Across neurodegeneration, oncology, and epilepsy—the underlying driver is metabolic. We're building the first platform to control it.
In Alzheimer's disease, FDG-PET shows glucose hypometabolism decades before symptoms appear. The brain is energy-starved long before plaques accumulate.
In immuno-oncology, 75–85% of patients don't respond to checkpoint inhibitors. The reason: T-cells exhaust in the metabolically hostile tumor microenvironment—they can't fuel themselves when tumor cells monopolize glucose.
In drug-resistant epilepsy, 30% of patients fail all medications. Yet metabolic intervention—the ketogenic diet—achieves 50–90% seizure reduction.
These are not three diseases. They are three manifestations of the same problem.
What if the drugs aren't failing? What if they're being deployed into the wrong metabolic state?