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Toxicology and Safety Pharmacology

Lower Risk Development Stems From Ncardia

When you need to increase confidence in your preclinical toxicology and safety pharmacology studies, partner with Ncardia, the proven iPSC experts.

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Cardiotoxicity Testing

Cardiotoxicity is a common cause of late-stage failures or postmarket withdrawals, making iPSC-derived cardiovascular cells essential tools for predicting and assessing cardiac risk before clinical trials.

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Cardiac Toxicology and Safety Pharmacology Assays

We offer a range of cardiac toxicology and safety assays — including custom assays — using iPSC-derived cardiomyocytes, enabling comprehensive evaluation of drug-induced heart effects in support of regulatory compliance and safer drug development:

  • Assays can be multiplexed for functional and structural cardiotoxicity assessments
  • Noninvasive assays allow both acute and chronic studies
Proliferation, adhesion & cell loss IncuCyte, ImageXpress Confocal, xCELLigence RTCA Cardio, CardioExcyte 96, Cytation
Gene expression BioRad Opus 384 qPCR, RNAseq, whole genome sequencing
Protein expression Western Blot, Spark Multimode Microplate Reader, NovoCyte Flow Cytometer, ImageXpress Confocal, MSD MESO Sector 600MM, Cytation
E-phys (MEA) Maestro MEA, CardioExcyte 96, LUMOS
Ca2+ transients FDSS µCell
Contractility xCELLigence RTCA Cardio, CardioExcyte 96
Metabolism assays Spark Multimode Microplate Reader (w/ Agilent MitoXpress), ImageXpress Confocal, Cytation (w/ mitochondrial dyes)

Neurotoxicity Assessments

Neural tissues are complex, sensitive and often slow to recover from injury, making neurotoxicity and safety pharmacology testing critical.

iPSC-derived neurons offer a highly relevant human-based platform for detecting and studying these toxic effects before they reach patients, supporting early detection of neurotoxic risks such as disrupted neurotransmission, dendritic damage or cell death, which may not be evident in traditional animal studies.

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Neurotoxicology Toxicology and Safety Pharmacology Assays

Ncardia’s customizable iPSC-based neurotoxicology and safety assay capabilities cover a spectrum of functional, structural and biochemical endpoints to detect subtle neural damage — improving the predictive power of safety evaluations:

  • Assays can be multiplexed for functional and structural cardiotoxicity assessments
  • Noninvasive assays allow both acute and chronic studies
Proliferation, adhesion & cell loss IncuCyte, ImageXpress Confocal, CardioExcyte 96, ECIS Z-Theta
Gene expression BioRad Opus 384 qPCR, RNAseq, whole genome sequencing
Protein expression Western Blot, Spark Multimode Microplate Reader, NovoCyte Flow Cytometer, ImageXpress Confocal, MSD MESO Sector 600MM
Metabolism Spark Multimode Microplate Reader, NovoCyte Flow Cytometer, ImageXpress Confocal
E-phys (MEA) Maestro MEA, LUMOS
Ca2+ transients FDSS µCell
Metabolism assays Spark Multimode Microplate Reader, NovoCyte Flow Cytometer, ImageXpress Confocal

Use Cardiotoxcitiy Testing to Select Preclinical Candidates

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When used in drug discovery, iPSC-based assays improve drug safety profiles and reduce costly failures by helping you:

  • Screen for safety more efficiently
  • Reduce your reliance on animal models
  • Better anticipate patient-specific vulnerabilities

Want a closer look at how cardiotoxicity testing supports drug discovery?

Use iPSC-Derived Neural Assays to Optimize Safety Pipelines

When used in drug discovery, iPSC-based neural assays enable more predictive, patient-specific evaluations, reduce reliance on less-representative models and support the development of safer therapeutics and chemicals.

  • Ncardia has developed a translational calcium assay for predicting in vivo toxicity based on iPSC derived human neuronal co-cultures.
  • Acute tolerability scores in mice correlate highly with calcium oscillation scores in human iPSC derived neurons (r2 > 0.8).
  • Assay is robust and scalable (384 well format) to enable assessment of your ASOs at any stage of the drug discovery process.

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Partner With the Proven iPSC Experts

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