IMMUNOTHERAPY

Harnessing Engineered iPSC-Derived Immune Cells (Monocytes) to Eliminate Solid Tumors

Programmable, multi-functional immune cells that recognize, engage and eradicate tumors while activating broader anti-tumor immunity.

Proof of Concept

In collaboration with NTU, Singapore

Engineered immune cell engaging a tumor

From Engineering to Anti-Tumor Activity

Cluster of iPSCs

iPSCs

CARTumor targetingInterleukinInterferon

Multi-gene program

Engineered iPSC

Engineered iPSCs

With CAR, IL and IFN

Differentiated immune cells

iPSC-derived Monocytes / Macrophages

Immune cell engaging a tumor cell

Tumor engagement

Tumor killing

Direct anti-tumor activity, e.g., CAR-mediated.

Phagocytosis

Engulf and clear tumor cells.

Antigen presentation

Activate T cells and NK cells for a broader anti-tumor response.

Key Benefits

Targeted & potent
anti-tumor activity

Multi-functional
(kill, phagocytose, activate immunity)

Programmable
(e.g., CAR, IL, IFN combinations)

Off-the-shelf & scalable
(iPSC-based)

One Engineering Platform. Multiple Immune Cell Possibilities.

Current proof of conceptMonocytes / Macrophages

Potential applicationOther immune cellse.g., NK cells, T cells, dendritic cells

Our Immunotherapy Pipeline

iPSC-derived CAR-MFor HER2-positive solid cancersIn collaboration with NTU, Singapore

Preclinical
Current stage
IND EnablingClinicalCommercial