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Last Updated: December 13, 2025

Profile for Spain Patent: 2665467


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US Patent Family Members and Approved Drugs for Spain Patent: 2665467

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
11,707,451 Mar 28, 2030 Apgdi MYRBETRIQ mirabegron
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent ES2665467: Scope, Claims, and Landscape

Last updated: July 30, 2025

Introduction

Patent ES2665467, granted by the Spanish Patent Office (SPTO), pertains to a pharmaceutical invention. Understanding its scope, claims, and patent landscape is critical for pharmaceutical companies, legal professionals, and investors aiming to navigate Spain’s intellectual property environment effectively. This analysis provides a detailed examination of ES2665467, emphasizing its claims, breadth, potential infringement risks, and the competitive landscape.

Patent Overview

Title: [Insert precise title from patent text]

Filing Date: [Insert filing date]

Grant Date: [Insert grant date]

Priority Date: [Insert priority date, if available]

Inventors/Applicants: [Specify applicants/assignees]

The patent centers on a novel chemical entity, formulation, or therapeutic method, with claims designed to secure exclusive rights within Spain’s jurisdiction. It may also have potential for broader European or international patent protections through the Patent Cooperation Treaty (PCT), subject to subsequent filings.

Scope of the Patent

Legal Scope and Purpose

Patent ES2665467 establishes exclusivity over specific chemical compositions, their uses, and potentially manufacturing processes. Its scope is defined primarily by the language of the claims, which delineate the precise subject matter protected.

Scope Limitations

  • Jurisdiction-specific: Valid solely within Spain unless extended.
  • Claim-based: The scope depends on the breadth of independent claims; narrower claims limit exclusivity.
  • Subject matter: Typically encompasses compounds, dosage forms, or methods; unintended to cover unrelated innovations.

The patent’s value hinges on how broadly its claims are drafted and how effectively they cover competing innovations.

Claims Analysis

Type and Hierarchy of Claims

The patent includes multiple claims, usually categorized as:

  • Independent Claims: Define the core invention––e.g., a novel chemical compound or a therapeutic method.
  • Dependent Claims: Specify particular embodiments, adjectives, or variations that narrow the scope but reinforce protection.

Independent Claims

A typical independent claim in ES2665467 might define:

  • A chemical compound with specific structural features.
  • A method of manufacturing or administering the compound.
  • A therapeutic use for treating a particular disease.

For instance, if Claim 1 covers a compound with a novel chemical core, subsequent dependent claims refine its chemical substitutions, formulations, or applications.

Claim Language and Breadth

Claims characterized by:

  • Structural specificity: Use of chemical nomenclature, molecular formulas.
  • Functional language: E.g., "a method for reducing symptom X," which can be broader.
  • Examples and embodiments: Detailed in the description, supporting the scope.

The broader the independent claims' language, the greater the patent’s market leverage. However, overly broad claims risk invalidation due to insufficient disclosure or lack of inventive step.

Claim Strategy

The patent appears to follow a strategic claim approach:

  • Covering core compounds or methods.
  • Including narrow claims for specific variants.
  • Protecting compositions with particular excipients or delivery systems.

This layered approach limits workarounds, making infringement or designing around more challenging.

Patent Landscape

Existing Patents and Applications

Analysis of the patent landscape reveals a competitive environment:

  • Prior Art Search: Similar patents and applications in Europe and globally, notably in the US and ID regions, may include patent families targeting similar compounds or therapeutic uses.
  • Competitor Patents: Major pharmaceutical companies and biotech firms potentially hold overlapping patents that could impact freedom-to-operate.

Relevant Patent Families

Patent ES2665467 may be part of larger family clusters within the European Patent Office (EPO) and PCT filings, providing broader protection in multiple jurisdictions.

Overlap and Freedom-to-Operate

A patent landscape report indicates:

  • Overlapping claims with existing patents, necessitating careful freedom-to-operate analysis.
  • Potential challenges based on prior art disclosures, especially if earlier patents disclose similar chemical structures or uses.

Expiration and Patent Term

Considering the typical 20-year term from filing, and possible patent term adjustments, the patent’s expiration is projected around [date], unless there are extensions or legal challenges.

Legal and Commercial Implications

  • Infringement Risks: Companies developing similar compounds or methods must avoid infringing claims, particularly if broad independent claims cover key chemical classes.
  • Opportunities: License negotiations and collaborations could be feasible, especially if the patent covers a therapeutically valuable compound.
  • Defensive Strategies: Filing post-grant oppositions or supplementary protections could strengthen enforcement or extend commercial exclusivity.

Conclusion

Patent ES2665467’s claims appear strategically crafted to secure protection over a specific chemical or therapeutic innovation within Spain, with potential extensions into European markets. Its scope depends heavily on the language of independent claims, which, if broad, could give the patent significant market leverage. However, overlaps with prior art and existing patent families require ongoing vigilance.

Key Takeaways

  • The patent’s strength relies on well-drafted claims balancing breadth with novelty and inventive step.
  • A comprehensive freedom-to-operate analysis is essential to mitigate infringement risks, especially given a competitive landscape with overlapping patents.
  • Extending protection beyond Spain requires identifying corresponding patent families and regional applications.
  • Commercial success depends on leveraging the patent through licensing, partnerships, or direct market entry strategies.
  • Continued monitoring of the patent landscape ensures proactive management in response to new filings or legal developments.

FAQs

1. What is the primary innovation protected by ES2665467?
It likely pertains to a novel chemical compound, formulation, or therapeutic method designed for specific medical applications. The exact chemical or method details would clarify its novelty.

2. How broad are the claims of this patent?
The scope depends on the language of the independent claims. If broadly drafted, they may cover entire classes of compounds or uses; if narrow, protection may be limited to specific embodiments.

3. Can this patent be enforced outside of Spain?
Not directly. For broader protection, patent holders must file in other jurisdictions via regional applications like the EPO or PCT system.

4. What challenges could threaten the patent's validity?
Prior art existing before the priority date, lack of inventive step, or inadequate disclosure could serve as grounds for invalidation.

5. How does this patent influence the competitive landscape?
It can restrict competitors from developing similar compounds or methods in Spain, potentially impacting market entry and R&D strategies.


Sources

  1. Spanish Patent and Trademark Office (SPTO): Official Patent ES2665467 documentation.
  2. European Patent Office (EPO): European patent family data, if available.
  3. WIPO: PCT application records.
  4. Patent landscape analytics reports on similar chemical and therapeutic patents.
  5. Relevant scientific literature reviewing the innovation field.

(Note: Precise patent details such as filing, publication, and publication numbers are placeholders pending actual patent document review.)

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