IP Library › Granted Patent US 7,041,680
Granted Patent B2
US 7,041,680 · App. 10/119,486 · Granted May 9, 2006

(R) and (S) isomers of substituted 2-(2,6-dioxopiperidin-3-yl) phthalimides and 1-oxoisoindolines and methods of using the same

Assignee: Celgene Corporation
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Quick Facts
Patent No.
US 7,041,680
App. No.
10/119,486
Granted
May 9, 2006
Kind
B2
Abstract

Substituted 2-(2,6-dioxopiperidin-3-yl) phthalimides and 1-oxo-2-(2,6-dioxopiperidin-3-yl) isoindolines reduce the levels of TNFα in a mammal. Typical embodiments are 1-oxo-2-(2,6-dioxo-3-methylpiperidin-3-yl)-4,5,6,7-tetrafluoroisoindoline and 1,3-dioxo-2-(2,6-dioxo-3-methylpiperidin-3-yl)-4-aminoisoindoline.

Claims (14)

1. A pharmaceutical composition comprising a therapeutically effective amount of the (S)-isomer of a compound of the formula:

or an acid addition salt of said isomer, wherein the (S) isomer is substantially free of its (R) isomer, in combination with a pharmaceutically and physiologically suitable carrier.

2. A single unit dosage form of the pharmaceutical composition according to claim 1 , wherein the dosage form is a powder, tablet, capsule or an injectable composition.

3. A pharmaceutical composition comprising a therapeutically effective amount of the (R)-isomer of a compound of the formula:

or an acid addition salt of said isomer, wherein the (R) isomer is substantially free of its (S) isomer, in combination with a pharmaceutically and physiologically suitable carrier.

4. A single unit dosage form of the pharmaceutical composition according to claim 3 , wherein the dosage form is as a powder, tablet, capsule or an injectable composition.

5. The pharmaceutical composition of claim 1 , wherein the (S) isomer has an optical purity of greater than 95%.

6. The pharmaceutical composition of claim 3 , wherein the (R) isomer has an optical purity of greater than 95%.

7. The pharmaceutical composition of claim 1 , wherein the composition is suitable for parenteral administration.

8. The pharmaceutical composition of claim 7 , which is a composition suitable for intravenous administration.

9. The pharmaceutical composition of claim 7 , which comprises a sterile injectable solution.

10. The pharmaceutical composition of claim 3 , wherein the composition is suitable for parenteral administration.

11. The pharmaceutical composition of claim 10 , which is a composition suitable for intravenous administration.

12. The pharmaceutical composition of claim 10 , which comprises a sterile injectable solution.

Continuity (5)
Continuation 0963390800 · Aug 7, 2000
Continuation 0954380900 · Apr 6, 2000
Division 0923038900 · May 7, 1999
Provisional Application 6004827800 · May 30, 1997
Related Publication 20020183360A1 · Dec 5, 2002