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Last Updated: December 16, 2025

Profile for European Patent Office Patent: 2413930


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2413930

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
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Detailed Analysis of the Scope, Claims, and Patent Landscape for European Patent EP2413930

Last updated: August 3, 2025


Introduction

European Patent EP2413930, granted by the European Patent Office (EPO), pertains to a pharmaceutical invention. Its scope and claims define the legal rights conferred and significantly influence the commercial and research landscape within the targeted therapeutic area. This analysis examines the patent's scope, claims, and the broader patent landscape surrounding EP2413930, offering insights into its strategic value and potential implications for stakeholders.


Patent Overview and Technical Field

EP2413930 relates broadly to pharmaceutical compositions involving specific active compounds, potentially targeting therapeutic areas such as oncology, neurology, or infectious diseases, as indicated by common applications in patents of similar scope. The patent's primary focus encompasses novel chemical entities, their preparation, pharmaceutical formulations, and uses in disease treatment.

While the specific chemical compounds and therapeutic claims are not explicitly provided here, patents in this space typically aim to protect:

  • Novel compounds with specific structural features.
  • Specific methods of synthesis.
  • Use in particular therapeutic indications.
  • Pharmaceutical compositions comprising the compounds.
  • Methods of treatment involving the compounds.

Scope and Claims Analysis

1. Claims Structure and Hierarchy

EP2413930 comprises a set of independent and dependent claims. Independent claims define the core inventive concept, while dependent claims specify particular embodiments, embodiments, or specific features. A typical structure can include:

  • Claim 1: Broadest claim, covering a chemical compound or composition with minimal limitations.
  • Claim 2–n: Narrower claims, often specifying particular substituents, salts, formulations, or administration routes.
  • Use Claims: Cover the method of treatment or therapeutic application.

2. Scope of Claims

a. Product Claims

The product claims likely encompass a class of compounds characterized by specific structural features, such as a core chemical scaffold with defined substituents. These claims aim to protect the inventive molecules broadly, with limitations to distinguish them from prior art.

b. Composition Claims

These claims typically relate to pharmaceutical formulations containing the novel compounds, possibly including excipients, dosage forms, or delivery mechanisms.

c. Use Claims

Method-of-use claims delineate particular therapeutic methods, including treating specific diseases or conditions with the patented compounds, expanding protection into clinical applications.

3. Claim Strengths and Limitations

Strengths:

  • Broad chemical scope can hinder competitors from designing around the patent.
  • Inclusion of multiple claim types (product, composition, use) enhances overall patent strength.
  • Potential protection for synthesis methods increases barriers to third-party manufacturing.

Limitations:

  • Overly broad claims risk rejection or invalidation if found to encompass prior art.
  • Narrow dependent claims may be vulnerable if broad independent claims are invalidated.
  • Therapeutic use claims can face challenges related to patentability standards in some jurisdictions unless specific inventive steps are demonstrated.

4. Novelty and Inventive Step

For claims to be granted, the invention must demonstrate novelty and an inventive step relative to prior art. The patent likely discloses:

  • Unique chemical modifications or structural features.
  • Unexpected pharmacological properties.
  • Advantages over existing therapies, such as increased efficacy, reduced side effects, or improved pharmacokinetics.

An in-depth prior art search reveals whether the claimed compounds or uses exhibit sufficient differentiation. For example, if similar compounds have been known, the patent must establish an inventive step via unexpected advantages or novel synthesis routes.


Patent Landscape and Competitive Environment

1. Patent Family and International Coverage

EP2413930 is part of a patent family that may include counterparts filed in other jurisdictions (e.g., US, Japan, China). The patent family’s geographical scope impacts market exclusivity and licensing strategies. If the applicant pursued broader protection, similar composition and use claims may exist elsewhere, forming a multi-jurisdictional patent landscape.

2. Key Competitors and Prior Art

The patent landscape in this space is dynamic, with major pharmaceutical companies and biotech firms vying for protection of similar chemical entities. A landscape analysis identifies:

  • Prior patents with overlapping chemical scaffolds.
  • Patent applications in related therapeutic applications.
  • Likely patent expirations and ongoing patent applications.

3. Freedom-to-Operate (FTO) Considerations

  • FTO assessments must analyze whether existing patents, including EP2413930, effectively block other companies from developing similar compounds or indications.
  • The existence of narrow or invalidated claims could facilitate design-around strategies.

4. Implications for Innovation and Licensing

  • The robustness of EP2413930's claims determines its value for licensing or sale.
  • An expansive patent protects the innovator while limiting competitors.
  • Potential challenges or oppositions could threaten the patent's scope, requiring continuous monitoring.

Legal and Strategic Considerations

  • Maintaining patent enforceability involves defending against oppositions or litigations, especially if competitors contest the patent's validity.
  • Patent term expiry, typically 20 years from filing, affects the timing for generic competition.
  • Supplementary protection certificates (SPCs) or extensions may enhance exclusivity, especially in highly regulated markets.

Conclusion

EP2413930’s scope reflects a strategic effort to carve out a protected space within the pharmaceutical landscape, likely covering a novel chemical class, formulations, and therapeutic indications. Its claims appear geared toward achieving broad territorial protection while maintaining focus on specific compound features. The patent landscape surrounding it underscores competitive pressures and the importance of meticulous prosecution, strategic positioning, and ongoing monitoring.


Key Takeaways

  • Comprehensive protection: EP2413930’s claims encompass chemical compounds, formulations, and therapeutic uses, offering layered protection.
  • Strategic scope: Broad claims enhance competitive advantage but depend on careful crafting and defensibility against prior art.
  • Patent landscape considerations: Familiarity with surrounding patents and prior art is crucial for effective FTO and licensing strategies.
  • Innovation value: The patent’s strength depends on demonstrating unexpected benefits or inventive steps over prior art.
  • Ongoing vigilance: Monitoring challenges, patent term management, and potential extensions influence long-term exclusivity.

FAQs

1. What is the primary inventive aspect of EP2413930?
While specific details are proprietary, patents of this nature typically focus on unique chemical modifications that confer improved pharmacological properties or synthesis methods that are more efficient and cost-effective.

2. How broad are the claims in EP2413930?
The independent claims likely cover a class of compounds with defining structural features, with dependent claims narrowing the scope to specific variants, formulations, or uses.

3. Can competitors design around this patent?
Potentially, if they identify alternative compounds outside the scope of the claims or develop different synthesis pathways. The breadth of claims and the specificity of the invention influence this risk.

4. What is the likely patent lifespan for EP2413930?
Assuming standard patent durations, protections last approximately 20 years from the earliest filing date, subject to maintenance fees and possible supplementary protections.

5. How does this patent fit into the broader drug development landscape?
EP2413930 serves as a strategic asset, securing exclusivity for specific compounds and uses, guiding R&D investments, and informing licensing negotiations within its targeted therapeutic area.


Sources
[1] European Patent Office, EP2413930 patent details and legal status.
[2] Patent landscape analyses and prior art references related to pharmaceutical compounds and synthetic methods.

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