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| CATEGORIES ABOUT ENFUVIRTIDE | |
| antiretroviral drugs | |
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Enfuvirtide is available only in injectable form since it is a peptide and would not survive digestion. The injections must be taken twice a day. This makes it inconvenient to take. With an estimated U.S. price of more than $25,000 for a year of Fuzeon, it is relatively expensive for an antiretroviral drug. Its inconvenience and price reserve it mostly for ''salvage'' therapy in patients with multi-drug resistant HIV. The most common side effect is injection site reaction. HISTORY Trimeris Inc. began development on enfuvirtide in 1996 and initially designated it T-20. Trimeris partnered with Hoffmann-La Roche in 1999 to complete the drug's development. The medication has several disadvantages that resulted in its slow progress. It is difficult to manufacture, and is only available in an injectable form. The injections must be taken twice a day. Its approval by the Food And Drug Administration (FDA) on March 13 , 2003 made it the first of the new Fusion Inhibitor class of antiretroviral drugs to be approved for use in the United States . It was approved on the basis of two studies (TORO 1 and TORO 2) which compared the effect of optimized regimens of antiretroviral medication with and without the addition of Fuzeon on serum Viral Load . MODE OF ACTION Enfuvirtide works by disrupting the HIV -1 molecular machinery at the final stage of fusion with the target Cell , preventing uninfected cells from becoming infected. A Biomimetic Peptide , Enfuvirtide was rationally designed to mimic components of the HIV -1 fusion machinery and displace them, preventing normal fusion. Drugs that disrupt fusion of Virus and target Cell are termed Entry Inhibitors . Greenberg, M. L. and N. Cammack (2004). "Resistance to enfuvirtide, the first HIV fusion inhibitor." J Antimicrob Chemother 54(2): 333-40. |
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