Enabling Next-Generation Treatments for Fibrosis & Infection 

Macrophages are among the most versatile and flexible immune cells we know today. Using iPSC-derived macrophages (iMAC) with superior process and phenotype control allows us to harness their full potential and unique properties. The unique properties of macrophages make iMAC a promising treatment option for chronic/acute infections and fibrosis, diseases with high mortality and currently limited treatment options.

iMAC Cell Therapy

  • Natural homing to infected, inflamed or fibrotic tissue
  • Immune-modulatory properties
  • Inactivation, killing and phagocytosis of cells with target molecules
  • Natural efferocytosis capacity
  • ECM remodeling and degradation
  • Suitable for high-risk patients e.g. cystic fibrosis or immuno-compromised patients
First image a new approach

Competitiveness of iMAC Cell Therapy

List of the competitiveness of iMAC cell therapy. Efficacy- Survival enhancing effect of autologous macrophages for patients with non-compensated liver fibrosis/cirrhosis demonstrated (MATCH Phase I / II trial). Safety- Clinical data demonstrated safety (MATCH Phase I / II trial). Low risk for adverse events/ Additional safety switch for therapeutic intervention. Affordability- Low cost per dose due to optimized manufacturing. Accessibility- Off-the-shelf availability of clonal cryopreserved drug product for large patient populations. No therapy delay. Full control- In-depth quality control of phenotype and genetic integrity. Flexibility- Rapid adaption to additional targets and indications via modular CARs.

Manufacturing iPSC-derived Macrophages

Genetically engineered or unmodified GMP‑grade iPSCs are differentiated into iMAC, which are subjected to comprehensive quality control and cryopreserved in a ready-to-infuse formulation. Their off‑the‑shelf availability and suitability for outpatient administration substantially enhance therapeutic accessibility.

Our proprietary manufacturing process delivers 40 x larger batch sizes compared to donor‑derived CAR T cells and is designed for seamless upscaling. With a low cost-of-goods (COGS) per dose, it offers a highly competitive treatment alternative.

Manufacturing process of iPSC-derived Macrophages

Our modular GMP-compatible Gene Editing Process Enables a Versatile iMAC Platform

Evotec’s modular GMP-compatible Gene Editing Process enables a versatile iMAC Platform
  1. Customizable exchangeable CAR for target specificity or combination with Immune Cell Engager (ICE) 
  2. Depletion of MHC surface display to prevent allorejection via T cells
  3. Inhibitory mechanism to prevent allorejection from NK cells  
  4. Further knock-ins to enhance function
  5. Safety switch for therapeutic intervention

Evotec’s Internal iMAC Programs

Evotec is currently developing two iMAC product candidates:

  1. Immune-shielded CAR-iMAC to treat fibrosis with a focus on liver and lung fibrosis
  2. Unedited iMAC to treat infections with a follow-up option including a CAR and/or anti-microbial edits
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.