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Chrdl1 is a preclinical-stage cardioprotective therapeutic being developed by Forcefield Therapeutics for the treatment of acute myocardial infarction and the prevention of heart failure. Identified through the FunSel screening platform in collaboration with King's College London, Chrdl1 is one of several secreted proteins found to protect cardiomyocytes from death following a heart attack. Its mechanism of action involves the activation of autophagy, prevention of cardiomyocyte apoptosis, and inhibition of cardiac fibrosis through the suppression of TGF-beta signaling. The program is being developed using two distinct modalities: a recombinant protein therapeutic for acute administration and an AAV-based gene therapy for sustained effect, the latter of which is being developed in partnership with Freeline Therapeutics.
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