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)phenyljurea
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 alkanesulphonate 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 the mammal in need thereof an effective amount of a clear 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 an alkanesulphonate salt thereof.
2 . The method of claim 1 , wherein the solution formulation comprises 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 methanesulphonate salt thereof, methanesulphonic acid and water, 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 at a solution concentration of from 6 to 30 mg/ml.
3 . The method of claim 1 , wherein the solution formulation comprises 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 an ethanesulphonate salt thereof, ethanesulphonic acid and water, 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 at a solution concentration of from 6 to 30 mg/ml.
4 . The method of claim 1 , wherein the solution formulation further comprises one or more cyclodextrins selected from the group consisting of beta-cyclodextrins, gamma-cyclodextrins, or a mixture thereof.
5 . The method of claim 4 , wherein the one or more cyclodextrins comprise hydroxypropyl-beta-cyclodextrin.
6 . The method of claim 4 , wherein the one or more cyclodextrins comprise sulphobutylether-beta-cyclodextrin.
7 . The method of claim 4 , wherein the one or more cyclodextrins comprise gamma-cyclodextrin.
8 . The method of claim 1 , wherein the pH of the solution formulation is from 3 to 8.
9 . The method of claim 1 , wherein the solution formulation is administered at a weekly dose in a range from 100 to 400 mg per week.
10 . A method of claim 1 , wherein the cancer is selected from the group consisting of 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.