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Predicting Human Liver Injury
Before It Reaches a Patient

Xellar’s Liver-on-a-Chip delivers mechanism-anchored, human-relevant DILI data — validated across 100+ compounds — so you can identify hepatotoxicity risk early, protect your clinical program, and move forward with confidence.

Animal models miss 50% of human DILI.
Standard panels miss the mechanism. You need human-relevant data — not an extrapolation.

The Challenge

Traditional Models Cannot Predict Human DILI

Hepatotoxicity is one of the most common — and most preventable — causes of clinical program failure. The models most teams rely on simply aren’t built for human liver biology.

The Xellar Liver-on-a-Chip

One Chip. Four Cell Types. The Liver as It Actually Works.

The Xellar DILI platform co-cultures primary human hepatocytes with liver sinusoidal endothelial cells, stellate cells, and Kupffer cells on OC-PLEX 32 & OC-PLEX 96 — reconstituting the liver microenvironment to generate mechanism-anchored, pharma-grade safety data.

Three Ways to Work With Xellar

Match the Assessment to Where Your Program Is Today

From rapid early-stage screening to IND-ready regulatory packages — choose the level of assessment your program needs.

The Xellar DILI Platform: Four Integrated Layers

This isn’t a DILI assay. It’s a DILI intelligence platform — four layers working together to deliver mechanism-anchored, decision-quality safety data.

DILI Assessment Workflow

From Compound Submission to Risk Report in 28 Days

A streamlined, end-to-end workflow — you ship your compounds, we deliver actionable DILI intelligence.

Why Xellar

The Platform That Outperforms Every Alternative

“We already run hepatocyte assays — why do we need this?” Here is what you’re missing.

Let’s Protect Your Next Program

A fraction of the cost of a Phase I surprise. A fraction of the time of a clinical hold.

Get Started

Your Compound Is Ready to Be Tested. So Are We.

Xellar offers a complimentary DILI Risk Review for your lead compound — a 30-minute conversation with our science team to assess your current safety data and identify where our platform can reduce your clinical risk.

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