< 5 min
Onset objective via intranasal CNS targeting
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.
Onset objective via intranasal CNS targeting
Catalytic turnover modulation over receptor blockade
State-management deployment, not chronic suppression
A coordinated translational architecture for delivery, safety, and responder precision.
Intranasal perineural transport through olfactory and trigeminal pathways is designed to align onset timing with acute phasic demand.
Soft-drug architecture supports bounded central activity with peripheral inactivation logic to reduce sustained off-target exposure risk.
Responder identification is anchored to kinetic mismatch signatures, including the Sensory-Autonomic Triad phenotype for cleaner cohort selection.
Therapeutics designed to work with endogenous clearance machinery to constrain signal radius and dwell-time, while preserving task-relevant phasic fidelity.