Fast-track NASH drug discovery with organ-on-a-chip studies
Our Non-Alcoholic Fatty Liver Disorder (NAFLD)/NASH In Vitro Services offer a preclinical tool to test therapeutics in a human-relevant model, replicating key clinical biomarkers to allow translatability to clinical trials.
Service overview:
We offer a collaborative approach, applying our extensive NASH expertise to designing an experiment that best suits your needs. Our established NAFLD/NASH assay can be adapted to investigate specific questions, focus on different endpoints, or provide samples for -omics analysis.
- Explore or validate the effect of your therapeutic in an industry-validated model
- Uses validated cells with known NASH-related genotypes
- Capture clinical markers with proven translatability
- Assess inflammation, fibrosis, steatosis, and cell health biomarkers
- Option to add -omics analysis of samples
- Full project report detailing methods and results and all raw data
Customer feedback
Working with CN Bio has been a pleasure, the team listened to our non-trivial requirements and made useful suggestions to help meet objectives. During the course of the project, the team were responsive and helpful. The results were delivered as agreed and helped us to move towards our goals.
Dr Giuseppe Ferrandino
Senior Translational Scientist at Owlstone Medical
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Inipharm is developing a drug that targets a genetic metabolic target which has metabolomics differences between mice and men. For this reason, we evaluated several different primary human testing systems that have features of NASH. We found CN Bio has developed a system that has steatotic, inflammatory, and fibrotic features that have been very useful in evaluating our lead compounds. The scientists at CN Bio are very knowledgeable and have worked with us on the study details to obtain the best quality of results in a timely manner.
Heather Hsu
Chief Scientific Officer, Inipharm
View more PhysioMimix reviews on SelectScience
How the service works:
Through the co-culture of primary human hepatocytes and non-parenchymal cells and the evaluation of multiple endpoints, our assay offers a complete assessment of NASH drug efficacy.
This service generates human-relevant data that captures the key pathophysiology of NASH, providing a complementary approach to murine models.
Your dedicated contact will work collaboratively with you from the start to the end of the project.
- Design and finalize experiment plan
- Customer supplies required amount of drug(s)
- Three to four weeks to complete cell culture
- Two to three weeks to run endpoint assays, analyze data and complete the report
- ~ two months to complete the study from receiving an order
Standard NASH cell culture timeline
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