Organamet Bio is advancing a sequential pipeline of bioengineered therapy candidates across the full spectrum of heart failure — led by Lami-Pro™, being developed as a potential first disease-modifying biologic for heart failure with preserved ejection fraction (HFpEF), a condition with no approved disease-modifying therapy today.
Our founding vision — a fully bioengineered, patient-specific heart — remains the endgame. But great science reaches patients only when it is sequenced wisely.
Organamet leads with the fastest, most capital-efficient product in our portfolio: Lami-Pro™, an injectable biologic for HFpEF. It reaches the clinic first, validates our intellectual-property platform, and generates the licensing revenue that funds and de-risks the larger prizes behind it — Ventri-Pro™ and Your-Heart™.
Why lead with Lami-Pro™? →One regenerative platform, anchored by the decellularization and bioengineering patents of Dr. Doris Taylor.
An injectable, patent-pending biologic delivered into cardiac muscle — designed to restore native proteins, reduce inflammation and fibrosis, and improve relaxation. Designed as a one-time treatment intended to reverse underlying disease processes.
A bioengineered cardiac-derived patch designed to slow dilated (HFrEF) heart-failure progression — intended to stabilize the heart, promote vascularization, and support an environment for regeneration before irreversible damage.
A fully bioengineered, patient-specific heart built from a patient's own cells — designed to reduce or eliminate the need for immunosuppression and to address the donor-supply ceiling. Our long-term aspiration for end-stage heart failure.
All Organamet Bio product candidates are investigational, have not been approved by FDA or any regulatory authority, and their safety and effectiveness have not been established.
Heart failure is the leading cause of death globally — and its largest segment has no disease-modifying therapy at all.