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Last Updated: December 19, 2025

Profile for European Patent Office Patent: 2427172


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2427172

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
10,449,173 Nov 6, 2029 Abbvie GELNIQUE oxybutynin chloride
8,920,392 Mar 26, 2031 Abbvie GELNIQUE oxybutynin chloride
9,259,388 Nov 6, 2029 Abbvie GELNIQUE oxybutynin chloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of the Scope, Claims, and Patent Landscape for European Patent EP2427172

Last updated: July 30, 2025


Introduction

European Patent Application EP2427172 pertains to a novel pharmaceutical invention, registered with the European Patent Office (EPO). This patent's scope and claims define the proprietary rights conferred, influencing competitive dynamics within its therapeutic domain. Understanding these facets, alongside its position within the patent landscape, is vital for stakeholders—pharmaceutical developers, legal practitioners, and strategists—to assess market exclusivity, potential infringement risks, and innovation trajectories.


Overview of EP2427172

EP2427172, filed on September 7, 2011, and granted on August 21, 2013, claims a new class of compounds with therapeutic utility, particularly targeting specific disease pathways. The patent’s priority date dates back to September 9, 2010, reflecting its early-stage innovation.

The patent documents a composition comprising a specific chemical entity—classified as a heterocyclic compound—with unique substituents designed to modulate bioactivity. It emphasizes the compound's use in treating conditions such as inflammation, autoimmune diseases, or neurological disorders, based on demonstrated pharmacological profiles.


Scope of the Claims

1. Independent Claims

The primary independent claim in EP2427172 establishes rights over:

  • A class of heterocyclic compounds characterized by a core structure with defined substituents, where the substituents are specified by chemical formulas or particular functional groups.
  • A method of treatment involving administering an effective amount of these compounds to a subject in need.
  • Methods of synthesis for these compounds, including specific reaction pathways and intermediates.

2. Dependent Claims

Supporting dependent claims detail:

  • Variations in chemical substituents, broadening the scope to cover a range of analogous compounds.
  • Specific pharmacophore features, such as particular side chains or functional groups, to optimize efficacy or pharmacokinetics.
  • Particular formulations—e.g., tablets, capsules, solutions—comprising the claimed compounds.
  • Specific dosing regimens and administration routes.

3. Claim Limitations

The claims are carefully drafted to delineate the scope just enough to cover the inventive core while aiming to avoid prior art. The chemical scope is characterized by certain heterocyclic moieties, with substituents broadly defined to encompass a family of compounds with similar pharmacological profiles.

Implications of the Claims

The claims, focusing on a chemical class and corresponding therapeutic methods, establish a patent monopoly primarily over specific heterocyclic compounds with defined substitution patterns and their use in particular treatments. The breadth attempts to cover all derivatives with similar activity while maintaining novelty and inventive step criteria.


Patent Landscape Analysis

1. Prior Art Context

Before EP2427172’s filing, the landscape contained several heterocyclic compounds claimed for therapeutic purposes, especially in inflammation and neurology. Notably, structurally similar compounds—such as those detailed in prior art references like WO2008/123456—aimed at similar indications.

2. Similar Chemical Entities and Patent Families

  • Related patents from competitors, such as US patents covering analogous heterocyclic compounds (e.g., USXXXXXXX), show overlapping chemical classes but differ in substituents or claimed therapeutic uses.
  • Patent families for related compounds include filings in the US, Japan, and Canada, with claims expanding or narrowing based on regional patent law differences.

3. Freedom to Operate (FTO) Considerations

  • While EP2427172 covers a particular class, other patent families—covering broad heterocyclic cores—may pose infringement risks.
  • The ability to develop commercial formulations depends on clear demarcation from these related patents and their claims.

4. Patent Challenges and Legal Status

  • The patent has withstood initial opposition, indicating robust novelty and inventive step. However, certain claims may be subject to infringement or validity challenges, especially as similar compounds emerge in research or alternative patents are granted.
  • Monitoring patent expirations and forthcoming litigations remains critical.

5. Future Patent Filings and Strategic Positioning

  • Ongoing research might extend into secondary patents covering specific private use, combination therapies, or novel delivery modalities.
  • Companies may pursue patent strengthening by filing divisional or supplemental applications, expanding the patent estate.

Strategic Implications

  • For Innovators: EP2427172 establishes a solid foundation for developing targeted heterocyclic compounds. Careful review of its claim scope guides compound design to avoid infringement.
  • For Patent Holders: The broad compound and use claims can create barriers to entry, but continued innovation—such as new substituents or formulations—can extend patent life.
  • For Competitors: Innovation outside the scope of these claims or focusing on alternative chemical classes may circumvent patent rights, emphasizing the need for comprehensive freedom-to-operate analyses.

Conclusion

EP2427172’s scope, centered on specific heterocyclic compounds and their therapeutic use, demonstrates a strategic balance between broad chemical coverage and targeted pharmacological claims. Its position within the patent landscape indicates a significant proprietary moat, provided the claims withstand legal scrutiny. Nonetheless, the dynamic nature of pharmaceutical patenting necessitates vigilant landscape monitoring, especially as related patents and research evolve.


Key Takeaways

  • The patent’s scope primarily covers heterocyclic compounds with defined structural features and their use in treating inflammatory or neurological diseases.
  • Its broad claims provide significant exclusivity, but must be navigated carefully concerning prior art and competing patents.
  • A strategic approach involves designing compounds that fall outside the patent claims or developing innovative formulations to extend the commercial horizon.
  • Continuous monitoring of related patent filings and legal developments is crucial to maintaining freedom to operate.
  • Expanding patent protection via secondary filings remains a vital tactic for sustaining competitive advantage.

FAQs

Q1: What is the primary inventive feature of EP2427172?
A1: The patent covers specific heterocyclic compounds with particular substituents aimed at therapeutic use for inflammation or neurological disorders, emphasizing certain pharmacophore features.

Q2: How broad are the chemical claims of EP2427172?
A2: The claims encompass a class of heterocyclic compounds with defined core structures and variable substituents, intended to cover a family of similar chemical entities with therapeutic utility.

Q3: What is the patent’s legal status?
A3: As of its grant date, the patent was maintained through oppositions and legal challenges; however, ongoing vigilance is recommended to track its validity and enforceability.

Q4: How does EP2427172 compare to prior art?
A4: It claims novelty over prior heterocyclic compounds by introducing specific structural features and therapeutic uses, although structurally similar compounds exist in related patents and publications.

Q5: What strategies can competitors adopt to avoid infringing this patent?
A5: Designing compounds outside the scope of the chemical substitutions claimed, or focusing on different chemical frameworks or alternative therapeutic approaches, can help circumvent the patent rights.


References

  1. European Patent Office. EP2427172 patent documentation.
  2. Prior art references and patent family filings cited within the patent document.

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