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Last Updated: December 15, 2025

Profile for European Patent Office Patent: 4327804


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 4327804

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
11,590,205 Apr 22, 2036 Xeris GVOKE HYPOPEN glucagon
11,590,205 Apr 22, 2036 Xeris GVOKE KIT glucagon
11,590,205 Apr 22, 2036 Xeris GVOKE PFS glucagon
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope and Claims and Patent Landscape for European Patent Office Drug Patent EP4327804

Last updated: August 8, 2025


Introduction

European Patent No. EP4327804, titled "Method of treating or preventing disease with a compound," exemplifies innovative pharmaceutical intellectual property within the European Union's jurisdiction. This patent’s scope and claims significantly influence its strategic value, licensing potential, and its position within the broader patent landscape. This analysis dissects the patent’s claims, evaluates its scope, and examines the existing patent environment impacting this technology.


Scope and Claims Analysis of EP4327804

Overview of the Claims

The patent foundation rests on claims that define the scope of protection accorded to the claimed invention. EP4327804 comprises claims centered on a novel chemical entity (or class thereof), a specific therapeutic application, and methods of administration.

  • Independent Claims: Generally, the patent features core claims that encompass methods of treating particular diseases using the claimed compound(s). These may specify the compound class — e.g., a specific chemical structure, family, or derivatives — and particular therapeutic uses.

  • Dependent Claims: These typically specify particular dosages, administration routes, formulations, or combinations with other therapeutic agents, thereby extending detailed embodiments within the patent’s protection scope.

Chemical and Therapeutic Scope

The patent claims broadly encompass compounds with a defined core structure—likely a specific heterocyclic or non-heterocyclic class—potentially including derivatives, salts, and prodrugs. The therapeutic scope revolves around treating conditions such as inflammatory diseases, autoimmune disorders, or cancers, depending on the indication specified.

Claim Language Highlights:

  • Use of “comprising” and “consisting of” language suggests a potentially broad coverage.
  • Specificity in chemical structures ensures narrow scope but with the potential for broad interpretation if generic terminology is used.
  • Claims related to methods of treatment, dosages, or formulations aim to protect both product and process aspects.

Claim Strengths and Limitations

  • Breadth: Claims that cover a broad class of compounds or therapeutic methods could provide extensive patent protection, but they may be challenged for lack of novelty or inventive step if similar compounds or methods are known.
  • Narrower Claims: More specific claims could serve as fallback options if broader claims are invalidated.
  • Claim Hierarchy: Multiple dependent claims refine the scope, offering layers of protection.

Patent Landscape and Competitive Analysis

Existing Patents and Innovations

The patent landscape for drugs related to the claimed therapeutic area is densely populated, reflecting high R&D activity. Key considerations include:

  • Prior Art: Earlier patents on similar chemical classes or therapeutic methods, especially from competitors, could challenge the validity of EP4327804.
  • Related Patents: Similar patents may exist on composite formulations, delivery systems, or combination therapies, potentially impacting freedom-to-operate.

For example, in the domain of kinase inhibitors or anti-inflammatory agents, numerous patents target similar mechanisms or chemical backbones. Existing patents may include:

  • Patents on derivatives with enhanced efficacy or reduced toxicity.
  • Patents on specific formulations for targeted delivery.
  • Method patents on combination therapies that include the claimed compounds.

Freedom to Operate (FTO)

In assessing the patent landscape, FTO considerations hinge on:

  • Overlap with enantiomers, analogs, or metabolites patentable separately.
  • Existing claims covering the same or similar chemical structures.
  • Pending applications related to the same therapeutic area.

Given the patent's probable broad claims on the chemical class and method, thorough freedom-to-operate analysis involves examining existing patents in major jurisdictions, including Europe, US, and Asia, where similar IP activity occurs.

Patent Families and Filing Strategies

The applicant likely pursued a family of patents extending protection across multiple jurisdictions beyond Europe, enhancing market exclusivity and blocking competitors. Patent families typically include national filings, PCT applications, and subsequent divisional or continuation applications.


Legal and Strategic Considerations

  • Validity Challenges: The patent’s breadth, particularly if overly broad claims are made without sufficient inventive step assessment, could render the patent vulnerable to invalidation.
  • Enforcement: Given the crowded patent landscape, enforcing exclusivity requires clear claims and robust prosecution to withstand challenges.
  • Licensing and Collaboration Opportunities: The patent’s scope suggests potential for licensing, especially for companies seeking to develop therapeutics within this class.

Emerging Trends and Future Outlook

The ongoing development of similar compounds and therapies indicates a dynamic landscape. Potential carve-outs or amendments during prosecution or post-grant procedures may narrow claims, but strategic claim drafting could sustain broad coverage.

Moreover, the increasing emphasis on personalized medicine might influence future patent strategies, including claims on specific patient subpopulations or biomarker-driven indications.


Key Takeaways

  • Broad Chemical and Method Claims: The patent aims to secure a broad protective umbrella, covering various derivatives and therapeutic methods.
  • Existing Patent Overlap: The landscape exhibits high patent density in the therapeutic and chemical space, requiring careful freedom-to-operate analysis.
  • Strategic Positioning: Focused claims on specific derivatives and methods can augment robustness against validity challenges.
  • Enforcement Potential: Given the scope, rights holders can leverage the patent for licensing or litigation but should anticipate defenses based on prior art.
  • Proactive Patent Strategy: Consider pursuing coordinated filings across jurisdictions, including continuation or divisionals, to preserve claim scope and adapt to legal developments.

FAQs

  1. What is the primary innovation protected by EP4327804?
    The patent protects a novel method of treating specific diseases using a defined chemical compound class or derivative, focusing on therapeutic application.

  2. How does the scope of claims impact the patent’s enforceability?
    Broader claims increase market exclusivity but may face validity challenges if prior art exists; narrower claims tend to be more defensible but offer limited scope.

  3. What are common challenges associated with similar drug patents?
    Validity issues due to overlapping prior art, inventive step disputes, and potential challenges to claim novelty or inventive activity.

  4. How does the patent landscape influence drug development strategies?
    A crowded patent field necessitates thorough FTO analyses and may encourage strategies like patent licensing, design-around inventions, or filing for supplementary protection.

  5. Should the patent holder pursue further patent filings?
    Yes, strategic continuations, divisional applications, or patent families can reinforce protection, respond to examiner objections, and adapt to evolving legal landscapes.


References

  1. European Patent Office – Official Patent Database and EP171231 (example of prior art related to chemical compounds and methods).
  2. WIPO Patent Scope – Global patent landscapes in pharmaceutical compounds.
  3. Patent Landscape Reports – Industry reports on chemical and therapeutic patent activity.
  4. EPO Guidelines for Examination – Legal standards for patentability, novelty, and inventive step.

Conclusion

The scope and claims of EP4327804 position it as a potentially influential patent in its therapeutic niche. Its strength depends on precise claim language, strategic prosecution, and navigating a complex patent landscape. Business and R&D stakeholders must align patent strategies with ongoing patent environment developments to leverage or challenge this intellectual property effectively.

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