ReCode Combines With TranscripTx, Raises $80m For Novel RNA Drugs
Executive Summary
ReCode, whose platform allows for organ-specific delivery of RNA therapies, plans to start clinical trials in 2022 for its two lead programs in primary ciliary dyskinesia and cystic fibrosis.
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The Next Big Thing In Gene Therapy Might Not Be Gene Therapy
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Gene therapy remains attractive when data show new technologies can advance the field, but gene regulation, editing and RNA therapies are grabbing investors’ attention, panelists said at ARM’s Cell and Gene Meeting on the Mesa.