim 16, wherein the anti-diabetic agent is selected from the group consisting of:

(a) an orally ingestible insulin;

(b) an injectible insulin;

(c) a sulfonylurea;

(d) a biguanide; and

(e) an alpha-glucosidase inhibitor.

21. A method for the treatment of diabetes mellitus comprising administering to a person afflicted with diabetes mellitus a therapeutic amount of an insulin sensitizer with a therapeutic amount of an orally ingestible anti-diabetic agent, wherein

(1) the insulin sensitizer is selected from the group consisting of:

BRL-49653, Pioglitazone HCL, Troglitazone, MC 555, ALRT 268, LGD 1069, Chromic Picolinate and V-411, and wherein

(2) the anti-diabetic agent is selected from the group consisting of;

an orally ingestible insulin;

an injectible insulin;

a sulfonylurea;

a biguanide; and

an alpha-glucosidase inhibitor.

22. The method of claim 21, wherein the insulin sensitizer is V-411.

23. The method of claim 21, wherein the anti-diabetic agent is an orally ingestible anti-diabetic agent.

24. The method of claim 22 wherein the anti-diabetic agent is an orally ingestible insulin.