Transforming Mental Health

in the Genetic Age

Precision Neurogenetics for a New Era in Mental Health

Cognigenics is developing the first RNAi-based therapeutics for psychiatry—engineered for precise, reversible modulation of neural circuits.

Our lead candidate in development, COG-301, is a short-interfering RNA (siRNA) therapeutic, delivered via lipid nanoparticles (LNPs) and administered intranasally. COG-301 is designed to selectively downregulate 5-HT2a receptor expression in targeted brain regions implicated in the limbic hyperactivity associated with anxiety and psychosis in Parkinson’s Disease Psychosis (PDP).

With intended weekly dosing, COG-301, based on promising preclinical results, aims to provide durable, non-sedating symptom relief while preserving cognitive function. The therapy is being developed for self-administration and cold storage at home, offering a potential alternative to current systemic treatments.

WHY IT MATTERS

Small-molecule drugs, a legacy technology developed over a century ago, rely on protein binding and often affect multiple receptor systems indiscriminately, leading to sedation, emotional blunting, and metabolic side effects. At Cognigenics, we are advancing a new era of neuropsychiatric treatment with RNA therapeutics that act upstream at the mRNA level, enabling precise, durable, and cell-specific modulation of neural targets. This approach results in fewer off-target effects, improved tolerability, and non-sedating, next-generation interventions.

COGNIGENICS

Our approach targets a single validated receptor, 5-HT2a, using siRNA-mediated gene silencing that reduces polypharmacy risk.

THERAPEUTIC AND COMMERCIAL CASE RESULTS THAT SET A NEW STANDARD

In our previous preclinical models of anxiety and perceptual dysregulation, COG-201, an shRNA neuromodulator outperformed leading pharmaceutical benchmarks on both behavioral and electrophysiological endpoints. Our therapy demonstrated:

  • Improved memory and anxiety outcomes
  • Appears to be well tolerated with no observed off-target effects
  • Regionally selective silencing of target genes

These results, validated by third-party laboratories, lay the foundation for a first-in-class RNAi therapeutic in psychiatry, backed by a delivery system that is scalable, targeted, and regulatory-track ready.

Developing Therapeutics with Speed and Precision

Cognigenics operates with a lean, translational model. It outsources manufacturing, safety, and toxicology to world-class CROs and CMOs while maintaining scientific leadership in target design, formulation, and delivery. This accelerates timelines and reduces burn without compromising rigor.

We’re not just building drugs. We’re building a platform for scalable, precision psychiatry in the Genetic Age.

COMPETITION

Attributes

Today’s Pharma (SSRIs)

Cognigenics COG-201

Efficacy

Shows limited effectiveness; often compared to a “sledgehammer” strategy with widespread systemic impact.

Delivers high precision in targeting specific
neuronal receptors, ensuring optimal effectiveness.

Tolerance

Associated with significant side effects, leading to patient withdrawal or resistance to treatment.

Experimental results to date reveal no significant side effects, indicating high tolerance.

Technology

Based on monomolecular compounds such as Xanax, Valium, Librium, Klonopin
(developed in the 1990s).

Utilizes advanced neurogenetic modulation technology, reflecting recent, cutting-edge developments in RNA therapeutics.

Business

Characterized by massive overhead costs including facilities, staff, and internal laboratories; typically slow, risk-averse, and established.

Operates with minimal overhead, leveraging Contract Research Organizations (CROs) and Contract Manufacturing Organizations (CMOs); known for its rapid, entrepreneurial approach and disruptive impact in the field.

Regulatory Disclaimer
This product is currently under development and has not been approved for sale or distribution in the United States. It is not available for purchase or use and has not been evaluated by the U.S. Food and Drug Administration (FDA) for safety or efficacy. For informational purposes only.