Trofinetide: First Approval
- PMID: 37191913
- DOI: 10.1007/s40265-023-01883-8
Trofinetide: First Approval
Abstract
Trofinetide (DAYBUE™), an oral, small molecule, synthetic analog of glycine-proline-glutamate [GPE; the N-terminal tripeptide derivative of insulin like growth factor-1 (IGF-1)], is being developed by Neuren Pharmaceuticals and Acadia Pharmaceuticals for the treatment of rare childhood neurodevelopmental disorders. Trofinetide was approved in March 2023 in the USA for the treatment of Rett syndrome in adult and pediatric patients 2 years of age and older. This article summarizes the milestones in the development of trofinetide leading to this first approval for Rett syndrome.
© 2023. The Author(s), under exclusive licence to Springer Nature Switzerland AG.
References
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- Neul JL, Percy AK, Benke TA, et al. Design and outcome measures of LAVENDER, a phase 3 study of trofinetide for Rett syndrome. Contemp Clin Trials. 2022. https://doi.org/10.1016/j.cct.2022.106704 . - DOI - PubMed
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- Neuren Pharmaceuticals Ltd. Annual Report 2021; 2022. https://www.neurenpharma.com/ . Accessed 28 Mar 2023.
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