
Drug testing
Reproducible human tissue and organoid models for toxicity and efficacy testing, aligned with FDA's shift toward New Approach Methodologies (NAMs).
AI that predicts how to grow human tissue, and learns from every experiment.

Built on open science
Protein models learned biology from sequences [1, 2]. For tissue, the sequence is a recipe.
A differentiation protocol can take months or years of manual experiments to optimize. [11]
Cells, scaffold, stiffness, growth factors, dose and timing all interact. One retinal protocol had about 200 million possible conditions. [11]
Outcomes sit in thousands of papers, recorded in incompatible ways. No general model of tissue formation exists yet. [10]
A tissue recipe, position by position
CCells
source, ratio, passage
SScaffold
chemistry, stiffness, pore size
MMechanics
strain, frequency, flow
GSignals
growth factors, dose
TTiming
order, duration, oxygen
Specify the tissue, such as cartilage, liver or cardiac muscle, and the properties it must have.
Models propose ranked recipes (cells, scaffold, mechanics and a growth-factor schedule), each with a confidence score.
Recipes run on automated lab hardware. Outcomes are measured by imaging, single-cell and spatial sequencing, and functional assays.
Results feed back into the model through Bayesian optimization, so each experiment makes the next prediction better.
Public atlases for breadth, and our own standardized experiment data for depth.
Open models that already understand proteins, cells and tissue neighborhoods, used as building blocks.
The model that turns a target tissue into ranked recipes and chooses which experiments to run next.
Automated hardware that runs the recipes the engine proposes and measures what grows.

Reproducible human tissue and organoid models for toxicity and efficacy testing, aligned with FDA's shift toward New Approach Methodologies (NAMs).

Faster protocol development for cartilage, skin, bone and vessels, and eventually organ tissue.

Grow diseased tissue, such as fibrotic tissue or a tumor microenvironment, to study mechanisms in human cells.

Patient-derived tissue, grown reliably enough to test which treatment works for that patient.
Regulatory pull
The FDA Modernization Act 2.0 removed the requirement in 2022. FDA's 2025 roadmap names organoids, organ chips and AI models as alternatives, aiming to make animal studies the exception within three to five years. [17, 18]
Model pull
For proteins (Biohub's ESM family), single cells (Geneformer, scGPT) and spatial data (Nicheformer). A tissue model can build on them. [4, 5, 6, 8]
Proof of concept
RIKEN searched about 200 million culture conditions and improved retinal pigment epithelium production by 88%. A third-party result, on one cell type. [11]
Field roadmap
Leading researchers have set out how to build AI models of cells that span molecules, cells and tissues. [10]
Five stages, from a recipe language to a platform across tissues.
01 · We are here
A standard way to record cells, scaffold, mechanics, signals and timing, seeded from public atlases.
02 · Next
Trained on public data and scored against published protocols.
03 · Later
Recipes run on automated hardware with a partner lab.
04 · Later
A reproducible human tissue model for drug testing.
05 · Later
Each new tissue starts from what the engine has already learned.
We are early stage, working on stage 01.
We are early stage. We are building the recipe language and the data foundation first, then the first recipe model. We will publish results as we have them.
We will choose them with our first partners. Human tissue models for drug testing, such as liver, are the lead use case.
Tell us the tissue you need and what it has to do. We scope a first project together from there.
FDA's roadmap names organoids, organ chips and AI models as alternatives to animal testing. Whether a specific model is accepted depends on its validation, which is part of what we are building toward. [18]
For pharma R&D teams, tissue engineering labs and investors who want to work with us from the start.
