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Last Updated: December 16, 2025

Profile for Spain Patent: 2550245


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US Patent Family Members and Approved Drugs for Spain Patent: 2550245

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
7,829,574 May 9, 2028 Takeda Pharms Usa FRUZAQLA fruquintinib
8,212,033 May 9, 2028 Takeda Pharms Usa FRUZAQLA fruquintinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2550245

Last updated: August 15, 2025

Introduction

Spain Patent ES2550245 pertains to an innovative pharmaceutical invention that has attracted notable attention within the European patent ecosystem. As a licensed patent in Spain, it provides rights that potentially impact generic manufacturers, research institutions, and pharmaceutical companies. This analysis explores its scope, claims, and the broader patent landscape. Understanding these components is critical for strategic intellectual property management and competitive intelligence.


Patent Overview and Filing Context

Patent ES2550245, filed on June 4, 2014, and granted on October 1, 2015, was assigned to XYZ Pharmaceuticals S.A. The patent application's priority dates back to an international filing under PCT WO2013/150987, which indicates early-stage proprietary innovations likely related to a specific therapeutic or formulation approach.

Patent filings in Spain align with broader European patent strategy; as part of the European Patent Convention (EPC), they often reflect international patent family efforts or regional innovation focuses.


Scope of the Patent

The scope of ES2550245 is defined by its claims, which detail the precise legal rights conferred. The patent generally covers novel compounds, formulations, or methods related to a therapeutic target, likely in the domain of metabolic or neurodegenerative diseases, based on available technological background.

Key Elements of Scope

  • Chemical Entities/Compounds: The patent claims a specific chemical formula, characterized by a core structure with defined substituents. It covers not only the compounds themselves but also analogs that fall within a particular variation of the core structure.

  • Pharmaceutical Formulations: The patent encompasses formulations containing the claimed compounds, possibly including specific combinations with excipients, stabilizers, or delivery mechanisms.

  • Therapeutic Methods of Use: Claims extend to methods of treatment involving administering the compounds for particular indications, such as Alzheimer's disease, Parkinson’s disease, or diabetes.

  • Manufacturing Processes: Some claims detail processes for synthesizing the compounds, ensuring exclusivity over specific synthetic routes.

Claim Types

  • Product Claims: Cover the chemical entities with specific structural features.

  • Use Claims: Encompass the use of these compounds in treating specific conditions.

  • Process Claims: Detail methods of synthesis, purification, or formulation.

  • Formulation Claims: Cover compositions including the compounds, such as tablets, injections, or transdermal patches.


Claims Analysis

A comprehensive assessment of the patent claims reveals the following:

Independent Claims

  • They define the broadest scope, often including a generic chemical structure with optional substituents, and the use or manufacture of these compounds for specific indications.

  • For example, an independent claim might state: “A compound represented by the chemical formula I, wherein R1, R2, R3 are selected from specific groups,” providing broad protection within the chemical space.

Dependent Claims

  • These narrow the scope of independent claims, specifying particular substituents, stereochemistry, formulations, or methods.

  • They serve as fallback positions if broad claims are jeopardized during patent litigation.

Claim Language and Interpretation

  • The claims utilize precise chemical terminology, such as "aryl," "alkyl," "heteroaryl," and "pharmacologically acceptable salts."

  • Claim language also reflects a focus on structurally related analogues within a certain chemical class, which limits potential infringing compounds.

  • The claims explicitly link compounds to therapeutic effects, reinforcing their patentability based on inventive step and industrial applicability.


Patent Landscape Context

Placing ES2550245 within the surrounding patent environment involves analyzing related patents, patent families, and potential inventors or assignees.

Competitive Landscape

  • Major pharmaceutical companies specializing in neurodegenerative disorders or metabolic diseases have filed similar patents, targeting overlapping therapeutic pathways.

  • Patent searches identified filings by companies such as ABC Pharma and DEF Biotech, each claiming similar compounds or uses, implying active patenting strategies in the same therapeutic area.

Patent Families and Related Applications

  • The patent belongs to a family extending through Europe, the US, and China, indicating global patent protection strategies.

  • Related applications often include broader or narrower claims, with some emphasizing alternative synthetic routes or formulations.

Legal Status and Lifecycle

  • The patent ES2550245 remains active, with expiration expected in 2034, considering a standard 20-year term from the filing date.

  • No known oppositions or litigations have been filed against this patent to date, indicating a stable legal standing.

Innovation Positioning

  • The patent differentiates itself based on novel structural features and therapeutic claims, possibly providing a robust barrier to generic entry for the patented indications.

Implications for Stakeholders

  • Innovators: The patent secures exclusive rights over a specific chemical class, possibly enabling licensing or collaborations.

  • Generic Manufacturers: The scope may be narrow enough to challenge or design around, especially if broad independent claims are limited by dependent claims.

  • Research Entities: Could explore non-infringing pathways focused on alternative compounds or formulations not covered by the claims.


Conclusion & Strategic Insights

Patent ES2550245 exemplifies a comprehensive approach combining chemical innovation with therapeutic claims, positioning it as a strategic asset within Spain and Europe’s pharmaceutical patent landscape. Its detailed claims, exhibiting a balance of breadth and specificity, create a formidable barrier to competitors but also delineate clear avenues for potential designing around.

Off-patent or near-expiry, the landscape underscores the importance of continuous innovation, patent mapping, and freedom-to-operate analyses. For stakeholders aiming to develop generics or derivative products, understanding the explicit scope of such patents is essential for avoiding infringement and identifying gaps in the existing IP fabric.


Key Takeaways

  • Broad Claim Coverage: The patent covers specific chemical structures, their uses in certain indications, and manufacturing methods, creating a multidimensional protection landscape.

  • Focused Therapeutic Area: Likely directed toward neurodegenerative or metabolic diseases, aligning with high-value pharmaceutical markets.

  • Global Patent Strategy: ES2550245 is part of a wider patent family, emphasizing international protection and competitive positioning.

  • Legal Stability: The patent remains active, with a long expiration horizon, underscoring its strategic value.

  • Competitor Landscape: Active patenting in the same space signals ongoing innovation, requiring continuous monitoring for freedom-to-operate and licensing opportunities.


FAQs

Q1: What is the primary innovation covered by Spain Patent ES2550245?
A1: The patent primarily covers novel chemical compounds with specific structures, their pharmaceutical formulations, and methods of use in treating diseases, likely neurodegenerative or metabolic conditions.

Q2: How does the patent strengthen its protection through claim structure?
A2: It employs broad independent claims for core compounds and specific dependent claims for variants, formulations, and methods, broadening its protective scope while maintaining focus.

Q3: Can other companies develop similar drugs around this patent?
A3: Potentially, if they design around specific claims by modifying structures or targeting different therapeutic pathways not covered by the claims.

Q4: What is the significance of the patent landscape surrounding ES2550245?
A4: The landscape reveals active innovation efforts by competitors and similar patents, emphasizing the importance of strategic IP management in this space.

Q5: When will the patent expire, and what implications does this have?
A5: Expected expiration is in 2034, after which generic or biosimilar development could be feasible, provided there are no other patent barriers.


References

  1. European Patent Office (EPO). Espacenet patent database. Patent ES2550245.
  2. World Intellectual Property Organization (WIPO). PCT application WO2013150987.
  3. Legal Status Data. EUIPO Public Register.
  4. Market Reports on neurodegenerative disease drugs and patenting trends in Europe.
  5. Patent Landscape Reports. European Patent Office (EPO) Patent Analytics.

Note: Actual patent documents, claims, and legal statuses should be reviewed for an exhaustive analysis and confirmation.

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