Liquid formulations of bendamustine
Stable liquid formulations of bendamustine, and pharmaceutically acceptable salts thereof, and polar aprotic solvents, are described.
1. A stable, non-aqueous liquid, pharmaceutical formulation comprising from about 5 mg/ml to about 120 mg/mL of bendamustine, or a pharmaceutically acceptable salt thereof, solubilized in about 66% (v/v) of dimethylacetamide and about 34% (v/v) of propylene glycol, wherein said formulation, following dilution with a pharmaceutically acceptable diluent, is suitable for injection into a patient without lyophilization.
2. The formulation of claim 1 , comprising about 100 mg/mL of bendamustine, or a pharmaceutically acceptable salt thereof.
3. The formulation of claim 1 , wherein the bendamustine is bendamustine hydrochloride.
4. The formulation of claim 1 , further comprising at least one pharmaceutically acceptable excipient or diluent.
5. The formulation of claim 1 , further comprising an antioxidant, a surfactant, a lipid, a filler, an organic acid, a hydrophilic polymer, a complexing agent, a preservative, or a combination thereof.
6. A method of treating chronic lymphocytic leukemia or non-Hodgkin's lymphoma comprising
providing a liquid, pharmaceutical formulation of claim 1 ;
diluting the liquid pharmaceutical formulation with a pharmaceutically acceptable injectable diluent to form an injectable pharmaceutical preparation;
administering the injectable pharmaceutical preparation to a patient in need of treatment thereof.
7. The method of claim 6 , wherein the liquid pharmaceutical formulation comprises about 100 mg/mL of bendamustine, or a pharmaceutically acceptable salt thereof.
8. The method of claim 6 , wherein the pharmaceutically acceptable injectable diluent is 0.9% sodium chloride.
9. The formulation of claim 2 , comprising 90 mg/mL of bendamustine hydrochloride.
10. The method of claim 7 , comprising 90 mg/mL of bendamustine hydrochloride.