Chemical structure of abacavir.
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Ziagen

Abacavir (ABC) is the most powerful nucleoside analog reverse transcriptase inhibitor (NARTI) used to treat HIV and AIDS. It has been well tolerated, its main side effect being hypersensitivity reactions, which can be dangerous. It is available under the trade name Ziagen™ by GlaxoSmithKline and the combination drug Trizivir™. more...

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Abacavir is one of the most deadly NARTIs, due its ability to trigger to hypersensitivity reactions that lead to sudden death in certain individuals. However, a genetic test is now available that, while not perfect, has reasonable accuracy in predicting whether an individual will be hypersensitive. Over 90% of patients can safely take abacavir.

Strains that are resistant to zidovudine (AZT) or lamivudine (3TC) are generally sensitive to abacavir, whereas strains that are resistant to AZT and 3TC are not as sensitive to abacavir.

History

Abacavir was approved by the Food and Drug Administration (FDA) on December 18, 1998 and is thus the fifteenth approved antiretroviral drug in the United States. Its patent will expire in the United States on 2009-12-26.

Mechanism of action

ABC is an analog of guanosine. It is capable of crossing the blood-brain barrier.

Abacavir is given orally and has a high bio-availability of 83%. It is metabolised primarily through alcohol dehydrogenase or gluconyl transferase.

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FDA panel recommends agency OK of Ziagen for HIV therapy
From Drug Store News, 12/14/98

A Food and Drug Administration advisory panel has recommended accelerated approval of Glaxo Wellcome Inc.'s Ziagen (abacavir sulfate), a nucleoside analogue reverse transcriptase inhibitor for the treatment of HIV. The Antiviral 9rugs Advisory Committee voted to recommend the drug for adult and pediatric use after review of various studies involving Ziagen in combination with Epivir (lamivudine), also known as 3TC, and Retrovir (zidovudine, AZT), as well as limited data involving Ziagen in combination with other antiretroviral drugs, including protease inhibitors. The FDA sought the review because of concern over serious allergic or hypersensitivity reactions which have been observed in patients using the drug. Approximately 9,000 HIV patients in the United States have received Ziagen through an expanded access program. Through this program, patients who are not maintaining viral suppression with their current drug combinations can access Ziagen for use in constructing a new treatment regimen.

COPYRIGHT 1998 Lebhar-Friedman, Inc.
COPYRIGHT 2000 Gale Group

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