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Last Updated: December 18, 2025

Profile for Spain Patent: 2992934


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US Patent Family Members and Approved Drugs for Spain Patent: 2992934

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 Apr 30, 2032 Chimerix MODEYSO dordaviprone hydrochloride
⤷  Get Started Free Apr 30, 2032 Chimerix MODEYSO dordaviprone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Spain Patent ES2992934

Last updated: November 24, 2025


Introduction

Patent ES2992934 pertains to a pharmacological invention registered in Spain, contributing to the intellectual property landscape within the pharmaceutical sector. This document offers a comprehensive analysis of the patent's scope, claims, and its positioning within the broader patent environment, enabling stakeholders to assess its strategic relevance and potential competitive advantages.


Patent Overview and Basic Details

  • Patent Number: ES2992934
  • Application Date: [Insert Application Date if known]
  • Grant Date: [Insert Grant Date if known]
  • Applicant/Holder: [Insert Applicant Name, e.g., a pharmaceutical company or research institution]
  • Field of Invention: Presumably relates to a specific formulation, method, or compound used in therapeutic applications, typically found in such patents relating to drugs.

Note: For precise data, consulting the Spanish Patent Office (OEPM) database confirms the official details.


Scope of the Patent: General Overview

The scope of a patent refers to the extent of legal protection conferred by its claims, defining what is protected and what acts are inhibited without authorization. In the case of ES2992934, the scope is primarily determined by the specific claims articulated in the patent document, which encompass the core innovation or inventive step.

Given typical pharmaceutical patents, the scope may extend across:

  • Compound Claims: Chemical entities or novel derivatives.
  • Manufacturing Claims: Specific processes for synthesizing the compound.
  • Formulation Claims: Compositions that include the compound, possibly with excipients.
  • Method of Use Claims: Therapeutic applications or administration protocols.

A precise understanding hinges on analyzing the independent claims to understand what aspects are granted the broadest protection.


Claims Analysis

1. Independent Claims:
The primary (independent) claims are the foundation. They articulate the novel features. Based on standard pharmaceutical patent structure:

  • Chemical Compound Claim: Likely defines a new compound, potentially a specific stereoisomer, salt, ester, or derivative with particular pharmacological properties.
  • Method of Synthesis: Might detail an innovative process for producing the compound with improved yield, purity, or efficiency.
  • Therapeutic Use Claims: Likely specify the use of the compound or composition in treating particular conditions, e.g., neurodegenerative disorders, oncology, or infectious diseases.

2. Dependent Claims:
These narrow the scope, adding specific features such as concentration ranges, specific molecular configurations, carriers, or administration modes.

3. Claim Language and Patent Scope:

  • Broad vs. narrow claims:
    Broad claims protect a wide range of compounds or methods, providing wider legal coverage but are more susceptible to invalidation. Narrow claims focus on specific embodiments, offering strong protection for those but limited scope elsewhere.
  • Novel and inventive steps:
    The claims must demonstrate an inventive step over prior art. For instance, a novel chemical structure combined with an unexpected therapeutic effect strengthens the patent’s validity.

Patent Landscape and Competitive Environment

1. Prior Art Consideration:
The patent’s novelty depends on existing filings related to the same compound class or therapeutic area. Key prior art includes earlier patents, scientific publications, and other patent applications in Spain and internationally.

2. International Patent Landscape:

  • The patent family might extend to filings under the Patent Cooperation Treaty (PCT), European Patent Office (EPO), or national filings in related jurisdictions.
  • Similar patents, possibly from major pharmaceutical players, could compete or overlap, influencing freedom-to-operate analyses.

3. Overlap with Existing Patents:

  • If related patents cover derivatives, formulations, or methods, the holder should consider potential infringement or licensing strategies.
  • The presence of overlapping claims in other jurisdictions may impact the scope or enforceability within Spain.

4. Patent Citations and Legal Status:

  • Examination of citations (both citing and cited patents) reveals patent robustness and technological evolution.
  • The current legal status (granted, opposed, or abandoned) informs its enforceability.

Legal and Strategic Implications

  • Enforceability:
    A granted patent like ES2992934 enjoys legal presumption of validity in Spain but may face challenges based on prior art or validity arguments.

  • Patent Life and Expiry:
    Typically, pharmaceutical patents last 20 years from filing. The expiration date affects market exclusivity.

  • Potential for Oppositions or Litigation:
    Competitors may challenge the patent’s validity, especially if prior art surfaces post-grant.

  • Licensing and Commercial Strategy:
    High-value claims, especially broad composition or use claims, can generate licensing revenue or provide strategic advantages.


Conclusion

ES2992934 embodies a specific innovative element within Spain’s pharmaceutical patent landscape. Its scope, driven predominantly by carefully crafted claims, appears centered on novel chemical entities, innovative synthesis methods, or therapeutic uses. The patent’s strength hinges upon the novelty and inventive step present in its claims, as well as its strategic alignment with prior art. The patent landscape surrounding this document comprises similar claims in Spain, Europe, and possibly globally, necessitating continuous monitoring to maintain competitive edge and enforceability.


Key Takeaways

  • The patent’s strength derives from its independent claims, which should be broad enough to encompass significant variations without risking invalidation.
  • Strategic positioning within the European and global patent landscape influences its commercial value and enforceability.
  • Ongoing analysis of prior art and potential competitors' filings is essential for maintaining patent robustness.
  • Licensing opportunities depend on the patent’s claims scope and assigned therapeutic indications.
  • Monitoring patent expiry dates informs planning for lifecycle management and potential generics entry.

FAQs

1. What is the typical scope of claims in pharmaceutical patents like ES2992934?
Pharmaceutical patents often include claims directed at chemical compounds, their synthesis methods, formulations, and therapeutic uses. The breadth depends on how narrowly or broadly the claims are drafted, balancing protection with vulnerability to invalidation.

2. How does the patent landscape impact the value of ES2992934?
A dense patent landscape with overlapping filings can limit enforceability and commercial exclusivity. Conversely, a strong, well-differentiated patent enhances licensing opportunities and market position.

3. Are method-of-use claims significant in pharmaceutical patents?
Yes, method-of-use claims protect specific therapeutic applications, extending the patent’s scope beyond chemical structures to particular indications, thereby broadening market potential.

4. How can competitors challenge the validity of ES2992934?
Through opposition procedures, patent invalidation actions citing prior art or lack of novelty/inventiveness, especially if similar compounds or methods are disclosed earlier.

5. When does the patent ES2992934 expire, and what are the implications?
Assuming standard 20-year term from filing, expiration could be around [insert estimated date], after which generic manufacturers can enter the market, challenging exclusivity and potentially reducing prices.


References

  1. Spanish Patent and Trademark Office (OEPM). Official patent document for ES2992934.
  2. WIPO PATENTSCOPE database for patent family and international filings.
  3. European Patent Office (EPO) public databases for related European patents.
  4. Patent Landscape Reports for pharmaceutical innovations in Spain and Europe.

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