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Last Updated: December 30, 2025

Profile for Spain Patent: 2524370


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US Patent Family Members and Approved Drugs for Spain Patent: 2524370

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 Dec 14, 2027 Glaxosmithkline ANORO ELLIPTA umeclidinium bromide; vilanterol trifenatate
⤷  Get Started Free Dec 14, 2027 Glaxo Grp Ltd BREO ELLIPTA fluticasone furoate; vilanterol trifenatate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2524370

Last updated: August 2, 2025

Introduction

Patent ES2524370 pertains to a medicinal invention filed in Spain, with potential implications within the pharmaceutical landscape. This analysis provides a comprehensive examination of its scope, claims, and the broader patent landscape. Such insights are instrumental for stakeholders including pharmaceutical companies, generic manufacturers, patent attorneys, and R&D entities aiming to delineate patent protections, freedom-to-operate, and competitive positioning within Spain and possibly broader jurisdictions.

Patent Overview

Patent Number: ES2524370
Application Filing Date: 2012 (Exact date typically warrants verification from the patent document)
Priority Date: Likely around 2011, considering Spanish patent application norms
Publication Date: Usually follows within 18 months of filing, approximate period 2013-2014

The patent title or abstract (if available) should specify the inventive subject matter; however, in absence of explicit details, this analysis will focus on typical patent structures, potential claim scope, and patent landscape factors relevant to medicinal patents filed in Spain.


Scope of the Patent

Legal Scope

The scope of patent ES2524370 is defined primarily through its claims, which delineate the legal protections conferred by the patent. The scope encompasses:

  • Product Claims: Covering specific chemical entities, formulations, or compositions disclosed within the patent.
  • Method Claims: Covering administration methods, production techniques, or therapeutic applications.
  • Use Claims: Encompassing novel therapeutic indications or specific treatment regimes.

The patent's scope hinges upon whether it claims:

  • A new active pharmaceutical ingredient (API) or a novel combination of known components,
  • A unique formulation or delivery system,
  • A distinct therapeutic method or specific use of the active compounds.

Technical Scope

The inventive scope, especially in medicinal patents, often extends to structural chemical claims, pharmaceutical formulations, or method-of-use claims. The scope's breadth determines the patent's strength against potential patent challenges and generic entry.

Claim Hierarchy and Strategy

Most patents contain a set of independent claims supported by narrower dependent claims that specify particular embodiments. The breadth of independent claims influences the patent’s enforceability and risk of design-arounds by competitors.


Claims Analysis

A detailed claim-by-claim analysis necessitates access to the official patent document, including its claims section. In general terms:

Type of Claims

  • Compound Claims: Cover specific chemical structures or derivatives. The scope depends on how broad the chemical genus covered is, often referencing a core scaffolding with variations.
  • Formulation Claims: Encompass specific compositions, excipients, or delivery forms.
  • Method Claims: Include novel methods of manufacturing, administering, or using the compound for particular indications.

Claim Language and Limitations

Effective claim language balances broad protection with clarity. Claims overly narrow limit the scope, increasing the risk of design-around strategies, while overly broad claims may be vulnerable to invalidation.

Novelty and Inventive Step

The claims must be rooted in a novel and inventive step over prior art, considering existing patents, scientific literature, and known therapeutic agents in Spain and abroad. For medicinal patents, this includes assessment against prior disclosures in databases such as Espacenet or the European Patent Office.

Claim Dependencies

Dependent claims specify particular embodiments, providing fallback positions if broader claims are invalidated. The strategic drafting of dependent claims enhances enforceability and provides flexibility in licensing negotiations.


Patent Landscape in Spain for Therapeutic Agents

Major Patent Families and Competitors

Spain is part of the European patent system, and many pharmaceutical patents are lodged through the European Patent Office (EPO); however, national filings like ES2524370 are critical in establishing the localized patent rights.

  • Major players: Multinational pharmaceutical corporations and biotech firms actively file in Spain, often with parallel filings in the EPO.
  • Patent clusters: Innovations around similar therapeutic areas such as oncology, neurology, cardiovascular health, and biologics are prevalent.

Technology Classes and International Classification

Patent ES2524370 likely falls into IPC classes relevant to pharmaceuticals, such as:

  • A61K (Preparation for medical, dental, or pharmaceutical purposes), which covers medicinal compounds, formulations, and their use.

The patent classification can influence the scope of prior art searches and patent scope assessments.

Legal Status and Outstanding Oppositions

As of current publicly available data, the patent's legal status—granted, pending, or challenged—is pivotal in assessing its enforceability and the risk of infringement.

  • Challenges could arise from prior art citations or oppositions filed within Spain or via European proceedings.
  • The patent's lifespan—generally 20 years from filing—affects the remaining patent term, influencing commercialization strategies.

European and International Patent Considerations

Given Spain’s membership in the European Patent Convention, patentees often pursue a broader patent portfolio through European and international filings, which significantly impact the scope and landscape around patent ES2524370. Evaluating whether equivalents or extensions exist in other jurisdictions helps in understanding the competitive landscape.


Implications and Strategic Considerations

Freedom-to-Operate (FTO)

  • Assessment: Validation whether other patents or prior art restrict the commercialization of similar compounds or methods.
  • Design-arounds: Identifying structural or functional modifications that avoid infringing on the claims without diluting therapeutic efficacy.

Patent Strength and Weaknesses

  • Strengths: Clear, specific claims with broad structural coverage and robust prosecution history.
  • Weaknesses: Narrow claims, prior art overlapping, or ambiguous claim language may limit enforceability.

Enforcement and Licensing

  • The patent can serve as a springboard for licensing negotiations or enforcement actions within Spain and potentially in Europe, provided the claims hold broad protection.

Key Takeaways

  • Scope clarity is pivotal: Precise, well-drafted claims that balance breadth with defensibility underpin robust patent protection.
  • Landscape awareness: Continuous monitoring of related patents, prior art, and competitors’ filings ensures strategic positioning.
  • Patent strength varies: Broad, specific, and well-supported claims enhance enforceability; weaknesses invite challenges.
  • Legal status matters: Active patents with maintained validity sustain market exclusivity and bargaining power.
  • Broader patent strategy: Alignment with European and global patent families can maximize commercial and defensive benefits.

FAQs

1. What is the primary inventive aspect of Spain patent ES2524370?
Without the specific claims and abstract, the inventive aspect likely involves a new chemical entity, formulation, or therapeutic method—details contingent on the patent document. Confirming requires directly reviewing the granted claims.

2. How does this patent relate to the broader patent landscape in Europe?
If filed through the EPO, similar or identical inventions may be protected across multiple European jurisdictions, providing extensive market exclusivity and potential for cross-border enforcement.

3. Can generic manufacturers challenge the validity of this patent?
Yes. Generic companies can file invalidity proceedings based on prior art or lack of novelty/inventive step, especially before patent expiry or if licensing is unavailable.

4. What strategic advantages does owning this patent offer to a pharmaceutical company?
It secures exclusive rights for specific therapeutic agents or methods within Spain, enabling market differentiation, negotiating licensing deals, and deterring competitors.

5. How might future patent filings impact the protection conferred by ES2524370?
Filing divisional or continuation applications could extend patent coverage or sharpen claim scope, reinforcing market position. Conversely, new prior art could threaten its validity.


References

[1] Spanish Patent and Trademark Office (OEPM). Official patent publication database.
[2] European Patent Office (EPO). Espacenet patent database.
[3] World Intellectual Property Organization (WIPO). PATENTSCOPE database.

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