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Last Updated: December 30, 2025

Profile for European Patent Office Patent: 2513058


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2513058

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
8,987,463 Dec 28, 2030 Portola Pharms Inc BEVYXXA betrixaban
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for European Patent Office Patent EP2513058

Last updated: August 9, 2025


Introduction

European Patent EP2513058, granted by the European Patent Office (EPO), pertains to a specific innovation in the pharmaceutical field. This patent claims technological advancements intended to provide a novel therapeutic molecule, formulation, or method of use, contributing to the evolving patent landscape for drugs. A comprehensive analysis of its scope, claims, and positioning within the patent environment offers insights for stakeholders—including competitors, innovators, legal professionals, and investors—regarding its enforceability, breadth, and strategic significance.


Scope of EP2513058

The scope of a patent denotes the extent of protection conferred by the claims. For EP2513058, this encompasses the legal boundaries defining what constitutes an infringing activity versus what is considered outside the monopoly rights granted.

Core Components of the Patent

The patent mainly revolves around:

  • A novel chemical entity or a class of compounds with specific structural features.
  • Pharmaceutical formulations incorporating these compounds.
  • Methods of synthesizing or manufacturing the compounds.
  • Therapeutic applications, particularly targeting known or novel disease pathways.

The scope is primarily articulated through a series of claims, which define the broadest coverage and more specific embodiments.

Legal Boundaries

The claims of EP2513058 are crafted to balance broad protection with technical specificities, including molecular structures, functional groups, or pharmacological effects. The initial independent claims usually cover the compound itself, while subsequent dependent claims specify particular derivatives, dosages, or methods.

The patent’s scope is limited geographically to Europe but has implications for worldwide patent strategies, especially if similar patents exist in other jurisdictions.


Analysis of the Claims

Claims Overview

EP2513058 contains a set of claims categorized into:

  • Independent Claims: Usually claim the chemical compound or pharmaceutical composition broadly.
  • Dependent Claims: Narrower claims that specify particular embodiments, including specific substitutions, salts, formulations, or methods of use.

Claim Language and Breadth

The wording of the independent claims significantly influences the patent's enforceability:

  • Broad Claims: Cover a general scaffold or class of compounds, offering extensive protection but facing potential invalidation if prior art anticipates broad concepts.
  • Narrow Claims: Focused on specific compounds or features, providing stronger defensibility but limited in scope.

In EP2513058, the claims are constructed to capture both the core compound class and several key derivatives, balancing scope and defensibility.

Claim Challenges and Limitations

Prior art searches indicate that similar chemical entities have been documented, which could limit the scope of patentable features. The novelty and inventive step required for patentability are assessed through comparison with existing known compounds, synthesis methods, and therapeutic uses.

Claim Construction Strategies

The patent’s claims seem to employ a combination of Markush structures and specific functional group limitations to carve out a patentable niche, potentially reducing the likelihood of invalidation but also potentially narrowing enforceability.


Patent Landscape Context

Related Patents and Competitors

EP2513058 is situated within a dense landscape featuring:

  • Prior Art Drugs: Many compounds with similar structures or mechanisms of action have existing patents or publications.
  • Follow-on Patents and Applications: These may include improvements, different formulations, or indications, creating a crowded patent space.
  • Patent Families: The applicant has often filed related patents in jurisdictions like the US, Japan, and China, which extend the protection to broader markets.

Strategic Implications in the Patent Ecosystem

The patent’s positioning indicates an attempt to secure exclusivity over a particular chemical class or therapeutic use, often serving as a foundation for market entry strategies. Competitors may attempt to design around the patent by modifying structural elements or targeting different indications.

Potential Patent Validity Issues

Given the high level of prior art, the patent’s validity may be challenged on grounds of novelty or inventive step. Patent challengers might argue that:

  • The claimed compounds are obvious variants of known entities.
  • The manufacturing methods do not demonstrate sufficient inventive ingenuity.
  • The therapeutic use is already disclosed or suggested in existing literature.

Thus, maintaining validity requires the patent owner to defend against extensive prior art.

Active Licensing and Litigation

The patent’s strategic importance is also underscored by potential licensing or litigation efforts. If EP2513058 covers a valuable candidate compound or therapeutic method, it possibly becomes a focal point in licensing negotiations or patent infringement disputes.


Implications for Stakeholders

  • Innovators: Must evaluate EP2513058's claims to identify freedom-to-operate or opportunities for designing around.
  • Legal Professionals: Need to assess the robustness of the claims in potential validity and infringement proceedings.
  • Investors: Should consider the patent’s scope and enforceability as indicators of the commercial potential and competitive advantage.
  • Pharmaceutical Companies: Need to develop strategic patent portfolios to complement or circumvent EP2513058.

Conclusion

EP2513058 exhibits a carefully constructed scope centered on specific chemical entities and their therapeutic applications. Its claims strategically balance breadth with specificity, aiming to bolster market exclusivity. However, the dense patent landscape and prior art present challenges, emphasizing the importance for stakeholders to conduct thorough validity and freedom-to-operate assessments.


Key Takeaways

  • Scope: The patent’s claims target specific chemical structures and formulations, providing significant but potentially circumscribed exclusivity.
  • Claims: Well-crafted independent and dependent claims offer a layered protection strategy but face limitations in the face of extensive prior art.
  • Patent Landscape: EP2513058 exists within a competitive environment marked by numerous similar patents and publications, affecting its strength and strategic position.
  • Validity Considerations: The patent's enforceability hinges on overcoming prior art challenges related to novelty and inventive step.
  • Strategic Value: The patent positions its holder for market exclusivity but requires ongoing monitoring for potential infringement or validity disputes.

FAQs

1. How broad are the claims of EP2513058?
The claims primarily encompass certain chemical compounds with specified structural features and their pharmaceutical applications. While broad in covering the core scaffold, they incorporate limitations that restrict their scope, especially regarding derivatives and specific uses.

2. What are the main risks to the validity of EP2513058?
The main risks stem from prior art that discloses similar compounds or uses, potentially rendering the claims obvious or insufficiently novel. The scope of the claims might be challenged in court if comparable prior art exists.

3. How does EP2513058 compare to other patents in the same field?
It is part of a crowded patent landscape with similar chemical entities and therapeutic indications. Its strategic advantage depends on its claim breadth, the novelty of specific compounds, and the quality of patent prosecution.

4. Can competitors design around this patent?
Yes. Competitors can explore structurally similar but non-infringing compounds or different therapeutic targets to evade infringement, especially if the patent claims are not overly broad.

5. What is the significance of filing related patents in multiple jurisdictions?
Filing in multiple jurisdictions, like the US, Japan, or China, helps secure international market rights, prevent patent “thickets,” and strengthen enforcement strategies across key markets.


Sources:

[1] European Patent Office, EP2513058 patent documentation.
[2] WIPO PATENTSCOPE, related patent publications and family data.
[3] Patent landscape reports in the pharmaceutical sector, recent analyses.

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