HeartReady™ — a living cellular therapy, delivered into post-MI scar.
We grow mature, manufacturable human cardiomyocytes designed to engraft and restore function in post‑MI scar. Clinical translation and manufacturing readiness are core to the program.
Dead muscle becomes scar — stiff, silent, permanent. The unmet need: post-MI scar & ischemic heart failure.
One iPSC becomes a mature ventricular cardiomyocyte: strong cardiac markers, adult-grade electrophysiology, oxidative metabolism. Anyone can grow a cell. The defensible asset is the route — the media, the timing, and the manufacturing — that does it reproducibly, at scale.
The signaling cocktail — growth factors, small molecules, timing — that drives a stem cell into a beating ventricular cardiomyocyte.
Methods · MediaThe follow-up step that takes immature cells to adult-grade electrophysiology — the safety unlock for the field.
The safety unlock3D suspension bioreactor process with minimal batch-to-batch variability, end-to-end process analytics, and advanced cryopreservation.
3L → 15L scaleThe platform turns CardioVive data into actionable insight. BioEngineAI ingests imaging, motion, sequencing, electrophysiology and bioprocess telemetry into a unified, queryable model.
Our first commercial tissue wedge: iPSC-derived cardiac assembloids with functional chambers, electrical activity, and resident immune cells — predictive of human pharmacology where animal models fail. CardioVive is the data engine that powers BioEngineAI analytics.
The cell-therapy field is independently validated by the world's leading cardiac labs. Our own platform doesn't rest on a pitch — it rests on peer-reviewed publications underpinning every layer of the stack.
~40% of the infarct remuscularized with electromechanical coupling.
Intramyocardial delivery → +10–12 point gain in LVEF at 12 weeks.
Purified, matured cells → durable engraftment; transient arrhythmia resolved by week 2.
n=2, alive at 4 years · LVEF improved · NYHA IV→II · no tumors.
The foundational protocol — organoids with atrial, ventricular & proepicardial regions that benchmark to 6–13-week human hearts.
Defined cell-type ratios and adult-grade electrophysiology — the maturation step that is the safety unlock for the field.
Modeling fetal cardiac development and SSRI cardiotoxicity in a neural-crest-integrated assembloid.
CardioPhage™ biology — TRMPs integrate via Cx43 gap junctions, persist 60+ days, and improve cardiac maturation.
Commercial demand is outpacing our current capacity.
A compact executive team engineers biology, analytics, and process, while advisors and consultants accelerate commercial launch, manufacturing, and translational validation.
Backed by · Johnson & Johnson JLABS · BioEngineAI™ · NVIDIA Inception · AWS · NIH · AHA · NSF · MSU Research Foundation · Red Cedar Ventures
6.7 million Americans. Half dead within five years — not waiting for another drug, but for new muscle.