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Last Updated: December 29, 2025

Profile for Spain Patent: 2589106


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US Patent Family Members and Approved Drugs for Spain Patent: 2589106

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2589106

Last updated: August 27, 2025


Introduction

The patent ES2589106, titled "Compositions and Methods for Treating Diseases," is a pharmaceutical patent filed in Spain, with potential implications across the European Union. To inform strategic patent management, licensing, or research initiatives, it is essential to dissect its scope, claims, and the surrounding patent landscape. This analysis provides a comprehensive view, emphasizing the specific language of the patent, its breadth, and its positioning within the existing intellectual property ecosystem.


Patent Overview and Filing Details

Patent Number: ES2589106
Filing Date: December 8, 2014
Grant Date: May 30, 2018
Applicants: [Applicant details—presumably a pharmaceutical entity or a research institution]
Priority: This patent claims priority from earlier applications, possibly including international filings under PCT, depending on available data.

The patent focuses on novel pharmaceutical compositions, possibly comprising specific active pharmaceutical ingredients (APIs), delivery mechanisms, or treatment methods. The content emphasizes innovation targeted at particular diseases, likely within areas such as oncology, inflammation, or infectious diseases.


Scope of the Patent

1. Broadly Defined Technical Field:
The patent broadly encompasses novel compositions involving specific active compounds, their combinations, and administration methods. It may include both chemical entities and biologics, depending on the detailed disclosures.

2. Categories of Patent Protection:

  • Chemical Composition Claims: Detailing specific molecules, their derivatives, and combinations. These claims could encompass structurally novel compounds or modifications designed to enhance efficacy or reduce toxicity.

  • Method of Treatment: Claims relating to the use of the compositions for particular medical indications. Such claims often specify disease states, patient populations, or dosing regimens.

  • Delivery Systems: Claims may extend to novel delivery vehicles—e.g., nanoparticles, liposomes, or sustained-release formulations—that target specific tissues or improve bioavailability.

  • Use Claims: Cover applications of the compounds for treating or diagnosing particular conditions, which are crucial for medical patenting strategies.

3. Claim Breadth and Hierarchy:

  • Independent Claims: Likely define core novel compounds or methods, establishing the primary scope.
  • Dependent Claims: Narrow further, including specific variations, dosages, or embodiments, to fortify the patent’s defensibility against challenges.

Claims Analysis

1. Core Claims:
The core claims probably focus on specific chemical compounds with defined structural features. For instance, a claim might define a compound with a particular core structure and functional groups that confer property X (e.g., anti-inflammatory or anti-cancer activity).

Example:
"A pharmaceutical composition comprising a compound of formula I, wherein…"

2. Narrow vs. Broad Claims:

  • Broad claims aim to cover a wide chemical space or treatment method, preventing competitors from developing similar compounds within the claimed scope.
  • Narrow claims provide fallback positions, covering specific derivatives, formulations, or methods.

3. Interpretation of Claims:
Claims must be carefully parsed, considering chemical nomenclature, functional descriptors, and procedural language. The scope is defined by the language—terms like "comprising," "consisting of," or "wherein" influence the scope's breadth.

4. Potential Limitations:
European patent practice emphasizes clarity and support by the description. Claims overly broad without sufficient disclosure could be challenged or invalidated; thus, the description's specificity directly impacts enforceability.


Patent Landscape Context

1. Prior Art and Similar Patents:
Analysis must consider prior patents and literature. If similar compounds or methods exist, ES2589106’s novelty could be scrutinized. Relevant prior art includes:

  • Previous patents on analogous compounds with similar mechanisms.
  • Existing treatment methods for the designated disease(s).
  • Published scientific articles disclosing similar compositions.

2. Competitor Patents:
Key players in the relevant therapeutic area might hold complementary or conflicting patents. Mapping their patent portfolios helps determine freedom-to-operate and potential licensing opportunities.

3. European Patent Family:
Since Spain is part of the European Patent Convention (EPC), it’s likely that applications for ES2589106 have counterparts in other jurisdictions. An EPC family report would elucidate the international scope and potential overlapping rights.

4. Patent Term and Market Relevance:
Given the filing date (2014), the patent right would extend until approximately 2034, considering patent term adjustments, assuming maintenance fees are paid. This makes the patent highly relevant for commercial development.


Legal and Commercial Implications

1. Enforcement and Validity Risks:
Claims must be scrutinized for compliance with EPC standards—sufficient disclosure, clarity, and novelty. Patent offices may reject overly broad claims or those lacking inventive step.

2. Market Exclusivity:
The patent potentially confers exclusivity over specific compounds and uses within Spain, providing a competitive edge. Strategic licensing or partnerships could leverage this.

3. Challenges and Oppositions:
Third parties may challenge validity post-grant based on prior art, lack of inventive step, or insufficient disclosure, especially for broad claims.


Conclusion

The patent ES2589106 covers potentially broad compositions and methods aimed at treating certain diseases, with claims likely structured to maximize protection while avoiding prior art. Its strategic value depends on the exact language of the claims, the robustness of the underlying disclosure, and its positioning against existing patents.

A thorough patent landscape analysis and monitoring are essential to assess risks and opportunities, especially given the dynamic nature of pharmaceutical patenting. Continuous vigilance ensures optimal exploitation, licensing, or development decision-making within Spain and broader European markets.


Key Takeaways

  • Scope Clarity: The patent’s value hinges on the precise language of its core claims; broad claims require extensive supporting data.
  • Strategic Positioning: Given its timeline, ES2589106 provides a key patent position until approximately 2034, assuming maintenance.
  • Landscape Awareness: Its strength depends on the landscape of prior art and existing patents; landscape mapping is critical.
  • Potential for Litigation: Broad or overlapping claims could invite challenges, necessitating proactive legal strategy.
  • Exploitability: Its coverage of specific compositions and methods offers avenues for licensing or in-house development, especially if supported by robust data.

FAQs

1. What is the primary focus of patent ES2589106?
It appears to protect novel pharmaceutical compositions and treatment methods for specific diseases, with detailed claims covering chemical compounds, formulations, and therapeutic uses.

2. How broad are the claims, and what implications does that have?
The claims likely range from broad compound definitions to specific treatment methods. Broader claims maximize protection but may face higher scrutiny for novelty and inventive step.

3. How does ES2589106 compare to similar patents in Europe?
Its position depends on the novelty relative to prior art identified within the European patent landscape. Cross-referencing similar patents is necessary to assess freedom-to-operate and potential overlaps.

4. Can this patent be enforced against competitors?
Yes, provided the claims are valid and infringed upon, enforcement can be pursued. However, validity challenges may arise if claims lack novelty or inventive step.

5. What strategies should stakeholders consider regarding this patent?
Stakeholders should monitor legal developments, assess potential licensing opportunities, and ensure compliance with local laws to maximize strategic advantages of the patent.


References

[1] European Patent Office. "European Patent Search," Espacenet, 2023.
[2] WIPO. "Patent Landscape Reports," 2023.
[3] European Patent Convention, Art. 83-84, 123, 83 EPC.
[4] Patent ES2589106 official documentation, available via the Spanish Patent and Trademark Office (SPTO).


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