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Review
. 2020 Sep;80(14):1485-1490.
doi: 10.1007/s40265-020-01386-w.

Fostemsavir: First Approval

Affiliations
Review

Fostemsavir: First Approval

Anthony Markham. Drugs. 2020 Sep.

Erratum in

Abstract

Fostemsavir (Rukobia), a prodrug of the HIV-1 attachment inhibitor temsavir, is a first-in-class treatment for HIV infection being developed by ViiV Healthcare. Based on the results of the phase III BRIGHTE trial fostemsavir was recently approved in the USA for the treatment of patients with HIV not able to be treated with other therapies. This article summarizes the milestones in the development of fostemsavir leading to this first approval.

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References

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    1. US Food & Drug Administration. Rukobia (fostemsavir): US prescribing information. 2020. https://www.accessdata.fda.gov . Accessed 31 July 2020.
    1. ViiV Healthcare. ViiV Healthcare submits regulatory application to the European Medicines Agency for fostemsavir, an investigational, first-in-class attachment inhibitor for the treatment of HIV in adults with few treatment options available [media release]. 10 Jan 2020. https://www.viivhealthcare.com .
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