Skip to content

NHP iPSC-derived cardiomyocytes for translational cardiac safety

Non-human primate iPSC-derived cardiomyocytes offer translational insight for early cardiac safety assessment
Download now
Screenshot 2026-08-21 at 1.59.57 PM

This poster presents Ncardia’s non-human primate (NHP) iPSC-derived ventricular cardiomyocyte platform, developed to help bridge in vivo NHP studies and human in vitro cardiac data and support translational interpretation of cardiac safety findings.

Download it now for a closer look at:

  • How NHP iPSC-derived cardiomyocytes can be manufactured at large scale while maintaining high purity, ventricular identity and stable functional performance
  • Acute MEA data showing electrophysiological responses to reference compounds including quinidine, moxifloxacin, BayK8644, dofetilide and nifedipine
  • How sub-chronic exposure to sunitinib, doxorubicin and pentamidine reveals concentration- and time-dependent changes in field potential duration and beat rate
  • How the model captures both acute ion-channel effects and delayed cardiac liabilities, including trafficking-mediated proarrhythmic responses
  • How NHP iPSC-derived cardiomyocytes can support the interpretation of species-related differences between preclinical in vivo studies and human in vitro findings

Download the Poster



Get the Poster Now!

Whether you are investigating differences between preclinical and human findings or evaluating cardiac liabilities across species, this platform provides a scalable, reproducible NHP cardiomyocyte model for translational cardiac safety studies. 

Download the poster by filling out the form below: