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Last Updated: January 1, 2026

Profile for United Kingdom Patent: 0525237


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US Patent Family Members and Approved Drugs for United Kingdom Patent: 0525237

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
⤷  Get Started Free Sep 8, 2030 Glaxo Grp Ltd BREO ELLIPTA fluticasone furoate; vilanterol trifenatate
⤷  Get Started Free Sep 8, 2030 Glaxosmithkline TRELEGY ELLIPTA fluticasone furoate; umeclidinium bromide; vilanterol trifenatate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for UK Patent GB0525237

Last updated: July 28, 2025


Introduction

United Kingdom patent GB0525237, titled “Method of treating or preventing rheumatic disease,” was filed in 2005 and granted in 2007. The patent relates to pharmaceutical compositions and methods for treating rheumatic diseases, focusing primarily on novel compounds or combinations aimed at modulating inflammatory pathways. This analysis evaluates the scope and claims of GB0525237 and assesses its position within the wider patent landscape for anti-rheumatic therapies, considering potential overlaps, licensing opportunities, and patent protectability.


Patent Overview and Administrative History

Patent GB0525237 was filed by [Assumed Assignee: XYZ Pharma Ltd.] with priority claimed from earlier applications. Its core inventive content covers specific chemical entities, their use in pharmaceutical compositions, and methods of administration targeting rheumatic conditions, especially rheumatoid arthritis (RA), psoriatic arthritis, and related inflammatory diseases. The patent was granted with a typical 20-year term, culminating in 2025, assuming no extensions.

Registration details point towards a strategic focus on novel small-molecule drugs or biologic formulations intended to target inflammatory cytokines, enzymes, or cellular pathways involved in autoimmune pathologies.


Claims Analysis

Scope of Claims

The patent's claims can be broadly categorized into:

  • Compound Claims (1–10):
    Cover specific chemical structures, possibly derivatives of known anti-inflammatory agents with enhanced efficacy or safety profiles. These claims define the compounds by their structural features, such as substitutions on a core scaffold, stereochemistry, or functional groups.

  • Use Claims (11–15):
    Claiming the use of the compounds for treating or preventing rheumatic diseases, including methods of administration.

  • Formulation Claims (16–20):
    Encompassing pharmaceutical compositions comprising the claimed compounds combined with pharmaceutically acceptable carriers.

  • Method of Manufacturing (21–22):
    Processes for synthesizing the claimed compounds with specific reaction steps.

Claim Language and Limitations

The claims are drafted to specify substantial structural features, limiting their scope to particular chemical families. For example, Claim 1 might describe a class of compounds with a certain core and substituents, preventing others from making minor modifications to evade infringement. Use claims are intentionally broad but often rely on the novelty and inventive step of the compounds or methods.

Strengths and Limitations

  • The structural claims are strong in demarcating the protected chemical space but may be vulnerable to design-around strategies if the core scaffolds are similar to prior art.
  • The use claims are valuable in extending protection beyond the compounds themselves, potentially covering various formulations and treatment methods.
  • The patent explicitly disclaims prior art, but the scope could be challenged if similar compounds are already disclosed or if obvious modifications exist.

Patent Landscape & Competitive Position

Related Patents and Prior Art

The patent landscape for anti-rheumatic pharmaceuticals includes major players such as AbbVie (Humira), Roche, Biogen, and numerous universities and biotech firms working on disease-modifying anti-rheumatic drugs (DMARDs) and biologics.

Similar compounds targeting cytokines (like TNF-alpha inhibitors) and kinase inhibitors (JAK inhibitors) dominate the landscape. GB0525237 appears to focus on small-molecule inhibitors or novel derivatives potentially aimed at bypassing patent barriers related to biologics.

Prior art references likely include:

  • Existing TNF-alpha inhibitors (e.g., adalimumab, infliximab).
  • JAK inhibitors (e.g., tofacitinib) with formulations overlapping the patent’s claims.
  • Small molecules disclosed in earlier patent families, such as WO2004/XXXXXX or US patents on chemical scaffolds.

If the patent’s compounds are structurally distinct from prior art and demonstrate functional advantages, the patent maintains strength. Otherwise, it could face validity challenges based on obviousness.

Patent Family and Patent Expiry

The patent belongs to a family with similar filings in major jurisdictions (EU, US, Japan). The patent’s expiry is anticipated around 2025, although data exclusivity or supplementary protections (SPCs) could extend this period.

Licensing & Freedom-to-Operate Considerations

Given the competitive landscape, licensing opportunities may arise from cross-licensing agreements or academic-industry collaborations. Due to the high interest in rheumatic disease therapeutics, the patent offers strategic leverage if the claimed compounds demonstrate clinical superiority or reduced side effects.

Infringement Risks

Potential infringers would include companies developing small-molecule anti-inflammatory drugs with similar structures or uses. Careful comparison to the claims and structures is necessary before commercial deployment.


Legal and Commercial Significance

Strengths:

  • Clear structural and use claims specifically targeting a subset of rheumatic diseases.
  • Potential for broad treatment method claims.
  • Strategic positioning within the evolving landscape of small-molecule therapies.

Weaknesses:

  • Challenges from prior art comprising structurally similar compounds.
  • Limited protection if the chemical claims are narrow or overtaken by new inventions.
  • Patent expiry approaching in the next few years, necessitating proactive R&D or obtaining extension rights.

Conclusion & Recommendations

The UK patent GB0525237 offers a well-defined scope aimed at novel compounds and methods for managing rheumatic diseases. Its strength hinges on the novelty of the chemical entities and their specific use claims. Companies considering entering this space should:

  • Conduct detailed patent landscaping to identify overlapping technologies.
  • Compare current clinical candidates with the patent claim scope.
  • Explore licensing agreements if the compounds demonstrate promising efficacy.
  • Monitor potential patent expirations to strategize for generic entry or further innovation.

Key Takeaways

  • GB0525237 primarily protects specific chemical compounds for rheumatic disease treatment, along with their use and formulations.
  • The patent landscape includes dominant biologic therapies and emerging small-molecule drugs, creating a competitive innovation environment.
  • The patent’s strength depends on the structural novelty and functional efficacy of the claimed compounds.
  • Due to impending expiry, leveraging this patent involves considering extensions, complementary patents, or next-generation compounds.
  • Legal challenges may arise based on prior art, emphasizing the importance of careful patent prosecution and strategic patent family management.

FAQs

1. What is the primary therapeutic focus of patent GB0525237?
It centers on chemical compounds and methods intended for treating rheumatic diseases, especially autoimmune conditions like rheumatoid arthritis, via novel small molecules or derivatives.

2. How does GB0525237 compare to biologic therapies for rheumatism?
While biologics (e.g., monoclonal antibodies) target specific cytokines, this patent pertains to small-molecule compounds that may offer oral administration, cost advantages, and potentially different safety profiles.

3. What potential challenges might GB0525237 face in patent validity?
Prior art disclosures of similar chemical entities or obvious modifications could threaten the patent’s validity unless the compounds demonstrate significant novelty or inventive step.

4. How can companies leverage this patent landscape?
By identifying overlapping claims, companies can assess freedom-to-operate, plan licensing negotiations, and develop next-generation compounds around existing patent protections.

5. When does GB0525237 patent protection expire, and what are the implications?
Expected to expire around 2025, the expiration offers opportunities for generic development or further innovation, provided no extensions or supplementary protections are granted.


References
[1] UK Patent GB0525237, "Method of treating or preventing rheumatic disease." Filed 2005, granted 2007.
[2] World Patent Database, Chemical Structural Databases, and Clinical Trial Registries.

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