Pushing Beyond the Limits of Today's CAR T Therapies

Successful CAR T therapy means remission that lasts. To get there, CAR T cells must expand, persist, and stay powerful — even without toxic pre‑conditioning chemotherapy. They need to stay active in the tumor microenvironment, target cancer from multiple angles, and resist immune rejection. iPSC‑derived CAR T cells can be engineered to do exactly that — built for durability and long‑term tumor control.

iPSC‑derived CAR T cells tackle current cell therapy limitations.

Manufacturing iPSC-CAR T Cells

GMP‑grade iPSCs are genetically engineered and differentiated into iPSC‑derived CAR T cells, which are subsequently expanded, cryopreserved, and subjected to comprehensive quality control. Their off‑the‑shelf availability and suitability for outpatient administration substantially enhance therapeutic accessibility.

Our proprietary manufacturing process delivers batch sizes on par with donor‑derived CAR T cells and is designed for seamless upscaling. With projected production costs below €2,000 per dose, it offers a highly competitive alternative to in vivo CAR T approaches.

Manufacturing of iPSC-derived CAR T cells.

CAR iγδ T Cells - A Powerful Cell Therapy Modality

At Evotec, we are developing a versatile iPSC-derived CAR γδ T cells (CAR iγδ T) platform designed to use as cell therapy modality in both oncology and immunology.

γδ T cells are particularly well suited for cell therapy because they:

Advantages of our versatile iPSC-derived CAR γδ T cells platform for both oncology and immunology applications.

ICE: Immune cell engager. 
TME: Tumor microenvironment.

  • Pose a lower risk of graft‑versus‑host disease thanks to their MHC‑independent antigen recognition.
  • Reduce the likelihood of tumor escape by recognizing multiple tumor antigens through their natural receptors.
  • Naturally infiltrate solid tumors with high efficiency.
  • Have demonstrated clinical efficacy with a favorable safety profile and minimal adverse events.

Evotec's Immune-Shieled iγδ T Cell Platform

Evotec’s GMP-compatible gene editing process enables a versatile iγδ T cell platform:

GMP-compatible gene editing process to enable a versatile iγδ T cell platform.
  1. Depletion of MHC surface display to prevent allorejection via T cells
  2. Inhibitory mechanism to prevent allorejection via NK cells
  3. Customizable (exchangeable) CAR for target specificity or combination with Immune Cell Engager (ICE)
  4. Safety switch for therapeutic intervention
  5. γδTCR to recognize natural tumor antigens
  6. Gene edits(s) for persistency and TME-resistance

Evotec’s CAR iγδ T cells to treat liver cancer

Evotec is currently developing an immune-shielded CAR iγδ T cell product candidate against liver cancer.

Competitiveness of CAR iγδ T Cells

Unique selling points of our CAR iγδ T cells for cancer treatment
Efficacy

Efficient infiltration and killing of tumor cells despite hostile tumor microenvironment and tumor heterogeneity

Tolerability and long-term tumor control

Efficient tumor control with no or low dose chemotherapy

Efficient expansion of CAR T cells with no or low dose lymphodepletion

Increased persistence and metabolic fitness or long-term survival

Safety

Reduced risk for adverse events and graft-versus-host-disease. Safety switch for therapeutic intervention. Well tolerated even in high doses. Minimized patient hospitalization.

Affordable

Low cost per dose due to optimized manufacturing process and high expansion

Availability and accessibility

Off-the-shelf availability of clonal cryopreserved drug product. No therapy delay. Accessibility independent of geography.

Full control

In-depth quality control of product phenotype and genetic integrity

Flexible applicability

Rapid iteration using modular exchangeable CARs for various indications
Andreas Scheel

Andreas Scheel, PhD

EVP, Head of Cell Therapy

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Evotec has the right technologies & disease understanding to meet our partners' evolving needs: a comprehensive disease knowledge at the molecular level, cutting-edge technologies & platforms to translate this expertise into effective precision medicines.