Advertisement
The Body: The Complete HIV/AIDS Resource
Follow Us Follow Us on Facebook Follow Us on Twitter Download Our App
Professionals >> Visit The Body PROThe Body en Espanol
  
  • Email Email
  • Printable Single-Page Print-Friendly
  • Glossary Glossary

Manufacturer Ends Adefovir Development

April 2000

A note from TheBody.com: Since this article was written, the HIV pandemic has changed, as has our understanding of HIV/AIDS and its treatment. As a result, parts of this article may be outdated. Please keep this in mind, and be sure to visit other parts of our site for more recent information!

Gilead Sciences has stopped development of its drug, adefovir, for use against HIV infection. This news came after the Food and Drug Administration (FDA) informed Gilead that adefovir would not be approved based on existing data and that additional studies would be necessary if it wants the FDA to reconsider the matter. The Antiviral Drugs Advisory Committee to the FDA had earlier recommended that the drug not be approved on the grounds that its potential serious side effects outweighed its potential benefits.

Contrary to the company's claims, the FDA analysis of the adefovir studies concluded that in three studies the drug did not provide any significant anti-HIV activity, while evidence of marginal activity was seen in two other studies. The FDA, like the advisory committee, was troubled by the side effect problems, most notably kidney toxicity. In addition, the FDA analysis concluded that the company had not made a convincing case that the drug would be useful in people who had developed resistance to multiple nucleoside analogue drugs such as AZT, ddI and 3TC.

Participants in studies with adefovir will be rolled over into the existing expanded access program, but the expanded access program will otherwise not accept new requests to supply the drug. For those already receiving the drug, the program will continue for as along as the individuals and their healthcare providers feel they are benefiting from it.

Gilead officials have now concluded that they can better use their resources in developing another drug, tenofovir (PMPA), which is in the final stages of studies. Project Inform and some other AIDS advocacy groups made a similar recommendation to the company almost three years ago. Results to date suggest that tenofovir may be more potent and have fewer side effects than adefovir. Gilead will continue its development program for adefovir as a potential treatment for hepatitis B virus.

Advertisement
The rejection of adefovir by the FDA represents something of a milestone in AIDS research. It is the first time in recent years that the FDA has rejected a request for the approval of an AIDS drug, and it is the first time that most AIDS advocacy groups did not rally to the drug's defense. While adefovir might have been approved had it appeared on the scene in earlier years, today's environment already offers a wide spectrum of AIDS drugs, many of which are clearly more potent and less troublesome than adefovir. But whether this means that the overall standard for approval of AIDS drugs has been raised is unclear.


Back to the Project Inform Perspective April 2000 contents page.

A note from TheBody.com: Since this article was written, the HIV pandemic has changed, as has our understanding of HIV/AIDS and its treatment. As a result, parts of this article may be outdated. Please keep this in mind, and be sure to visit other parts of our site for more recent information!



  
  • Email Email
  • Printable Single-Page Print-Friendly
  • Glossary Glossary

This article was provided by Project Inform. It is a part of the publication Project Inform Perspective. Visit Project Inform's website to find out more about their activities, publications and services.
 
See Also
Talk to a Physician About HIV/Hepatitis Coinfection in Our "Ask the Experts" Forums
More News and Research on Hepatitis B Prevention and Treatment

Tools
 

Advertisement