IP Library Patent Application 11792905
Patent Application
App. No. 11/792,905

Treatment Of Hepatitis C In The Asian Population With Interferon-Beta

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Quick Facts
Patent No.
US None
App. No.
11/792,905
Abstract

The invention relates to the use of IFN-beta in the manufacture of a medicament for the treatment of an HCV infection in a treatment-naïve patient belonging to the Asian population.

Claims (17)

1 - 16 . (canceled)

17 . A method of treatment of a interferon-α-naïve patient belonging to the Asian population with a hepatitis C virus (HCV) infection, comprising administering to the patient an effective amount of interferon-β (IFN-β), or a mutein, functional derivative, active fragment or fusion protein thereof, having IFN-β activity.

18 . The method according to claim 17 , wherein the patient has not been treated with a combination of IFN-α and ribavirin.

19 . The method according to claim 17 , wherein the HCV infection is a chronic HCV infection.

20 . The method according to claim 17 , wherein the HCV is selected from genotype 1, 4, 5 or 6.

21 . The method according to claim 17 , wherein the patient has a high viral load of over 2×10 6 copies/ml.

22 . The method according to claim 17 , wherein the patient has a sustained viral response.

23 . The use according to any of the preceding claims, wherein IFN-β is recombinant IFN-β.

24 . The method according to claim 17 , wherein the IFN-β is IFN-β-1a.

25 . The method according to claim 17 , wherein the IFN-β functional derivative comprises one or more polyethyleneglycol (PEG) moieties.

26 . The method according to claim 17 , wherein the IFN-β fusion protein is an immunoglobulin fusion protein.

27 . The method according to claim 17 , wherein the IFN-β is administered subcutaneously.

28 . The method according to claim 17 , wherein dosages and regimens of the treatment are selected from the group consisting of: 12 MIU (44 mcg) three times a week, 12 MIU (44 mcg) daily, 24 MIU (88 mcg) three times a week, and 24 MIU (88 mcg) daily.

29 . The method according to claim 17 , further comprising treating the patient with ribavirin.

30 . The method according to claim 29 , wherein the ribarivin is administered orally.

31 . The method according to claim 30 , wherein the ribavirin is administered at about 800 to 1400 mg per person per day.

32 . A method of treatment of a interferon-α-naïve patient belonging to the Asian population with a hepatitis C virus (HCV) infection, comprising administering to the patient an effective amount of a pharmaceutical composition comprising interferon-β (IFN-β), or a mutein, functional derivative, active fragment or fusion protein thereof, having IFN-β activity, together with a pharmaceutically acceptable excipient.

Assignments (4)
CHANGE OF NAME Recorded Dec 3, 2009
From: LABORATOIRES SERONO SA
To: MERCK SERONO SA
Reel/Frame 023601/0311 →
CORRECTIVE ASSIGNMENT TO CORRECT THE BRIEF TO "MERGER"; REMOVE PAGES OF THE ORIGINAL DOCUMENT; AND TO REMOVE INCORRECT SERIAL NUMBERS ON THE ATTACHED SCHEDULE A PREVIOUSLY RECORDED ON REEL 023000 FRAME 0862. ASSIGNOR(S) HEREBY CONFIRMS THE MERGER AGREEMENT OF ENTIRE INTEREST. Recorded Oct 8, 2009
From: LABORATOIRES SERONO S.A.
To: LABORATOIRES SERONO SA
Reel/Frame 023412/0643 →
CHANGE OF NAME Recorded Jul 24, 2009
From: LABORATOIRES SERONO S.A.
To: MERCK SERONO SA
Reel/Frame 023000/0862 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 22, 2007
From: PARSONS, IAN; GIN, THEODOR WEE TIT
To: LABORATOIRES SERONO S.A.
Reel/Frame 019731/0837 →