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Fostemsavir: First Approval

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A Correction to this article was published on 09 September 2020

This article has been updated

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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Change history

  • 09 September 2020

    The original article can be found online

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Acknowledgements

During the peer review process, the manufacturer of fostemsavir was also offered an opportunity to review this article. Changes resulting from comments received were made on the basis of scientific and editorial merit.

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Correspondence to Anthony Markham.

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The preparation of this review was not supported by any external funding.

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A. Markham is a contracted employee of Adis International Ltd/Springer Nature, and declares no relevant conflicts of interest. All authors contributed to the review and are responsible for the article content.

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Not applicable.

Additional information

The original article has been update: Due to Acknowledgement update.

Enhanced material for this AdisInsight Report can be found at https://doi.org/10.6084/m9.figshare.12792599.

This profile has been extracted and modified from the AdisInsight database. AdisInsight tracks drug development worldwide through the entire development process, from discovery, through pre-clinical and clinical studies to market launch and beyond.

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Markham, A. Fostemsavir: First Approval. Drugs 80, 1485–1490 (2020). https://doi.org/10.1007/s40265-020-01386-w

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