Pharmaceutical composition, methods for treating and uses thereof
The present invention relates to certain SGLT-2 inhibitors for treating and/or preventing metabolic disorders, such as type 1 or type 2 diabetes mellitus or pre-diabetes, in patients with renal impairment or chronic kidney disease (CKD).
1. A method for improving glycemic control in a patient with type 2 diabetes mellitus comprising administering empagliflozin to the patient if the eGFR of the patient is ≥45 ml/min/1.73 m 2 and <60 ml/min/1.73 m 2 , wherein empagliflozin is administered orally once daily as a pharmaceutical composition comprising 10 mg or 25 mg of empagliflozin, wherein the glycemic control in said patient is improved, and discontinuing empagliflozin if the eGFR of the patient falls below 45 ml/min/1.73 m 2 .
2. The method according to claim 1 , wherein said pharmaceutical composition comprises 10 mg of empagliflozin.
3. The method according to claim 1 , wherein said pharmaceutical composition comprises 25 mg of empagliflozin.
4. A method for improving glycemic control in a patient with type 2 diabetes mellitus comprising:
a) assessing the renal function of a patient;
b) administering empagliflozin to the patient if the eGFR of the patient is ≥45 ml/min/1.73 m 2 and <60 ml/min/1.73 m 2 , wherein empagliflozin is administered orally once daily as a pharmaceutical composition comprising 10 mg or 25 mg of empagliflozin,
wherein the glycemic control in said patient is improved;
c) discontinuing empagliflozin if the eGFR of the patient falls below 45 ml/min/1.73 m 2 .
5. The method according to claim 4 , wherein said pharmaceutical composition comprises 10 mg of empagliflozin.
6. The method according to claim 4 , wherein said pharmaceutical composition comprises 25 mg of empagliflozin.
7. A method of treating type 2 diabetes mellitus in a patient comprising administering empagliflozin to the patient if the eGFR of the patient is ≥45 ml/min/1.73 m 2 and <60 ml/min/1.73 m 2 , wherein empagliflozin is administered orally once daily as a pharmaceutical composition comprising 10 mg or 25 mg of empagliflozin, wherein the glycemic control in said patient is improved, and discontinuing empagliflozin if the eGFR of the patient falls below 45 ml/min/1.73 m 2 .
8. The method according to claim 7 , wherein said pharmaceutical composition comprises 10 mg of empagliflozin.
9. The method according to claim 7 , wherein said pharmaceutical composition comprises 25 mg of empagliflozin.
10. A method of treating type 2 diabetes mellitus comprising:
a) assessing the renal function of a patient with type 2 diabetes mellitus;
b) administering empagliflozin to the patient if the eGFR of the patient is ≥45 ml/min/1.73 m 2 and <60 ml/min/1.73 m 2 , wherein empagliflozin is administered orally once daily as a pharmaceutical composition comprising 10 mg or 25 mg of empagliflozin, wherein the glycemic control in said patient is improved;
c) discontinuing empagliflozin if the eGFR of the patient falls below 45 ml/min/1.73 m 2 .
11. The method according to claim 10 , wherein said pharmaceutical composition comprises 10 mg of empagliflozin.
12. The method according to claim 10 , wherein said pharmaceutical composition comprises 25 mg of empagliflozin.