IP Library Granted Patent US 10,610,516
Granted Patent B2
US 10,610,516 · App. 16/125,571 · Granted Apr 7, 2020

Methods of using (+)- 2-[1-(3-ethoxy-4-methoxyphenyl)-2-methylsulfonylethyl]-4-acetylaminoisoindoline-1, 3-dione

Inventors: George W. Muller (Rancho Sante Fe, CA); Peter H. Schafer (Belle Mead, NJ); Hon-Wah Man (Princeton, NJ); Chuansheng Ge (Belle Mead, NJ)
Assignee: AMGEN INC.
A61K31/4035A61K45/06C07C317/28C07D209/48C07B2200/07Y02A50/411
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Quick Facts
Patent No.
US 10,610,516
App. No.
16/125,571
Granted
Apr 7, 2020
Kind
B2
Abstract

Stereomerically pure (+)-2-[1-(3-Ethoxy-4-methoxyphenyl)-2-methylsulfonylethyl]-4-acetylaminoisoindoline-1,3-dione, substantially free of its (−) isomer, and prodrugs, metabolites, polymorphs, salts, solvates, hydrates, and clathrates thereof are discussed. Also discussed are methods of using and pharmaceutical compositions comprising the (+) enantiomer of 2-[1-(3-Ethoxy-4-methoxyphenyl)-2-methylsulfonylethyl]-4-acetylaminoisoindoline-1,3-dione 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 method of treating myelodysplastic syndrome, myeloproliferative disease, and complex regional pain syndrome, which comprises administering to a patient a therapeutically effective amount of stereomerically pure (+)-2-[1-(3-ethoxy-4-methoxyphenyl)-2-methanesulfonylethyl]-4-acetylaminoisoindolin-1,3-dione:

or a pharmaceutically acceptable salt thereof.

2. The method of claim 1 , wherein the stereomerically pure (+)-2-[1-(3-ethoxy-4-methoxyphenyl)-2-methylsulfonylethyl]-4-acetylaminoisoindoline-1,3-dione is substantially free of the (−) isomer.

3. The method of claim 1 , wherein the compound is administered orally.

4. The method of claim 3 , wherein the compound is administered in the form of a tablet or capsule.

5. The method of claim 1 , wherein the compound is administered in the amount of from about 1 mg to about 1,000 mg per day.

6. The method of claim 5 , wherein the compound is administered in the amount of from about 5 mg to about 500 mg per day.

7. The method of claim 6 , wherein the compound is administered in the amount of from about 10 mg to about 200 mg per day.

8. The method of claim 5 , wherein the compound is administered in the amount of about 1, 5, 10, 15, 20, 25, 30, 40, 50, 60, 75, or 100 mg per day per day.

9. The method of claim 8 , wherein the compound is administered in the amount of about 1, 5, 10, 15, 20, 25 or 30 mg twice per day.

10. The method of claim 8 , wherein the compound is administered in the amount of about 40 mg once daily.

11. The method of claim 1 , further comprising administering to a patient in need of such treatment a therapeutically effective amount of an antihistamine, anti-inflammatory drug, non-steroid anti-inflammatory drug, or steroid.

12. The method of claim 1 wherein the patient is a mammal.

13. The method of claim 1 , wherein the stereomerically pure compound comprises greater than about 90% by weight of the (+) isomer based on the total weight percent of the compound.

14. The method of claim 1 , wherein the stereomerically pure compound comprises greater than about 95% by weight of the (+) isomer based on the total weight percent of the compound.

15. The method of claim 1 , wherein the stereomerically pure compound comprises greater than about 97% by weight of the (+) isomer based on the total weight percent of the compound.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 4, 2019
From: SCHAFER, PETER H.; MULLER, GEORGE W.; MAN, HON-WAH; GE, CHUANSHENG
To: CELGENE CORPORATION
Reel/Frame 051185/0985 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 4, 2019
From: CELGENE CORPORATION
To: AMGEN INC.
Reel/Frame 051181/0038 →
Continuity (11)
Continuation 15629678 · Jun 21, 2017
Continuation 15016856 · Feb 5, 2016
Continuation 14316160 · Jun 26, 2014
Continuation 13682652 · Nov 20, 2012
Continuation 12630788 · Dec 3, 2009
Continuation 12098379 · Apr 4, 2008
Division 11170308 · Jun 28, 2005
Division 10392195 · Mar 19, 2003
Provisional Application 60438450 · Jan 7, 2003
Provisional Application 60366515 · Mar 20, 2002
Related Publication 20190000804A1 · Jan 3, 2019