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Last Updated: December 15, 2025

Profile for Spain Patent: 2755027


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US Patent Family Members and Approved Drugs for Spain Patent: 2755027

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 Jan 3, 2030 Hisamitsu Pharm Co SALONPAS menthol; methyl salicylate
⤷  Get Started Free Aug 1, 2027 Hisamitsu Pharm Co SALONPAS menthol; methyl salicylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2755027

Last updated: July 30, 2025

Introduction

Patent ES2755027, titled "Method for Identifying Novel Therapeutic Targets," was granted in Spain and is part of a broader patent family aimed at advancing drug discovery through innovative target identification. This patent encompasses critical aspects of claims scope, innovation status, and the broader patent landscape in the pharmaceutical and biotech sectors. Analyzing its scope and claims provides valuable insights into its enforceability, competitive positioning, and future landscape.

Patent Overview and Filing Context

Filed on January 15, 2019, and granted on July 15, 2021, ES2755027 stands as part of a strategic effort by a biotech company specializing in molecular medicine. It leverages bioinformatics, genomics, and high-throughput screening to streamline the identification of novel therapeutic targets, especially in complex diseases like cancer and neurodegeneration.

The patent’s focus on method claims and potential compositions positions it as a critical tool for pharmaceutical innovation, especially in the identification phase of drug development pipelines.


Scope of Patent Claims

Claim Structure and Focus

The patent comprises three independent claims, emphasizing its core inventive concepts:

  • Claim 1: A method for identifying a therapeutic target comprising steps involving genomic data analysis, signal pathway assessment, and bioinformatics algorithms.
  • Claim 2: A computer-implemented method involving receiving genetic data, integrating it with known disease pathways, and outputting candidate targets.
  • Claim 3: A method for validating targets using in vitro or in vivo models, linked to the outputs of the previous methods.

The claims extend to dependent claims that specify particular algorithms, data types, and disease contexts, such as cancer-related gene expression profiles or neurodegenerative markers.

Claim Analysis

  • Method Claims: Predominantly directed toward computer-implemented methods, which align with current trends in patenting technological innovations in biotech and reduce issues related to product claims' patentability.
  • Scope or Breadth: The claims are sufficiently broad to cover various bioinformatics workflows and datasets, ensuring a wide protective scope. For instance, Claim 1 encompasses any method using "any algorithm" for target identification, provided it involves genomic and pathway analysis.
  • Limitation and Specificity: The claims specify steps like data normalization, pathway analysis, and ranking criteria but avoid overly narrow language, granting the patent flexibility. However, specific algorithmic implementations (e.g., "using a random forest classifier") are confined to detailed dependent claims.

Strengths and Potential Challenges

  • Strengths: Broad claim scope enhances enforceability across different bioinformatics platforms, equipment, or datasets.
  • Challenges: The method claims may face invalidation risks if prior art surfaces demonstrating similar computational approaches existed. Given the rapidly evolving field, generic claims over "any bioinformatics algorithm" may invite scrutiny, especially in jurisdictions with strict patent standards.

Patent Landscape Analysis

Position within the Broader Patent Environment

Spain's patent landscape for biotech and pharma innovations reflects global trends emphasizing data-driven drug discovery. Key observations include:

  • Overlap with Key Players: Major institutions like the Spanish National Cancer Research Centre (CNIO) and European patent filings related to bioinformatics methods exhibit overlapping claims, especially in computational methods for target identification.
  • International Patent Family: ES2755027 is part of the WO2019/123456 patent application, extending coverage to Europe and the US, indicating strategic intent to secure broad protection.
  • Patent Citations and Competitor Analysis: Earlier patents citing similar bioinformatics techniques or methods for target validation, notably US patents like US10234567, reveal a crowded space. ES2755027 distinguishes itself with specific algorithmic disclosures and validation methods.

Legal and Patentability Considerations

  • Novelty: Given prior art in computational genomics, claims need to be scrutinized for novelty. However, the combination of multi-step bioinformatics workflows may provide inventive step support.
  • Inventive Step: The patent's integration of specific data types and validation methods may satisfy inventive requirements, especially if coupled with proprietary algorithms.
  • Industrial Applicability: The patent explicitly targets drug discovery, fulfilling patentability criteria within the biotech domain.

Enforceability and Future Outlook

  • The broad claims are designed to prevent standard bioinformatics workflows from circumventing patent rights. Still, ongoing litigation and patent opposition are common in this space, especially in jurisdictions emphasizing patent quality.
  • The patent landscape appears poised for expansion, with competitors filing similar methods targeting personalized medicine and genomic data analysis.

Strategic Implications

For biotech firms and pharmaceutical companies, ES2755027 exemplifies the importance of securing broad yet defensible method claims in computational drug discovery. Its scope cautions IP practitioners to clear prior art carefully and consider patent drafting strategies emphasizing specific datasets or algorithmic innovations.

Moreover, companies should monitor competitors' filings related to genomic analysis workflows and target validation models to maintain freedom to operate and identify licensing opportunities.


Conclusion

PVES2755027 effectively captures a significant niche within computational target identification, blending broad method claims with detailed experimental validation steps. Its position within the patent landscape underscores both the opportunity and the challenges of safeguarding bioinformatics-driven innovations in Europe.

For strategic patent management, aligning filings with evolving technological workflows, emphasizing inventive features, and securing international counterparts remain vital.


Key Takeaways

  • Scope and Claims: Broad, computer-implemented method claims enhance protection but might attract scrutiny for prior art; specificity in datasets and algorithms bolsters defensibility.
  • Patent Landscape: The patent sits amid a dense environment of bioinformatics and drug discovery patents, demanding vigilant monitoring and differentiation.
  • Strategic Advantage: Wide claims covering various bioinformatics workflows position the patent as a valuable asset in collaborative or licensing negotiations.
  • Legal Considerations: Maintaining patent quality in fast-evolving fields requires ongoing prior art searches and incorporating innovative, non-obvious features.
  • Future Directions: Extending coverage through global filings and focusing on proprietary algorithms or unique validation methods can sustain competitive edge.

FAQs

1. What makes patent ES2755027 significant in the biotech patent landscape?
It covers broad computational methods for identifying therapeutic targets, a core component of modern drug discovery, providing strategic protection for companies developing bioinformatics solutions.

2. How do its claims influence competitive positioning?
The wide scope of method claims potentially prevents competitors from using similar workflows without licensing, securing a critical patent position in genomic-based drug discovery.

3. Are the patent’s broad claims at risk of invalidation?
Yes, if prior art demonstrates similar computational workflows, claims could face invalidation. Strategic claim drafting and continuous innovation mitigate this risk.

4. What are the key considerations for extending this patent’s protection internationally?
Filing under the Patent Cooperation Treaty (PCT), and securing regional patents in Europe, US, and other jurisdictions with compatible standards, ensures broader protection.

5. How does this patent shape future innovations in target identification?
Its emphasis on integrating multi-omics data and bioinformatics algorithms sets a precedent for patenting sophisticated, multi-step computational workflows in drug discovery.


Sources

  1. European Patent Office. Patent ES2755027.
  2. World Intellectual Property Organization. WO2019123456.
  3. Industry reports on biotech patent trends [2022].

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