PHARMACEUTICAL COMPOSITIONS FOR MODULATING A KINASE CASCADE AND METHODS OF USE THEREOF
The invention relates to a pharmaceutical composition comprising 2-(5-(4-(2-morpholinoethoxy)phenyl)pyridin-2-yl)-N-benzylacetamide or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier.
1 . A pharmaceutical composition for oral, intravenous, intramuscular, or subcutaneous administration comprising an amount of compound (I):
or a pharmaceutically acceptable salt thereof, ranging from 2 mg to 400 mg per dose administered two or three times daily and a pharmaceutically acceptable carrier.
2 . The pharmaceutical composition according to claim 1 , wherein the amount is from 10 mg to 300 mg, from 20 mg to 250 mg, from 40 mg to 200 mg, or from 60 mg to 160 mg.
3 .- 5 . (canceled)
6 . A pharmaceutical composition for oral, intravenous, intramuscular, or subcutaneous administration comprising an amount of compound (I):
or a pharmaceutically acceptable salt thereof ranging from 4 mg to 800 mg per dose administered once daily and a pharmaceutically acceptable carrier.
7 . The pharmaceutical composition according to claim 6 , wherein the amount is from 20 mg to 600 mg, from 40 mg to 500 mg, from 80 mg to 400 mg, from 120 mg to 320 mg.
8 .- 10 . (canceled)
11 . The pharmaceutical composition according to claim 1 , wherein the composition comprises the mesylate salt of compound (I).
12 .- 15 . (canceled)
16 . The pharmaceutical composition according to claim 1 , wherein the dose is administered two times daily.
17 . The pharmaceutical composition according to claim 1 , wherein the dose is administered three times daily.
18 . The pharmaceutical composition according to claim 1 , wherein the composition is administered in combination with one or more anti-cancer treatments or anti-cancer agents.
19 . The pharmaceutical composition according to claim 18 , wherein the composition is administered in combination with the anti-cancer agent gemcitabine.
20 . The pharmaceutical composition according to claim 18 , wherein the composition is administered in combination with the anti-cancer agent oxaliplatin.
21 . A method of treating or preventing a condition or disorder selected from cancer, cell proliferative disorder, microbial infection, hyperproliferative disorder, macular edema, osteoporosis, cardiovascular disorder, eye disease, immune system disfunction, type II diabetes, obesity, transplant rejection, hearing loss, stroke, athrosclerosis, chronic neuropathic pain, hepatitis B, and autoimmune disease comprising administering the pharmaceutical composition according to claim 1 .
22 . The method according to claim 21 , wherein the condition or disorder is cancer.
23 . The method according to claim 22 , wherein the cancer is selected from renal, prostate, liver, lung, pancreatic, brain, breast, colon, leukemia, ovarian, epithelial, and esophageal.
24 . The method according to claim 22 , wherein the cancer is selected from an advanced malignancy, a solid tumor, and lymphoma.
25 . The method according to claim 21 , wherein the condition or disorder is a cell proliferative disorder.
26 . The method according to claim 25 , wherein the cell proliferative disorder is selected from psoriasis, diabetic retinopathy, and macular degeneration.
27 . The method according to claim 21 , wherein the condition or disorder is a microbial infection.
28 . The method according to claim 27 , wherein the microbial infection is selected from bacterial, fungal, parasitic, and viral.
29 . The method according to claim 21 , wherein the disorder or condition is selected from hyperproliferative disorder, macular edema, osteoporosis, cardiovascular disorder, eye disease, immune system disfunction, type II diabetes, obesity, transplant rejection, hearing loss, stroke, athrosclerosis, chronic neuropathic pain, hepatitis B, and autoimmune disease.
30 . A method of regulating immune system activity comprising administering the pharmaceutical composition according to claim 1 .