Transforming Mental Health
in the Genetic Age

Cognigenics is pioneering the first non-invasive genetic medicine for the brain, using intranasal RNAi to precisely silence disease‑driving genes and restore neural balance in psychiatric and neurodegenerative disorders.
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 conjugates 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.
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.

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.
Our Science
Neuronal Hyperactivity in various brain regions is associated with anxiety, depression, and other neurocognitive disorders and psychiatric conditions.

Article by Dean Radin, Ph.D., Chairman and Co-founder
in Springer Nature | Resarch Communities
Toward a new class of genetic therapeutics for mental health disorders
Read Article
RNA Therapeutics, Engineered for Precision Neuromodulation
At Cognigenics, we are building the next generation of psychiatric treatments by integrating molecular genetics, neuroscience, and targeted delivery technologies.
Our unique AcuGen platform centers on short interfering RNA (siRNA)—a highly selective therapeutic modality that allows us to modulate gene expression with unprecedented spatial and temporal precision. Delivered via lipid conjugates, our therapeutics reach the brain noninvasively through intranasal administration, bypassing the blood-brain barrier.
Target: 5-HT2a Receptor
Decades of pharmacological and imaging research have implicated 5-HT2a receptor overactivation in limbic and cortical circuits as a key mechanism underlying hallucinations and psychosis, particularly in Parkinson's Disease Psychosis. The clinical efficacy of selective 5-HT2a antagonists and evidence of upregulated receptor density in affected brain regions support this.
Our approach is a fundamental change. Instead of the outside-in approach of traditional small-molecule drugs, we're developing an inside-out approach, modulating only specific neuronal receptors in the brain.
COG-301 silences 5-HT2a gene expression at the mRNA level using siRNA, enabling receptor-specific downregulation without polypharmacology.
Cognigenics Therapeutic Strategy – An Evolution
Our scientific development has progressed through three strategic phases:
- CRISPR Knockout
Used to establish causality between specific gene targets and behavioral phenotypes. - shRNA Gene Silencing
Provided long-duration suppression and validated therapeutic impact in preclinical models. - siRNA + Lipid Conjugates Delivery (Current Focus)
Enables tunable, reversible modulation. Ideal for dynamic conditions like PDP with co-occurring anxiety, allowing dose control and flexible treatment schedules.

THE COGNIGENICS PLATFORM
Our intranasal delivery platform offers a novel way to provide permanent (via DNA) or long-lasting (via RNA) treatments for mental health disorders associated with hyperactive neurons. The platform can accommodate a wide range of genetic therapeutics, enabling precise treatments that can be customized for individual needs.
Precision Delivery via Intranasal Lipid Conjugates
Our patent-pending lipid conjugates formulation will enable nose-to-brain targeting—a direct path to the limbic and cortical regions implicated in psychiatric illness. Intranasally delivered, this formulation is designed to:
- Avoid systemic exposure
- Enable weekly dosing
- Require no implanted hardware or infusion devices
- Allow at-home patient administration and cold storage in a standard refrigerator
This approach balances efficacy, safety, and scalability in a way conventional psychiatric treatments cannot.
Advancing a New Class of CNS Therapeutics
We believe Cognigenics is defining a new category of neurotherapeutics:
Precise. Reversible. RNA-based.
COG-301, our lead candidate under development, embodies this innovation. It's a first-in-class RNAi therapy for anxiety and perceptual symptoms in PDP—and it lays the foundation for broader expansion across psychiatric and neurodegenerative indications.
Our Team
Scientific, Strategic, and Operational Leadership in Precision Psychiatry
At Cognigenics, we bring together a cross-disciplinary team of scientists, clinicians, entrepreneurs, and technologists to advance the future of RNA therapeutics for neuropsychiatric disease. Our leadership spans neuroscience, genetic medicine, biotech commercialization, and venture strategy, all aligned around one goal: transforming brain health through precision genetic modulation.

Outcomes
Transformative Outcomes of Cognigenics Therapeutics
Empowering Lives Through Precision Neurogenetics
At Cognigenics, we are advancing a new class of therapeutics that aims to redefine treatment outcomes for neuropsychiatric disorders. Our siRNA-based therapies, delivered via intranasal lipid conjugates, are designed to target the molecular drivers of psychiatric and cognitive symptoms, in order to offer safe, reversible modulation of brain circuits without systemic exposure.
MEASURABLE IMPACT, MEANINGFUL CHANGE
Improved Mental and Emotional Balance
By modulating activity in the interpeduncular–ventral hippocampus pathway, our therapeutics show promise in restoring emotional regulation, enhancing mood, and increasing stress resilience.


Our Goal: A Better Experience for Patients
Noninvasive, At-Home Administration
Our delivery system is designed for simplicity: a once-weekly, self-administered intranasal spray that may reduce the need for daily pills or clinical procedures.
Empowering Patient Control
Ease of use promotes adherence and places therapeutic management back in the hands of the individual.
A Foundation in Science, A Vision for Impact
Third-Party Validation
Our outcomes are validated through studies performed at independent, AAALAC-accredited laboratories utilizing behavioral assays, immunohistochemistry, qPCR, and electrophysiology, and confirmed through peer-reviewed evaluation.
A Platform for Broader Transformation
While we begin with Parkinson's Disease Psychosis with Anxiety, our AcuGen platform is scalable across cognitive impairment, neurodegeneration, and anxiety spectrum conditions.

Our Vision
We envision a future where genetic medicine delivers not only symptom relief but a renewal of well-being—where patients once burdened by anxiety and cognitive disruption regain clarity, joy, and autonomy. With continued collaboration across the scientific, medical, and regulatory communities, Cognigenics is committed to unlocking this future.
A Broad-Based Pipeline for the Future
Advancing siRNA Therapeutics for Neuropsychiatric Disease
Cognigenics is developing a platform of precision RNA therapeutics for neuropsychiatric and neurodegenerative conditions. Each candidate is built on our core technology: short interfering RNA (siRNA) delivered via intranasal lipid conjugates, enabling targeted receptor modulation in the brain without systemic exposure.
Our lead candidate, COG-301, exemplifies this strategy. It is currently being developed for Parkinson's Disease Psychosis with Anxiety, an area of high unmet medical need with limited therapeutic options.
Pipeline Overview

* Pipeline programs under preclinical investigation for future expansion. Subject to refinement as clinical data emerges.
Lead Candidate: COG-301
COG-301 is a weekly siRNA therapeutic targeting 5-HT2a, a receptor implicated in the limbic hyperactivity seen in Parkinson's Disease Psychosis. Our goals:
- Selective gene silencing without the side effects of systemic antipsychotics
- Durable symptom relief without sedation or tolerance
- Noninvasive, intranasal dosing suitable for at-home administration
- COG-301 is being developed under a neurology/psychiatry regulatory path, with plans for first-in-human trials following IND-enabling studies in 2025.
Platform Expansion
COG-301 leads our clinical path, and our siRNA + lipid conjugates platform is designed to be modular and scalable.
Programs address:
- Cognitive impairment in aging and early neurodegeneration
- Anxiety spectrum disorders across populations
- Genetic modulation of other serotonin, glutamate, or GABA receptor subtypes
Our pipeline reflects not only individual therapeutics but a broader strategy to redefine neuropsychiatry through gene-level control.
Investors
A New Investment Frontier in Genetic Psychiatry
Cognigenics offers investors access to a high-potential, de-risked therapeutic platform at the intersection of neuroscience, RNA therapeutics, and noninvasive delivery.
Market Rationale
- ~1 million patients with Parkinson's in the U.S.; 40–50% of advanced-stage patients develop psychosis or severe anxiety
- No targeted RNA-based therapies exist for psychiatric indications
- First-mover advantage in intranasal siRNA delivery targeting CNS receptors
Capital Use
Next-stage capital will fund:
- COG-301 NEW design and testing (in vitro and in vivo)
- Final GLP tox and dose-ranging studies
- IND submission and Phase I trial readiness
- Expanded IP filings and manufacturing scale-up
Ethics
Responsibility at the Forefront of Innovation
At Cognigenics, we approach neurogenetic innovation with a firm ethical framework:
- We adhere to all relevant FDA, EMA, and AAALAC guidelines for preclinical and clinical work.
- All animal studies are conducted under approved IACUC protocols, ensuring humane, justified use.
- Our intranasal delivery system is designed to minimize patient burden, support autonomy, and eliminate unnecessary systemic exposure.
As we develop the world's first psychiatric siRNA platform, we remain committed to transparency, safety, and patient-centered design.
Genetic modulation of cognition and emotion must be approached with technical sophistication, compassion, and caution.










