CardioVive™
Proprietary cardiac biology. Ground truth no competitor can source.
HeartReady™ — a living cellular therapy, delivered into post-MI scar.
Data generation → AI monetization → venture-scale optionality.
Proprietary cardiac biology. Ground truth no competitor can source.
Analytics licenses selling today. 80% gross margin.
Allogeneic cell therapy for ischemic heart disease.
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. CytoHub.AI 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 CytoHub.AI 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 · CytoHub.AI™ · 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.