A Breakthrough Platform That Goes Where Others Can’t

Safe, targeted gene therapy — delivered directly to the brain.

Most therapies can’t effectively reach the brain. Our platform combines precision gene editing, RNA therapeutics, and an intranasal delivery system to bypass the brain’s protective blood barriers.

CRISPR-based Prime Editing

Repairs DNA mutations with unmatched accuracy — without cutting. Designed to minimize off-target effects for safer gene therapy.

RNA Formulations

Enables precise and intended gene expression with targeted control to treat complex neurological conditions like Alzheimer’s and Parkinson’s.

Intranasal Nano-Delivery

Delivers prophylactic and therapeutic agents directly to targeted brain cells—bypassing invasive injections and minimizing systemic side effects and off-target risks.

Precise Gene Editing

CRISPR-based prime editing system targets genetic mutations with high precision by introducing biologics known as the prime editors, to the intended site enabling safer and more efficient genome modification.

Science That Reaches the Brain

Our patented intranasal nano-delivery system bypasses the blood-brain barrier to deliver treatment directly—no injections required.

From Lab Bench to Bedside

We work with globally recognized scientists to turn clinical research into therapies that transform patient outcomes.

A New Standard in Precision Gene Therapy

NanoMedX’s advanced nanocarrier achieves over 98.67% transfection efficiency in preclinical murine models—far surpassing the 5–30% seen with traditional lipid nanoparticles (LNPs).

98.67%

Transfection success rate using NanoMedX's nano-delivery system

37.94%

LNP transfection rate in the same model

Partner With Us to Bring Groundbreaking Therapies to Life

Join us in transforming neurological care through co-development, licensing, or investment. Let’s solve the unsolved—together.