IP Library Granted Patent US 8,003,684
Granted Patent B2
US 8,003,684 · App. 11/709,299 · Granted Aug 23, 2011

Crystal form and pharmaceutical compositions of (+)-R-zileuton

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Quick Facts
Patent No.
US 8,003,684
App. No.
11/709,299
Granted
Aug 23, 2011
Kind
B2
Abstract

Crystalline forms of (+)-R-zileuton, which may be used in pharmaceutical applications, are disclosed. Particular single crystalline forms of (+)-R-zileuton are characterized by a variety of properties and physical measurements. As well, methods of producing crystalline (+)-R-zileuton, and using it to inhibit 5-lipoxygenase activity in subjects to treat a number of diseases, are also discussed.

Claims (18)

1. A composition comprising (+)-R-zileuton represented by the following structural formula:

wherein at least 70% by weight of the composition is the single crystalline form Form I of (+)-R-zileuton, characterized by major x-ray powder diffraction peaks at 2θ angles of 4.5°, 9.1°, 16.3°, 17.3°, 17.9°, 20.3°, 22.2° and 24.0°.

2. The composition of claim 1 , wherein the single crystalline form is characterized by x-ray powder diffraction peaks at 2θ angles of 4.5°, 9.1°, 16.3°, 17.3°, 17.9°, 20.3°, 22.2°, 22.7° and 24.0°.

3. The composition of claim 1 , wherein the single crystalline form is characterized by x-ray powder diffraction pattern of FIG. 1 .

4. The composition of claim 1 , wherein the single crystalline form is characterized by a single endothermic transition at 151° C. in the differential scanning calorimetry profile with a scanning rate of 10° C./minute or the single crystalline form is anhydrous.

5. A pharmaceutical composition comprising a pharmaceutically acceptable carrier or diluent and the composition of claim 1 .

6. The pharmaceutical composition of claim 1 , wherein the single crystalline form is characterized by x-ray powder diffraction peaks at 2θ angles of 4.5°, 9.1°, 16.3°, 17.3°, 17.9°, 20.3°, 22.2°, 22.7° and 24.0°.

7. The pharmaceutical composition of claim 1 , wherein the single crystalline form is characterized by x-ray powder diffraction pattern of FIG. 1 .

8. The pharmaceutical composition of claim 1 , wherein the single crystalline form is characterized by a single endothermic transition at 151° C. in the differential scanning calorimetry profile with a scanning rate of 10° C./minute or the single crystalline form is anhydrous.

9. The pharmaceutical composition of claim 5 wherein at least 99% by weight of the (+)-R-zileuton is the single crystalline form.

10. The pharmaceutical composition of claim 5 wherein at least 99.9% by weight of the (+)-R-zileuton is the single crystalline form.

11. A composition comprising (+)-R-zileuton represented by the following structural formula:

wherein at least 70% by weight of (+)-R-zileuton is a single crystalline form Form II of (+)-R-zileuton characterized by major x-ray powder diffraction peaks at 2θ angles of 4.6°, 9.2°, 16.1°, 16.3°, 17.6°, 18.6°, 19.9°, 21.3°, 23.4° and 23.7°.

12. The composition of claim 11 , wherein the single crystalline form is characterized by x-ray powder diffraction pattern of FIG. 4 .

13. A pharmaceutical composition comprising a pharmaceutically acceptable carrier or diluent and the composition of claim 11 .

14. The pharmaceutical composition of claim 13 , wherein the single crystalline form is characterized by x-ray powder diffraction pattern of FIG. 4 .

15. A method of treating asthma or nasal polyposis in a subject in need thereof comprising administering to the subject an effective amount of a pharmaceutical composition comprising a pharmaceutically acceptable carrier or diluent and (+)R-zileuton represented by the following structural formula:

wherein at least 70% by weight of the (+)-R-zileuton is crystalline Form I of (+)-R-zileuton characterized by major x-ray powder diffraction peaks at 2θ angles of 4.5°, 9.1°, 16.3°, 17.3°, 17.9°, 20.3°, 22.2° and 24.0°, or crystalline Form II of (+)-R-zileuton characterized by major x-ray powder diffraction peaks at 2θ angles of 4.6°, 9.2°, 16.1°, 16.3°, 17.6°, 18.6°, 19.9°, 21.3°, and 23.4°.

Assignments (2)
CHANGE OF NAME Recorded Jan 5, 2009
From: CRITICAL THERAPEUTICS, INC.
To: CORNERSTONE THERAPEUTICS, INC.
Reel/Frame 022052/0747 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 30, 2007
From: HANKO, JASON A.
To: CRITICAL THERAPEUTICS, INC,
Reel/Frame 020184/0595 →