Eli Lilly has signed a $1.9 billion agreement with Ascidian Therapeutics to advance a pipeline of RNA exon editors specifically targeting inherited kidney diseases. This massive investment highlights a growing industry focus on high-precision genetic medicines that modify RNA rather than altering the underlying DNA sequence. Biotech developers should also note the simultaneous release of new open-source protein biology models, which are set to streamline the design of binders and protein function mapping in drug discovery.
Read the full article at Genetic Engineering News
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