Century Therapeutics Announces Upcoming Poster Presentations at the 2024 American Society of Hematology (ASH) Annual Meeting

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Century Therapeutics, Inc.
Century Therapeutics, Inc.

– Company to share preclinical data across diverse pipeline of iNK, γδ iT, and αβ iT cell therapy programs for oncology and autoimmune disease (AID) –

– Preclinical data on development of iPSC-derived CD4+ and CD8+ CAR T cells that demonstrate function comparable to primary αβ CAR-T cells, allowing for control of tumors in vivo without the need for exogenous or engineered cytokines

– Posters include demonstration of advances in gene editing and transgene design that enable greater control and improved functionality of iPSC derived immune cells –

PHILADELPHIA, Nov. 05, 2024 (GLOBE NEWSWIRE) -- Century Therapeutics (NASDAQ: IPSC), an innovative biotechnology company developing induced pluripotent stem cell (iPSC)-derived cell therapies in immuno-oncology and autoimmune disease, today announced that preclinical data from the Company’s iPSC-derived cell therapy platform will be presented in five posters at the 2024 ASH Annual Meeting to be held in San Diego, CA from December 7-10, 2024.

“We are pleased to spotlight continued achievement across our pre-clinical pipeline as we develop a diverse portfolio of iNK, γδ iT, and αβ iT-cell programs spanning oncology and autoimmune diseases,” said Chad Cowan, Ph.D., Chief Scientific Officer at Century Therapeutics. “Most notably, we will be showcasing what we believe to be the first iPSC-derived CD4+ and CD8+ CAR T cells that demonstrate function comparable to primary αβ CAR-T cells. The engineerability of iPSC-derived immune effector cells, which is a core benefit of the Company’s platform, will also be highlighted at ASH. This includes data relating to our enhanced Allo-Evasion™ via a novel CD300a TASR that demonstrated universal protection from NK cells, advanced CAR endo-domains that improve cytotoxicity and persistence, and differentiation-stage-specific promoters that allow for selective control of gene expression. Furthermore, we are encouraged by data demonstrating our CAR iNK and γδ iT cells’ potent preclinical ability to treat B-cell-mediated autoimmune diseases. We believe the breadth of these pre-clinical findings further underscores the compelling rationale behind our iPSC-derived cell therapies across multiple indications.”

Details of the posters being presented are as follows:

Successful Generation of iPSC-Derived CD4+ and CD8+ CAR T Cells with αβ-like T Cell Function, Including Antigen-Dependent Expansion and IL-2 Production
Publication Number4819
Session Title703. Cellular Immunotherapies Other than CAR-T Cells: Basic and Translational: Poster III
Session Date & TimeMonday, December 9, 2024, at 6:00 PM - 8:00 PM PT