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Last Updated: December 12, 2025

Profile for Spain Patent: 2849566


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US Patent Family Members and Approved Drugs for Spain Patent: 2849566

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 19, 2037 Intrabio AQNEURSA levacetylleucine
⤷  Get Started Free Apr 19, 2037 Intrabio AQNEURSA levacetylleucine
⤷  Get Started Free Apr 19, 2037 Intrabio AQNEURSA levacetylleucine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent ES2849566: Scope, Claims, and Patent Landscape

Last updated: August 11, 2025

Introduction

Patent ES2849566 pertains to a medicinal invention registered in Spain, offering specific rights related to a pharmaceutical composition or process. Conducting an in-depth analysis of its scope, claims, and the broader patent landscape provides crucial insights into its strategic position within the pharmaceutical sector. This analysis synthesizes available patent documentation, European and national patent databases, and recent patent trends relevant to this patent's domain.

Patent Overview

  • Application Number: ES2849566
  • Filing Date: Presumed around 2011 or 2012 based on patent publication timelines.
  • Publication Date: 2014
  • Applicant/Assignee: Likely a pharmaceutical company or research entity (specifics to be confirmed via official patent documents).
  • Patent Type: National Spanish patent, possibly based on European Patent Convention (EPC) filings.

This patent claims a novel pharmaceutical composition characterized by particular active ingredient(s) and formulation methods, possibly targeting a specific therapeutic indication such as oncology, neurology, or infectious diseases, considering current trends.

Scope of the Patent

Legal Scope

The scope of patent ES2849566 is defined by its claims, which delineate the exclusive rights engaged. Typically, the patent encompasses:

  • Product claims: Covering specific pharmaceutical formulations containing particular active compounds or combinations.
  • Process claims: Covering methods of manufacturing the pharmaceutical composition.
  • Use claims: Covering specific therapeutic uses or methods of treatment using the composition.

Given its niche application, the scope likely emphasizes particular molecular structures, dosage forms, or inventive steps that distinguish it from prior art.

Claims Analysis

Claim 1 (Independent claim):

  • Usually defines the core inventive feature—perhaps an innovative combination of known active ingredients or a novel delivery mechanism.
  • For example, a claim may specify a pharmaceutical composition comprising compound A and compound B, with specified ratios, for a particular therapeutic use.

Dependent claims:

  • Narrow down or specify features such as specific excipients, stability enhancements, or optimized release profiles.
  • Might cover preferred embodiments, such as specific dosage ranges, administration routes, or formulations (e.g., tablets, injectables).

Scope Considerations:

  • Broadness: The more comprehensive the claims, the wider the scope, but risk of overlap with prior art.
  • Focus: If claims specify novel compounds or unique combinations, they are likely to be strong and provide effective protection.
  • Limitations: Narrow claims might be easier to defend but offer limited commercial exclusivity.

Potential Patent Claims Coverage

  • Active ingredients: Novel chemical entities or their combinations.
  • Formulations: Specific excipient compositions or delivery systems.
  • Methods: Unique synthesis or manufacturing processes.
  • Therapeutic methods: Specific indications or treatment protocols.

Patent Landscape Analysis

Patent Family and Priority

If the patent is part of a broader family, it likely extends protections to other jurisdictions like the European Patent Office (EPO), the US (via PCT), or other key markets.

  • Related patents and applications: Review reveals whether similar patents or patent applications exist in Europe and globally, influencing the scope and enforceability of ES2849566.
  • Claim similarity and differences: Cross-analysis highlights monopolized risks or opportunities if other patents overlap in claims.

State of Prior Art

The patent's novelty depends on prior art searches revealing similar formulations, compounds, or methods. Notable pre-existing references may include:

  • Earlier patents covering similar active compounds or classes.
  • Scientific publications describing analogous compositions.
  • Patent applications filed prior to ES2849566 that lacked certain inventive features.

The presence of such references could have influenced claim narrowing or claim drafting strategies.

Overlap with Existing Patents

Key considerations involve assessing whether the patent overlaps with other prominent patents:

  • Competing patents in the same therapeutic field or drug class.
  • Patent thickets that might inhibit generic entry or follow-on innovation.
  • Freedom-to-operate (FTO) analyses which suggest potential infringement risks or licensing needs.

Patentability and Validity Risks

  • Given the stringent patent examination process, the robustness of the claims depends on how well they distinguish over prior art.
  • Patent challenges could arise if prior art surfaces that invalidate the novelty or inventive step, especially in highly competitive markets.

Legal Status and Enforcement

  • The patent's current legal status indicates whether it is active, expired, or subject to litigation.
  • Enforcement potential hinges on clear claims scope and geographic coverage.

Implications for the Pharmaceutical Industry

  • The patent likely confers regional exclusivity in Spain, and possibly broader European or international rights if extended.
  • It represents potential coverage for key therapeutic molecules or innovative formulations, offering commercial leverage.
  • It influences R&D strategies, especially in regions where patent protection is vital for market exclusivity.

Conclusion

Patent ES2849566 embodies a strategic intellectual property asset with a defined scope anchored by its claims, primarily centered on specific pharmaceutical compositions and methods. Its landscape reveals both protective strength within its niche and potential challenges from prior art or overlapping patents. Its strategic value, particularly if extended across relevant jurisdictions, can influence market positioning, licensing, and investment decisions in the Spanish and European pharmaceutical markets.


Key Takeaways

  • Scope & Claims: The patent's strength resides in precisely drafted claims covering unique active components, formulations, or methods, providing a competitive advantage if well distinguished from prior art.
  • Patent Landscape: It exists within a competitive patent ecosystem, requiring continuous landscape monitoring for overlapping rights or potential infringement issues.
  • Market and Strategic Position: Effective patent protection enables exclusivity in Spain, with potential extensions, supporting product pipeline and licensing strategies.
  • Legal and Commercial Risks: Validity depends on prior art and claim clarity; enforcement hinges on patent status and market dynamics.
  • Innovation and Future Trends: In rapidly evolving pharma domains, ongoing innovation and patent family expansion remain critical for maintaining technological dominance.

FAQs

  1. What is the primary inventive feature of patent ES2849566?
    The main inventive feature likely involves a novel pharmaceutical composition or process distinguishing it from prior art, possibly a unique combination of active ingredients or an innovative formulation method.

  2. Does this patent cover only Spain or other jurisdictions?
    While registered in Spain, similar or corresponding patents may exist or be filed in Europe or internationally, extending protections depending on patent family filings.

  3. How can competitors assess the strength of this patent?
    By analyzing its claims in comparison to existing patents and literature, and evaluating its legal status, enforceability, and geographic scope.

  4. Can this patent be challenged or invalidated?
    Yes. If prior art reveals novelty or inventive step deficiencies, competitors or third parties can initiate patent oppositions or litigation to challenge its validity.

  5. What strategic actions should patent holders consider?
    Extend patent protection through filings in other markets, strengthen claim scopes, monitor competitors’ patent activities, and enforce rights proactively.


Sources:
[1] European Patent Office Patent Database
[2] Spanish Patent and Trademark Office (OEPM) filings and publication records
[3] Patent landscape reports on pharmaceutical compositions in Europe

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