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A new once-daily dose of the protease inhibitor fosamprenavir, marketed in the United States as Lexiva, has been approved by the US Food and Drug Administration.

The new indication offers patients new to HIV treatment the option of taking fosamprenavir as a once daily dose of two 700mg tablets with a single booster dose of 100mg of ritonavir. This represents a halving of the ritonavir booster dose, and says manufacturer GlaxoSmithKline, it should result in better toleration of fosamprenavir treatment.

A study in healthy volunteers showed that while the lower ritonavir dose did not result in significantly lower fosamprenavir levels, volunteers who received the 100mg ritonavir dose experienced fewer side-effects.

Once-daily dosing of fosamprenavir is not recommended for protease inhibitor-experienced patients, because of a concern that lower trough levels that occur with once-daily dosing will not be enough to overcome any existing resistance to protease inhibitors. Instead a twice daily dose of one 700mg tablet and 100mg of ritonavir is recommended.

In Europe fosamprenavir is marketed as Telzir and is licensed for use in both treatment-naïve and tretament-experienced patients at a dose of 700mg twice daily plus 100mg of ritonavir twice daily.

Keith Alcorn

Keith Alcorn

Editorial Consultant

Keith joined the editorial team of the National AIDS Manual (NAM) in 1991, launched the aidsmap website in 1998 and was the Senior Editor of NAM and aidsmap until 2018. He now contributes news and conference reports as a freelancer.