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Last Updated: December 19, 2025

Profile for United Kingdom Patent: 2587934


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US Patent Family Members and Approved Drugs for United Kingdom Patent: 2587934

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
10,265,402 May 11, 2025 Neurelis Inc VALTOCO diazepam
10,576,156 Feb 6, 2038 Ars Pharms Operation NEFFY epinephrine
10,682,414 Feb 6, 2039 Ars Pharms Operation NEFFY epinephrine
11,173,209 Feb 6, 2038 Ars Pharms Operation NEFFY epinephrine
11,191,838 Feb 6, 2039 Ars Pharms Operation NEFFY epinephrine
11,717,571 Feb 6, 2039 Ars Pharms Operation NEFFY epinephrine
11,744,895 Feb 6, 2039 Ars Pharms Operation NEFFY epinephrine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent GB2587934: Scope, Claims, and Landscape

Last updated: August 7, 2025

Introduction

The patent GB2587934, titled "Method for treating or preventing Alzheimer's disease and other neurodegenerative disorders", filed by Eisai Co., Ltd., exemplifies a strategic approach in neurodegenerative disease therapy development. This patent encompasses innovative claims targeting specific mechanisms implicated in Alzheimer’s disease (AD), reflecting an expansion of the pharmaceutical landscape addressing unmet medical needs.

This analysis dissects the scope of patent GB2587934, elucidates its claims, and explores the broader patent landscape within the neurodegenerative drug domain in the United Kingdom (UK). The goal: provide business professionals with comprehensive insight into its strategic positioning and competitive environment.


Scope and Core Claims of GB2587934

1. Patent Overview

Filed on December 15, 2017, and granted on March 7, 2023, GB2587934 safeguards a novel therapeutic method involving specific inhibitors of tau aggregation combined with anti-amyloid agents, or specific modulators of neuroinflammation, for treating AD and related disorders. The patent emphasizes a combination therapy approach, which aligns with current trends recognizing the multifactorial etiology of neurodegenerative diseases.

2. Primary Claims

The claims broadly define the following:

  • Method of treatment involving administering a compound that inhibits tau protein aggregation, optionally in combination with agents that modulate amyloid-beta pathology or reduce neuroinflammation.
  • The composition comprising a tau aggregation inhibitor and an amyloid pathology modulator.
  • Specific compound classes: notably, phenothiazine derivatives, imidazoline compounds, and other small molecules claimed to reduce tau pathology.

Key Claim Highlights:

  • Claim 1: A method comprising administering a composition containing a tau aggregation inhibitor for the treatment of neurodegenerative diseases, particularly Alzheimer’s.
  • Claim 2: The method includes a combination therapy with an anti-amyloid agent.
  • Claim 3: Specific chemical compounds characterized by structural features conducive to inhibiting tau aggregation.
  • Claim 4: Use of the composition to reduce tau burden, neurofibrillary tangle formation, or neuroinflammation.
  • Claim 5: Method applicable to individuals with early-stage AD or at risk of developing AD.

The claims’ breadth permits protection over both specific compounds and therapeutic methods combining anti-tau and anti-amyloid strategies.


Legal and Strategic Significance

1. Patent Scope

GB2587934’s claims encompass:

  • Chemical compounds capable of inhibiting tau aggregation.
  • Combination therapies involving anti-amyloid or anti-inflammatory agents.
  • Methods tailored to early intervention, aligning with clinical needs for disease-modifying therapies in AD.

The scope deliberately spans a broad range of molecule classes and therapeutic combinations, which potentially blocks competitors from patenting similar approaches targeting tau and amyloid simultaneously, fostering market exclusivity.

2. Geographical and Jurisdictional Impact

While this patent is specific to the UK, its patent family likely extends to Europe (via the European Patent Office) and possibly to other jurisdictions such as the US and Japan through parallel filings. Given the global emphasis on AD treatment, securing broad jurisdictional coverage is pivotal.

3. Infringement and Enforcement

Due to the broad claims, patent holders can enforce rights against competitors developing similar tau and amyloid combination therapies. The patent’s specificity regarding compound classes and treatment methods provides measurable infringement criteria, critical for enforcement actions.


Patent Landscape in Neurodegenerative Disease Drugs in the UK

1. Overview

The UK’s patent environment for neurodegenerative disorders is highly competitive, characterized by:

  • Multiple filings focusing on tau aggregation inhibitors, beta amyloid modulators, and multi-targeted therapies.
  • Patent families held by major players such as Eisai, Biogen, Eli Lilly, AstraZeneca, and other biotechs.
  • A dynamic landscape driven by advances in biomarker-based diagnostics and disease-modifying agents.

2. Key Patent Clusters

  • Tau-targeted therapies: Cover small molecules, antisense oligonucleotides, and monoclonal antibodies aimed at tau pathology. Several patent families focus on small-molecule inhibitors patented by Eisai (GB patents, e.g., GB2587934).
  • Amyloid-targeted agents: Including antibody-based therapies and BACE inhibitors.
  • Combination therapies: Patents reflecting multi-mechanism approaches, similar to GB2587934, are increasingly prevalent.
  • Biomarker and diagnostic patents: Supporting targeted application and early diagnosis.

3. Notable Patent Filings and Prior Art

Previous filings include US patents by Lilly and Biogen, with claims extending to tau immunotherapies (e.g., Aducanumab) and beta-secretase inhibitors. The novelty of GB2587934 lies in:

  • The specific combination of tau inhibitors with anti-amyloid strategies,
  • The structural scope of chemical compounds,
  • The focus on early intervention, which remains a critical market segment.

4. Patent Trends and Strategic Considerations

The landscape emphasizes:

  • Multi-targeted approaches as an innovative direction, reflected in GB2587934.
  • The need for broad claim scopes to prevent workaround strategies.
  • The importance of clinical data to bolster patent claims, especially for combination therapies.

Implications for Commercial and R&D Strategies

Patent GB2587934 signals a deepening emphasis on multi-modal treatment strategies for Alzheimer’s, aligning with:

  • Clinical paradigm shifts favoring combination therapies over monotherapies.
  • The necessity for robust patent protection to secure market exclusivity amidst prolific R&D activity.
  • The potential for licensing negotiations or strategic partnerships for compounds covered under GB2587934.

Furthermore, emerging patent applications in the same space increasingly target next-generation tau aggregation inhibitors and bi-specific antibodies, which may threaten or supplement the protection offered by GB2587934.


Key Takeaways

  • Scope and Claims: GB2587934’s claims are broad, targeting the inhibition of tau aggregation and combination therapy with amyloid or anti-inflammatory agents, with specific chemical structures and therapeutic methods.
  • Strategic Importance: It fortifies Eisai’s position within the UK and potentially broader European markets in the growing realm of multi-mechanism neurodegenerative drugs.
  • Patent Landscape Context: The patent sits within a highly competitive environment, where combination therapies and multi-targeted approaches are gaining prominence.
  • Innovation Focus: Emphasis on early-stage intervention and structural diversity of chemical compounds enhances its competitive edge.
  • Business Implication: Patent rights can underpin licensing, collaborations, and clinical development, offering a significant strategic advantage in the Alzheimer’s therapeutics market.

FAQs

1. Does GB2587934 protect specific chemical compounds or just methods?
GB2587934 primarily protects both specific chemical compounds capable of inhibiting tau aggregation and methods of treatment involving these compounds, including combination therapies.

2. How broad are the claims within GB2587934?
The claims are designed to be broad, covering multiple classes of tau aggregation inhibitors, combination therapies with anti-amyloid or anti-inflammatory agents, and various treatment methods, thus providing extensive protection.

3. Can competitors develop similar therapies around this patent?
Potentially, if they modify chemical structures significantly or target different mechanisms not encompassed by specific claims. However, the broad scope of the claims limits such workaround strategies.

4. How does this patent fit into the global patent landscape?
GB2587934 likely forms part of an international patent family, complementing European and US filings. It aligns with the global shift toward multi-targeted, disease-modifying therapies for AD.

5. What does the patent landscape imply for future drug development in neurodegenerative diseases?
It indicates a trend toward combination approaches targeting multiple pathological features, emphasizing the importance of broad, multi-mechanistic claims and early intervention focus, with substantial patent protection vital for commercial success.


References

  1. Eisai Co., Ltd.. "Method for treating or preventing Alzheimer’s disease and other neurodegenerative disorders." GB2587934 patent publication.
  2. European Patent Office. Patent family data and related filings.
  3. Biogen and Lilly patent families focusing on tau and amyloid therapies.
  4. Clinical trials and patent strategies in neurodegeneration from industry reports.

In conclusion, GB2587934 illustrates strategic patenting in neurodegenerative disease therapeutics, emphasizing combination approaches with broad compound and method claims, aligning with evolving scientific insights and market priorities in Alzheimer’s research.

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