Innovating Tomorrow's Medicine
What if we could silence disease-causing proteins not by targeting the protein itself, but by preventing its mRNA from ever being translated—using small-molecule drugs? In this episode, David Weitz, Co-founder, President and CEO of Syrna Therapeutics, shares how his company is pioneering a revolutionary approach: 3D structure-guided drug discovery for mRNA, coupled with covalent translation inhibitors that block disease-causing proteins before they're even made. What we discuss: • Why mRNA represents an untapped class of small-molecule drug targets • How covalent translation inhibitors work to silence protein expression • 3D structure-guided drug discovery: revealing druggable domains in mRNA • Lead programs in immunology and neurodegeneration • The universal mechanism that can be applied to any mRNA with a druggable structured domain • Coming out of stealth: building Syrna and attracting top-tier investors • Personal reflections on pioneering a fundamentally new drug discovery approach This isn't traditional RNA therapeutics. This is small-molecule drug discovery targeting mRNA—a completely new frontier in precision medicine. About the Guest: David Weitz is Co-founder, President and CEO of Syrna Therapeutics, a biotechnology company pioneering 3D structure-guided drug discovery for mRNA targets using covalent translation inhibitors. About the Show: Innovating Tomorrow's Medicine features conversations with biotech leaders, researchers, and innovators who are transforming bold ideas into real-world impact in healthcare and life sciences. 🔗 Connect: • Syrna Therapeutics: [https://www.syrnatx.com/] • David Weitz: [https://linkedin.com/in/david-weitz-25ba] • Host Jeff Trickett: [https://www.linkedin.com/in/jeff-trickett] 📧 Questions or guest suggestions? [jeffreytrickett@gmail.com] #Biotech #mRNA #DrugDiscovery #SmallMolecule #Immunology #Neurodegeneration #PrecisionMedicine #Innovation #RNATherapeutics
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