IP Library Granted Patent US 10,548,890
Granted Patent B2
US 10,548,890 · App. 16/014,908 · Granted Feb 4, 2020

Parenteral formulations of lipophilic pharmaceutical agents and methods for preparing and using the same

Inventors: Borje S. Andersson (Houston, TX); Benigno C. Valdez (Missouri City, TX); Jeffrey Tarrand (Houston, TX)
Assignee: Platform Brightworks Two, Ltd.
A61K31/496A61K9/0019A61K9/08A61K9/1075A61K31/255A61K47/02A61K47/10A61K47/26
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Quick Facts
Patent No.
US 10,548,890
App. No.
16/014,908
Granted
Feb 4, 2020
Kind
B2
Abstract

There may be provided compositions of lipophilic pharmaceutical agents with improved solubility and stability. For example, there may be provided a non-aqueous composition that comprises a lipophilic pharmaceutical agent, and an amphiphilic polymeric solvent such as PEG400 but essentially free of organic solvents and non-solubilized particles. The composition may be further diluted with a desired aqueous diluent such as an infusion fluid for parenteral administration to a subject such as a human. The compositions may be useful for the treatment for diseases or conditions that are sensitive to lipophilic agents, such as infectious diseases, malignant or autoimmune diseases.

Claims (13)

1. A non-aqueous, homogeneous solution comprising a solubilized lipophilic pharmaceutical agent and an amphiphilic liquid polymeric solvent, the formulation being substantially free of non-polymeric organic solvents, water and non-solubilized particles, wherein the solubilized lipophilic pharmaceutical agent has a concentration of at least about 0.5 mg/mL, wherein the lipophilic pharmaceutical agent is busulfan and further wherein the solution is pharmaceutically acceptable for administration to a human patient.

2. The non-aqueous, homogeneous solution of claim 1 , wherein the solution remains stable and free of non-solubilized particles for at least 40 days when stored at room temperature.

3. An aqueous, homogeneous, pharmaceutically-acceptable parenteral formulation, prepared by a process comprising obtaining a solution in accordance with claim 1 , and diluting the solution with a desired aqueous diluent.

4. The solution of claim 1 , wherein the solubilized lipophilic pharmaceutical agent has a concentration of about 1 to 10 mg/mL.

5. The solution of claim 4 , wherein the solubilized lipophilic pharmaceutical agent has a concentration of about 3 to 9 mg/mL.

6. The solution of claim 1 , wherein the solution does not comprise a surfactant.

7. The solution of claim 1 , wherein said amphiphilic liquid polymeric solvent is comprised of a single polymer.

8. The solution of claim 1 , wherein said amphiphilic liquid polymeric solvent is polyethylene glycol (PEG).

9. The solution of claim 8 , wherein said PEG is selected from the group consisting of PEG-100, PEG-200, PEG-300, PEG-400, PEG-600 and PEG-800.

10. The solution of claim 1 , wherein the solution further comprises a protonating agent.

11. The solution of claim 10 , wherein the protonating agent is an acid, alcohol or acidified alcohol.

12. The solution of claim 11 , wherein the acid is HCl, citric acid, acetic acid or glutamic acid.

13. The solution of claim 1 , wherein the solution has a pH of from about 1 to about 6.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 1, 2023
From: PLATFORM BRIGHTWORKS TWO, LTD.
To: GREENJAY THERAPEUTICS, INC.
Reel/Frame 063820/0336 →
Continuity (5)
Continuation 15451748 · Mar 7, 2017
Division 15154919 · May 13, 2016
Continuation 13452033 · Apr 20, 2012
Provisional Application 61480259 · Apr 28, 2011
Related Publication 20180296556A1 · Oct 18, 2018
Cited By (2)
US 12,544,336 US 12,661,407