Treatment of hepatitis C in the Asian population with subcutaneous interferon-beta
View Patent ↗The present invention relates to the use of recombinant IFN-beta for the production of a medicament for the treatment of HCV infection by subcutaneous administration to patients of Asian race, which failed to respond to a previous treatment with interferon-alpha, is herein reported. According to a preferred embodiment of the invention, this treatment can be better and further focused to those patients which after at least 4 weeks of initial treatment with IFN-beta show HCV RNA clearance.
1. A method of treating hepatitis C virus infections comprising the subcutaneous administration of an effective amount of a composition comprising interferon-beta (IFN-β) to Asian patients that had failed to respond to a previous treatment with interferon-α.
2. The method according to claim 1 , wherein said patients which failed to respond to a previous treatment with interferon-α have undergone at least 12 weeks of treatment with IFN-α at a dose of at least 3 Million International Units (MIU) 3 times a week, with one of the following outcomes: (a) failure to normalise serum alanine aminotransferase (ALT), or (b) normalisation of ALT followed by breakthrough (ALT elevation) before the end of therapy and said IFN-β is administered according to a schedule selected from the group consisting of: 12 MIU (44 mcg) IFN-β-1a three times a week, 12 MIU (44 mcg) IFN-β-1a daily, 24 MIU (88 mcg) IFN-β-1a three times a week, and 24 MIU (88 mcg) IFN-β-1a daily.
3. The method according to claim 1 , wherein said IFN-β is administered according to a schedule selected from the group consisting of: 12 MIU (44 mcg) IFN-β-1a three times a week, 12 MIU (44 mcg) IFN-β-1a daily, 24 MIU (88 mcg) IFN-β-1a three times a week, and 24 MIU (88 mcg) IFN-β-1a daily.
4. The method according to claim 1 , wherein said composition comprises IFN-β and an additional anti-viral agent.
5. The method according to claim 4 , wherein said IFN-β is administered according to a schedule selected from the group consisting of: 12 MIU (44 mcg) IFN-β-1a three times a week, 12 MIU (44 mcg) IFN-β-1a daily, 24 MIU (88 mcg) IFN-β-1a three times a week, and 24 MIU (88 mcg) IFN-β-1a daily.
6. The method according to claim 1 , wherein the IFN-β is recombinant IFN-β-1a.
7. The method according to claim 6 , wherein said recombinant IFN-β-1a is administered according to a schedule selected from the group consisting of: 12 MIU (44 mcg) recombinant IFN-β-1a three times a week, 12 MIU (44 mcg) recombinant IFN-β-1a daily, 24 MIU (88 mcg) recombinant IFN-β-1a three times a week, and 24 MIU (88 mcg) recombinant IFN-β-1a daily.