Claims for Patent: 10,688,155

Summary for Patent: 10,688,155

Title:	Combination of dopamine agonists plus first phase insulin secretagogues for the treatment of metabolic disorders
Abstract:	The present invention is directed to a method of treating a metabolic disorder or key elements of a metabolic disorder such method comprising the use of an agent(s) that increases central dopaminergic activity plus a first-phase insulin secretagouge.
Inventor(s):	Cincotta; Anthony H. (Tiverton, RI)
Assignee:	VeroScience LLC (Tiverton, RI)
Application Number:	15/874,430
Patent Claims:	1. A method of treating a metabolic disorder or key elements of a metabolic disorder such method comprising the step of administering to a subject having a metabolic disorder or a patient in need thereof, (a) a dopamine receptor agonist; and (b) a first-phase insulin secretagogue selected from the group consisting of glucagon like peptide-1 (GLP-1) or an analog thereof, a dipeptidyl peptidase inhibitor, gastric inhibitory polypeptide (also known as glucose-dependent insulinotropic peptide), a meglitinide, repaglinide, nateglinide, postprandial insulin, a thiazolidinedione and short acting insulin, wherein the dosage of each of said dopamine receptor agonist and first-phase insulin secretagogue in combination, provides a therapeutic effect greater than the additive effect of administering the same dosage of each of said dopamine receptor agonist and first-phase insulin secretagogue alone, and wherein the dopamine receptor agonist and the first-phase insulin secretagogue are administered at the same time. 2. The method of claim 1, wherein said dopamine receptor agonist and the first-phase insulin secretagogue are administered within 4 hours of waking in the morning. 3. The method of claim 1, wherein said dopamine receptor agonist is a dopamine D2 receptor agonist selected from the group consisting of bromocriptine, lisuride, hydergine, dihydroergotoxine, and other dopamine D2 receptor agonists with low or no serotonin 2B receptor agonist activity. 4. The method of claim 1, wherein the metabolic disorder is selected from the group consisting of pre-diabetes, Impaired Fasting Glucose, Impaired Glucose Tolerance and Type 2 diabetes. 5. The method of claim 1, wherein the metabolic disorder is selected from the group consisting of metabolic syndrome, Type 2 diabetes, obesity, prediabetes, insulin resistance, hyperinsulinemia, cardiovascular disease, elevated plasma norepinephrine, elevated cardiovascular-related inflammatory factors or potentiators of vascular endothelial dysfunction, hyperlipoproteinemia, atherosclerosis, hyperphagia, hyperglycemia, hyperlipidemia, hypertension, and high blood pressure. 6. The method of claim 1, wherein the key elements of metabolic disorders are selected from the group consisting of impaired fasting glucose, impaired glucose tolerance, increased waist circumference, increased visceral fat content, increased fasting plasma glucose, increased fasting plasma triglycerides, increased fasting plasma free fatty acids, decreased fasting plasma high density lipoprotein level, increased systolic or diastolic blood pressure, increased plasma postprandial triglyceride or free fatty acid levels, increased cellular oxidative stress or plasma indicators thereof, increased circulating hypercoagulative state, arteriosclerosis, coronary artery disease, peripheral vascular disease, congestive heart failure, hepatic steatosis, renal disease including renal insufficiency, and cerebrovascular disease. 7. The method of claim 1, wherein the metabolic disorder is selected from the group consisting of glucose intolerance or insulin resistance. 8. The method of claim 1, wherein the metabolic disorder is Type 2 diabetes or pre-diabetes. 9. The method of claim 1, wherein the dosage of the dopamine receptor agonist is insufficient to effectively treat said disorder or key elements of said disorder without co-administration of the first-phase insulin secretagogue. 10. The method of claim 1, wherein the dosage of the first-phase insulin secretagogue is insufficient to effectively treat the disorder or key elements of the disorder without co-administration of the dopamine receptor agonist. 11. The method of claim 1, wherein the dosage of each of the dopamine receptor agonist and the first-phase insulin secretagogue in combination are effective to treat the disorder or key elements of the disorder. 12. The method of claim 1, wherein the dopamine receptor agonist is selected from the group consisting of quinpirole, quinelorane, talipexole, ropinirole, apomorphine, terguride, fenoldopam, dihydroergocryptine and combinations thereof. 13. The method of claim 1, wherein the dosage of said first-phase insulin secretagogue effective to treat said disorder when administered with said dopamine receptor agonist is less than the dosage of said secretagogue effective to treat said disorder when administered without said dopamine receptor agonist. 14. The method of claim 1, wherein the dopamine receptor agonist is a combination of a dopamine D1 receptor agonist and a dopamine D2 receptor agonist. 15. The method of claim 1, wherein the dopamine receptor agonist is bromocriptine or a pharmaceutically acceptable salt thereof. 16. The method of claim 15, wherein the dopamine receptor agonist is bromocriptine mesylate. 17. The method of claim 1, wherein the subject is a mammal. 18. The method of claim 17, wherein the mammal is a human. 19. The method of claim 1, wherein the dopamine receptor agonist and the first phase insulin secretagogue are administered at the same time. 20. The method of claim 1, wherein the dopamine receptor agonist and the first phase insulin secretagogue are administered together in a single dosage form. 21. The method of claim 1, wherein the dopamine receptor agonist and the first phase insulin secretagogue are administered together in a single dosage form. 22. A method of treating glucose intolerance or insulin resistance in a mammal in need of such treatment, such method comprising: administering to a mammal suffering from glucose intolerance or insulin resistance (a) bromocriptine or a pharmaceutically acceptable salt thereof; and (b) a first-phase insulin secretagogue selected from the group consisting of GLP-1 or an analog thereof and insulin, wherein the dosage of each of bromocriptine or a pharmaceutically acceptable salt thereof and first-phase insulin secretagogue in combination, provides a therapeutic effect greater than the additive effect of administering the same dosage of each of said bromocriptine or a pharmaceutically acceptable salt thereof and said first-phase insulin secretagogue alone and wherein the bromocriptine or a pharmaceutically acceptable salt thereof and the first-phase insulin secretagogue are administered at the same time. 23. The method of claim 22, wherein said bromocriptine or a pharmaceutically acceptable salt thereof and the first-phase insulin secretagogue are administered to a human to increase central dopaminergic activity within 4 hours of waking in the morning. 24. The method of claim 22, wherein the salt is mesylate. 25. The method of claim 22, wherein the mammal is suffering from type 2 diabetes. 26. A method of treating a metabolic disorder or key elements of a metabolic disorder such method comprising the step of administering to a patient having a metabolic disorder or a patient in need thereof, (a) a dopamine receptor agonist; and (b) a first-phase insulin secretagogue selected from the group consisting of glucagon like peptide-1 (GLP-1) or an analog thereof, a dipeptidyl peptidase inhibitor, gastric inhibitory polypeptide (also known as glucose-dependent insulinotropic peptide), a meglitinide, repaglinide, nataglinide, postprandial insulin, a thiazolidinedione and short acting insulin, wherein the dosage of each of said dopamine receptor agonist and first-phase insulin secretagogue in combination, provides a therapeutic effect greater than the additive effect of administering the same dosage of each of said dopamine receptor agonist and first-phase insulin secretagogue alone and wherein the dopamine receptor agonist and first phase insulin secretagogue are administered at the same time. 27. The method of claim 26, wherein the dopamine receptor agonist is selected from the group consisting of bromocriptine, lisuride, hydergene, dihydroergotoxine, and other dopamine D2 receptor agonists with low or no serotonin 2B receptor agonist activity. 28. The method of claim 26, wherein metabolic disorder is selected from the group consisting of pre-diabetes, Impaired Fasting Glucose, Impaired Glucose Tolerance and Type 2 diabetes. 29. The method of claim 26, wherein the metabolic disorder is selected from the group consisting of the metabolic syndrome, Type 2 diabetes, obesity, prediabetes, insulin resistance, hyperinsulinemia, cardiovascular disease, elevated plasma norepinephrine, elevated cardiovascular-related inflammatory factors or potentiators of vascular endothelial dysfunction, hyperlipoproteinemia, atherosclerosis, hyperphagia, hyperglycemia, hyperlipidemia, hypertension, and high blood pressure. 30. The method of claim 26, wherein the key elements of metabolic disorders are selected from the group consisting of impaired fasting glucose, impaired glucose tolerance, increased waist circumference, increased visceral fat content, increased fasting plasma glucose, increased fasting plasma triglycerides, increased fasting plasma free fatty acids, decreased fasting plasma high density lipoprotein level, increased systolic or diastolic blood pressure, increased plasma postprandial triglyceride or free fatty acid levels, increased cellular oxidative stress or plasma indicators thereof, increased circulating hypercoagulative state, arteriosclerosis, coronary artery disease, peripheral vascular disease, congestive heart failure, hepatic steatosis, renal disease including renal insufficiency, and cerebrovascular disease. 31. The method of claim 26, wherein said dopamine receptor agonist and first-phase insulin secretagogue are administered to a patient to increase central dopaminergic activity within 4 hours of waking in the morning. 32. The method of claim 26, wherein the dosage of the dopamine receptor agonist is insufficient to effectively treat said disorder or key elements of said disorder without co-administration of the first-phase insulin secretagogue. 33. The method of claim 26, wherein the dosage of the first-phase insulin secretagogue is insufficient to effectively treat said disorder or key elements of said disorder without co-administration of the dopamine receptor agonist. 34. The method of claim 26, wherein the dosage of each of the dopamine receptor agonist and the first-phase insulin secretagogue in combination are effective to treat said disorder or key elements of said disorder. 35. The method of claim 26, wherein the dopamine receptor agonist is selected from the group consisting of quinpirole, quinerolane, talipexole, ropinirole, apomorphine, terguride, fenoldopam, dihydroergocryptine and combinations thereof. 36. The method of claim 26, wherein the dosage of said first-phase insulin secretagogue effective to treat said disorder when administered with said dopamine receptor agonist is less than the dosage of said secretagogue effective to treat said disorder when administered without said dopamine receptor agonist. 37. The method of claim 26, wherein the dopamine receptor agonist is a combination of a dopamine D1 receptor agonist and a dopamine D2 receptor agonist. 38. The method of claim 26, wherein the dopamine receptor agonist is bromocriptine or a pharmaceutically acceptable salt thereof. 39. The method of claim 38, wherein the dopamine receptor agonist is bromocriptine mesylate. 40. The method of claim 26, wherein the dopamine receptor agonist and the first phase insulin secretagogue are administered at the same time. 41. The method of claim 26, wherein the dopamine receptor agonist and the first phase insulin secretagogue are administered together in a single dosage form. 42. A method of treating glucose intolerance or insulin resistance in a mammal in need of such treatment, such method comprising: administering to a mammal suffering from glucose intolerance or insulin resistance (a) a dopamine D2 receptor agonist selected from the group consisting of bromocriptine, lisuride, hydergene, dihydroergotoxine, and other dopamine D2 receptor agonists with low or no serotonin 2B receptor agonist activity; and (b) a first-phase insulin secretagogue selected from the group consisting of glucagon like peptide-1 (GLP-1) or an analog thereof, a dipeptidyl peptidase inhibitor, gastric inhibitory polypeptide (also known as glucose-dependent insulinotropic peptide), a meglitinide, repaglinide, nataglinide, postprandial insulin, a thiazolidinedione and short acting insulin, wherein the dosage of each of said dopamine D2 receptor agonist and first-phase insulin secretagogue in combination provides a therapeutic effect greater than the additive effect of administering the same dosage of each of said dopamine D2 receptor agonist and first-phase insulin secretagogue alone and wherein the dopamine receptor agonist and first phase insulin secretagogue are administered at the same time. 43. The method of claim 42, wherein said dopamine receptor agonist and first phase insulin secretagogue are administered to a human to increase central dopaminergic activity within 4 hours of waking in the morning. 44. A method of treating a metabolic disorder or key elements of a metabolic disorder such method comprising the step of administering to a patient having a metabolic disorder or a patient in need thereof, (a) a dopamine receptor agonist; and (b) a first-phase insulin secretagogue selected from the group consisting of glucagon like peptide-1 (GLP-1) or an analog thereof, a dipeptidyl peptidase inhibitor, gastric inhibitory polypeptide (also known as glucose-dependent insulinotropic peptide), a meglitinide, repaglinide, nataglinide, postprandial insulin, a thiazolidinedione and short acting insulin, wherein the dosage of each of said dopamine receptor agonist and first-phase insulin in combination, provides a therapeutic effect greater than the additive effect of administering the same dosage of each of said dopamine receptor agonist and first-phase insulin secretagogue alone and wherein said dopamine receptor agonist and said first phase insulin secretagogue are administered at the same time. 45. The method of claim 44, wherein the dopamine receptor agonist is selected from the group consisting of bromocriptine, lisuride, hydergene, dihydroergotoxine, and other dopamine D2 receptor agonists with low or no serotonin 2B receptor agonist activity. 46. The method of claim 44, wherein the metabolic disorder is selected from the group consisting of pre-diabetes, Impaired Fasting Glucose, Impaired Glucose Tolerance and Type 2 diabetes. 47. The method of claim 44, wherein the metabolic disorder is selected from the group consisting of the metabolic syndrome, Type 2 diabetes, obesity, prediabetes, insulin resistance, hyperinsulinemia, cardiovascular disease, elevated plasma norepinephrine, elevated cardiovascular-related inflammatory factors or potentiators of vascular endothelial dysfunction, hyperlipoproteinemia, atherosclerosis, hyperphagia, hyperglycemia, hyperlipidemia, hypertension, and high blood pressure. 48. The method of claim 44, wherein the key elements of metabolic disorders are selected from the group consisting of impaired fasting glucose, impaired glucose tolerance, increased waist circumference, increased visceral fat content, increased fasting plasma glucose, increased fasting plasma triglycerides, increased fasting plasma free fatty acids, decreased fasting plasma high density lipoprotein level, increased systolic or diastolic blood pressure, increased plasma postprandial triglyceride or free fatty acid levels, increased cellular oxidative stress or plasma indicators thereof, increased circulating hypercoagulative state, arteriosclerosis, coronary artery disease, peripheral vascular disease, congestive heart failure, hepatic steatosis, renal disease including renal insufficiency, and cerebrovascular disease. 49. The method of claim 44, wherein said dopamine receptor agonist is administered to a patient to increase central dopaminergic activity within 4 hours of waking in the morning. 50. The method of claim 44, wherein the dosage of the dopamine receptor agonist is insufficient to effectively treat said disorder or key elements of said disorder without co-administration of the first-phase insulin secretagogue. 51. The method of claim 44, wherein the dosage of the first-phase insulin secretagogue is insufficient to effectively treat said disorder or key elements of said disorder without co-administration of the dopamine receptor agonist. 52. The method of claim 44, wherein the dosage of each of the dopamine receptor agonist and the first-phase insulin secretagogue in combination are effective to treat said disorder or key elements of said disorder. 53. The method of claim 44, wherein the dopamine receptor agonist is selected from the group consisting of quinpirole, quinerolane, talipexole, ropinirole, apomorphine, terguride, fenoldopam, dihydroergocryptine and combinations thereof. 54. The method of claim 44, wherein the dosage of said first-phase insulin secretagogue effective to treat said disorder when administered with said dopamine receptor agonist is less than the dosage of said secretagogue effective to treat said disorder when administered without said dopamine receptor agonist. 55. The method of claim 44, wherein the dopamine receptor agonist is a combination of a dopamine D1 receptor agonist and a dopamine D2 receptor agonist. 56. The method of claim 44, wherein the dopamine receptor agonist is bromocriptine or a pharmaceutically acceptable salt thereof. 57. The method of claim 44, wherein the dopamine receptor agonist is bromocriptine mesylate.