Claims for Patent: 11,666,590

Summary for Patent: 11,666,590

Title:	Pharmaceutical composition, methods for treating and uses thereof
Abstract:	The present invention relates to certain SGLT-2 inhibitors for treating, preventing, protecting against and/or delaying the progression of chronic kidney disease in patients, for example patients with prediabetes, type 1 or type 2 diabetes mellitus.
Inventor(s):	Uli Christian BROEDL, Odd-Erik JOHANSEN, Eric Williams Mayoux, Nima Soleymanlou, Maximilian von EYNATTEN, Hans-Juergen Woerle, David Z.I. CHERNEY, Bruce A. PERKINS
Assignee:	Boehringer Ingelheim International GmbH
Application Number:	US17/094,037
Patent Claims:	1. A method of treating, reducing the risk of, delaying the occurrence of and/or delaying the progression of chronic kidney disease in a patient, said method comprising administering to the patient a pharmaceutially effective amount of empagliflozin, optionally in combination with one or more other therapeutic substances. 2. The method according to claim 1, wherein the progression of said chronic kidney disease is the progression to end stage renal disease/kidney failure, or renal death in the patient. 3. The method according to claim 1, wherein said patient is at risk for renal disease. 4. The method according to claim 1, wherein the patient is a patient with prediabetes, type 1 or type 2 diabetes mellitus. 5. The method according to claim 4, wherein the patient is a patient with type 2 diabetes mellitus. 6. The method according to claim 1, wherein the patient has or is at risk of a cardiovascular disease. 7. The method according to claim 1, wherein the patient is a patient with prediabetes, type 1 or type 2 diabetes mellitus and with or at risk of a cardiovascular disease. 8. The method according to claim 1, wherein the patient has a loss of eGFR of less than 50%. 9. The method according to claim 1, wherein the patient is a patient with one or more cardiovascular risk factors selected from the group consiting of A), B), C) and D): A) previous or existing vascular disease selected from the group consisting of myocardial infarction, coronary artery disease, percutaneous coronary intervention, coronary artery by-pass grafting, ischemic or hemorrhagic stroke, congestive heart failure, and peripheral occlusive arterial disease, B) advanced age>/=60-70 years, C) one or more cardiovascular risk factors selected from the group consisting of advanced type 1 or type 2 diabetes mellitus>10 years duration, hypertension, current daily cigarette smoking, dyslipidemia, obesity, age>/=40, metabolic syndrome, hyperinsulinemia or insulin resistance, and hyperuricemia, erectile dysfunction, polycystic ovary syndrome, sleep apnea, or family history of vascular disease or cardiomyopathy in first-degree relative, D) one or more of the following: confirmed history of myocardial infarction, unstable angina with documented multivessel coronary disease or positive stress test, multivessel Percutaneous Coronary Intervention, multivessel Coronary Artery By-pass Grafting (CABG), history of ischemic or hemorrhagic stroke, or peripheral occlusive arterial disease. 10. The method according to claim 1, wherein the one or more other therapeutic substances are selected from other antidiabetic substances. 11. The method according to claim 1, comprising administering empagliflozin in combination with metformin, with linagliptin or with metformin and linagliptin. 12. The method according to claim 1, wherein the one or more other therapeutic substances is a renin angiotensin aldosterone system (RAAS) inhibitor. 13. The method according to claim 1, wherein the one or more other therapeutic substances is a direct renin inhibitor, an Angiotensin-Converting Enzyme (ACE) inhibitor and/or an angiotensin II receptor blocker (ARB). 14. The method according to claim 1, comprising administering empagliflozin in combination with a renin angiotensin aldosterone system (RAAS) inhibitor. 15. The method according to claim 1, comprising administering empagliflozin in combination with a direct renin inhibitor, an Angiotensin-Converting Enzyme (ACE) inhibitor and/or an angiotensin II receptor blocker (ARB). 16. The method according to claim 1, wherein empagliflozin is administered orally in a total daily amount of 10 mg or 25 mg. 17. The method according to claim 1, wherein empagliflozin is administered as a pharmaceutical composition comprising 10 mg or 25 mg of empagliflozin. 18. The method according to claim 1, wherein the method protects against or delays the loss of estimated glomerular filtration rate (eGFR) in the patient. 19. The method according to claim 1, wherein the method reduces the progression to end stage renal disease/kidney failure in the patient. 20. The method according to claim 1, wherein the method reduces the risk of progression to renal death in the patient. 21. The method according to claim 1, wherein the patient is a patient with chronic kidney disease. 22. The method according to claim 21, wherein the patient is a patient with stage 3 chronic kidney disease. 23. The method according to claim 21, wherein the patient is a patient with stage 3B chronic kidney disease. 24. The method according to claim 21, wherein the patient is a patient with stage 4 chronic kidney disease. 25. The method according to claim 1, wherein the method protects against or delays the loss of estimated glomerular filtration rate (eGFR) in the patient, and wherein the patient has chronic kidney disease. 26. The method according to claim 1, wherein the method reduces the progression to end stage renal disease/kidney failure in the patient, and wherein the patient has chronic kidney disease. 27. The method according to claim 1, wherein the method reduces the risk of progression to renal death in the patient, and wherein the patient has chronic kidney disease. 28. A method for treating a patient having chronic kidney disease, the method comprising administering to the patient a pharmaceutically effective amount of empagliflozin, optionally in combination with one or more other therapeutic substances, wherein: the method protects against or delays the loss of estimated glomerular filtration rate (eGFR) in the patient, the method reduces the progression to end stage renal disease/kidney failure in the patient, and/or the method reduces the risk of progression to renal death in the patient. 29. A method for treating a patient having chronic kidney disease, the method comprising administering to the patient a pharmaceutically effective amount of empagliflozin, optionally in combination with one or more other therapeutic substances, wherein the method protects against or delays the loss of estimated glomerular filtration rate (eGFR) in the patient. 30. A method for treating a patient having chronic kidney disease, the method comprising administering to the patient a pharmaceutically effective amount of empagliflozin, optionally in combination with one or more other therapeutic substances, wherein the method reduces the progression to end stage renal disease/kidney failure in the patient. 31. A method for treating a patient having chronic kidney disease, the method comprising administering to the patient a pharmaceutically effective amount of empagliflozin, optionally in combination with one or more other therapeutic substances, wherein the method reduces the risk of progression to renal death in the patient. 32. A method for treating, reducing the risk of and/or delaying the progression of chronic kidney disease in a patient with chronic kidney disease, said method comprising administering to the patient a pharmaceutically effective amount of empagliflozin, optionally in combination with one or more other therapeutic substances.