Quick Search 
Drugs of the Future
Register or sign in

Drugs Fut 2021, 46(1): 29
ISSN 0377-8282
Copyright 2021 Clarivate
CCC: 0377-8282
DOI: 10.1358/dof.2021.46.1.3208246
Trofinetide. Glycine-proline-glutamate (GPE) analogue, Treatment of Rett syndrome, Treatment of fragile X syndrome
Collins, B.E., Neul, J.L.
Insulin-like growth factor 1 (IGF-1) is neuroprotective and ameliorates features of neurodevelopmental disorders (NDD) in preclinical models, but potential mitogenic effects limit its therapeutic potential. Glycine-proline-glutamate (GPE) is the N-terminal tripeptide of IGF-1 that confers similar therapeutic effects but is highly unstable. Trofinetide, a methylated GPE analogue, has an improved pharmacokinetic profile and has demonstrated efficacy for individuals with genetically caused NDD, specifically Rett syndrome (RTT) and fragile X syndrome (FXS). Despite an understanding of the genetic basis and availability of disease models, there are no approved therapeutics addressing core features of either disease. Phase II trials of oral trofinetide for RTT and FXS found that the studied doses were generally safe and well tolerated and found improvement on both caregiver- and clinician-based efficacy outcome measures. A phase III trofinetide trial in children and adolescents with RTT is ongoing, which will be critical for determination of efficacy in RTT.

Full Text: PDF 

© Clarivate. All rights reserved.
Copyright NoticeTerms of UsePrivacy StatementCookie PolicyManage cookie preferences