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The once-daily HIV treatment would greatly increase effectiveness for patients, but Gilead Sciences and Merck and Co. have failed to register it
in countries where it is needed most
LOS ANGELES, Sept. 10 /PRNewswire-USNewswire/ -- AIDS Healthcare Foundation (AHF) today called on Gilead Sciences and Merck to immediately register and distribute the three-in-one, once daily lifesaving HIV treatment, Atripla, in developing countries. When Atripla first received approval from the Food and Drug Administration (FDA) in July of 2006, advocates like AHF applauded the production of a single, once-a-day drug as a landmark step in treating HIV. However, since its approval, little progress has been made in expanding the availability of the treatment in the developing world, where only 28% of those in need of treatment were able to access it as of December 2006. Efforts made by AHF to clarify what countries currently can purchase Atripla at the announced $613 per patient per year access price have gone unanswered.
"This treatment is a standard therapy in the United States. It is on
the World Health Organization's Essential Medicines List, and is an
antiretroviral drug regimen that could greatly benefit patients everywhere
while reducing costs in the long term," said Michael Weinstein, AIDS
Healthcare Foundation President. "The fact that Gilead and Merck appear to
be unable or unwilling to make it available in resource-poor countries is
deeply troubling, and causing unnecessary suffering. Gilead and Merck
should immediately begin making this treatment available to the rest of the
world, or license it out to a generic drug manufacturer, such as Cipla,
which already produces a generic version in India, that will. In the
instances where the registration process has been initiated such as in the
European Union, governments must also recognize their roles and streamline
the necessary approval processes to facilitate quick distribution of these
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