FORMULATIONS OF BENDAMUSTINE
Methods of treatment using bendamustine formulations designed for small volume intravenous administration are disclosed. The methods conveniently allow shorter administration time without the active ingredient coming out of solution as compared to presently available formulations.
1 . A method of treating chronic lymphocytic leukemia in a subject comprising parenterally administering to the subject, over a period of less than or equal to about 20 minutes, a volume of about 325 mL or less of a liquid composition comprising:
from about 0.05 to about 6 mg/ml of bendamustine or a pharmaceutically acceptable salt thereof; and
a parenterally acceptable diluent comprising Water for Injection, 0.9% saline, 0.45% saline, or 2.5% dextrose/0.45% saline.
2 . The method of claim 1 , wherein the liquid composition comprises from about 0.05 to about 3.2 mg/ml of bendamustine.
3 . The method of claim 1 , wherein the subject is administered a bendamustine dosage amount ranging from about 25 mg/m 2 to about 100 mg/m 2 .
4 . The method of claim 1 , wherein the subject is administered a bendamustine dosage amount of about 100 mg/m 2 .
5 . The method of claim 1 , wherein the volume administered is 325 ml+/−10%.
6 . The method of claim 1 , wherein the volume administered is 250 ml+/−10%.
7 . The method of claim 1 , wherein the volume administered is 100 ml+/−10%.
8 . The method of claim 1 , wherein the volume administered is 50 ml+/−10%.
9 . The method of claim 1 , wherein the liquid composition is administered over a period of about 15 minutes.
10 . The method of claim 1 , wherein the liquid composition is administered over a period of about 10 minutes.
11 . The method of claim 1 , wherein the liquid composition is administered intravenously in a volume of about 50 mL in about 10 minutes or less on days 1 and 2 of a 28 day cycle.
12 . The method of claim 11 , wherein the method is repeated for up to 6 cycles.
13 . A method of treating indolent B cell non-Hodgkin's lymphoma in a subject comprising parenterally administering to the subject, over a period of less than or equal to about 20 minutes, a volume of about 325 mL or less of a liquid composition comprising:
from about 0.05 to about 6 mg/ml of bendamustine or a pharmaceutically acceptable salt thereof; and
a parenterally acceptable diluent comprising Water for Injection, 0.9% saline, 0.45% saline, or 2.5% dextrose/0.45% saline.
14 . The method of claim 13 , wherein the liquid composition comprises from about 0.05 to about 3.2 mg/ml of bendamustine.
15 . The method of claim 13 , wherein the subject is administered a bendamustine dosage amount ranging from about 60 mg/m 2 to about 120 mg/m 2 .
16 . The method of claim 13 , wherein the subject is administered a bendamustine dosage amount of about 120 mg/m 2 .
17 . The method of claim 13 , wherein the subject is administered a bendamustine dosage amount of about 100 mg/m 2 .
18 . The method of claim 13 , wherein the volume administered is 325 ml+/−10%.
19 . The method of claim 13 , wherein the volume administered is 250 ml+/−10%.
20 . The method of claim 13 , wherein the volume administered is 100 ml+/−10%.
21 . The method of claim 13 , wherein the volume administered is 50 ml+/−10%.
22 . The method of claim 13 , wherein the liquid composition is administered over a period of about 15 minutes.
23 . The method of claim 13 , wherein the liquid composition is administered over a period of about 10 minutes.
24 . The method of claim 13 , wherein the liquid composition is administered intravenously in a volume of about 50 mL in about 10 minutes or less on days 1 and 2 of a 21 day cycle.
25 . The method of claim 24 , wherein the method is repeated for up to 8 cycles.