Entrada Therapeutics, Inc. · NASDAQ:TRDA

Entrada Therapeutics — PPMD 2023 Annual Conference

9 slides from Entrada Therapeutics's conference presentation, 2023

  1. Slide 1: Endosomal Escape Vehicle (EEV) Platform for Delivery of Oligonucleotides in Duchenne Muscular Dystrophy

    Endosomal Escape Vehicle (EEVTM) Platform for Delivery of Oligonucleotides in Duchenne Muscular Dystrophy Nerissa Kreher, MD, MBA WANT TO LEARN MORE? Chief Medical Officer Scan the QR code for access to our recent publications and Entrada Therapeutics, Inc. conference presentations. 1 PPMD 2023 Annu

  2. Slide 2: Disclaimer

    DISCLAIMER This presentation includes express and implied “forward-looking statements. Forward looking statements include all statements that are not historical facts, and in some cases, can be identified by terms such as “may,” “might,” “will,” “could,” “would,” “should,” “expect,” “intend,” “plan,

  3. Slide 3: Our Commitment to the Duchenne Community

    OUR COMMITMENT TO THE DUCHENNE COMMUNITY Our partnerships with community leaders and patient advocacy organizations are at the heart of our work to bring innovative therapies to people living with serious diseases ENTR-601WeeweWe-44ENTR-601-44 We appreciate the Duchenne community’s PURSUING TREATMEN

  4. Slide 4: Our Endosomal Escape Vehicle (EEV) Platform

    OUR ENDOSOMAL ESCAPE VEHICLE (EEV TM) PLATFORM We are developing EEV-oligonucleotide conjugates for the treatment of Duchenne • EEV-oligonucleotide conjugates are cyclic Prolonged duration of effect Improved entry into the cell 3 peptides attached to oligonucleotides (intracellular depot) 1 (~90% up

  5. Slide 5: ENTR-601-44 Is Our Exon Skipping Clinical Candidate

    ENTR-601-44 IS OUR EXON 44 SKIPPING CLINICAL CANDIDATE A single IV dose of ENTR-601-44 resulted in robust exon skipping in both skeletal and cardiac muscles in non-human primates (NHP), as well as prolonged duration of effect for at least 12 weeks Exon Skipping in Muscles at Day 7 Duration of Effect

  6. Slide 6: Preclinical Data Support Advancement of ENTR-601-44 to the Clinic

    PRECLINICAL DATA SUPPORT ADVANCEMENT OF ENTR-601-44 TO THE CLINIC Results show: Effective exon Robust dystrophin Prolonged duration of skipping seen in production observed effect, which may skeletal, in skeletal muscle translate to diaphragm and cells from patients administration of drug heart muscl

  7. Slide 7: ENTR-601-45 Effective in Skeletal and Cardiac Muscle Cells

    ENTR-601-45 EFFECTIVE IN SKELETAL AND CARDIAC MUSCLE CELLS ENTR-601-45 showed robust exon skipping and dystrophin production in skeletal and cardiac muscle cells from patients living with Duchenne who are amenable to exon 45 skipping ENTR-601-45 in Skeletal Muscle Cells ENTR-601-45 in Cardiac Muscle

  8. Slide 8: In Summary

    IN SUMMARY Entrada lead programs are advancing new therapeutic options for people living with exon 44 and exon 45 skip amenable Duchenne • ENTR-601-44 produced robust exon skipping and dystrophin production in cell and animal models of Duchenne • We observed robust exon skipping over 12+ weeks from

  9. Slide 9: Thank You From Our Whole Team

    THANK YOU FROM OUR WHOLE TEAM Please visit us at the resource fair in the Lonestar Foyer! WANT TO LEARN MORE? Scan the QR code for access to our recent publications and conference presentations. For questions, contact: Regan Sherman, Head of Patient Advocacy, rsherman@entradatx.com 9 PPMD 2023 Annua

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