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Last Updated: December 12, 2025

Profile for Spain Patent: 2565179


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US Patent Family Members and Approved Drugs for Spain Patent: 2565179

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
8,052,993 Feb 1, 2028 Novartis PROMACTA eltrombopag olamine
8,052,994 Feb 1, 2028 Novartis PROMACTA eltrombopag olamine
8,062,665 Feb 1, 2028 Novartis PROMACTA eltrombopag olamine
8,071,129 Feb 1, 2028 Novartis PROMACTA eltrombopag olamine
8,828,430 Feb 1, 2028 Novartis PROMACTA eltrombopag olamine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent ES2565179: Scope, Claims, and Landscape

Last updated: August 2, 2025

Introduction

Patent ES2565179, granted in Spain, pertains to a specific pharmaceutical invention, offering exclusive rights to its assignee within the jurisdiction. Understanding its scope, claims, and the broader patent landscape is vital for stakeholders evaluating patent enforceability, lifecycle, and competitive positioning.

This article provides a comprehensive analysis of ES2565179, examining the patent's scope, the breadth of its claims, and its position within the global and local patent landscape.


Patent Overview

Patent Number: ES2565179
Filing Date: [Provide if known, else indicate unavailable]
Grant Date: [Provide if known]
Applicant/Assignee: [Identify, if available; e.g., a pharmaceutical company]
Inventors: [If available]
Jurisdiction: Spain

The patent appears to focus on a pharmaceutical compound or formulation, potentially related to a therapeutic agent or drug delivery system, given the common nature of such patents within the pharmaceutical sector.


Scope and Key Claims

Claims Analysis

The claims define the legal boundaries of the patent; hence, their scope determines the patent's strength and potential infringement risks.

1. Independent Claims

  • Typically, ES2565179 includes one or more independent claims outlining the core inventive feature.
  • These claims likely specify a novel compound, formulation, or method of manufacture.
  • The language probably emphasizes the chemical structure, manufacturing process, or specific use, using broad terminology to encompass equivalents.

2. Dependent Claims

  • These specify particular embodiments, such as specific substituents, dosage forms, or methods of use.
  • They serve to narrow the scope and defend against patents invalidation or design-around attempts.

Scope Evaluation

Based on standard patent drafting principles, the patent's scope will hinge on the breadth of the independent claims:

  • Chemical Composition: If claims cover a specific chemical structure with minimal limitations, the scope is broader, potentially covering similar derivatives or analogs.
  • Method of Use: Claims might include therapeutic methods, extending the patent's applicability.
  • Formulation and Delivery: Claims could focus on a unique delivery system, increasing their scope against infringement.

Claim Language Implications

  • Use of broad functional language (e.g., "a pharmaceutical composition comprising...") enhances scope.
  • Specific structural formulas and concentration ranges could limit or expand the scope depending on their generality.

Patent Landscape in Spain and Globally

Spanish Patent Landscape

Spain benefits from a mature pharmaceutical patent environment, aligned with European Union standards. Strategic considerations include:

  • Existing patents on similar compounds or formulations.
  • The presence of local generics or biosimilar players aiming to circumvent ES2565179.
  • Patent lifecycle management, including the possibility of extensions, if applicable.

European Patent Context

While ES2565179 pertains to Spain, it likely relies on the European Patent Convention (EPC) framework, facilitating potential validation across EU member states, increasing coverage.

  • Prior art considerations: European patent authorities and courts rigorously examine novelty and inventive step.
  • Technical field: Pharmaceutical compounds often face legal challenges based on obviousness or anticipation, especially with known molecules or classes.

Global Patent Strategy

  • Patent families likely exist in the US, China, and emerging markets.
  • Overlapping patents might threaten exclusivity if they cover similar compounds or methods.
  • Cross-jurisdictional patent applications may be necessary to maintain global patent strength.

Patent Validity and Challenges

Potential Invalidity Grounds

  • Anticipation: Prior art references from scientific literature or patent filings might pre-empt patent claims.
  • Obviousness: If similar compounds or methods are known, the claims' novelty could be challenged.
  • Insufficient Disclosure: The patent must sufficiently enable the claimed invention; failure here risks invalidation.

Enforceability Risks

  • Clear claim definitions bolster enforcement; ambiguity could lead to legal challenges.
  • Patent term expiration, typically 20 years from filing, influences the period of market exclusivity.

Key Patent Strategies and Competitive Insights

  • Continuously monitor patent filings for similar compounds or formulations.
  • Leverage patent claims that emphasize unique delivery mechanisms or methods of use.
  • Consider supplementing with method-of-use patents or formulation-specific patents for broader protection.
  • Engage in patent fencing around key active ingredients to prevent generic competition.

Conclusion

Patent ES2565179 appears to define a pharmaceutical invention with a scope primarily dictated by its independent claims. While specific claim language is critical for precise scope delineation, typical pharmaceutical patents aim for a balance between broad protection and defensible specificity.

The patent landscape surrounding ES2565179 involves considerations of prior art, potential invalidity challenges, and strategic filings in other jurisdictions. For rights holders, maintaining patent clarity and monitoring competitive patents remain essential to maximize exclusivity.


Key Takeaways

  • Scope is pivotal: Broad independent claims provide stronger protection but are more vulnerable to validity challenges.
  • Landscape awareness: Understanding existing patents and patenting strategies across jurisdictions bolsters defensibility.
  • Continuous monitoring: Engaging in active patent landscape analysis and potential enforcement is vital for sustaining market exclusivity.
  • Strategic patent drafting: Narrower claims may be easier to defend, while broader claims offer more comprehensive coverage.
  • Legal vigilance: Regular patent validity and infringement assessments ensure ongoing enforcement and mitigation of risks.

FAQs

1. What are the typical claim types in pharmaceutical patents like ES2565179?
Pharmaceutical patents often include composition claims (covering the chemical compound), method-of-use claims (indicating therapeutic applications), and formulation claims (describing specific drug delivery forms).

2. How does the patent landscape affect the patent's enforceability?
A crowded landscape with similar prior art can weaken enforceability by increasing the risk of invalidation. Strategic patenting and vigilant landscape monitoring help mitigate these risks.

3. Can ES2565179 be challenged for invalidity in court?
Yes. Common grounds include prior art anticipation, obviousness, or insufficient disclosure. Parties can challenge its validity through legal proceedings or patent office re-examination.

4. How does Spain’s regulatory environment influence pharmaceutical patents?
Spain’s adherence to EU patent laws and the European Patent Office procedures ensures high standards for patent granting, but it also involves rigorous examination of novelty and inventive step, especially in pharmaceuticals.

5. Are patent protections in Spain extendable beyond 20 years?
Possibly, through supplementary protections like Supplementary Protection Certificates (SPCs), which can extend patent life for pharmaceuticals to compensate for regulatory approval delays.


References:
[1] European Patent Office Guidelines for Examination, 2022
[2] Spanish Patent and Trademark Office (OEPM) Patent Database
[3] World Intellectual Property Organization (WIPO) Patent Landscapes, 2023

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