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| Hepatitis B
and C (MIV-210) Over a million people every year die as a
consequence of hepatitis B, with some 400 million people chronically
infected. Asia and Africa have the most sufferers. There are some 200
million people chronically affected by HCV worldwide, most of them in the
industrial world. Hepatitis B is exceptionally contagious and spread via blood. Extremely
small amounts of virus are enough to cause infection. The virus can also
spread through other body fluids. Although there are HBV vaccines available, they only function on people
who are not infected. There are two approved HBV drugs, interferon – which
influences the immune system but gives rise to significant side-effects –
and lamivudine, which functions well, but eventually causes resistance. HBV researchers agree that a combination treatment against the disease is
imperative, similar to that used against HIV, to circumvent resistance
development and achieve enhanced efficacy. HCV is another readily changeable virus, which will imply problems during
the development of pharmaceuticals and vaccines. |
MIV-210 against hepatitis B In vitro experiments proved that MIV-210 is active against lamivudine-resistant HBV. Comparative studies in in vivo models demonstrated MIV-210’s superior efficacy over lamivudine (the market’s currently predominant HBV pharmaceutical). In vitro trials demonstrated that MIV-210 also is effective against multiresistant HIV. Methods to produce the pharmaceutical grade MIV-210 were enhanced, resulting in better yields and reduced production costs. The pharmaceutical has been formulated in capsules for phase I trials; development of a tablet formulation commenced. Current phase I trials have demonstrated the compound’s very good oral uptake, when administered as capsules. No drug-dependent side-effects were demonstrated. |
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Copyright 2003. Medivir AB. Changed: 2003-11-19.
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