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Adefovir dipivoxil

Hepsera 




Article: Adefovir

[[Image:|220px|Adefovir chemical structure]]
Adefovir
Systematic (IUPAC) name
[2-(6-aminopurin-9-yl)ethoxymethyl- (2,2-dimethylpropanoyloxymethoxy) phosphoryl]oxymethyl 2,2-dimethylpropanoate
Identifiers
CAS number 142340-99-6
ATC code J05AF08
PubChem 60871
DrugBank APRD00781
Chemical data
Formula C20H32N5O8P
Mol. weight 501.471 g/mol
Pharmacokinetic data
Bioavailability  ?
Metabolism  ?
Half life  ?
Excretion  ?
Therapeutic considerations
Pregnancy cat.

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Legal status
Routes  ?
1707-adefovir-dipivoxil-adefovir-dipivoxil.png
Adefovir dipivoxil
1708-adefovir-adefovir-dipivoxil.png
Adefovir

Adefovir dipivoxil, previously called bis-POM PMEA, with trade names Preveon® and Hepsera®, is an orally-administered nucleotide analog reverse transcriptase inhibitor (ntRTI) used for treatment of Hepatitis B. It is a failed treatment for HIV.

History

Adefovir was invented in Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic by Antonin Holy, and the drug was developed by Gilead Sciences for HIV with the brand name Preveon. However, in November 1999, an expert panel advised the U.S. Food and Drug Administration (FDA) not to approve the drug due to concerns about the severity and frequency of kidney toxicity when dosed at 60 or 120mg. The FDA followed that advice, refusing to approve adefovir as a treatment for HIV.

Gilead Sciences discontinued its development for HIV treatment in December 1999 but continued to develop the drug for Hepatitis B (HBV), where it is effective with a much lower dose. FDA approval for use in the treatment of Hepatitis B was granted on September 20, 2002, and adefovir is sold for this indication under the brand name Hepsera.

Adefovir became an approved treatment for HBV in the United States in September 2002 and in the European Union in March 2003.

Mechanism of action

Adefovir works by blocking reverse transcriptase, an enzyme that is crucial for the hepatitis B virus (HBV) to reproduce in the body.

It is approved for the treatment of chronic hepatitis B in adults with evidence of active viral replication and either evidence of persistent elevations in serum aminotransferases (primarily ALT) or histologically active disease.

Adefovir is a failed treatment for HIV due to the severity and frequency of kidney toxicity when dosed at 60 or 120mg. However, trials have found the 10mg dose of adefovir to be an effective and safe treatment for HBV.

The main benefit of adefovir over lamivudine (the first NRTI approved for the treatment of hepatitis B) is that it takes a much longer period of time before the virus develops resistance to it.

Resources



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December 4, 2009



Page Updated: July 22, 2006
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