Abstract 4365373: An Innovative Human iPSC Cardiomyocyte Platform to Accelerate Cardiac Drug Discovery and Target Validation

B Benjamin Fsicher (Evotec SE, Hamburg, Germany) H Hanna Schubert (Evotec SE, Hamburg, Germany) F Fatima Kahlid (Evotec SE, Hamburg, Germany) K Kamran Honarnejad (Evotec SE, Hamburg, Germany) S Shadaan Zulfiqar (Evotec SE, Hamburg, Germany) C Caroline Imse (Evotec SE, Hamburg, Germany) S Sophie Luellau (Evotec SE, Hamburg, Germany) A Ambuj Gore (Evotec SE, Hamburg, Germany) C Claudia Ploetzky (Evotec SE, Hamburg, Germany) A Anna Carbone (Evotec SE, Hamburg, Germany) D Doerte Fust (Evotec SE, Hamburg, Germany) S Sandra Lubitz (Evotec SE, Hamburg, Germany) B Bastian Zimmer (Evotec SE, Hamburg, Germany)

Abstract

Background: Effective treatment of cardiac diseases requires a deep understanding of disease-relevant cellular mechanisms that drive pathology in the human heart. Traditional cell lines often lack the complexity and genetic context necessary to capture these mechanisms. Human induced pluripotent stem cell (iPSC)-derived cardiomyocytes provide a physiologically relevant and genetically diverse platform to model human cardiac disease biology. Evotec’s iPSC platform enables detailed study of disease processes critical for identifying therapeutic targets and developing novel treatments. Methods&Results: We developed a robust, scalable human iPSC-based cardiomyocyte platform integrating a genetically diverse bank of well-characterized iPSC lines and optimized cardiac differentiation protocols. The platform enables the generation of multiple human-relevant cardiac cell types and model systems, including cardiomyocytes, cardiac fibroblasts, 2D co-cultures of these cell types, 3D cardiac spheroids, and engineered heart tissue (EHT). Genome editing technologies, including CRISPR/Cas9 and RNA interference, are routinely applied at both iPSC and cardiomyocyte stages. These tools enable the introduction of disease-relevant mutations to model specific cardiac pathologies, as well as the validation and exploration of novel target gene functions within a human cellular context. To assess disease mechanisms and potential target effects, we use multi-electrode arrays (MEA) for electrophysiology, xCELLigence and FlexCyte for contractility, and calcium transient assays. This enables high-throughput, quantitative, and physiologically relevant phenotyping. Pharmacological testing with well-characterized compounds confirms the platform’s sensitivity to cardiac functional changes. Conclusion: Evotec’s iPSC cardiomyocyte platform, combined with the Evotec Heart Atlas, offers a human-relevant system for cardiac disease modeling, drug target validation, and mechanistic insights. Together, these platforms accelerate cardiovascular therapy discovery and increase clinical success through improved human and disease relevance.

Article Details

Journal Circulation
Volume / Issue Vol. 152, Issue Suppl_3
Published November 04, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (13)

B

Benjamin Fsicher

Evotec SE, Hamburg, Germany

H

Hanna Schubert

Evotec SE, Hamburg, Germany

F

Fatima Kahlid

Evotec SE, Hamburg, Germany

K

Kamran Honarnejad

Evotec SE, Hamburg, Germany

S

Shadaan Zulfiqar

Evotec SE, Hamburg, Germany

C

Caroline Imse

Evotec SE, Hamburg, Germany

S

Sophie Luellau

Evotec SE, Hamburg, Germany

A

Ambuj Gore

Evotec SE, Hamburg, Germany

C

Claudia Ploetzky

Evotec SE, Hamburg, Germany

A

Anna Carbone

Evotec SE, Hamburg, Germany

D

Doerte Fust

Evotec SE, Hamburg, Germany

S

Sandra Lubitz

Evotec SE, Hamburg, Germany

B

Bastian Zimmer

Evotec SE, Hamburg, Germany