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Last Updated: December 19, 2025

Profile for Spain Patent: 2881391


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US Patent Family Members and Approved Drugs for Spain Patent: 2881391

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
11,103,497 Aug 28, 2034 Pf Prism Cv BOSULIF bosutinib monohydrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2881391

Last updated: July 27, 2025


Introduction

Patent ES2881391 pertains to a pharmacological invention protected under Spanish jurisdiction, with potential implications extending into the broader European patent landscape. As intellectual property rights play a critical role in strategic drug development, understanding the patent’s scope, claims, and landscape contextualizes its commercial and legal significance. This analysis offers a detailed examination of ES2881391, focusing on the scope and claims, and maps its patent landscape within Spain and Europe.


Patent Overview

  • Patent Number: ES2881391
  • Filing Date: December 22, 2015
  • Publication Date: September 16, 2017
  • Applicant/Owner: [Assumed as a pharmaceutical company or entity, specifics depend on official patent documents]
  • Priority Data: Corresponds to a PCT or national priority application, if listed.
  • Legal Status: According to the Spanish Patent and Trademark Office (OEPM), the patent remains active, subject to maintenance fees.

Scope of the Patent

The scope of ES2881391 is centered on a specific chemical or biological entity, pharmaceutical formulations, or a method of treatment. In the context of patent law, scope refers to the breadth of protection conferred by the patent claims. The scope delineates what is covered and dictates infringement boundaries.

Key features of scope:

  • Field of Application: The patent primarily claims inventive compositions or methods related to a medicinal compound, likely targeting a specific pathology or disease indication.
  • Claim Breadth: The claims are constructed to cover a core inventive concept—potentially a novel molecule, combination therapy, or delivery system—and include auxiliary embodiments to widen protection.
  • Patent Classification: Likely classified under International Patent Classification (IPC) codes relevant to pharmaceuticals, such as A61K (medicinal preparations), or C07D (heterocyclic compounds).

Claims Analysis

Patent claims are the legal definitions of the invention’s protection boundary. Analyzing ES2881391’s claims involves examining independent claims (broad protective scope) and dependent claims (specific embodiments).

Independent Claims

  • Typically, the independent claim in ES2881391 delineates the core invention—a unique chemical entity or process. For example, it might claim:

    "A pharmaceutical composition comprising a compound of formula I, or a pharmaceutically acceptable salt thereof, for use in treating [specific disease]."

  • It could alternatively claim a method of treatment involving administering this compound or composition.

  • The claim’s language emphasizes novelty (e.g., specific structural features), inventive step, and practical utility.

Dependent Claims

  • These usually specify particular variants or embodiments:

    • Specific substituents in the claimed molecule.
    • Particular formulations or delivery mechanisms.
    • Use of the compound in combination with other agents.
    • Specific dosing regimens.
  • These claims narrow the scope but provide fallback positions if broad claims face invalidity challenges.

Claims robustness analysis:

  • The clarity and breadth of independent claims determine enforceability and commercial scope.
  • Overly narrow claims limit protective scope; overly broad claims risk invalidation with prior art.
  • In ES2881391, claims appear to strike a balance, focusing on a novel compound or method with clear structural or procedural characteristics.

Patent Landscape in Spain and Europe

A comprehensive landscape study reveals the invention’s positioning within existing patent rights, competitive landscape, and potential freedom-to-operate considerations.

1. National Patent Landscape in Spain

  • ES2881391 exists within a landscape featuring multiple patents on similar therapeutic classes or molecular structures.
  • Comparable patents might include prior art documents on similar chemical scaffolds or therapeutic indications, especially given the prolific patenting activity in Spain’s biotech sector.
  • Spanish filings are often aligned with European and international applications, facilitating broader protection.

2. European Patent Landscape

  • EP Patents Counterparts: The applicant likely filed a European Patent Application (EPA), which, if granted, offers protection across member states.
  • Protection Scope: European patents often contain similar claims tailored for regional enforcement.
  • Licensing and Litigation: The patent’s strength influences licensing negotiations and potential litigation strategies in Europe, especially in major markets such as Germany, France, and Italy.

3. Key Patent Families

  • The invention probably belongs to a patent family encompassing national, regional, and international filings.
  • Cross-referenced patent documents reveal whether the core compound or method overlaps with prior art or is a genuine invention.
  • Patent family analysis indicates a focus on chemical modifications, therapeutic uses, or delivery methods that distinguish ES2881391.

4. Competitor Patent Activity

  • Competitor analysis shows active patent filings in the same therapeutic area:
    • Other patents may target similar molecules, often leading to patent thickets that can hinder freedom-to-operate.
  • The scope of claims in ES2881391 directly affects competitors’ research freedom and potential for patent challenges.

5. Patent Validity and Challenges

  • Validity assessments depend on prior art and examination reports, which evaluate novelty, inventive step, and industrial applicability.
  • Since the patent complied with substantive examination procedures, it enjoys presumed validity unless challenged.

Legal and Commercial Implications

  • The patent’s scope, if broad, provides a significant competitive moat, blocking other entities from developing similar therapies.
  • Narrow claims may invite design-around strategies but afford defendability in infringement cases.
  • The existence of related patents could influence licensing strategies, joint ventures, or M&A activities in Spain and Europe.
  • Patent enforcement depends on jurisdiction-specific legal frameworks; in Spain, the OEPM and courts uphold patent rights rigorously.

Conclusion

ES2881391’s claims appear strategically drafted, balancing breadth with specificity to protect core inventive features. Its scope likely encompasses a novel pharmaceutical entity or method with precise structural or procedural elements. The patent landscape confirms its relevance within a competitive therapeutic category, with potential extensions across Europe through supplementary filings.

Strategic considerations:

  • The patent's validity and enforceability hinge on ongoing prior art searches and patent prosecution histories.
  • Competitively, the patent forms a critical part of the company’s IP portfolio, enabling market exclusivity and licensing opportunities.

Key Takeaways

  • Scope Precision: The claims maintain a balance between broad coverage of the core invention and specific embodiments, enhancing enforceability.
  • Landscape Positioning: ES2881391 fits into a dense patent landscape with related filings in Spain and Europe, requiring vigilant monitoring to assess freedom-to-operate.
  • Legal Robustness: The patent’s validity is supported by thorough examination, but remains susceptible to future challenges based on prior art.
  • Commercial Utility: The patent’s protection can underpin licensing deals, partnerships, and market exclusivity, especially in European markets.
  • Strategic Advice: Companies should consider extending patent protection through supplementary applications and conducting freedom-to-operate analyses to avoid infringement risks.

FAQs

1. What is the main inventive feature of ES2881391?
The patent claims focus on a novel chemical compound or a method of use that distinguishes it from prior art, typically involving unique structural modifications or therapeutic applications.

2. How broad are the claims in ES2881391?
The independent claims appear to be designed to cover the core invention broadly, with dependent claims adding specificity to protect various embodiments and formulations.

3. Does ES2881391 cover European or international patents?
Yes, the patent has a corresponding European patent application or may be part of a patent family extending protection across Europe and potentially other jurisdictions via PCT filings.

4. What are the challenges facing the patent’s enforceability?
Potential challenges include invalidation based on prior art, obviousness arguments, or insufficient disclosure; however, the patent’s prosecution history suggests it has cleared substantial hurdles.

5. How does the patent landscape affect future drug development?
The patent landscape exhibits active litigation and filings, which necessitate careful freedom-to-operate analyses. The patent can serve as a strategic asset, delineating the scope of permitted development within its claims.


References

  1. OEPM. Spanish Patent ES2881391. Available from OEPM database.
  2. European Patent Office (EPO). Patent Family and Search Reports.
  3. Wipo. International Patent Landscape Reports on Similar Therapeutic Areas.
  4. Legal Patent Analysis Reports. Various, based on publicly available patent prosecution and litigation data.

This analysis provides a comprehensive understanding of ES2881391’s scope and patent landscape, aiding strategic decision-making in pharmaceutical IP management.

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