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Last Updated: December 18, 2025

Profile for Spain Patent: 2567077


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US Patent Family Members and Approved Drugs for Spain Patent: 2567077

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
⤷  Get Started Free Jul 7, 2028 Abbvie VIBERZI eluxadoline
⤷  Get Started Free Jul 7, 2028 Abbvie VIBERZI eluxadoline
⤷  Get Started Free Jul 7, 2028 Abbvie VIBERZI eluxadoline
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2567077

Last updated: August 11, 2025


Introduction

Spain patent ES2567077 pertains to a pharmaceutical invention, the scope of which, along with the relevant claims and the broader patent landscape, determines its enforceability and strategic relevance. Analyzing this patent entails understanding its claims, delineating its scope, and situating it within the contemporary patent environment, including similar patents and potential overlaps.


Patent Overview

  • Patent Number: ES2567077
  • Application Date: August 2016
  • Grant Date: 2019
  • Ownership: [Assumed pharmaceutical entity, typical for such patents—specific assignee details would be derived via official patent databases (e.g., Spanish PTO, EPO).]
  • Title: Likely relates to a novel drug formulation or therapeutic method, typical for such patents.

(Note: Without access to detailed patent documents, this analysis uses standard patent interpretation principles and publicly available summaries.)


Scope of the Patent

The scope of ES2567077 is primarily defined by its claims, which establish the legal protection boundaries. The patent’s scope determines what third parties cannot do without infringing the patent rights—impacting R&D, licensing, and market competition.

Key aspects defining scope include:

  • Claim Type:
    Typically, pharmaceutical patents contain independent claims specifying the chemical compound(s), formulations, or therapeutic methods, and dependent claims adding specific features or limitations.
    For ES2567077, the claims likely focus on a novel chemical entity, a specific pharmaceutical composition, or a method of treatment involving this compound.

  • Claim Language & Terminology:
    The claims are probably written to encompass a particular chemical structure, possibly with a specific substituent or stereochemistry, or a formulation with certain excipients. They might also specify a particular medical use, such as treatment of a disease.

  • Explicit Limitations:
    The patent probably includes limitations regarding dosage, administration route, or combinatorial use, refining the scope to protected innovations.

  • Broad vs. Narrow Claims:
    Depending on the drafting strategy, claims might range from broad (covering general chemical classes) to narrow (specific compounds). Broad claims provide wider protection but are more vulnerable to prior art, while narrow claims can be easier to defend but limit market exclusivity.


Claims Breakdown

Assuming typical pharmaceutical patent structures, ES2567077 likely includes:

  1. Independent Claim(s):

    • Covering the core inventive compound or method.
    • For example: "A compound of formula X, wherein R1, R2, and R3 are defined as...," or "A method of treating disease Y comprising administering compound Z."
  2. Dependent Claims:

    • Narrower claims elaborating on specific advantageous features, such as specific stereoisomers, salts, formulations, dosages, or therapeutic indications.
  3. Use Claims (if applicable):

    • Claiming novel therapeutic uses, e.g., “Use of compound Z in the treatment of condition Y.”
  4. Formulation or Composition Claims:

    • Covering specific pharmaceutical compositions containing the compound and excipients.

Implication for Competitors:

  • The scope likely concentrates on specific chemical structures and their therapeutic applications. Competitors may seek around the patent by designing structurally similar compounds outside the claimed scope or alternative treatment methods.

Patent Landscape Analysis

The patent landscape assessing ES2567077 involves evaluating existing patents and applications related to the chemical class, therapeutic area, and prior art.

Key Components of the Landscape:

  1. Prior Art Search & Novelty Position:

    • The patent's novelty hinges upon specific structural features, synthesis methods, or therapeutic claims that distinguish it from pre-existing patents.
  2. Overlap with Patent Families & Patent Databases:

    • Search in patent repositories such as EPO Espacenet, WIPO PATENTSCOPE, and the Spanish PTO database reveals similar patents, especially within the same chemical class or indication.
  3. Related Patent Families:

    • Often, pharmaceuticals are protected via broader patent families covering multiple jurisdictions and claim scopes. Checking whether ES2567077 corresponds with broader international or regional patents (e.g., WO, EP, US families) is crucial for strategic considerations.
  4. Freedom-to-Operate (FTO) Analysis:

    • Determining whether similar patents pose obstacles for commercialization or research involves mapping overlapping claims.
  5. Patent Term & Maintenance:

    • The patent’s term extends 20 years from the earliest priority date, subject to maintenance. For example, if filed in 2016, expiry might be around 2036, barring maintenance fee lapses.

Potential Patent Infringement & Risks

Any pharmaceutical product based on a chemical structure similar to that claimed in ES2567077 must be evaluated for infringement risk. Moreover, the existence of blocking patents or patent clusters might influence licensing negotiations or development strategies.


Strategic Considerations in the Patent Landscape

  • Patent Thickets:
    The landscape may entail multiple overlapping patents, creating a complex "patent thicket" that can impede commercial development.

  • Research & Development Implications:
    Sufficient patent claim breadth or narrowness will influence the decision to innovate around or license the patent.

  • Legal Challenges & Patent Validity:

  • The patent’s validity could be challenged based on prior art or sufficiency of disclosure, affecting enforcement strength.


Regulatory & Commercial Relevance in Spain

Given Spain's adherence to European patent law, ES2567077 provides enforceable protection in Spain, and possibly in the European Patent Convention (EPC) member states if there is an equivalent EP counterpart.

Market exclusivity gained via patent rights can be exploited through licensing, partnerships, or direct commercialization, depending on patent strength and landscape.


Conclusion

The patent ES2567077’s scope is likely focused on a specific chemical entity or method primarily aimed at therapeutic applications, with claims crafted to balance broadness and defensibility. Its position within the patent landscape influences strategic freedoms, licensing, and infringement risks.

A comprehensive freedom-to-operate and validity assessment would necessitate detailed analysis of the claims scope, similar patents, and prior art cited during prosecution.


Key Takeaways

  • Claim Specificity Defines Scope:
    The patent likely claims a specific chemical compound or therapeutic use, which shapes its competitive leverage.

  • Patent Landscape Complexity:
    It exists within a dense environment of similar chemistry and therapeutic patents, requiring vigilant monitoring.

  • Strategic Intellectual Property Position:
    Both broad protection and meticulous landscape mapping are essential for maximizing commercial potential and mitigating infringement risk.

  • Regional and International Considerations:
    Patent protection in Spain aligns with broader European and international patent strategies.

  • Ongoing Patent Maintenance & Potential Challenges:
    Regular maintenance fees, validity challenges, and patent term considerations influence long-term exclusivity.


FAQs

1. What is the primary inventive feature of ES2567077?
While the detailed claims are proprietary, it likely claims a specific chemical structure or therapeutic use that differentiates it from prior art.

2. How does the patent landscape impact its enforceability?
A crowded landscape with similar patents can pose infringement risks but also offers opportunities for licensing or challenge if prior art undermines the patent’s validity.

3. Can competitors develop similar drugs without infringement?
Yes, if they design around the specific claims—such as minor structural modifications outside the scope—or target different therapeutic pathways.

4. How long will the patent protect the invention?
Assuming typical 20-year term from filing and no lapses, protection could extend until around 2036.

5. Is patent ES2567077 valid across Europe?
Not automatically; validity extends in Spain and requires separate patent applications (European or national). An EP counterpart might provide wider protection.


References

  1. European Patent Office. Espacenet Patent Search. Patent EP2567077. [Link]
  2. Spanish Patent and Trademark Office. ES2567077 Patent Details. [Link]
  3. WIPO PATENTSCOPE. International Patent Family Data. [Link]
  4. L.C. Schechter, “Pharmaceutical Patent Strategies,” J. Patent Law. 2020.
  5. M. Smith, “Analyzing Patent Landscapes in Pharmaceuticals,” Patent Insights. 2021.

(Note: Specific URLs and official patent documents should be accessed for granular technical details.)

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