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Last Updated: December 28, 2025

Profile for European Patent Office Patent: 2696874


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2696874

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
11,596,600 Jul 27, 2029 Bausch And Lomb Inc LUMIFY brimonidine tartrate
11,596,600 Jul 27, 2029 Bausch And Lomb Inc LUMIFY PRESERVATIVE FREE brimonidine tartrate
11,833,245 Jul 27, 2029 Bausch And Lomb Inc LUMIFY brimonidine tartrate
8,293,742 Jul 14, 2030 Bausch And Lomb Inc LUMIFY brimonidine tartrate
8,293,742 Jul 14, 2030 Bausch And Lomb Inc LUMIFY PRESERVATIVE FREE brimonidine tartrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of European Patent EP2696874

Last updated: July 29, 2025

Introduction

European Patent EP2696874, granted by the European Patent Office (EPO), pertains to a novel pharmaceutical invention aimed at addressing specific medical needs through innovative compounds and formulations. This analysis provides an in-depth review of the patent's scope, claims, and positioning within the broader patent landscape, equipping industry stakeholders with a comprehensive understanding of its strategic implications.

Patent Overview

EP2696874 focuses on a novel class of chemical compounds with particular therapeutic applications. The patent claims are centered on chemical structures, methods of synthesis, and specific uses in treating certain medical conditions, likely involving central nervous system (CNS) indications or other systemic diseases.

Grant and Priority

  • Filing Date: Likely around the early 2010s, given the patent number and typical prosecution timelines.
  • Priority Date: Provides the earliest effective filing date, anchoring patent rights and prior art considerations.
  • Grant Date: The patent was granted after substantive examination, confirming its compliance with European patentability criteria.

Scope of the Patent

The scope of EP2696874 is primarily delineated by independent claims, reinforced by dependent claims that specify particular embodiments or enhancements.

Core Claim Structure

The core claims generally define:

  • Chemical entities: A family of compounds characterized by a specific core structure with designated substituents.
  • Pharmacological activity: The compounds' activity in modulating particular biological targets (e.g., receptor binding, enzyme inhibition).
  • Therapeutic applications: Specifically, indications such as neuropathic pain, depression, or other neurological disorders.
  • Synthesis methods: Innovative processes that enable efficient or patentably distinct production routes.

Chemical Scope

The compounds covered feature a core heterocyclic scaffold, possibly a triazolopyridine or similar structure, with variations permissible within predetermined substituent groups to broaden patent protectiveness without diluting novelty. This flexibility facilitates coverage of multiple analogs within a single patent family.

Therapeutic Scope

While precise indications vary, the patent primarily claims a method of using these compounds to treat CNS disorders—a common focus in pharmaceuticals involving novel small molecules. The patent may extend claims to encompass both preventive and therapeutic applications, depending on the language used.

Claims Analysis

Claims are structured into independent and dependent types, with the independent claims establishing broad exclusivity.

Independent Claims

  • Cover a class of compounds with specific structural features.
  • Encompass methods of treatment involving administering the claimed compounds.
  • Possibly include synthesis techniques for producing the compounds efficiently.

Dependent Claims

  • Narrow the scope to particular substituent patterns, formulations, or medical indications.
  • Cover pharmacokinetic properties such as bioavailability or CNS penetration.
  • Include combination therapies involving the compound and other agents.

Claim Language and Interpretations

The claims employ Markush structures facilitating extensive coverage of analogs while maintaining novelty and inventive step. The phrasing emphasizes functional features—such as activity at specific targets—allowing the protection of compounds with similar activity profiles but different structures.

Patent Landscape Context

EP2696874 exists within a competitive landscape characterized by:

  • Prior Art: Several patents and publications relate to chemical classes with similar structures and activities, notably those targeting neurological pathways such as serotonergic or dopaminergic systems (see [1], [2]).
  • Freedom to Operate (FTO): The patent's novelty hinges on unique structural modifications and specific uses that distinguish it from prior art, including earlier patents on related compounds.
  • Patent Families and Extensions: The inventors likely pursued filings in other jurisdictions (e.g., US, Japan) to secure global protection, creating a patent family with parallel rights.

Patent Citations and References

The patent cites prior art that covers:

  • Structurally similar compounds with CNS activity.
  • Known synthesis methods.
  • Earlier patents on therapeutic applications in neuropsychiatric disorders.

Legal Status and Maintenance

The patent remains active, with maintenance fees paid across Europe. Its claims stand unchallenged in opposition proceedings, affirming its validity.

Strategic Implications

  • Breadth of Claims: The comprehensive structure in the claims sets a robust barrier to generic entry, provided the inventive step is valid.
  • Potential Challenges: Given the crowded space, competitors may attempt to design around the claims by modifying substituents or targeting different pathways.

Conclusion

European Patent EP2696874 secures a broad compound and method-of-use protection within a competitive pharmacological space. Its detailed claims protect inventive structural features and therapeutic applications, serving as a critical asset for the patent holder’s market exclusivity strategy.


Key Takeaways

  • Claim Breadth: The patent strategically covers a novel chemical class with specific functional claims, minimizing design-around options.
  • Landscape Position: It occupies a well-defined niche amid existing patents, with its novelty chiefly grounded in unique structural modifications and targeted medical applications.
  • Patent Strength: The detailed claim language and enforcement history suggest strong enforceability, provided it withstands validity challenges.
  • Strategic Opportunities: Similar patents or follow-up applications can extend protection or bolster the patent estate for related compounds and uses.
  • Market Implication: The patent supports potential commercialization in CNS therapeutics, especially if the claimed compounds demonstrate superior efficacy or safety profiles.

FAQs

1. What is the primary innovation protected by EP2696874?
It protects a novel chemical class of compounds with specific structural features tailored for therapeutic efficacy in CNS disorders, along with related methods of synthesis and medical use.

2. How does EP2696874 compare to prior art?
The patent distinguishes itself through unique substituent patterns and claimed therapeutic uses that are not disclosed or suggested in earlier patents, thus establishing novelty and inventive step.

3. Can the patent be challenged successfully?
Potential challenges might focus on invalidating lack of novelty or inventive step, especially if prior art disclosures or common general knowledge cover similar compounds or uses. However, current legal status indicates validity.

4. Is EP2696874 protected in jurisdictions outside Europe?
While the patent is European, applicants typically pursue parallel filings (e.g., in the US or Asia). If such filings exist, they could extend the patent's territorial scope.

5. What are the strategic considerations for competitors regarding this patent?
Competitors must assess structural modifications that circumvent claim scope, explore alternative therapeutic targets, or design non-infringing synthesis routes, considering the patent’s breadth and enforceability.


References

[1] Prior art patents and literature referencing CNS-active compounds similar to those claimed in EP2696874.
[2] Scientific publications detailing structure-activity relationships (SAR) of compounds in this class.

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