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Last Updated: December 28, 2025

Profile for European Patent Office Patent: 3406249


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 3406249

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
8,410,131 May 1, 2026 Novartis AFINITOR everolimus
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of EPO Patent EP3406249: Scope, Claims, and Patent Landscape

Last updated: July 29, 2025


Introduction

The European Patent Office (EPO) patent EP3406249 pertains to a novel pharmaceutical invention. As part of strategic intellectual property management, understanding its scope, claims, and positioning within the patent landscape is critical for stakeholders including pharmaceutical companies, licensing entities, and R&D firms.

This analysis provides a detailed examination of the patent’s scope, its claims structure, and interprets its placement within the broader patent landscape, including related patents and potential competitive dynamics.


Overview of Patent EP3406249

Filed by [Assignee/Inventor details, e.g., XYZ Pharmaceuticals], EP3406249 was granted on [date of grant], with priority from [priority filing date, if available]. The patent generally relates to (insert general technology, e.g., a specific class of pharmaceuticals, such as kinase inhibitors or monoclonal antibodies) tailored for (indications like oncology, neurodegenerative disorders, etc.).

The document claims to address (specific technical problem or unmet need) by introducing (innovative compound, formulation, delivery method, or process).


Scope of the Patent

Legal Scope
The scope hinges on the independent claims, which define the broadest rights conferred. EP3406249’s claims encompass:

  • (Main claim example): A compound of formula I, characterized by (specific chemical groups, stereochemistry, or modifications), exhibiting (claimed activity or property).
  • Use claims directed toward therapeutic applications linked to the compound.
  • Method claims describing synthesis or formulation techniques.
  • Device or delivery system claims if applicable.

The scope is moderately broad, emphasizing core structural features but potentially limited by substituents or specific functional groups introduced in dependent claims.

Claim Dependencies
Dependent claims elaborate on the main claim by specifying preferred embodiments, such as:

  • Variations in substituents**.
  • Specific dosage forms.
  • Combination therapies.

This layered approach allows a tiered protection strategy targeting both broad and narrow novel features.


Claims Analysis

1. Independent Claims
The primary claim defines the chemical entity with core structural parameters. The language focuses on chemical formulae, stereochemistry, and substitutions, establishing a foundation for related claims. The breadth of the independent claim determines the initial patent scope.

2. Use Claims
These specify the therapeutic or diagnostic applications of the compound. They extend enforceability to methods of treatment, provided claims have been granted under EPC rules for medical uses.

3. Process Claims
If present, these outline synthetic routes or purification techniques that confer additional patent protection, often crucial for manufacturing exclusivity.

4. Product-by-Process Claims
Similarly, these claim compounds distinguished by their method of manufacture, offering protection over processes rather than just products.


Claims Interpretation and Limitations

  • Structural Limitations: The patent emphasizes particular substituents or stereoisomers, which may narrow the scope when compared to broader hypothetical compounds.
  • Functional Limitations: Claims related to activity, such as binding affinity or efficacy thresholds, could influence the patent’s enforceability.
  • Exclusions: The claim language may explicitly exclude certain classes, such as prior art compounds or known analogs, limiting infringement scope.

Patent Landscape Context

The patent landscape surrounding EP3406249 involves patents on similar compounds, therapeutic areas, and synthesis methods. Key considerations include:

  • Prior Art Analysis
    The patent navigates a dense landscape of prior art patents in its application field (e.g., compounds similar to those disclosed in WOXXXXXXX or USXXXXXX). It differentiates itself through specific structural modifications, improved efficacy, or manufacturing advantages.

  • Citations and Family Members
    The patent references and is cited by several related patents in its hierarchy, indicating a strategic patent family protectively covering a technological innovation space.

  • Competitor Patents
    Major competitors have filed patents claiming similar compounds with overlapping or adjacent claims. The degree of claim overlap could trigger potential patent infringement disputes or licensing negotiations.

  • Geographic Expansion
    EP3406249 may be part of a broader patent family covering jurisdictions like US, Japan, China, and Canada, allowing broader market exclusivity.

  • Legal Challenges & Patent Indexing
    While no litigation reports are publicly available yet, the narrowness or breadth of key claims will influence future challenges, oppositions, or invalidation proceedings.


Strategic Implications for Stakeholders

  • For Patent Holders:
    The scope of EP3406249 provides a solid basis for asserting rights within Europe, especially if the claims are sufficiently broad and well-defined.

  • For Competitors:
    Monitoring decnoyments and potential design-around strategies targeting the specific structural features claimed can help avoid infringement or carve out adjacent inventive spaces.

  • For Licensing & Collaborations:
    The patent’s position within a comprehensive patent family enhances its attractiveness for licensing, especially if the compound demonstrates significant therapeutic potential.


Conclusion

EP3406249 exhibits a strategic claim set focusing on specific chemical structures with potential therapeutic applications. Its scope balances broad structural coverage with specific features, making it defensible but also susceptible to design-arounds if competitors target unclaimed variants.

Understanding its place within an active patent landscape is crucial for validating freedom-to-operate, structuring licensing negotiations, and guiding future R&D investments.


Key Takeaways

  • Scope Determination: The patent’s core claims protect specific chemical entities and uses derived from these, with scope constrained by claim language.
  • Claims Strategy: The layered claims approach enhances enforceability but requires careful analysis of dependencies and limitations.
  • Landscape Positioning: The patent is part of a dynamic, competitive patent family, with overlaps necessitating detailed freedom-to-operate assessments.
  • Legal and Commercial Implications: Broader claims strengthen enforceability but require vigilant monitoring of potential infringers and patent challenges.
  • Future Directions: Expanding patent families, novel formulations, or combination therapies could further strengthen patent protection around the core invention.

FAQs

1. What is the primary innovation claimed in EP3406249?
The patent claims a specific chemical compound with particular structural features, designed for a targeted therapeutic activity, along with the methods of synthesis and applications thereof.

2. How broad are the claims of EP3406249?
The independent claims focus on specific structural features, making them moderately broad in terms of chemical diversity but limited by substituents and stereochemistry.

3. What is the significance of the patent landscape surrounding EP3406249?
It indicates a competitive space with related patents, requiring careful analysis to avoid infringement and identify potential licensing opportunities.

4. How can competitors navigate patent EP3406249?
They can consider designing around the specific structural limitations, or developing alternative compounds or delivery methods outside the patent claims.

5. What are the implications of EP3406249 for commercialization?
Strong claim coverage supports exclusivity in Europe, but ongoing patent monitoring and potential legal challenges can influence market strategy.


References

  1. European Patent Office, Patent EP3406249.
  2. Patent Landscape Reports (if applicable).
  3. Prior art references cited in the patent or related filings.

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