Formulations of a PI3K/mTOR-inhibitor for intravenous administration
The present invention relates to a pharmaceutical aqueous formulation comprising 1-(4-{[4-(dimethylamino)piperidin-1-yl]carbonyl}phenyl)-3-[4-(4,6-dimorpholin-4-yl-1,3,5-triazin-2-yl)phenyl]urea, or a pharmaceutically acceptable salt thereof, that is a clear solution. Such a formulation is particularly suitable for intravenous or parenteral administration to a patient.
1. A method of treating cancer in a mammal, comprising administering to said mammal an effective amount of a second pharmaceutical aqueous solution formulation obtained as a clear solution by reconstitution or constitution a lyophilized formulation, said lyophilized formulation obtained by freeze drying a first pharmaceutical aqueous solution formulation comprising:
1-(4-{[4-(dimethylamino)piperidin-1-yl]carbonyl}phenyl)-3-[4-(4,6-dimorpholin-4-yl-1,3,5-triazin-2-yl)phenyl]urea, or a lactate salt thereof, lactic acid and water, wherein said 1-(4-{[4-(dimethylamino)piperidin-1-yl]carbonyl}phenyl)-3-[4-(4,6-dimorpholin-4-yl-1,3,5-triazin-2-yl)phenyl]urea is present at a solution concentration of less than 6 mg/ml and sufficient lactic acid is present to provide a clear solution.
2. The method of claim 1 , wherein said 1-(4-{[4-(dimethylamino)piperidin-1-yl]carbonyl}phenyl)-3-[4-(4,6-dimorpholin-4-yl-1,3,5-triazin-2-yl)phenyl]urea is present in the first pharmaceutical aqueous solution formulation at a solution concentration of from 5.0 to 5.5 mg/ml and at least 2.5 mole equivalents of lactic acid are present.
3. The method of claim 1 , wherein said 1-(4-{[4-(dimethylamino)piperidin-1-yl]carbonyl}phenyl)-3-[4-(4,6-dimorpholin-4-yl-1,3,5-triazin-2-yl)phenyl]urea is present in the first pharmaceutical aqueous solution formulation at a solution concentration of about 5 mg/ml and at least 2.5 mole equivalents of lactic acid are present.
4. The method of claim 1 , wherein said 1-(4-{[4-(dimethylamino)piperidin-1-yl]carbonyl}phenyl)-3-[4-(4,6-dimorpholin-4-yl-1,3,5-triazin-2-yl)phenyl]urea is present in said first pharmaceutical aqueous solution formulation at a solution concentration of about 5 mg/ml, and at least 1.5 mole equivalents of lactic acid are present and in an amount sufficient to ensure a clear solution is formed.
5. The method of claim 1 , wherein 1-(4-{[4-(dimethylamino)piperidin-1-yl]carbonyl}phenyl)-3-[4-(4,6-dimorpholin-4-yl-1,3,5-triazin-2-yl)phenyl]urea is present in said first pharmaceutical aqueous solution formulation at a solution concentration of about 5 mg/ml, and about 4.1 mole equivalents of lactic acid are present and in an amount sufficient to ensure a clear solution is formed with a pH of no greater than 3.7.
6. The method of claim 1 , wherein said 1-(4-{[4-(dimethylamino)piperidin-1-yl]carbonyl}phenyl)-3-[4-(4,6-dimorpholin-4-yl-1,3,5-triazin-2-yl)phenyl]urea is present in said first pharmaceutical aqueous solution formulation at a solution concentration of from 2.5 to 5.5 mg/ml, and from above 2.5 to 8.0 mole equivalents of lactic acid are present and in an amount sufficient to ensure a clear solution is formed.
7. The method of any of claims 1 and 2 - 6 wherein DL-lactic acid, L-lactic acid or D-lactic acid is used in the first pharmaceutical aqueous solution formulation.
8. The method of any of claims 1 and 2 - 6 , wherein the cancer is selected from leukemia, skin cancer, bladder cancer, breast cancer, uterus cancer, ovary cancer, prostate cancer, lung cancer, colon cancer, pancreas cancer, renal cancer, gastric cancer and brain cancer.
9. The method of claim 8 wherein the cancer is breast cancer.
10. The method of claim 8 wherein the cancer is prostate cancer.