Kinetic Precision in
Neurotherapeutics

A first-in-class NET positive allosteric modulation program targeting the kinetics of synaptic clearance, rather than the volume of neurotransmitter presence.

Current treatment paradigms primarily manipulate concentration. Our framework targets processing efficiency within endogenous clearance pathways.

< 5 min

Onset objective via intranasal CNS targeting

kcat

Catalytic turnover modulation over receptor blockade

Pulsatile

State-management deployment, not chronic suppression

Three Program Pillars

A coordinated translational architecture for delivery, safety, and responder precision.

I

Direct CNS Targeting

Intranasal perineural transport through olfactory and trigeminal pathways is designed to align onset timing with acute phasic demand.

II

Retrometabolic Safety

Soft-drug architecture supports bounded central activity with peripheral inactivation logic to reduce sustained off-target exposure risk.

III

Biomarker Stratification

Responder identification is anchored to kinetic mismatch signatures, including the Sensory-Autonomic Triad phenotype for cleaner cohort selection.

From chronic suppression to acute restoration.

Therapeutics designed to work with endogenous clearance machinery to constrain signal radius and dwell-time, while preserving task-relevant phasic fidelity.