IP Library Granted Patent US 7,893,101
Granted Patent B2
US 7,893,101 · App. 12/079,615 · Granted Feb 22, 2011

Solid forms comprising (+)-2-[1-(3-ethoxy-4-methoxyphenyl)-2-methylsulfonylethyl]-4-acetylaminoisoindoline-1,3-dione, compositions thereof, and uses thereof

Assignee: Celgene Corporation
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Quick Facts
Patent No.
US 7,893,101
App. No.
12/079,615
Granted
Feb 22, 2011
Kind
B2
Abstract

Solid forms comprising (+)-2-[1-(3-Ethoxy-4-methoxyphenyl)-2-methylsulfonylethyl]-4-acetylaminoisoindoline-1,3-dione, compositions comprising the solid forms, methods of making the solid forms and methods of their use are disclosed. The methods include methods of treating and/or preventing disorders ameliorated by the reduction of levels of TNF-α or the inhibition of PDE4.

Claims (16)

1. A Form B crystal form of the compound of Formula (I):

which is enantiomerically pure, and which has an X-ray powder diffraction pattern comprising peaks at about 10.1, 13.5, 20.7, and 26.9 degrees 2θ.

2. The crystal form of claim 1 , which has an X-ray powder diffraction pattern further comprising peaks at about 12.4, 15.7, 18.1, and 24.7 degrees 2θ.

3. The crystal form of claim 2 , which has an X-ray powder diffraction pattern further comprising peaks at about 16.3, 22.5, 26.2, and 29.1 degrees 2θ.

4. The crystal form of claim 1 , which has an X-ray powder diffraction pattern matching the pattern depicted in FIG. 5 .

5. The crystal form of claim 1 , which has a differential scanning calorimetry plot comprising an endothermic event with an onset temperature of about 154° C.

6. The crystal form of claim 1 , which has a differential scanning calorimetry plot matching the plot depicted in FIG. 6 .

7. The crystal form of claim 1 , which has a thermal gravimetric analysis plot comprising a mass loss of less than about 1% when heated from about 25° C. to about 140° C.

8. The crystal form of claim 7 , wherein the mass loss is about 0.25%.

9. The crystal form of claim 1 , which has a thermal gravimetric analysis plot matching the plot depicted in FIG. 7 .

10. The crystal form of claim 1 , which exhibits a mass increase of less than about 1% when subjected to an increase in relative humidity from about 0% to about 95% relative humidity.

11. The crystal form of claim 10 , wherein the mass increase is about 0.6%.

12. The crystal form of claim 1 , which has a moisture sorption isotherm plot matching the plot depicted in FIG. 8 .

13. The crystal form of claim 1 , which is stable upon exposure to about 40° C. and about 75% relative humidity for about 4 weeks.

14. The crystal form of any one of claims 1 and 2 to 13 , which is substantially pure.

15. A solid pharmaceutical composition comprising the crystal form of any one of claims 1 and 2 to 13 .

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 4, 2019
From: CELGENE CORPORATION
To: AMGEN INC.
Reel/Frame 051181/0038 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 9, 2008
From: MULLER, GEORGE W.; SCHAFER, PETER H.; MAN, HON-WAH; GE, CHUANSHENG; XU, JEAN
To: CELGENE CORPORATION
Reel/Frame 021103/0728 →
Continuity (5)
Continuation In Part 11106142 · Apr 13, 2005
Division 10392195 · Mar 19, 2003
Provisional Application 60366515 · Mar 20, 2002
Provisional Application 60438450 · Jan 7, 2003
Related Publication 20080234359A1 · Sep 25, 2008