IP Library Granted Patent US 7,799,322
Granted Patent B2
US 7,799,322 · App. 10/583,370 · Granted Sep 21, 2010

Use of IL-6 in liver injury

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Quick Facts
Patent No.
US 7,799,322
App. No.
10/583,370
Granted
Sep 21, 2010
Kind
B2
Abstract

The invention relates to the use of IL-6 in liver cirrhosis.

Claims (18)

1. A method for treating hepatic fibrosis, comprising administering to a patient in need thereof an effective dose of IL-6 or IL-6 fused to another protein or polypeptide, optionally together with a pharmaceutically acceptable carrier to treat hepatic fibrosis, wherein the dose is in the range of 0.1 to 10 mcg/kg weight.

2. The method according to claim 1 , wherein the method of treatment comprises liver resection.

3. The method according to claim 1 , wherein the dose is about 0.1 mcg/kg or about 1 mcg/kg or about 10 mcg/kg.

4. The method according to claim 1 , wherein the IL-6 or IL-6 fused to another protein or polypeptide is administered daily or administered once a week or administered three times per week.

5. The method according to claim 1 , wherein the IL-6 is glycosylated at one or more sites.

6. The method according to claim 1 , wherein the IL-6 is not glycosylated.

7. The method according to claim 1 , wherein the other protein or polypeptide to which IL-6 is fused is an immunoglobulin (Ig) or a fragment thereof.

8. The method according to claim 1 , wherein the other protein or polypeptide to which IL-6 is fused is gp80 or a fragment thereof.

9. The method of claim 1 , wherein the hepatic fibrosis is caused by hepatotoxic agents.

10. A method for treating hepatic fibrosis which comprises resection, comprising administering to a patient in need thereof an effective dose of IL-6, or IL-6 fused to another protein or polypeptide to treat hepatic fibrosis including resection, wherein the dose is in the range of 0.1 to 10 mcg/kg weight.

11. The method according to claim 10 , wherein the administration is carried out before during and/or after resection treatment.

12. The method of claim 10 , wherein the hepatic fibrosis is caused by hepatotoxic agents.

13. The method according to claim 10 , wherein the other protein or polypeptide to which IL-6 is fused is an immunoglobulin (Ig) or a fragment thereof.

14. The method according to claim 10 , wherein the other protein or polypeptide to which IL-6 is fused is gp80 or a fragment thereof.

15. A method for treating hepatic fibrosis followed by engraftment, comprising administering to a patient in need thereof an effective dose of IL-6, or IL-6 fused to another protein or polypeptide to treat hepatic fibrosis, wherein the dose is in the range of 0.1 to 10 mcg/kg weight.

16. The method of claim 15 , wherein the hepatic fibrosis is caused by hepatotoxic agents.

17. The method according to claim 15 , wherein the other protein or polypeptide to which IL-6 is fused is an immunoglobulin (Ig) or a fragment thereof.

18. The method according to claim 15 , wherein the other protein or polypeptide to which IL-6 is fused is gp80 or a fragment thereof.

Assignments (3)
CHANGE OF NAME Recorded Nov 25, 2009
From: LABORATOIRES SERONO SA
To: MERCK SERONO SA
Reel/Frame 023569/0120 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 7, 2008
From: DREANO, MICHEL; TIBERIO, GUIDO A.M.; GAROTTA, GIANNI; SCHIAFFONATI, LUISA
To: APPLIED RESEARCH SYSTEMS ARS HOLDING N.V.
Reel/Frame 020475/0020 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 11, 2007
From: APPLIED RESEARCH SYSTEMS ARS HOLDING N.V.
To: LABORATOIRES SERONO SA
Reel/Frame 019966/0026 →