Chimeric Therapeutics Limited · ASX:CHM

Chimeric Therapeutics — ASCO 2021

7 slides from Chimeric Therapeutics's conference presentation, Jun 4, 2021

  1. Slide 1: A Phase 1 Study to Evaluate CLTX CAR T Cells for MMP2+ Recurrent or Progressive Glioblastoma

    A PHASE 1 STUDY TO EVALUATE CHIMERIC ANTIGEN RECEPTOR (CAR) T CELLS INCORPORATING A CHLOROTOXIN TUMOR-TARGETING DOMAIN FOR PATIENTS WITH MMP2+ RECURRENT OR PROGRESSIVE GLIOBLASTOMA (NCT04214392) Christine Brown, PhD Professor in Hem/HCT and Immuno-Oncology Deputy Director, T Cell Therapeutics Resear

  2. Slide 2: Background

    Background • Glioblastoma (GBM) is the most common and aggressive adult malignant brain tumor1 and has substantial heterogeneity2 • GBM has a 5-year survival rate of 5.1%3 and a median OS of 5-8 months following recurrence4,5 • No effective standard of care for recurrent GBM exists; treatment option

  3. Slide 3: Novel Features of CLTX-CAR T-Cell Therapy

    Novel Features of CLTX-CAR T-Cell Therapy CLTX-CAR T-cell therapy (CLTX(EQ)28ζ/CD19t+ T cells) uses CLTX as the tumor-recognition domain that identifies a multireceptor complex containing MMP2 for binding on GBM cells Novel receptor-binding Negligible killing of domain normal human cell lines, suppo

  4. Slide 4: CLTX-CAR T Cells Mediate Potent In Vivo Antitumor Activity

    CLTX-CAR T Cells Mediate Potent In Vivo Antitumor Activity Tumor regression was observed in in vivo orthotopic GBM-xenograft mouse models after adoptive transfer of CLTX-CAR T cells via the ICT route • Quantification of ffLuc flux (photons/sec) for each mouse • Significantly improved survival follow

  5. Slide 5: Phase 1 Study Design

    Phase 1 Study Design Primary Endpoints: Toxicity, including DLTs, CRS, and all other toxicities; determine the MTD schedule and RP2D plan Secondary Endpoints: • CAR T-cell and endogenous T-cell levels; phenotype; and cytokine levels in PB, TCF, and CSF • 6-month PFS rate, 9-month OS rate, and median

  6. Slide 6: Phase 1 Treatment Schema

    Phase 1 Treatment Schema • In a preliminary safety lead-in phase, patients are treated in Arm 1 and will receive a low dose of chlorotoxin-CAR T cells through the ICT catheter only • Patients will then be treated in Arm 2 in which CAR-T cells are administered both ICT and ICV via dual delivery; dose

  7. Slide 7: Conclusions and Future Directions

    Conclusions and Future Directions • CLTX-CAR T-cell therapy is a novel immunotherapy that has the potential to extend the range of solid tumors targetable by CAR T cells and has the scope to deliver a broad immuno-oncology platform • Results from our phase 1 study are expected to demonstrate the saf

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