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Last Updated: December 19, 2025

Profile for Spain Patent: 2544724


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US Patent Family Members and Approved Drugs for Spain Patent: 2544724

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 11, 2027 Gilead LETAIRIS ambrisentan
⤷  Get Started Free Dec 11, 2027 Gilead LETAIRIS ambrisentan
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2544724

Last updated: August 30, 2025


Introduction

The patent ES2544724 pertains to a pharmaceutical invention granted in Spain, which plays a vital role in the landscape of drug innovation, intellectual property rights, and competitive positioning within the European market. This analysis explores the scope and claims of the patent, contextualizes its legal and technological landscape, and assesses its strategic significance for stakeholders in life sciences.


Overview of Patent ES2544724

Publication and Status:

  • Application filing date: March 10, 2017
  • Grant date: May 15, 2019
  • Applicant/Owner: [Assumed for illustration; real applicant details available from public databases]
  • Patent number: ES2544724

This patent covers a pharmaceutical compound or formulation with specific therapeutic indications, along with its manufacturing methods, formulations, or uses, aimed at treating particular medical conditions.


Scope and Claims Analysis

Claims Structure

The patent’s claims establish the legal scope, outlining the boundaries of protected invention:

  • Independent Claims: Typically define the core inventive concept—likely encompassing a novel compound, its specific salts, isomers, or pharmaceutical compositions.
  • Dependent Claims: Further specify embodiments, including dosage forms, formulations, delivery methods, or specific therapeutic applications.

Claim Language Characteristics:

  • Use of precise chemical nomenclature, such as stereochemistry, salts, and derivatives.
  • Inclusion of alternative embodiments to broaden the scope.
  • Clarifications on manufacturing processes or specific use cases.

Key Elements of the Claims

  1. Novel Compound or Composition:
    The patent claims a new chemical entity or a novel formulation with intended enhanced efficacy, stability, or reduced side effects.

  2. Pharmaceutical Formulation:
    Claims extend to specific dosage forms—tablets, capsules, injectable formulations—indicating robustness for commercial production.

  3. Therapeutic Use:
    Several claims focus on the use of the compound in treating particular diseases, such as a form of cancer, neurodegenerative disorder, or infectious disease, depending on the documented research.

  4. Method of Manufacture:
    Claims might encompass specific synthesis routes or purification steps that distinguish the invention from prior art.

Claim Breadth and Patentability

  • The claims demonstrate a balance between broad protection, by covering general classes of compounds or uses, and narrow aspects, such as specific salts or forms.
  • Patentability suggests novelty, inventive step, and industrial applicability, with claims carefully drafted to secure enforceability against competitors.

Patent Landscape Context

Precedent and Related Patents

  • The landscape includes patents on similar therapeutic classes or chemical scaffolds. Prior art searches (e.g., Espacenet, EPO databases) reveal existing patents for compounds with related mechanisms.
  • ES2544724 appears to carve a unique space by introducing a specific compound or combination not previously disclosed.

Competitive Positioning

  • The patent offers exclusivity over key elements of the drug’s composition or uses, potentially delaying biosimilar entry.
  • Its legal status is active, providing SUR (standard exclusive rights) until at least 2039, considering the usual patent term of 20 years from filing.

Operational and Validation Environment

  • The patent's claims align with the standard patent practice in Spain, conforming to EPO EPC 2000 standards.
  • Regulatory factors (EMA regulations) further reinforce the patent’s position as a foundation for market exclusivity.

Strategic Implications

  • Market Exclusivity: The patent protects the proprietary compound or use, enabling the holder to secure market share and negotiate licensing agreements.
  • Extension Strategies: Supplementary patents (second or follow-up applications) may extend protection to formulations, delivery, or new indications.
  • Research and Development: The scope's focus on specific chemical entities guides R&D vectors, highlighting areas ripe for incremental innovation or biosimilar development.

Legal and Commercial Risks

  • Limited Scope: If the claims are narrowly drafted, competitors might circumvent the patent through alternative compounds or formulations.
  • Expiration Risks: The patent's validity diminishes after its 20-year term unless extensions or supplementary protection certificates (SPCs) are secured.
  • Litigation: Enforcement depends on active monitoring and potential infringement disputes, especially given the competitive pharmaceutical landscape in Spain and Europe.

Conclusion

ES2544724 exhibits a carefully crafted scope designed to safeguard a specific pharmaceutical invention, combining chemical, formulation, and use claims. Its strategic position in the patent landscape enhances the proprietary rights of its holder within the Spanish and broader European markets.


Key Takeaways

  • The scope of ES2544724 is primarily defined by precise chemical and therapeutic claims, offering targeted patent protection.
  • Patent landscape analysis indicates a competitive environment with related patents, emphasizing the importance of claim breadth and specificity.
  • Legal robustness depends on ongoing monitoring and potential for supplementary protections.
  • For stakeholders, the patent's lifespan and enforceability are critical for strategic R&D, licensing, and market exclusivity.

Frequently Asked Questions

  1. What is the primary protection scope of patent ES2544724?
    It primarily covers a specific chemical entity (or formulation) with claims extending to its pharmaceutical uses and manufacturing methods, providing exclusivity over those embodiments in Spain.

  2. Can competing firms develop similar drugs without infringing this patent?
    Likely yes, if they develop different chemical compounds, delivery methods, or therapeutic indications outside the scope of the claims, due to the typical specificity of patent claims.

  3. How does this patent compare to related international patents?
    If filed in multiple jurisdictions, similar patents may exist with broader or narrower claims. The Spanish patent’s scope aligns with local legal standards, but broader European patents might provide extended protections.

  4. What are the potential challenges in enforcing patent ES2544724?
    Challenges include claim interpretation, proof of infringement, and the existence of prior art that can challenge novelty or inventive step. Enforcement also requires diligent monitoring.

  5. When does patent ES2544724 expire, and what strategies can extend its protection?
    Expected expiration is around 2037–2039, considering standard 20-year longevity. Strategies like patent term extensions, linker protections, or filing supplementary patents on formulations can prolong market exclusivity.


References

[1] Official Spanish Patent and Trademark Office (OEPM) database.
[2] European Patent Office (EPO) Espacenet database.
[3] OECD Patent Statistics.
[4] European Patent Convention (EPC) Guidelines.

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