Mechanism: Social threat and stress circuits are overactive; V1b antagonism may reduce amygdala to HPA overdrive and excessive fear learning.
Severity: Avoidance of school, dating, and work; isolation; higher depression and substance use; lower earnings and quality of life.
US Demographics: About 15-20 million adults; often begins in adolescence and persists for years.
NILU-002
Limerence
V1aR Antagonist
Discovery
Pre-Clinical
Phase I-II
Phase III
Mechanism: V1a signaling can lock intrusive romantic salience and jealousy loops; antagonism aims to reduce obsessive attachment and stress coupling.
Severity: Obsessions, insomnia, anxiety, impaired focus and work, impulsive choices that harm relationships and finances.
US Demographics: No formal count; clinically severe cases are modeled at roughly 1-3 million with major functional impairment.
NILU-003
Peri-Op Cognitive Disorder
PDE4/PDE10 Inhibitor, MIF Antagonist
Discovery
Pre-Clinical
Phase I-II
Phase III
Mechanism: Open chest surgeries can trigger neuroinflammation, microglial activation, and microvascular injury; our drug is proven to lower proinflammatory cytokines, suppresses microglia, and supports neurotrophic pathways.
Severity: Memory and attention problems, slower processing, mood changes, loss of independence, reduced employability, increased hospitalization cost, caregiver burden.
US Demographics: About 150-200k CABG procedures each year; persistent impairment in 10-20 percent, or about 15-40k new patients annually.
NILU-004
Visual Snow Subtype
ASIC1a Antagonist
Discovery
Pre-Clinical
Phase I-II
Phase III
Mechanism: ASIC1a overactivity may sustain cortical hyperexcitability and abnormal sensory gain; antagonism targets normalization of thalamocortical signaling.
Severity: Constant, debilitating visual static with intrusive tinnitus; poor sleep; anxiety; lower productivity; social withdrawal and depressed mood.
US Demographics: Estimated 100-200k individuals.
NILU-005
DNA-Protectant
Polyamine Analog
Discovery
Pre-Clinical
Phase I-II
Phase III
Mechanism: Tautomeric proton shifts cause base mispairing and raise DNA mutation rate; this analog aims to stabilize base pairing and reduce replication errors.
Severity: Genomic instability drives cancer, neurodegeneration, and faster biological aging, reducing independence and mental well being.
US Demographics: Universal in principle; every person accrues mutations. Older adults 65 plus, about 62 million, face the highest annual burden.