Developer docs
API playgroundTry for free, no card

Search company profiles

Cognition Therapeutics

Full company profile

uuid000051l

Namestring
Cognition Therapeutics
Legal namestring
Cognition Therapeutics, Inc.
Websiteurl
cogrx.com
Company typeenum
Public
Founded yearint
2007
Descriptiontext

Cognition Therapeutics, Inc. (NASDAQ: CGTX) is a clinical-stage biopharmaceutical company headquartered in Pittsburgh, Pennsylvania, developing therapeutics for Alzheimer's disease, dementia with Lewy bodies (DLB), and historically dry age-related macular degeneration. The company employs 11–50 people and is led by CEO Lisa Ricciardi, who joined the board in 2019, was appointed CEO in 2020, and led the company through its initial public offering.

The company's entire portfolio is built around a single investigational small molecule, zervimesine (also known as CT1812), a once-daily, oral, brain-penetrant first-in-class antagonist of the sigma-2 receptor (TMEM97) complex designed to displace toxic amyloid-beta and alpha-synuclein oligomers from neuronal synapses, thereby protecting synaptic integrity and function. Zervimesine achieves CSF concentrations consistent with greater than 80% estimated brain receptor occupancy and is being evaluated across six clinical programs — START (Phase 2, early Alzheimer's, 540-participant target, enrollment completed November 2025), SHINE (Phase 2, mild-to-moderate Alzheimer's, completed), SHIMMER (Phase 2, DLB, completed with 86% slowing of neuropsychiatric decline on NPI-12), SEQUEL (Phase 2 EEG synaptic function study, completed), SPARC (Phase 1 PET synaptic density study, completed), SNAP (Phase 1b target engagement study, completed), and MAGNIFY (Phase 2 in geographic atrophy, voluntarily discontinued to prioritize AD and DLB). A 32-participant Expanded Access Program for zervimesine in DLB reached full enrollment in December 2025.

Cognition Therapeutics is pre-revenue, generating no product sales; its operating capital comes from approximately $112M of cumulative NIA/NIH grant funding, a $30M registered direct offering closed in September 2025 with two new fundamental institutional investors, a prior $6M public offering in November 2022, philanthropic donations supporting the DLB EAP, and earlier angel and seed financing. The company has secured FDA alignment on two registrational paths — a biomarker-enriched (plasma p-tau217) Phase 3 design for Alzheimer's disease and a pivotal Phase 3 program in DLB psychosis expected to begin mid-2027 — and holds a Notice of Allowance on a polymorphic crystalline form patent providing IP protection through 2045 (potentially 2050). Commercialization has not yet commenced and the go-to-market model (self-launch versus partnership/licensing) remains undisclosed.

Short descriptiontext

Cognition Therapeutics (NASDAQ: CGTX) is a clinical-stage Pittsburgh-based biopharmaceutical company developing zervimesine (CT1812), a once-daily oral sigma-2 receptor modulator, as a disease-modifying therapy for Alzheimer's disease and dementia with Lewy bodies psychosis, currently advancing toward FDA-aligned Phase 3 registrational trials.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersPittsburgh, United States
HQ citystring
Pittsburgh
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Keyword5 values
neurodegenerative disease therapeutics, Alzheimer's disease treatment, Lewy body dementia therapy, small molecule drug development, synaptic protection therapy
Industry1 code
1Cognitive & Behavioral Neurology (Dementia/Memory Disorders)
CodeHLAKAIAHPrimaryYes
NAICS code1 code
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
Product category
Neurodegenerative disease therapeutics
GTM motion3 records

Each record includes

Type, Description, Source

Revenue model4 records
1Pre-revenue clinical-stage development
TypeLicensing Royalties
Description

Cognition Therapeutics is a clinical-stage biopharmaceutical company with no approved products and no product revenue; future revenue model is expected to derive from commercialization of zervimesine following regulatory approval, supplemented by potential licensing or partnership deals.

cogrx.com
2Equity financings (registered direct and public offerings)
TypeTransaction Fee
Description

Funded primarily through equity issuances, including a $30 million registered direct offering closed in September 2025 to two new fundamental institutional investors led by Titan Partners Group, and a prior $6 million public offering closed in November 2022.

globenewswire.com
3Non-dilutive grant funding (NIA/NIH)
TypeManaged Services
Description

Receives non-dilutive grant funding from the National Institute on Aging (NIA), including a $2.14 million grant for the SEQUEL study, a $30 million NIA grant supporting the SHIMMER Phase 2 study, and an approximately $81 million NIA grant supporting the START Phase 2 study.

biospace.com
4Philanthropic donations
TypeAffiliate Referral
Description

Has received philanthropic donations (e.g., from Jeffrey Pechter, founding partner of Mindful Capital) to extend the Expanded Access Program (EAP) for zervimesine in dementia with Lewy bodies.

stocktitan.net
Cost components3 values
Technology or R&D, Personnel, Marketing or Sales
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Cognition Therapeutics is developing zervimesine (CT1812), an investigational, first-in-class, once-daily, oral small-molecule sigma-2 receptor modulator designed to displace toxic amyloid-beta and alpha-synuclein oligomers from neuronal synapses and preserve synaptic integrity. The company's lead clinical programs target early Alzheimer's disease and dementia with Lewy bodies, with additional exploratory activity historically in dry age-related macular degeneration / geographic atrophy.

Differentiator
Functional benefit
Problem solved
Product overview1 text field

Cognition Therapeutics is a clinical-stage neuroscience company that has built its entire product offering around a single investigational lead asset — zervimesine (also known as CT1812) — a once-daily, brain-penetrant small-molecule oral sigma-2 receptor modulator designed to displace toxic amyloid beta and alpha-synuclein oligomers from synapses to protect neuronal integrity in age-related neurodegenerative diseases. The portfolio is structured as one core compound (zervimesine) evaluated across multiple named clinical programs: the Phase 2 START (COG0203) program in early Alzheimer's disease, the completed Phase 2 SHINE (COG0201) and SEQUEL (COG0202) programs in mild-to-moderate Alzheimer's disease, the completed Phase 2 SHIMMER (COG1201) program in dementia with Lewy bodies (now supporting a Phase 3 registrational program in DLB psychosis), the completed Phase 1 SPARC (COG0105) and SNAP (COG0104) studies, the voluntarily discontinued Phase 2 MAGNIFY (COG2201) program in geographic atrophy, and an Expanded Access Program in DLB. These named studies together form a platform-like development strategy around the zervimesine molecule, targeting Alzheimer's disease, DLB psychosis, and (historically) dry AMD, with biomarker-driven Phase 3 trials aligned with the FDA.

Product and service2 records
1Zervimesine (CT1812)
CategoryInvestigational small-molecule drug (CNS)
2Zervimesine Expanded Access Program (DLB)
CategoryExpanded access / patient program
Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Clinical-stage biopharmaceutical company developing small-molecule therapeutics for Alzheimer's disease, Rett syndrome, and other neurodegenerative diseases. Highly comparable to Cognition as a small-cap, late-stage CNS biotech with a single-asset-focused pipeline targeting similar indications.

TypeDirect peer
Description

Clinical-stage biotechnology company developing simufilam for Alzheimer's disease. Directly comparable to Cognition as a small-cap, single-asset-focused AD therapeutics developer with similar regulatory and capital-raising dynamics.

TypeDirect peer
Description

Clinical-stage biotechnology company developing protein dysregulation-targeted therapies for neurodegenerative diseases including Alzheimer's and Parkinson's. Comparable to Cognition in neurodegenerative disease focus, pipeline breadth within CNS, and clinical-stage development profile.

TypeDirect peer
Description

Clinical-stage biopharmaceutical company developing therapeutics and diagnostics for neurodegenerative diseases, with multiple programs targeting Alzheimer's pathology. Comparable to Cognition in AD-focused pipeline and small-cap clinical-stage status.

TypeDirect peer
Description

Clinical-stage biotechnology company developing small-molecule therapeutics for neurodegenerative diseases including Alzheimer's. Comparable to Cognition in clinical-stage AD focus, single-asset concentration, and small-cap profile.

TypeDirect peer
Description

Clinical-stage biotechnology company developing therapeutics for neurodegenerative diseases including Parkinson's and Alzheimer's. Comparable to Cognition in CNS/neurodegenerative disease focus and clinical-stage development approach.

TypeDirect peer
Description

Was a clinical-stage biopharmaceutical company developing therapeutics targeting neurodegenerative disease pathogenesis, including for Alzheimer's. Comparable to Cognition in AD-targeted clinical-stage development and small-cap biotech profile (note: company underwent significant restructuring).

TypeBroad incumbent
Description

Commercial-stage CNS biopharmaceutical company with approved products (Zurzuvae) and pipeline in depression, epilepsy, and other neurological conditions. Broader incumbent in CNS therapeutics with overlapping neuroscience expertise, though focused on different indications than Cognition.

TypeBroad incumbent
Description

Large established biopharmaceutical company commercializing Leqembi (lecanemab) with Eisai for early Alzheimer's disease. Major incumbent in AD therapeutics whose approved anti-amyloid antibody sets the competitive benchmark Cognition must differentiate against.

TypeBroad incumbent
Description

Large established Japanese pharmaceutical company with Leqembi (lecanemab) for Alzheimer's disease and a broad neurology pipeline. Major incumbent competitor in AD therapeutics whose commercial presence and regulatory experience shape the market Cognition is entering.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses2 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Ideal customer profile2 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature4 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles11 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
Compliance1 record

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds23 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors17 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Cognition Therapeutics

Neurodegenerative disease therapeuticscogrx.com

Cognition Therapeutics (NASDAQ: CGTX) is a clinical-stage Pittsburgh-based biopharmaceutical company developing zervimesine (CT1812), a once-daily oral sigma-2 receptor modulator, as a disease-modifying therapy for Alzheimer's disease and dementia with Lewy bodies psychosis, currently advancing toward FDA-aligned Phase 3 registrational trials.

What Cognition Therapeutics does

Cognition Therapeutics, Inc. (NASDAQ: CGTX) is a clinical-stage biopharmaceutical company headquartered in Pittsburgh, Pennsylvania, developing therapeutics for Alzheimer's disease, dementia with Lewy bodies (DLB), and historically dry age-related macular degeneration. The company employs 11–50 people and is led by CEO Lisa Ricciardi, who joined the board in 2019, was appointed CEO in 2020, and led the company through its initial public offering.

The company's entire portfolio is built around a single investigational small molecule, zervimesine (also known as CT1812), a once-daily, oral, brain-penetrant first-in-class antagonist of the sigma-2 receptor (TMEM97) complex designed to displace toxic amyloid-beta and alpha-synuclein oligomers from neuronal synapses, thereby protecting synaptic integrity and function. Zervimesine achieves CSF concentrations consistent with greater than 80% estimated brain receptor occupancy and is being evaluated across six clinical programs — START (Phase 2, early Alzheimer's, 540-participant target, enrollment completed November 2025), SHINE (Phase 2, mild-to-moderate Alzheimer's, completed), SHIMMER (Phase 2, DLB, completed with 86% slowing of neuropsychiatric decline on NPI-12), SEQUEL (Phase 2 EEG synaptic function study, completed), SPARC (Phase 1 PET synaptic density study, completed), SNAP (Phase 1b target engagement study, completed), and MAGNIFY (Phase 2 in geographic atrophy, voluntarily discontinued to prioritize AD and DLB). A 32-participant Expanded Access Program for zervimesine in DLB reached full enrollment in December 2025.

Cognition Therapeutics is pre-revenue, generating no product sales; its operating capital comes from approximately $112M of cumulative NIA/NIH grant funding, a $30M registered direct offering closed in September 2025 with two new fundamental institutional investors, a prior $6M public offering in November 2022, philanthropic donations supporting the DLB EAP, and earlier angel and seed financing. The company has secured FDA alignment on two registrational paths — a biomarker-enriched (plasma p-tau217) Phase 3 design for Alzheimer's disease and a pivotal Phase 3 program in DLB psychosis expected to begin mid-2027 — and holds a Notice of Allowance on a polymorphic crystalline form patent providing IP protection through 2045 (potentially 2050). Commercialization has not yet commenced and the go-to-market model (self-launch versus partnership/licensing) remains undisclosed.

Cognition Therapeutics firmographics

Firmographics
Name
Cognition Therapeutics
Legal name
Cognition Therapeutics, Inc.
Website
https://cogrx.com
Company type
Public
Founded year
2007
Operating status
Operating
Headcount range
11–50 employees
Short description
Cognition Therapeutics (NASDAQ: CGTX) is a clinical-stage Pittsburgh-based biopharmaceutical company developing zervimesine (CT1812), a once-daily oral sigma-2 receptor modulator, as a disease-modifying therapy for Alzheimer's disease and dementia with Lewy bodies psychosis, currently advancing toward FDA-aligned Phase 3 registrational trials.
Ownership category
akta.pro rank

Cognition Therapeutics industry classification

Industry
Product category
Neurodegenerative disease therapeutics
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714)
akta.pro primary industry
Cognitive & Behavioral Neurology (Dementia/Memory Disorders) (HLAKAIAH)

Keywords

  • Neurodegenerative disease therapeutics
  • Alzheimer's disease treatment
  • Lewy body dementia therapy
  • Small molecule drug development
  • Synaptic protection therapy

Where Cognition Therapeutics is headquartered

Location

Headquarters

HQ city
Pittsburgh
HQ country
United States
HQ region
North America

Markets served

Cognition Therapeutics business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Personnel, Marketing or Sales

Revenue model

  1. Pre-revenue clinical-stage development: Cognition Therapeutics is a clinical-stage biopharmaceutical company with no approved products and no product revenue; future revenue model is expected to derive from commercialization of zervimesine following regulatory approval, supplemented by potential licensing or partnership deals.
  2. Equity financings (registered direct and public offerings): Funded primarily through equity issuances, including a $30 million registered direct offering closed in September 2025 to two new fundamental institutional investors led by Titan Partners Group, and a prior $6 million public offering closed in November 2022.
  3. Non-dilutive grant funding (NIA/NIH): Receives non-dilutive grant funding from the National Institute on Aging (NIA), including a $2.14 million grant for the SEQUEL study, a $30 million NIA grant supporting the SHIMMER Phase 2 study, and an approximately $81 million NIA grant supporting the START Phase 2 study.
  4. Philanthropic donations: Has received philanthropic donations (e.g., from Jeffrey Pechter, founding partner of Mindful Capital) to extend the Expanded Access Program (EAP) for zervimesine in dementia with Lewy bodies.

Go-to-market motion3 records

Cognition Therapeutics product offering

Product offering

Core offering

Cognition Therapeutics is developing zervimesine (CT1812), an investigational, first-in-class, once-daily, oral small-molecule sigma-2 receptor modulator designed to displace toxic amyloid-beta and alpha-synuclein oligomers from neuronal synapses and preserve synaptic integrity. The company's lead clinical programs target early Alzheimer's disease and dementia with Lewy bodies, with additional exploratory activity historically in dry age-related macular degeneration / geographic atrophy.

Product overview

Cognition Therapeutics is a clinical-stage neuroscience company that has built its entire product offering around a single investigational lead asset — zervimesine (also known as CT1812) — a once-daily, brain-penetrant small-molecule oral sigma-2 receptor modulator designed to displace toxic amyloid beta and alpha-synuclein oligomers from synapses to protect neuronal integrity in age-related neurodegenerative diseases. The portfolio is structured as one core compound (zervimesine) evaluated across multiple named clinical programs: the Phase 2 START (COG0203) program in early Alzheimer's disease, the completed Phase 2 SHINE (COG0201) and SEQUEL (COG0202) programs in mild-to-moderate Alzheimer's disease, the completed Phase 2 SHIMMER (COG1201) program in dementia with Lewy bodies (now supporting a Phase 3 registrational program in DLB psychosis), the completed Phase 1 SPARC (COG0105) and SNAP (COG0104) studies, the voluntarily discontinued Phase 2 MAGNIFY (COG2201) program in geographic atrophy, and an Expanded Access Program in DLB. These named studies together form a platform-like development strategy around the zervimesine molecule, targeting Alzheimer's disease, DLB psychosis, and (historically) dry AMD, with biomarker-driven Phase 3 trials aligned with the FDA.

Differentiator

Problem solved

Functional benefit

Products and services

  • Zervimesine (CT1812)
  • Zervimesine Expanded Access Program (DLB)

Companies that use Cognition Therapeutics

Customer profile

Ideal customer profiles2 records

Cognition Therapeutics technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

Cognition Therapeutics partnerships and signals

Strategic signal

Recent moves7 records

Expansion highlights6 records

Cognition Therapeutics competitors and assessment

Company assessment

Direct peers

  • Anavex Life Sciences: Clinical-stage biopharmaceutical company developing small-molecule therapeutics for Alzheimer's disease, Rett syndrome, and other neurodegenerative diseases. Highly comparable to Cognition as a small-cap, late-stage CNS biotech with a single-asset-focused pipeline targeting similar indications.
  • Cassava Sciences: Clinical-stage biotechnology company developing simufilam for Alzheimer's disease. Directly comparable to Cognition as a small-cap, single-asset-focused AD therapeutics developer with similar regulatory and capital-raising dynamics.
  • Prothena Corporation: Clinical-stage biotechnology company developing protein dysregulation-targeted therapies for neurodegenerative diseases including Alzheimer's and Parkinson's. Comparable to Cognition in neurodegenerative disease focus, pipeline breadth within CNS, and clinical-stage development profile.
  • AC Immune SA: Clinical-stage biopharmaceutical company developing therapeutics and diagnostics for neurodegenerative diseases, with multiple programs targeting Alzheimer's pathology. Comparable to Cognition in AD-focused pipeline and small-cap clinical-stage status.
  • Athira Pharma: Clinical-stage biotechnology company developing small-molecule therapeutics for neurodegenerative diseases including Alzheimer's. Comparable to Cognition in clinical-stage AD focus, single-asset concentration, and small-cap profile.
  • Denali Therapeutics: Clinical-stage biotechnology company developing therapeutics for neurodegenerative diseases including Parkinson's and Alzheimer's. Comparable to Cognition in CNS/neurodegenerative disease focus and clinical-stage development approach.
  • Cortexyme: Was a clinical-stage biopharmaceutical company developing therapeutics targeting neurodegenerative disease pathogenesis, including for Alzheimer's. Comparable to Cognition in AD-targeted clinical-stage development and small-cap biotech profile (note: company underwent significant restructuring).

Broad incumbents

  • Sage Therapeutics: Commercial-stage CNS biopharmaceutical company with approved products (Zurzuvae) and pipeline in depression, epilepsy, and other neurological conditions. Broader incumbent in CNS therapeutics with overlapping neuroscience expertise, though focused on different indications than Cognition.
  • Biogen: Large established biopharmaceutical company commercializing Leqembi (lecanemab) with Eisai for early Alzheimer's disease. Major incumbent in AD therapeutics whose approved anti-amyloid antibody sets the competitive benchmark Cognition must differentiate against.
  • Eisai: Large established Japanese pharmaceutical company with Leqembi (lecanemab) for Alzheimer's disease and a broad neurology pipeline. Major incumbent competitor in AD therapeutics whose commercial presence and regulatory experience shape the market Cognition is entering.

Market position

Strengths5 records

Weaknesses2 records

Competitive moat4 records

Key risks6 records

Key highlights7 records

Customer concentration

Cognition Therapeutics social profiles

Digital presence

Cognition Therapeutics compliance and trust

Trust signal

Compliance1 record

Cognition Therapeutics financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Cognition Therapeutics leadership team

Management profile

Number of profiles

Profiles11 records

Cognition Therapeutics funding detail

Funding detail

Funding overview

Funding rounds23 records

Investors17 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Cognition Therapeutics M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Cognition Therapeutics

What does Cognition Therapeutics do?

Cognition Therapeutics is developing zervimesine (CT1812), an investigational, first-in-class, once-daily, oral small-molecule sigma-2 receptor modulator designed to displace toxic amyloid-beta and alpha-synuclein oligomers from neuronal synapses and preserve synaptic integrity. The company's lead clinical programs target early Alzheimer's disease and dementia with Lewy bodies, with additional exploratory activity historically in dry age-related macular degeneration / geographic atrophy.

Is Cognition Therapeutics a public or private company?

Cognition Therapeutics is a public company. It is classified as public and is currently operating.

When was Cognition Therapeutics founded?

Cognition Therapeutics was founded in 2007. It employs 11 to 50 people.

Where is Cognition Therapeutics based?

Cognition Therapeutics is headquartered in Pittsburgh, United States, in the North America region.

How does Cognition Therapeutics make money?

Four revenue lines are on record. Pre-revenue clinical-stage development is the primary driver. The others are equity financings (registered direct and public offerings), non-dilutive grant funding (NIA/NIH) and philanthropic donations.

Who are Cognition Therapeutics's main competitors?

Direct peers on record are Anavex Life Sciences, Cassava Sciences, Prothena Corporation, AC Immune SA, Athira Pharma, Denali Therapeutics and Cortexyme. Broad incumbents are Sage Therapeutics, Biogen and Eisai.

Does Cognition Therapeutics have an API?

No public API is recorded for Cognition Therapeutics.

What industry is Cognition Therapeutics in?

Cognition Therapeutics's product category is Neurodegenerative disease therapeutics. Its primary akta.pro industry code is HLAKAIAH, Cognitive & Behavioral Neurology (Dementia/Memory Disorders). Its NAICS code is 541714.

Unlock the full company data

50 free credits on sign-up, no credit card required.

Contact sales
Live signals
Longevity.TechnologyCognition Therapeutics wins patent for zervimesine through 2045Cognition Therapeutics received a U.S. patent for a novel crystalline form of zervimesine (CT1812), expiring in 2045 with possible five-year extension. The patent covers the composition, production process, and therapeutic methods for Alzheimer's, dry AMD, and dementia with Lewy bodies. The company plans an FDA meeting to finalize endpoints for a registrational program in dementia with Lewy bodies.MarketBeatCognition Therapeutics, Inc. (NASDAQ:CGTX) Stock Has Average Target Price of $3.33Cognition Therapeutics shares rose 4% to $0.89, with an average analyst price target of $3.33 and a Moderate Buy consensus. Institutional investors hold 43.35% of the stock, and the company reported a quarterly loss of $0.04 per share, beating estimates.The future of tradingCognition Therapeutics wins US patent for new crystalline form of zervimesine through 2045Cognition Therapeutics won a U.S. patent for a new crystalline form of its lead candidate zervimesine, with protection through 2045 and potential FDA extension. The patent covers manufacturing and treatment methods for Alzheimer's, dry AMD, and dementia with Lewy bodies. Manufacturing is planned for Q1 2027, with an FDA meeting on registrational endpoints scheduled next week.Longevity.TechnologyFDA talks could set the bar for a Lewy body drugCognition Therapeutics will meet the FDA on 20 October to align on the primary endpoint for a Phase 3 trial of zervimesine in dementia with Lewy bodies. The company plans to measure psychosis, citing a Phase 2 study showing an 89% reduction in hallucinations and delusions. The outcome will set a regulatory path for the drug.Investing.comH.C. Wainwright reiterates Cognition Therapeutics stock rating ahead of FDA meetingH.C. Wainwright reiterated a Buy rating and $3.00 price target on Cognition Therapeutics, implying 222% upside from the $0.93 stock price. The company holds a $88 million market cap and a 7.03 current ratio. An FDA Type C meeting is scheduled for October 20, 2026, to align on the primary endpoint for zervimesine's Phase 3 study.Longevity.TechnologyCognition Therapeutics plans FDA meeting for Phase 3 Lewy body dementia trialCognition Therapeutics scheduled a Type C FDA meeting on October 20, 2026, to align on endpoints for a Phase 3 trial of Zervimesine in dementia with Lewy bodies with psychosis. The trial will enroll participants with hallucinations and delusions, randomizing them to 100 mg daily Zervimesine or placebo for nine months. A Phase 2 trial reported an 89% slowing of hallucination/delusion progression versus placebo.Ticker ReportCognition Therapeutics, Inc. (NASDAQ:CGTX) Stock Has Consensus Target Price of $3.33Cognition Therapeutics received a consensus 'Moderate Buy' rating from four analysts, with an average price target of $3.33. The stock opened at $0.95, and the company reported a quarterly loss of $0.04 per share, beating estimates. Institutional investors hold 43.35% of the stock.Markets DailyCognition Therapeutics (NASDAQ:CGTX) Posts Quarterly Earnings Results, Beats Expectations By $0.02 EPSCognition Therapeutics reported its quarterly earnings, posting a loss of $0.04 EPS, which beat analysts' expectations of a loss of $0.06 EPS. The stock has been trading at around $1.08 with a market cap of approximately $96.66 million. The company focuses on developing therapies for neurodegenerative disorders, particularly Alzheimer's disease, and its lead candidate has completed Phase 1 safety studies and preliminary Phase 2a trials.Quiver QuantitativeCognition Therapeutics Stock (CGTX) Opinions on biotech upside speculation | CGTX Stock NewsSocial media users have highlighted Cognition Therapeutics (CGTX) as an under-the-radar speculative biotech play, with discussions noting the stock trading around $1 or lower and the formation of dedicated investor forums. Three company executives, including the CFO, Chief Medical Officer, and CEO, purchased a combined 29,175 shares on the open market in the past six months. Institutional investor activity shows mixed sentiment, with 31 funds adding positions and 27 decreasing holdings in recent quarters, while no concrete catalysts or price targets have been established.BioSpaceCognition Therapeutics Reports Financial Results for the Second Quarter 2026 and Provides Business UpdateCognition Therapeutics reported Q2 2026 financial results, with a net loss of $3.9 million and cash of $34.8 million. The company plans to initiate its Phase 3 trial for DLB psychosis in mid-2027 with an improved tablet composition. It also received a Notice of Allowance for a new composition of matter patent.