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TauRx Pharmaceuticals

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uuid0000qwt

Namestring
TauRx Pharmaceuticals
Legal namestring
TauRx Therapeutics Management Limited
Company typeenum
Private
Founded yearint
2002
Descriptiontext

TauRx Pharmaceuticals is a privately held life sciences company founded in 2002 in Singapore, developing disease-modifying treatments and diagnostic tools for neurodegenerative diseases, with a primary focus on Alzheimer's disease and frontotemporal dementia. The company's core technology is a proprietary Tau Aggregation Inhibitor (TAI) platform based on hydromethylthionine mesylate (HMTM), an oral small-molecule compound discovered through research initiated by co-founder Prof Claude Wischik in 1988 and 1996. HMTM targets tau tangle pathology in the brain via a mechanism distinct from anti-amyloid approaches, and is administered as a film-coated tablet designed for early intervention in mild cognitive impairment (MCI) and mild-to-moderate Alzheimer's disease.

The company has completed Phase III clinical trials (LUCIDITY) involving approximately 3,000 patients across North America and Europe, demonstrating pharmacological activity on clinical decline and brain atrophy. In 2022, TauRx submitted HMTM to the UK Medicines and Healthcare products Regulatory Agency (MHRA) for approval and received an Innovation Passport acknowledging innovative potential; a confirmatory study was published in the Journal of Prevention of Alzheimer's Disease in 2024. The company is incorporated in Scotland (TauRx Therapeutics Management Limited, Registered Number SC531195) and operates from headquarters in Singapore with a UK operational base in Aberdeen. It has a leadership team led by Prof Claude Wischik (Co-Founder, Chairman and CEO), Dr Glenn Corr (COO/CBO), Prof Bjoern Schelter (Chief Analytics Officer), Prof John Storey (CTO), and Dr Richard Stefanacci (CMO).

TauRx is pre-commercial and pre-revenue, with no products currently generating sales. The planned business model upon regulatory approval is prescription pharmaceutical sales through healthcare systems, hospitals, and pharmacies, supported by the company's joint venture GT Diagnostics (with Genting Berhad) which develops digital diagnostic tools for early dementia detection and progression monitoring. The company has been funded through multiple private rounds totaling over $377 million since 2012, with Dundee Corporation holding approximately 1,007,008 shares at US$125/share as of 2024.

Short descriptiontext

TauRx Pharmaceuticals is a Singapore-headquartered, privately held life sciences company developing HMTM, an oral tau aggregation inhibitor for Alzheimer's disease and frontotemporal dementia, currently awaiting MHRA approval. It serves MCI and Alzheimer's patients via pharmaceutical sales and operates a diagnostic joint venture.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
501–1,000
akta.pro rankint
HeadquartersSingapore, Singapore
HQ citystring
Singapore
HQ countrystring
Singapore
HQ regionstring
Asia
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
tau aggregation inhibitors, Alzheimer's disease therapeutics, neurodegenerative disease treatment, clinical-stage pharmaceuticals, dementia drug development
Industry2 codes
1Neurology & Psychiatry (CNS) Pharmaceuticals
CodeHLAIAAAFPrimaryYes
2Neurology & CNS Specialty Pharmaceuticals
CodeHLAIACACPrimaryNo
NAICS code1 code
  • Medicinal and Botanical Manufacturing325411
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Alzheimer's Disease Therapeutics
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1HMTM Pharmaceutical Sales
TypeOne Time License
Description

Pre-commercial stage. HMTM has been submitted for regulatory approval to MHRA as a tablet to treat MCI and mild to moderate Alzheimer's disease. Once approved, the company will generate revenue through prescription pharmaceutical sales. The company states HMTM has a strong safety profile not requiring expensive tests or scans for routine monitoring, potentially offering cost advantages.

taurx.com
Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components4 values
Technology or R&D, Personnel, Operations, Marketing or Sales
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 2 records shown
1HMTM (Hydromethylthionine Mesylate)
Description

Oral tau aggregation inhibitor tablet for treatment of mild cognitive impairment and mild to moderate Alzheimer's disease

taurx.com
+1 more record
Core offering1 text field

TauRx Pharmaceuticals is developing hydromethylthionine mesylate (HMTM), an oral, film-coated tablet that acts as a Tau Aggregation Inhibitor (TAI) targeting tau pathology in the brain to modify disease progression in mild cognitive impairment (MCI) and mild-to-moderate Alzheimer's disease. The compound has completed Phase III clinical trials (LUCIDITY) and has been submitted to the UK's MHRA for regulatory approval as the company's first commercial product. Through its GT Diagnostics joint venture, the company also develops digital tools for early dementia diagnosis and progression monitoring.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • Phase III trials demonstrated pharmacological activity on clinical decline and brain atrophy in Alzheimer's disease and frontotemporal dementia
+2 more records
Product overview1 text field

TauRx Pharmaceuticals is a life sciences company focused on developing treatments for Alzheimer's disease and other neurodegenerative diseases caused by protein aggregation. The company's core product is HMTM (hydromethylthionine mesylate), an oral tau aggregation inhibitor tablet that has completed Phase III clinical trials (LUCIDITY) and was submitted for regulatory approval to the UK's MHRA in 2024. Complementary to its treatment pipeline, TauRx operates through a joint venture GT Diagnostics focused on digital diagnostic tools for dementia. The company was founded in 2002 in Singapore with roots in both Singapore and the United Kingdom.

Product and service1 record
1HMTM (Hydromethylthionine Mesylate)
CategoryAlzheimer's Disease Therapeutics
Description

Oral, film-coated tablet formulated as a Tau Aggregation Inhibitor (TAI) for early intervention in Alzheimer's disease to modify the underlying disease process and slow progression. Designed to dissolve tau tangles in the brain through a mechanism distinct from anti-amyloid therapies, with a strong safety profile requiring minimal routine monitoring (no expensive scans or tests). Targeted at patients with mild cognitive impairment and mild-to-moderate Alzheimer's disease, prescribed by neurologists, geriatricians, and primary care physicians.

Scale indicator4 records

Each record includes

Type, Value, Description, Source

Partnership1 partner
Strategic tierCoreTypeStrategic or Co-development Partner
Description

TauRx collaborates with Genting Berhad to create the joint venture GT Diagnostics, which aims to change the diagnostic landscape of dementia by developing tools for early diagnosis and monitoring progression. Focus on using digital tools to address bottlenecks in the diagnostic pathway, aiding clinicians to streamline dementia diagnosis. This is complementary to TauRx's research expertise focused on developing treatments.

Recent move3 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Late-stage clinical biopharma focused on a disease-modifying oral therapy (simufilam) for Alzheimer's disease, directly comparable in target indication, modality (oral small molecule), and pre-commercial regulatory stage.

TypeDirect peer
Description

Clinical-stage biopharma developing therapeutics and diagnostics targeting tau and other misfolded proteins in Alzheimer's and neurodegeneration, comparable in tau-pathology focus and integrated diagnostic-therapeutic strategy.

TypeDirect peer
Description

Clinical-stage biopharma developing small-molecule therapies for Alzheimer's disease and other neurodegenerative conditions, with a similar late-stage CNS profile and similar go-to-market through regulatory submissions in Alzheimer's.

TypeBroad incumbent
Description

Large pharma that developed and launched Kisunla (donanemab) for early symptomatic Alzheimer's disease, a direct therapeutic competitor to HMTM in the same target population.

TypeEmerging player
Description

Clinical-stage biopharma developing therapeutics for neurodegenerative diseases with an emphasis on biological targets and CNS delivery, comparable in neurodegeneration focus and platform-style pipeline approach.

TypeBroad incumbent
Description

Large Japanese pharmaceutical company co-developing and commercializing Leqembi (lecanemab), an approved anti-amyloid Alzheimer's therapy, making it the most direct large-pharma competitor for HMTM in the same disease.

TypeBroad incumbent
Description

Global neurology-focused biopharma co-marketing Leqembi and previously launching Aduhelm, representing the established Alzheimer's commercial competitor with deep payer and prescriber relationships.

TypeEmerging player
Description

Clinical-stage biopharma developing therapies for Alzheimer's disease and other neurological conditions, comparable in late-stage CNS pipeline and pre-commercial regulatory positioning.

TypeDirect peer
Description

Tau-pathology-focused clinical-stage biopharma developing vaccines and therapeutics for Alzheimer's and frontotemporal dementia, directly comparable in tau-targeting approach and neurodegenerative focus.

TypeDirect peer
Description

Clinical-stage CNS biopharma developing small-molecule therapies for Alzheimer's disease, sharing a similar late-stage private/early-public profile and oral small-molecule CNS modality.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat5 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

Named customers2 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment3 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile3 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
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles5 records

Each record includes

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

Subsidiaries1 record

Each record includes

Name, Acquired on, Relationship type, Type, Business focus

No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds6 records

Each record includes

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

Investors3 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 →

TauRx Pharmaceuticals

Alzheimer's Disease Therapeuticstaurx.com

TauRx Pharmaceuticals is a Singapore-headquartered, privately held life sciences company developing HMTM, an oral tau aggregation inhibitor for Alzheimer's disease and frontotemporal dementia, currently awaiting MHRA approval. It serves MCI and Alzheimer's patients via pharmaceutical sales and operates a diagnostic joint venture.

What TauRx Pharmaceuticals does

TauRx Pharmaceuticals is a privately held life sciences company founded in 2002 in Singapore, developing disease-modifying treatments and diagnostic tools for neurodegenerative diseases, with a primary focus on Alzheimer's disease and frontotemporal dementia. The company's core technology is a proprietary Tau Aggregation Inhibitor (TAI) platform based on hydromethylthionine mesylate (HMTM), an oral small-molecule compound discovered through research initiated by co-founder Prof Claude Wischik in 1988 and 1996. HMTM targets tau tangle pathology in the brain via a mechanism distinct from anti-amyloid approaches, and is administered as a film-coated tablet designed for early intervention in mild cognitive impairment (MCI) and mild-to-moderate Alzheimer's disease.

The company has completed Phase III clinical trials (LUCIDITY) involving approximately 3,000 patients across North America and Europe, demonstrating pharmacological activity on clinical decline and brain atrophy. In 2022, TauRx submitted HMTM to the UK Medicines and Healthcare products Regulatory Agency (MHRA) for approval and received an Innovation Passport acknowledging innovative potential; a confirmatory study was published in the Journal of Prevention of Alzheimer's Disease in 2024. The company is incorporated in Scotland (TauRx Therapeutics Management Limited, Registered Number SC531195) and operates from headquarters in Singapore with a UK operational base in Aberdeen. It has a leadership team led by Prof Claude Wischik (Co-Founder, Chairman and CEO), Dr Glenn Corr (COO/CBO), Prof Bjoern Schelter (Chief Analytics Officer), Prof John Storey (CTO), and Dr Richard Stefanacci (CMO).

TauRx is pre-commercial and pre-revenue, with no products currently generating sales. The planned business model upon regulatory approval is prescription pharmaceutical sales through healthcare systems, hospitals, and pharmacies, supported by the company's joint venture GT Diagnostics (with Genting Berhad) which develops digital diagnostic tools for early dementia detection and progression monitoring. The company has been funded through multiple private rounds totaling over $377 million since 2012, with Dundee Corporation holding approximately 1,007,008 shares at US$125/share as of 2024.

TauRx Pharmaceuticals firmographics

Firmographics
Name
TauRx Pharmaceuticals
Legal name
TauRx Therapeutics Management Limited
Website
http://taurx.com
Company type
Private
Founded year
2002
Operating status
Operating
Headcount range
501–1,000 employees
Short description
TauRx Pharmaceuticals is a Singapore-headquartered, privately held life sciences company developing HMTM, an oral tau aggregation inhibitor for Alzheimer's disease and frontotemporal dementia, currently awaiting MHRA approval. It serves MCI and Alzheimer's patients via pharmaceutical sales and operates a diagnostic joint venture.
Ownership category
akta.pro rank

TauRx Pharmaceuticals industry classification

Industry
Product category
Alzheimer's Disease Therapeutics
NAICS
Medicinal and Botanical Manufacturing (325411)
SIC
Pharmaceutical Preparations (2834)
akta.pro primary industry
Neurology & Psychiatry (CNS) Pharmaceuticals (HLAIAAAF)
akta.pro secondary industry
Neurology & CNS Specialty Pharmaceuticals (HLAIACAC)

Keywords

  • Tau aggregation inhibitors
  • Alzheimer's disease therapeutics
  • Neurodegenerative disease treatment
  • Clinical-stage pharmaceuticals
  • Dementia drug development

Where TauRx Pharmaceuticals is headquartered

Location

Headquarters

HQ city
Singapore
HQ country
Singapore
HQ region
Asia

Offices2 records

Markets served

TauRx Pharmaceuticals business model

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

Revenue model

  1. HMTM Pharmaceutical Sales: Pre-commercial stage. HMTM has been submitted for regulatory approval to MHRA as a tablet to treat MCI and mild to moderate Alzheimer's disease. Once approved, the company will generate revenue through prescription pharmaceutical sales. The company states HMTM has a strong safety profile not requiring expensive tests or scans for routine monitoring, potentially offering cost advantages.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels6 records

TauRx Pharmaceuticals product offering

Product offering

Core offering

TauRx Pharmaceuticals is developing hydromethylthionine mesylate (HMTM), an oral, film-coated tablet that acts as a Tau Aggregation Inhibitor (TAI) targeting tau pathology in the brain to modify disease progression in mild cognitive impairment (MCI) and mild-to-moderate Alzheimer's disease. The compound has completed Phase III clinical trials (LUCIDITY) and has been submitted to the UK's MHRA for regulatory approval as the company's first commercial product. Through its GT Diagnostics joint venture, the company also develops digital tools for early dementia diagnosis and progression monitoring.

Product overview

TauRx Pharmaceuticals is a life sciences company focused on developing treatments for Alzheimer's disease and other neurodegenerative diseases caused by protein aggregation. The company's core product is HMTM (hydromethylthionine mesylate), an oral tau aggregation inhibitor tablet that has completed Phase III clinical trials (LUCIDITY) and was submitted for regulatory approval to the UK's MHRA in 2024. Complementary to its treatment pipeline, TauRx operates through a joint venture GT Diagnostics focused on digital diagnostic tools for dementia. The company was founded in 2002 in Singapore with roots in both Singapore and the United Kingdom.

Differentiator

Problem solved

Functional benefit

Brands

  • HMTM (Hydromethylthionine Mesylate): Oral tau aggregation inhibitor tablet for treatment of mild cognitive impairment and mild to moderate Alzheimer's disease
  • GT Diagnostics

Products and services

  • HMTM (Hydromethylthionine Mesylate) Oral, film-coated tablet formulated as a Tau Aggregation Inhibitor (TAI) for early intervention in Alzheimer's disease to modify the underlying disease process and slow progression. Designed to dissolve tau tangles in the brain through a mechanism distinct from anti-amyloid therapies, with a strong safety profile requiring minimal routine monitoring (no expensive scans or tests). Targeted at patients with mild cognitive impairment and mild-to-moderate Alzheimer's disease, prescribed by neurologists, geriatricians, and primary care physicians.

Quantifiable outcome

  • Phase III trials demonstrated pharmacological activity on clinical decline and brain atrophy in Alzheimer's disease and frontotemporal dementia
  • +2 more outcomes

Companies that use TauRx Pharmaceuticals

Customer profile

Named customers2 records

Segments3 records

Ideal customer profiles3 records

TauRx Pharmaceuticals technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

TauRx Pharmaceuticals partnerships and signals

Strategic signal

Partnerships

One partnership is on record.

  • GT Diagnostics (Joint Venture with Genting Berhad)coreStrategic or Co-development PartnerTauRx collaborates with Genting Berhad to create the joint venture GT Diagnostics, which aims to change the diagnostic landscape of dementia by developing tools for early diagnosis and monitoring progression. Focus on using digital tools to address bottlenecks in the diagnostic pathway, aiding clinicians to streamline dementia diagnosis. This is complementary to TauRx's research expertise focused on developing treatments.

Scale indicators4 records

Recent moves3 records

Expansion highlights6 records

TauRx Pharmaceuticals competitors and assessment

Company assessment

Direct peers

  • Cassava Sciences: Late-stage clinical biopharma focused on a disease-modifying oral therapy (simufilam) for Alzheimer's disease, directly comparable in target indication, modality (oral small molecule), and pre-commercial regulatory stage.
  • AC Immune: Clinical-stage biopharma developing therapeutics and diagnostics targeting tau and other misfolded proteins in Alzheimer's and neurodegeneration, comparable in tau-pathology focus and integrated diagnostic-therapeutic strategy.
  • Anavex Life Sciences: Clinical-stage biopharma developing small-molecule therapies for Alzheimer's disease and other neurodegenerative conditions, with a similar late-stage CNS profile and similar go-to-market through regulatory submissions in Alzheimer's.
  • Axon Neuroscience: Tau-pathology-focused clinical-stage biopharma developing vaccines and therapeutics for Alzheimer's and frontotemporal dementia, directly comparable in tau-targeting approach and neurodegenerative focus.
  • Cognition Therapeutics: Clinical-stage CNS biopharma developing small-molecule therapies for Alzheimer's disease, sharing a similar late-stage private/early-public profile and oral small-molecule CNS modality.

Broad incumbents

  • Eli Lilly: Large pharma that developed and launched Kisunla (donanemab) for early symptomatic Alzheimer's disease, a direct therapeutic competitor to HMTM in the same target population.
  • Eisai: Large Japanese pharmaceutical company co-developing and commercializing Leqembi (lecanemab), an approved anti-amyloid Alzheimer's therapy, making it the most direct large-pharma competitor for HMTM in the same disease.
  • Biogen: Global neurology-focused biopharma co-marketing Leqembi and previously launching Aduhelm, representing the established Alzheimer's commercial competitor with deep payer and prescriber relationships.

Emerging players

  • Denali Therapeutics: Clinical-stage biopharma developing therapeutics for neurodegenerative diseases with an emphasis on biological targets and CNS delivery, comparable in neurodegeneration focus and platform-style pipeline approach.
  • BioVie: Clinical-stage biopharma developing therapies for Alzheimer's disease and other neurological conditions, comparable in late-stage CNS pipeline and pre-commercial regulatory positioning.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks6 records

Key highlights7 records

Customer concentration

TauRx Pharmaceuticals social profiles

Digital presence

TauRx Pharmaceuticals financial estimates

Financial estimate

Revenue estimate

Valuation estimate

TauRx Pharmaceuticals leadership team

Management profile

Number of profiles

Profiles5 records

TauRx Pharmaceuticals subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

TauRx Pharmaceuticals funding detail

Funding detail

Funding overview

Funding rounds6 records

Investors3 records

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

TauRx Pharmaceuticals 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 TauRx Pharmaceuticals

What does TauRx Pharmaceuticals do?

TauRx Pharmaceuticals is developing hydromethylthionine mesylate (HMTM), an oral, film-coated tablet that acts as a Tau Aggregation Inhibitor (TAI) targeting tau pathology in the brain to modify disease progression in mild cognitive impairment (MCI) and mild-to-moderate Alzheimer's disease. The compound has completed Phase III clinical trials (LUCIDITY) and has been submitted to the UK's MHRA for regulatory approval as the company's first commercial product. Through its GT Diagnostics joint venture, the company also develops digital tools for early dementia diagnosis and progression monitoring.

Is TauRx Pharmaceuticals a public or private company?

TauRx Pharmaceuticals is a private company. It is classified as venture growth investor backed and is currently operating.

When was TauRx Pharmaceuticals founded?

TauRx Pharmaceuticals was founded in 2002. It employs 501 to 1,000 people.

Where is TauRx Pharmaceuticals based?

TauRx Pharmaceuticals is headquartered in Singapore, Singapore, in the Asia region.

How does TauRx Pharmaceuticals make money?

One revenue line is on record: HMTM Pharmaceutical Sales.

Who are TauRx Pharmaceuticals's main competitors?

Direct peers on record are Cassava Sciences, AC Immune, Anavex Life Sciences, Axon Neuroscience and Cognition Therapeutics. Broad incumbents are Eli Lilly, Eisai and Biogen. Emerging players are Denali Therapeutics and BioVie.

Does TauRx Pharmaceuticals have an API?

No public API is recorded for TauRx Pharmaceuticals.

What industry is TauRx Pharmaceuticals in?

TauRx Pharmaceuticals's product category is Alzheimer's Disease Therapeutics. Its primary akta.pro industry code is HLAIAAAF, Neurology & Psychiatry (CNS) Pharmaceuticals, with a secondary code of HLAIACAC, Neurology & CNS Specialty Pharmaceuticals. Its NAICS code is 325411 and its SIC code is 2834.

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Live signals
DundeecorporationDundee Corporation Announces the Sale of 8,000 Shares of TauRx Pharmaceuticals Ltd. for Proceeds of US$1 MillionDundee Corporation announced the sale of 8,000 shares in TauRx Pharmaceuticals Ltd. to a private investor for US$1 million, with the transaction pending board approval. Dundee will retain its remaining stake of 1,007,008 shares following the completion of this deal.MarketScreenerDundee Corporation Announces the Sale of 8,000 Shares of TauRx Pharmaceuticals Ltd. for Proceeds of US$1 MillionDundee Corporation sold 8,000 shares of TauRx Pharmaceuticals Ltd. to a private investor for proceeds of US$1 million. The transaction is currently subject to approval from the TauRx board of directors. Upon completion, Dundee will retain its remaining stake of 1,007,008 shares in the pharmaceutical company.PR NewswireLUCIDITY phase 3 topline data presented at CTAD for HMTM - the only oral anti-Tau therapy in late-stage developmentTauRx Pharmaceuticals Ltd presented positive Phase 3 LUCIDITY topline data for HMTM, its oral tau aggregation inhibitor for Alzheimer's disease, at the CTAD conference in San Francisco on November 30, 2022. The trial demonstrated sustained cognitive improvement over 18 months over pre-treatment baseline in patients with MCI due to AD at the 16 mg/day dose, with a strong safety profile showing no amyloid-related imaging abnormalities. The company secured USD119 million in additional investment and is preparing regulatory submissions primarily in the UK, US, and Canada, with plans for China and other territories to follow.PR NewswireLUCIDITY phase 3 topline data presented at CTAD for HMTM - the only oral anti-Tau therapy in late-stage developmentTauRx Pharmaceuticals Ltd presented LUCIDITY Phase 3 topline data for its oral tau aggregation inhibitor HMTM at the CTAD conference in San Francisco on 30 November 2022, showing sustained cognitive improvement over 18 months in patients with mild cognitive impairment due to Alzheimer's disease at the 16 mg/day dose. The company reported a strong safety profile with no amyloid-related imaging abnormalities, positioning HMTM as a potential game-changing oral disease-modifying treatment, and secured USD119 million in additional investment triggered by the results. TauRx is preparing regulatory submissions primarily in the UK, US, and Canada, with completion of the 24-month study expected in mid-2023.GlobeNewswireDundee Corporation Portfolio Holding, TauRx Pharmaceuticals Ltd., Secures Funding for Regulatory Submissions of its Alzheimer’s TreatmentTauRx Pharmaceuticals raised $119 million through a warrant exercise at $45 per share to fund regulatory submissions for its Alzheimer's treatment in the UK, US, and Canada. Proceeds will also advance development for regulatory approval in China. The company will present Phase 3 LUCIDITY trial results at the CTAD conference on November 30.FinSMEsTauRx Raises Additional USD119M in FundingTauRx Pharmaceuticals raised USD119M in funding, with backers not disclosed. The company will use the funds to accelerate regulatory approval in China and plans to submit HMTM for approval in the UK, US, and Canada in 2023. The round followed Phase 3 LUCIDITY topline data and adds to USD64M raised in 2021.PR NewswireTauRx Announces Additional Investment of USD119 million following announcement of Phase 3 LUCIDITY Topline ResultsTauRx Pharmaceuticals Ltd secured USD 119 million through a warrants exercise triggered by positive Phase 3 LUCIDITY trial topline results announced in October 2022, with more than 99% of warrants exercised by shareholders. The investment will support regulatory submissions for HMTM, the company's oral tau aggregation inhibitor for Alzheimer's disease, in the UK, US, and Canada, as well as preparation for market availability. TauRx plans to present the Phase 3 findings at the CTAD conference in San Francisco on November 30, 2022, and submit HMTM for regulatory approval in 2023.PR NewswireTauRx Announces Additional Investment of USD119 million following announcement of Phase 3 LUCIDITY Topline ResultsTauRx Pharmaceuticals Ltd secured USD 119 million through a warrants exercise triggered by the announcement of positive Phase 3 LUCIDITY trial topline results in October 2022, with over 99% of warrants exercised. The investment will support regulatory submissions for HMTM, TauRx's oral tau aggregation inhibitor targeting Alzheimer's disease pathology, in the UK, US, and Canada, as well as preparation for market availability. The funding adds to USD 64 million raised in 2021 and represents a significant milestone for UK-based life sciences research, with regulatory submissions planned for 2023.GlobeNewswireDundee Corporation Portfolio Holding, TauRx Pharmaceuticals Ltd., Announces Results from Phase 3 Study, LUCIDITY, and Proceeds with Regulatory SubmissionsTauRx Pharmaceuticals announced Phase 3 results from its Alzheimer's study LUCIDITY, showing HMTM treatment improved cognition and reduced brain atrophy in early and mild-to-moderate AD. Dundee Corporation holds a 3.5% undiluted stake in TauRx. The company will present findings at CTAD and proceed with regulatory submissions.PR NewswireTauRx Announces Results from Phase 3 Alzheimer's Disease Study, LUCIDITY, Assuring Path for Regulatory SubmissionsTauRx Pharmaceuticals Ltd announced Phase 3 LUCIDITY trial results for Hydromethylthionine mesylate (HMTM), an oral tau aggregation inhibitor for Alzheimer's disease, showing sustained cognitive improvement over 18 months in early-stage patients and stabilization of disease progression in mild-to-moderate patients, compared against pre-treatment baselines and historical ADNI controls. The trial found no amyloid-related imaging abnormalities and no treatment-related serious adverse events, with the company now preparing regulatory submissions for the UK, US, and Canada in 2023. TauRx also appointed Dr Richard Stefanacci as Chief Medical Officer and has engaged strategic regulatory advisors as it advances HMTM toward commercialization.