IP Library Granted Patent US 7,868,011
Granted Patent B2
US 7,868,011 · App. 11/650,089 · Granted Jan 11, 2011

Use of reversible inhibitors of S-adenosyl-L-homocysteine hydrolase for treating lupus

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Quick Facts
Patent No.
US 7,868,011
App. No.
11/650,089
Granted
Jan 11, 2011
Kind
B2
Abstract

The present invention provides methods for suppressing autoimmunity in a patient in need of treatment for systemic lupus erythematosus by administering to the patient an effective amount of methyl 4-(Adenin-9-yl)-2-hydroxybutanoate or pharmaceutically acceptable salts thereof. In some embodiments, the claimed methods include co-administering an effective amount of an immunosuppressant.

Claims (21)

1. A method for suppressing autoimmunity in a patient in need of treatment for systemic lupus erythematosus, comprising administering to said patient an effective amount of methyl 4-(Adenin-9-yl)-2-hydroxybutanoate or a pharmaceutically acceptable salt thereof, thereby suppressing autoimmunity in said patient.

2. The method of claim 1 , wherein the patient is a human.

3. A method for suppressing autoimmunity in a patient in need of treatment for systemic lupus erythematosus, comprising administering to said patient an effective amount of a combination, wherein the combination comprises:

a) an effective amount of methyl 4-(Adenin-9-yl)-2-hydroxybutanoate or a pharmaceutically acceptable salt thereof; and

b) an effective amount of an immunosuppressant,

thereby suppressing autoimmunity in said patient.

4. The method of claim 3 , wherein the patient is a human.

5. A method for suppressing autoimmunity in a human in need of treatment for systemic lupus erythematosus, which method comprises administering to said human an effective amount of methyl 4-(Adenin-9-yl)-2-hydroxybutanoate or a pharmaceutically acceptable salt thereof in a oral, parenteral, intranasal, topical, or injectable dosage form, whereby autoimmunity is suppressed in said human.

6. A kit comprising an effective amount of methyl 4-(Adenin-9-yl)-2-hydroxybutanoate or a pharmaceutically acceptable salt thereof, and an instruction means for administering said compound or pharmaceutically acceptable salt thereof to a mammal having systemic lupus erythematosus.

7. The kit of claim 6 , further comprising an effective amount of an immunosuppressant.

8. The method of claim 2 , wherein the administration is oral, parenteral, intranasal, topical, or injectable.

9. The method of claim 2 , wherein methyl 4-(Adenin-9-yl)-2-hydroxybutanoate or a pharmaceutically acceptable salt thereof is formulated in a solid or liquid dosage form.

10. The method of claim 2 , wherein methyl 4-(Adenin-9-yl)-2-hydroxybutanoate or a pharmaceutically acceptable salt thereof is formulated for oral or injectable administration in a dosage ranging from about 0.1 to about 20 mg/kg per day.

11. The method of claim 10 , wherein said injectable administration is selected from the group consisting of intracavernous injection, subcutaneous injection, intravenous injection, intramuscular injection, and intradermal injection.

12. The method of claim 4 , wherein the administration is oral, parenteral, intranasal, topical, or injectable.

13. The method of claim 4 , wherein methyl 4-(Adenin-9-yl)-2-hydroxybutanoate or a pharmaceutically acceptable salt thereof is formulated in a solid or liquid dosage form.

14. The method of claim 4 , wherein methyl 4-(Adenin-9-yl)-2-hydroxybutanoate or a pharmaceutically acceptable salt thereof is formulated for oral or injectable administration in a dosage ranging from about 0.1 to about 20 mg/kg per day.

15. The method of claim 14 , wherein said injectable administration is selected from the group consisting of intracavernous injection, subcutaneous injection, intravenous injection, intramuscular injection, and intradermal injection.

16. The method of claim 5 , wherein methyl 4-(Adenin-9-yl)-2-hydroxybutanoate or a pharmaceutically acceptable salt thereof is formulated in a solid or liquid dosage form.

17. The method of claim 5 , wherein methyl 4-(Adenin-9-yl)-2-hydroxybutanoate or a pharmaceutically acceptable salt thereof is formulated for oral or injectable administration in a dosage ranging from about 0.1 to about 20 mg/kg per day.

18. The method of claim 17 , wherein said injectable administration is selected from the group consisting of intracavernous injection, subcutaneous injection, intravenous injection, intramuscular injection, and intradermal injection.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 13, 2017
From: ERAGON VENTURES, LLC
To: NINGBO ZIYUAN PHARMACEUTICALS, INC.
Reel/Frame 041243/0528 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 1, 2016
From: GENERAL ATOMICS
To: ERAGON VENTURES, LLC
Reel/Frame 038176/0890 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 9, 2007
From: YUAN, CHONG-SHENG
To: GENERAL ATOMICS
Reel/Frame 019271/0021 →