Cognition Therapeutics, Inc. (CGTX): History, Ownership, Mission, How It Works & Makes Money

Cognition Therapeutics, Inc. (CGTX): History, Ownership, Mission, How It Works & Makes Money

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When you look at Cognition Therapeutics, Inc. (CGTX), a clinical-stage biopharmaceutical company focused on neurodegenerative disorders, are you seeing a high-risk gamble or a differentiated investment in the future of Alzheimer's treatment?

The company's focus on its lead candidate, zervimesine (CT1812), an oral small molecule, has driven its $122.04 million market capitalization, but it still posted a Q3 2025 net loss of $4.9 million, which is typical for a business in this phase.

This is a story about a clinical-stage firm that generates revenue primarily from non-dilutive grant funding-like the $81 million National Institute on Aging (NIA) grant for its Phase 2 START study-not commercial sales, so you have to evaluate its value based on clinical progress, not just a balance sheet.

With its Phase 2 START study in early Alzheimer's disease now fully enrolled as of November 2025, we need to understand the history, the core mechanism of action, and the ownership structure that is funding this high-stakes race to market.

Cognition Therapeutics, Inc. (CGTX) History

You need a clear picture of Cognition Therapeutics, Inc.'s (CGTX) origins to understand its current valuation. The company has evolved from a small Pittsburgh-based biotech to a publicly traded, clinical-stage neuroscience firm with a dual-track strategy targeting major degenerative diseases. The story is one of persistent clinical development, fueled by significant non-dilutive grant funding from the US government.

Given Company's Founding Timeline

Year established

Cognition Therapeutics was founded in 2007. The focus from the start was on developing small-molecule therapeutics for age-related degenerative disorders of the central nervous system.

Original location

The company's initial operations were based in Pittsburgh, Pennsylvania. It has since established its corporate headquarters in Purchase, New York, reflecting its growth and transition to a public company.

Founding team members

The company was co-founded by a team of experienced scientists and executives, including Franz F. Hefti, Gilbert M. Rishton, and Dr. Susan M. Catalano, who continues to serve as Chief Science Officer. This mix of scientific and pharmaceutical industry expertise was defintely crucial for its early direction.

Initial capital/funding

While the exact seed capital isn't public, the company's early development was significantly supported by non-dilutive funding. For example, the National Institute on Aging (NIA) later provided an approximately $81 million grant to support its lead clinical program, the Phase 2 START study. This grant-based model is a core part of its financial history.

Given Company's Evolution Milestones

Year Key Event Significance
2018 Positive Phase 2 data for CT1812 in mild-to-moderate Alzheimer's disease. Demonstrated statistically significant improvement in the ADAS-Cog scale, validating the drug's mechanism of action.
2020 Raised $25 million in Series C financing. Secured a major private funding round to accelerate the clinical development of its lead candidate, zervimesine (CT1812).
2021 Completed Initial Public Offering (IPO) on NASDAQ. Transitioned to a public company, raising capital for further research and development. The issue price was $12.00 per share.
Q2 2025 Reported positive Phase 2 dry Age-Related Macular Degeneration (AMD) results. Showed a 28.6% reduction in Geographic Atrophy (GA) lesion growth at 18 months, opening a new potential indication.
Q3 2025 Closed a $30 million Registered Direct Offering. Strengthened the balance sheet with new institutional investment to specifically support the Phase 3 development of zervimesine.
November 2025 Completed enrollment in Phase 2 'START' study for early Alzheimer's disease. A critical operational milestone that sets the stage for topline data readout and further regulatory discussions.

Given Company's Transformative Moments

The company's trajectory has been defined by a few key moments that de-risked its lead asset, zervimesine (CT1812), and secured its financial runway. These moments shifted the company from a pure research entity to a clinical-stage firm preparing for pivotal trials.

  • Securing a Registrational Path: In mid-2025, the company received End-of-Phase 2 meeting minutes from the U.S. FDA, confirming alignment on a registrational path for zervimesine in Alzheimer's disease. This regulatory clarity is a massive step, moving the program closer to a Phase 3 trial.
  • The Non-Dilutive Grant Strategy: The company's ability to secure and maintain significant grant funding from the National Institute on Aging (NIA)-including the approximately $81 million for the START study-has been transformative. This funding model has allowed it to advance its pipeline while minimizing shareholder dilution, unlike many peers.
  • The Dual-Track Clinical Expansion: The strategic decision in 2025 to aggressively pursue both Alzheimer's disease and Dementia with Lewy Bodies (DLB) simultaneously, including applying for FDA Breakthrough Therapy Designation for DLB, broadened the potential market and increased the number of near-term catalysts.
  • Recent Financial Strengthening: The $30 million registered direct offering closed in September 2025, plus a reported Q3 2025 net loss of only $4.9 million, gives the firm a cash runway projected into the second quarter of 2027. This is a strong position for a biotech awaiting Phase 2 data.

To understand the strategic logic behind these clinical and financial moves, you should review the company's core principles: Mission Statement, Vision, & Core Values of Cognition Therapeutics, Inc. (CGTX).

Cognition Therapeutics, Inc. (CGTX) Ownership Structure

Cognition Therapeutics, Inc. (CGTX) is a clinical-stage biopharmaceutical company, meaning its ownership structure is typical of a high-risk, high-reward NASDAQ-listed entity, where a significant portion of shares is held by insiders and retail investors, plus a core of specialist institutional funds.

You need to know who is really calling the shots. Honestly, the company's direction is primarily steered by the large block of insider and retail ownership, giving management and founders a strong voice, but the institutional money still dictates market sentiment and liquidity, so you can't ignore them.

Cognition Therapeutics' Current Status

Cognition Therapeutics is a publicly traded company, listed on the NASDAQ exchange under the ticker symbol CGTX. It completed its Initial Public Offering (IPO) in October 2021.

As a clinical-stage biotech, the company's financial profile in the 2025 fiscal year reflects high R&D spending and no commercial revenue. For the third quarter of 2025, the company reported a net loss of $4.9 million (or $(0.06) per basic and diluted share). Still, the balance sheet is strong, with cash, cash equivalents, and restricted cash equivalents totaling approximately $39.8 million as of September 30, 2025, plus another $36.3 million in remaining grant funds from the National Institute of Aging (NIA). That cash runway is estimated to last into the second quarter of 2027.

Cognition Therapeutics' Ownership Breakdown

The company's ownership is a mix of insiders, institutional capital, and individual investors. This breakdown is crucial because it shows where the conviction-and the potential for large block sales-lies.

Shareholder Type Ownership, % Notes
Retail Investors 58.08% A large block of shares held by individual, non-professional investors.
Insiders 29.21% Includes executives, directors, and large affiliated shareholders like Aaron Gl Fletcher, who holds 11.64%.
Institutional Investors 12.71% Managed by funds like Bios Capital Management LP (6.80%) and The Vanguard Group, Inc..

The high insider ownership, nearly 30%, is a double-edged sword: it signals strong commitment from those closest to the drug development process, but it also means a large portion of the stock is defintely illiquid and subject to lock-up agreements or concentrated selling risk.

Cognition Therapeutics' Leadership

The leadership team is a blend of seasoned biotech and pharmaceutical veterans, which is what you want to see in a clinical-stage company navigating complex regulatory paths.

The organization is steered by its Chief Executive Officer, Lisa Ricciardi, who has been in the role since March 2020. Her total yearly compensation is reported at $1.51 million, reflecting a mix of salary and performance incentives.

  • Lisa Ricciardi: Chief Executive Officer, President & Director. She has a background in global corporate and business development at companies like Foundation Medicine and Pfizer Inc..
  • John Doyle: Chief Financial Officer. He joined in 2023 and has significant experience in raising capital and leading companies through the transition to commercialization.
  • Dr. Anthony O. Caggiano: Chief Medical Officer and Head of Research & Development. Dr. Caggiano has extensive experience in developing new medicines for neurological conditions from his time at Acorda Therapeutics.
  • Dr. Steven A. Weissman: Vice President and Head of Chemistry, Manufacturing, and Controls (CMC). He is responsible for the manufacturing oversight of the lead candidate, zervimesine (CT1812).

The Board of Directors, which includes Chairman Jack Khattar and Director Aaron Glenn Fletcher, provides oversight, with an average tenure of 6.0 years, suggesting a stable governance structure. To fully grasp the strategic direction this team is taking, you should review the Mission Statement, Vision, & Core Values of Cognition Therapeutics, Inc. (CGTX).

Cognition Therapeutics, Inc. (CGTX) Mission and Values

Cognition Therapeutics' core purpose extends beyond drug development-it is driven by the human cost of neurodegenerative disease, aiming to deliver a new class of oral, disease-modifying treatments. This patient-centric focus is the cultural DNA that underpins their scientific strategy, which is currently backed by a significant $81 million grant from the National Institute on Aging (NIA).

Cognition Therapeutics' Core Purpose

You're looking at a clinical-stage biotech, so their mission is less about quarterly profit and more about scientific validation. Honestly, the entire company's valuation, which stood at a market capitalization of roughly $214 million as of August 2025, hinges on this core purpose.

Official Mission Statement

The company's mission is fundamentally defined by the sheer burden of illness, a clear and empathetic starting point. They are not just chasing a blockbuster drug; they are responding to the massive unmet need of patients and caregivers affected by diseases like Alzheimer's and Dementia with Lewy Bodies (DLB).

  • Develop safe, effective, and easy-to-administer treatment options.
  • Slow the progression of life-altering neurodegenerative diseases.
  • Target the sigma-2 receptor complex to protect synapses from toxic oligomers.

Their focus is on changing the treatment landscape, not just adding another option. That's a powerful, defintely high-stakes goal.

Vision Statement

The vision for Cognition Therapeutics is a paradigm shift (a fundamental change in approach) in how we treat central nervous system (CNS) disorders. Their lead candidate, zervimesine (CT1812), is an oral, once-daily small molecule, which is a massive differentiator from the current invasive infusion treatments for Alzheimer's.

  • Create a treatment paradigm shift from invasive and burdensome to convenient and comfortable.
  • Restore cellular damage response processes like autophagy (cellular housekeeping) and protein trafficking.
  • Establish zervimesine as a foundational, orally delivered therapy for multiple neurodegenerative conditions.

The successful enrollment of 540 participants in the Phase 2 START Study, completed in November 2025, shows they are making that vision a near-term reality.

Cognition Therapeutics Slogan/Tagline

While the company does not prominently feature a single, catchy tagline in the way a consumer brand would, their operational mantra is clear and scientifically precise. You can see this reflected in their public-facing materials.

  • Preventing the Progression of CNS disorders.

This simple statement maps directly to their mechanism of action, which is about protecting neurons rather than just clearing plaques after the damage is done. For more on how they operationalize this, see: Mission Statement, Vision, & Core Values of Cognition Therapeutics, Inc. (CGTX).

Cognition Therapeutics, Inc. (CGTX) How It Works

Cognition Therapeutics, Inc. is a clinical-stage biopharmaceutical company that operates by discovering and developing small molecule drugs to treat age-related neurodegenerative disorders, primarily Alzheimer's disease and Dementia with Lewy bodies. Since it is a clinical-stage company, it does not yet have a commercial product, so it makes money by securing large government grants, like the $81 million from the National Institute of Aging (NIA), and through equity financing, such as the $30.0 million registered direct offering completed in Q3 2025.

You're looking for a clear picture of their value proposition, and it boils down to one molecule: zervimesine. This drug works by targeting the sigma-2 receptor complex (a multi-protein receptor on neuronal and retinal cells) to protect synapses-the critical connection points between neurons-from the toxicity caused by pathogenic proteins like amyloid-beta (Aβ) and alpha-synuclein (ɑ-synuclein). This mechanism is functionally distinct from the antibody-based approaches you see from competitors, which is a key differentiator.

Cognition Therapeutics, Inc.'s Product/Service Portfolio

Product/Service Target Market Key Features
Zervimesine (CT1812) Early Alzheimer's Disease (AD) and Mild Cognitive Impairment (MCI) Investigational, oral, once-daily pill; targets the sigma-2 receptor complex to protect synapses; Phase 2 'START' study completed enrollment of 540 participants in November 2025.
Zervimesine (CT1812) Dementia with Lewy Bodies (DLB) Oral, once-daily therapeutic; aims to slow disease progression by preserving neuronal function; Expanded Access Program (EAP) is ongoing for former Phase 2 participants and other patients.
NICE Discovery Platform Preclinical Pipeline Expansion Proprietary discovery engine (Novel Improved Conditioned Extraction) used to identify new small molecules for other neurodegenerative conditions.

Cognition Therapeutics, Inc.'s Operational Framework

The operational process is focused almost entirely on clinical execution and securing non-dilutive funding to advance zervimesine. This is typical for a clinical-stage biotech; success is measured by trial milestones, not sales. Here's the quick math: the company reported a net loss of $4.9 million for the third quarter of 2025. Their cash position, which includes cash and equivalents of approximately $39.8 million plus remaining NIA grant funds of $36.3 million as of September 30, 2025, is estimated to fund operations into the second quarter of 2027.

  • Clinical Trial Management: Execute large, multi-site studies like the Phase 2 'START' study, which completed enrollment of 540 participants in November 2025.
  • Grant Funding & Collaboration: Manage significant grants, including an $81 million grant from the NIA, and collaborate with partners like the Alzheimer's Clinical Trials Consortium (ACTC).
  • R&D Prioritization: Focus resources on the most promising indications; for example, the voluntary discontinuation of the dry AMD study in early 2025 to prioritize AD and DLB.
  • Regulatory Strategy: Engage with the FDA to achieve alignment on a registrational path for zervimesine in Alzheimer's disease and pursue potential Breakthrough Therapy Designation for DLB.

This streamlined focus on their lead candidate is defintely the right move for a company of their size.

Cognition Therapeutics, Inc.'s Strategic Advantages

In the crowded neurodegenerative space, Cognition Therapeutics, Inc. has carved out a few distinct advantages that are worth noting.

  • Novel Mechanism of Action: Zervimesine's targeting of the sigma-2 receptor complex is a new approach, protecting synapses directly, which differentiates it from the current commercialized amyloid-targeting monoclonal antibodies like Leqembi (lecanemab).
  • Oral, Once-Daily Dosing: As an oral pill, zervimesine offers a significant convenience advantage over infusion-based therapies, potentially increasing patient compliance and reducing healthcare system burden.
  • Strong Non-Dilutive Funding: The substantial grant support, totaling approximately $171 million in cumulative grants primarily from the NIA, dramatically offsets the high Research and Development (R&D) costs. For context, R&D expenses were $11.5 million in Q2 2025 alone.
  • Regulatory Acceleration: The FDA has granted zervimesine Fast Track designation for Alzheimer's disease, which can expedite the review process and potentially accelerate time to market.

If you want to dig deeper into the numbers behind these operations, you should read Breaking Down Cognition Therapeutics, Inc. (CGTX) Financial Health: Key Insights for Investors.

Cognition Therapeutics, Inc. (CGTX) How It Makes Money

As a clinical-stage biopharmaceutical company, Cognition Therapeutics, Inc. (CGTX) does not currently generate revenue from product sales; its financial engine runs almost entirely on non-dilutive government grants and capital raised through equity offerings to fund its drug development pipeline.

Cognition Therapeutics, Inc.'s Revenue Breakdown

The company is focused on advancing its lead candidate, zervimesine (CT1812), through clinical trials for neurodegenerative disorders like Alzheimer's disease, so its revenue is not from commercialized products. The primary revenue source is grant income, which is recognized as development costs are incurred.

Here's the quick math for the third quarter of 2025: Total expenses (Research and Development plus General and Administrative) were $6.4 million ($3.8 million + $2.6 million), and the reported net loss was $4.9 million. This means the total revenue (grant income) recognized for the quarter was approximately $1.5 million.

Revenue Stream % of Total (Q3 2025) Growth Trend
Grant Income (NIA/NIH) 100% Increasing/Stable (Project-Dependent)
Product Sales/Licensing 0% Stable (At Zero)

Business Economics

The core economic fundamental for Cognition Therapeutics is a high-risk, high-reward model common in early-stage biotech, where the current value is tied to the probability of clinical success, not current cash flow. The company's strategy is to use non-dilutive funding-primarily a significant, multi-year grant from the National Institute on Aging (NIA)-to finance its most expensive asset, the Phase 2 START study for zervimesine in Alzheimer's disease.

This grant funding is critical because it extends the company's operating runway without immediately diluting shareholder equity, which is a big plus. As of September 30, 2025, the total obligated grant funds remaining from the NIA were $36.3 million. That's essentially a committed revenue stream tied to the progress of the trial.

The ultimate pricing strategy, which is still years away, would likely involve a premium price point typical for novel, first-in-class treatments for chronic, debilitating diseases like Alzheimer's. The oral, once-daily formulation of zervimesine (CT1812) offers a potential market advantage over infusion-based therapies, which could defintely impact future market penetration and pricing power.

  • Maximize non-dilutive capital: Rely on grants to cover R&D, preserving cash for non-grant-supported activities.
  • Milestone-based valuation: Value creation hinges on advancing the drug pipeline, especially achieving FDA alignment on a registrational path for zervimesine, which happened recently.
  • Future revenue drivers: Potential future revenue streams will come from partnership/collaboration milestone payments or, eventually, direct product sales after regulatory approval.

For a deeper dive into who is betting on this model, check out Exploring Cognition Therapeutics, Inc. (CGTX) Investor Profile: Who's Buying and Why?

Cognition Therapeutics, Inc.'s Financial Performance

The company's financial health, as of November 2025, reflects a well-capitalized clinical-stage entity focused on managing its burn rate while pushing its lead candidate forward. The core metric to watch right now is cash runway, not profitability.

  • Cash and Equivalents: As of September 30, 2025, cash, cash equivalents, and restricted cash were approximately $39.8 million. This is a strong liquidity position, especially when combined with the remaining grant funds.
  • Recent Funding: A $30.0 million registered direct offering was completed in Q3 2025, significantly bolstering the balance sheet and enabling preparations for the next stage of zervimesine's development.
  • Estimated Cash Runway: Management estimates the current cash and committed grants can fund operations and capital expenditures into the second quarter of 2027. That's a solid 18-month-plus cushion.
  • Net Loss: The net loss for the third quarter ended September 30, 2025, was $4.9 million. This is an improvement from the $9.9 million net loss in the comparable 2024 period, mainly due to lower R&D expenses as some trials concluded.
  • R&D Spend: Research and development expenses were $3.8 million for Q3 2025, a substantial decrease from $11.4 million in Q3 2024. This drop is a one-time event reflecting the completion of certain Phase 2 trials (SHINE and SHIMMER), not a long-term reduction in drug development commitment.

What this estimate hides is the potential need for another large capital raise (dilution) to fund the expensive Phase 3 trials once the registrational path is finalized, but for the near-term, the balance sheet looks stable.

Cognition Therapeutics, Inc. (CGTX) Market Position & Future Outlook

Cognition Therapeutics, Inc. (CGTX) is positioned as a high-risk, high-reward clinical-stage biotech, currently holding 0% commercial market share but targeting a multi-billion-dollar Alzheimer's disease (AD) market with a novel, oral small molecule. The company's future trajectory hinges entirely on the success of its lead candidate, zervimesine (CT1812), particularly the forthcoming data from its Phase 2 'START' study.

The company has bolstered its financial runway into Q2 2027 with a recent $30 million direct offering and approximately $36.3 million in remaining National Institute on Aging (NIA) grant funds as of September 30, 2025, providing the capital needed to advance its registrational path in AD. This is a critical buffer, considering the Q3 2025 net loss of $4.9 million.

Competitive Landscape

In the neurodegenerative space, CGTX's zervimesine (CT1812) is a small molecule that targets the sigma-2 receptor complex (S2R complex), a mechanism distinct from the current market-leading monoclonal antibodies (DMTs). This difference is its core competitive advantage: an oral, non-antibody approach that avoids the infusion logistics and the amyloid-related imaging abnormalities (ARIA) risk associated with its rivals.

Company Market Share, % (2025 Estimate) Key Advantage
Cognition Therapeutics, Inc. (CGTX) 0% (Clinical Stage) Oral, Small Molecule, Novel Sigma-2 Receptor Target (Non-Amyloid/Tau)
Cholinesterase Inhibitors (e.g., Donepezil, Rivastigmine) ~45% Established Efficacy, Low Cost, Oral Dosing (Symptomatic Relief)
Eisai/Biogen (Leqembi) <5% (Emerging DMT) First FDA-Approved Anti-Amyloid Disease-Modifying Therapy (DMT)

Opportunities & Challenges

You need to be aware of the dual nature of this investment: the massive market opportunity versus the significant clinical-stage risk. The global Alzheimer's drug market is estimated at $4.69 billion to $5.64 billion in 2025, and a successful DMT could capture a substantial portion of that growth.

Opportunities Risks
Oral Dosing Advantage: Zervimesine is an oral drug, maximizing patient adherence and simplifying logistics compared to the bi-weekly or monthly intravenous (IV) infusions required for antibody DMTs. Clinical Trial Failure: The entire valuation hinges on positive Phase 2/3 results; any negative data could lead to a catastrophic loss of value.
Novel Mechanism of Action: Targeting the S2R complex to protect synapses offers a differentiated approach from amyloid-beta antibodies, potentially allowing for combination therapy or treating a broader patient population. Cash Burn & Dilution: Despite a runway into Q2 2027, the company is not revenue-generating (excluding grants); future large-scale Phase 3 trials will require substantial new capital, likely through equity dilution.
Pipeline Expansion: Positive Phase 2 results in dry Age-related Macular Degeneration (dry AMD) and an Expanded Access Program (EAP) for Dementia with Lewy Bodies (DLB) de-risk the company by validating the S2R mechanism across multiple neurodegenerative disorders. Regulatory Hurdles & Competition: The FDA's bar for approval remains high, and the market is rapidly filling with deep-pocketed rivals like Eli Lilly (Kisunla) and Eisai/Biogen (Leqembi).

Industry Position

Cognition Therapeutics is a niche player in the broader neurodegenerative therapeutics market, currently valued at a modest market capitalization of $136.83 million as of November 14, 2025. It is a clinical-stage company, meaning its industry standing is based on pipeline potential, not commercial sales.

  • Pipeline-Driven Valuation: The company's valuation has seen high volatility (Beta of 1.36) and is primarily driven by clinical milestones, such as the recent completion of enrollment for the 540-participant Phase 2 START study.
  • Strategic Alignment: The achievement of FDA alignment on a registrational path for zervimesine in Alzheimer's disease is a major strategic accomplishment, moving the drug closer to a pivotal Phase 3 trial.
  • Differentiation from DMTs: Its oral, small-molecule approach provides a distinct competitive profile against the first-generation anti-amyloid monoclonal antibodies (DMTs), which are costly and carry a significant risk of ARIA. This is defintely a key selling point.
  • Financial Resilience: The cash position of $39.8 million (as of Q3 2025) combined with the remaining NIA grant funding provides a strong liquidity position (current ratio of 6.44), giving it a longer operational runway than many peers.

For a deeper dive into who is backing this high-stakes play, you should be Exploring Cognition Therapeutics, Inc. (CGTX) Investor Profile: Who's Buying and Why?

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