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Kelonia Therapeutics has launched with $50 million in series A funding to develop genetic medicines using what it calls off-the-shelf in vivo gene delivery. Kelonia says existing gene therapies are complex, costly, and limited by complicated treatments and dose-limiting toxicities. It plans to use lentiviral vector-like particles discovered in Michael Birnbaum’s lab at the Massachusetts Institute of Technology to deliver genetic payloads for a broad range of diseases.
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