A two-component botanical drug candidate targeting immunosenescence and metabolic-mitochondrial decline. One component protects surviving cells; the other renews mitochondrial and stem-cell reserve. Advancing through the FDA Botanical Drug pathway.
Progressive loss of immune competence after age 55 drives multi-morbidity, infectious susceptibility, and accelerated biological aging — affecting more than 1.5 billion people globally.
No approved therapeutic simultaneously addresses the root mechanisms: oxidative stress driving aging, hematopoietic decline, chronic inflammaging, and failure of adaptive hormetic defenses.
NMN, resveratrol, and NAD+ products lead the category but lack patent protection, mechanistic precision, or validated clinical rationale.
The healthspan economy is enormous and still searching for its defining, defensible product.
One component protects the aging cell — antioxidant, anti-inflammatory, reserve-sparing. The other renews it — mitochondrial biogenesis, senescence delay. The specific combination, not any single known ingredient, is the inventive core.
Lowers ROS, MDA, AGEs; raises glutathione — reducing the oxidative damage that drives immunological aging.
Lowers IL-6, IL-8, IL-1β — suppressing the chronic low-grade inflammation that accelerates immune decline.
Normalizes immune indices under suppression — sparing and restoring the body's residual immune competence.
Activates PGC-1α / SIRT1 / TFAM axis — restores mitochondrial mass, membrane potential, and ATP under oxidative stress.
Protects quiescent hematopoietic stem cells from oxidative attrition via DNA-repair (PARP-1) — preserving the long-term immune-hematopoietic reserve.
Primary base protects existing mitochondria from oxidative damage; second component builds new ones. Supra-additive synergy pending combination study.
IP protection covers the specific two-component formulation, ratio, preparation method, and oral form. Defensibility rests on the specific combination — not any single publicly-known component.
1,000+ subjects studied in cyclophosphamide myelosuppression models. A 4-group mechanistic study and Colby synergy validation are planned, alongside a D-galactose aging model validation in Phase 1.
FDA Botanical Drug Guidance (2016) pathway toward IND for the aging indication. Free of cyanogenic glycosides; ICH Q1A(R2) 12-month stability claimed.
Serial entrepreneur with 15 years in banking and venture-building. Concurrently CEO of Immune-G Ltd. and DetentionPro.
Healthcare specialist leading preclinical research and formulation development.
Focused on botanical pharmacology and hematopoietic research underlying the platform's mechanism work.
Patent filed. FDA Botanical Drug pathway. We're sharing materials with investors who think about aging biology and execution-stage de-risking the same way we do.