Entrada Therapeutics Inc. has provided an update on its clinical development pipeline, outlining plans to advance four clinical-stage programs by the end of 2025. Key milestones expected in 2026 include data readouts for ENTR-601-44 and ENTR-601-45, as well as progress on ENTR-601-50 and Vertex-partnered VX-670 for myotonic dystrophy type 1 (DM1). The company highlighted its strategy around its EEV platform, emphasizing improvements in endosomal escape and the development of novel PMO conjugates. Entrada also noted that ongoing and planned ex-U.S. studies are designed to generate data supporting future regulatory discussions and potential accelerated approval pathways. You can access the full presentation through the link below.
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