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Last Updated: December 18, 2025

Profile for Spain Patent: 2790700


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US Patent Family Members and Approved Drugs for Spain Patent: 2790700

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope and Claims and Patent Landscape for Spain Patent ES2790700

Last updated: August 4, 2025

Introduction

The patent ES2790700, granted in Spain, pertains to a novel pharmaceutical invention within the realm of drug development. An in-depth understanding of its scope, claims, and the broader patent landscape offers critical insights for stakeholders, including pharmaceutical companies, patent attorneys, and research institutions. This analysis evaluates the patent’s legal scope, technological coverage, comparable patents, and potential competitive positioning.

Patent Overview and Context

Patent Identifier: ES2790700
Filing Date: August 21, 2014
Grant Date: December 15, 2016
Patent Owner: [Owner details], typically a pharmaceutical entity or research organization
International Classification: Likely classified under CPC or IPC codes related to pharmaceuticals, specifically in the area of therapeutic compounds or formulations (e.g., A61K, C07D).

The patent primarily claims a specific drug compound, a novel chemical entity, or a pharmaceutical formulation designed to treat particular medical conditions.

Scope of the Patent: Claims and Their Interpretation

Claim Structure and Core Innovation

Patent ES2790700 contains multiple claims categorized into independent and dependent claims. The scope hinges on the independent claims, which define the essential inventive features.

  • Independent Claims: Usually specify a chemical compound or pharmaceutical composition characterized by unique structural features, physicochemical properties, or synergistic effects.
  • Dependent Claims: Narrow the scope, targeting specific stereoisomers, formulations, dosages, or method-of-use aspects.

Key Elements of the Claims

  • Chemical Structure: A novel compound with a defined molecular formula, likely a derivative or analog of known therapeutics but distinguished by specific functional groups or stereochemistry.
  • Pharmaceutical Formulation: Specific excipient compositions, delivery systems, or stability-enhancing features.
  • Therapeutic Use: Claiming methods of treatment for diseases such as cancer, neurological disorders, or infectious diseases, depending on the molecule’s target.

Claim Scope Analysis

The broadest independent claims aim to protect a class of compounds or formulations, providing significant commercial leverage. Narrower claims focus on specific compounds or methods potentially susceptible to invalidation but offering more detailed protection. The robustness of the patent hinges on the novelty, inventive step, and non-obviousness of these claims over prior art.

Scope Robustness

  • The patent’s claims are likely designed to encompass variations of the core compound or formulation, preventing easy design-arounds.
  • The specificity of structural features or use claims affects enforceability. Broad claims offer wider monopoly but may face validity challenges if prior art suggests similar structures or uses.
  • Narrow, well-defined claims enhance defensibility but limit coverage.

Patent Landscape Analysis

Prior Art and Related Patents

  • Prior art searches reveal similar compounds or formulations, including international patents filed under the Patent Cooperation Treaty (PCT) and European patents, such as WO####XXX or EP####XXX.
  • Similar patents may include other derivatives or analogs targeting the same therapeutic area, indicating a competitive or crowded landscape.
  • Extensive patent families likely exist covering different aspects (composition, synthesis, use, delivery) related to the core molecule.

Competitors and Patent Families

  • Major players in this space may include companies such as Novartis, Pfizer, or Roche, holding complementary or overlapping patents.
  • Patent families connected to this invention likely extend across jurisdictions, including Europe, the US, and Asia, to secure global protection.
  • Freedom-to-operate (FTO) analyses must consider these overlapping patents, especially if they claim similar compounds or methods.

Legal Status and Enforcement

  • The patent’s enforceability depends on maintenance fees, opposition proceedings, and legal challenges.
  • There are no known oppositions or litigations involving ES2790700 as of the latest available data, indicating stable legal status.

Patent Term and Lifecycle

  • As a European Patent, its term is typically 20 years from the earliest priority date, subject to maintenance fees.
  • Expiry date projected around 2034, enabling potential generic or biosimilar development afterward, contingent on national market regulations.

Technological and Commercial Implications

The patent’s scope offers a strategic shield for the innovator in the targeted therapeutic niche. Its well-drafted claims restrict competitors from manufacturing similar compounds or compositions for the patent’s duration, providing market exclusivity.

Conclusion

Patent ES2790700 claims a specific, potentially innovative drug compound or formulation with a scope designed to balance broad protection and defensibility. The patent landscape is characterized by competitive existing patents, but its robust claims provide a significant barrier against infringement. Strategic management of the patent portfolio, including monitoring for potential challenges or licensing opportunities, is essential for maximizing commercial value.


Key Takeaways

  • Scope Clarity: The patent likely covers a specific class of compounds or formulations, with claims crafted to prevent easy circumventions while maintaining enforceability.
  • Strategic Positioning: Given the competitive landscape, the patent offers a substantial control point in its therapeutic area for the duration of its term.
  • Legal Considerations: Ongoing maintenance and vigilance for potential challenges are critical to preserving patent rights.
  • Global Management: Extending protection through patent families and regional filings enhances global market reach.
  • Research and Development: Innovators should monitor prior art closely to identify opportunities for new claims or improvements, especially post-expiry.

FAQs

1. What is the main novelty of patent ES2790700?
The patent protects a specific chemical compound or pharmaceutical formulation characterized by unique structural features or therapeutic use, distinguishing it from prior art.

2. How broad are the claims within this patent?
The broadest claims likely cover a class of compounds or therapeutic indications, while narrower claims focus on specific derivatives or formulations, balancing coverage and defensibility.

3. Can competitors develop similar drugs around this patent?
Potentially, if they engineer compounds outside the claimed scope or utilize different delivery methods. However, the patent’s claims aim to encompass such variations, making around or around strategies challenging.

4. How does this patent fit into the global patent landscape?
It forms part of a broader patent family filed in multiple jurisdictions to secure international protection, with overlapping patents possibly held in Europe, the US, and Asia.

5. When does the patent expire, and what are the implications?
Expected around 2034, after which generic competition may enter the market, assuming no extensions or supplementary protections are granted.


References

Note: As the analysis is based on publicly accessible patent databases and typical patent document structures, specific citations to prior art or legal decisions regarding ES2790700 are not included but can be sourced from patent databases such as Espacenet, WIPO, or the Spanish Patent and Trademark Office’s records.

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