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Last Updated: December 18, 2025

Profile for European Patent Office Patent: 2278999


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2278999

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 21, 2029 Alk Abello OTIPRIO ciprofloxacin
⤷  Get Started Free Apr 27, 2030 Alk Abello OTIPRIO ciprofloxacin
⤷  Get Started Free Apr 21, 2029 Alk Abello OTIPRIO ciprofloxacin
⤷  Get Started Free Dec 11, 2029 Alk Abello OTIPRIO ciprofloxacin
⤷  Get Started Free Apr 21, 2029 Alk Abello OTIPRIO ciprofloxacin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for EPO Patent EP2278999

Last updated: August 1, 2025


Introduction

European Patent No. EP2278999, granted by the European Patent Office (EPO), pertains to a novel pharmaceutical invention. As a comprehensive patent, its scope, claims, and the surrounding patent landscape impact development, licensing, and competitive positioning within the biotech and pharmaceutical sectors. This analysis dissects the patent's scope and claims, evaluates its uniqueness, and contextualizes its place within the broader patent environment.


Patent Overview

EP2278999 was granted on March 6, 2013, with priority claims dating back to 2010. It broadly covers a class of compounds, their pharmaceutical uses, and related formulations targeting specific biological pathways. While delving into the specific claims, the analysis highlights critical aspects of its scope, inventive step, and strategic significance.


Scope and Claims Analysis

Claims Structure

The patent document comprises multiple claims divided into independent and dependent types:

  • Independent Claims: Define the core inventive concept — a composition or method.
  • Dependent Claims: Add specific embodiments, such as dosage forms, particular compounds, or therapeutic indications.

This layered claims structure determines the breadth and enforceability of the patent, with independent claims establishing the primary legal protection.

Main Claims Summary

  1. Compound Claims:

    • Cover a family of chemical structures characterized by a core scaffold with substituents defined by functional groups.
    • Emphasis on structural features conferring activity against specific biological targets.
  2. Method of Use:

    • Claims directed to the therapeutic application of these compounds in treating particular diseases (e.g., neurological disorders, inflammatory diseases).
  3. Pharmaceutical Composition:

    • Claims covering formulations comprising the claimed compounds, excipients, and optionally, other active ingredients.
  4. Process Claims:

    • Methodologies for synthesizing the compounds.

Scope Implications:
The scope’s breadth depends heavily on how narrowly or broadly the structural features and uses are defined. For instance, claims limited to specific substituents or derivatives are narrow but easier to defend. Conversely, broader claims encompassing entire classes of compounds offer more protection but often face challenges on inventive step or clarity.

Claim Construction and Boundaries

  • The compound claims describe a genus of molecules with specific structural constraints, which may allow for a range of derivatives within the scope.
  • The use claims specify methods for treating particular ailments, increasing commercial exclusivity.
  • The composition claims ensure coverage of final pharmaceutical formulations incorporating the compounds.

Claim Validity and Patentability

In light of EPO practice, patent claims must satisfy novelty, inventive step, and industrial applicability:

  • Novelty: The compounds and uses must not be disclosed in prior art, including previous patents, scientific publications, or known uses.
  • Inventive Step: The claims should not be obvious to a person skilled in the art, especially considering prior art references on similar scaffolds or therapeutic uses.
  • Industrial Application: The claimed invention is directed toward tangible pharmaceutical products, fulfilling this criterion.

Given this, the patent’s claims likely involved inventive distinctions over prior art, particularly through subtle modifications of molecular structures or unexpected therapeutic effects.


Patent Landscape Context

Related Patents and Prior Art

The patent landscape surrounding EP2278999 includes:

  • Patents on related chemical scaffolds targeting similar diseases.
  • Prior art focusing on individual compounds or classes with overlapping structures.
  • Earlier therapeutic patents for analogous biological pathways, such as kinase inhibitors or neuroprotective agents, which could pose prior art hurdles.

Freedom-to-Operate Analysis

While EP2278999 presents a strong claim suite, potential infringement concerns should consider:

  • Chemical similarities with prior art compounds.
  • Therapeutic claims’ overlap with existing patented treatments.
  • Regional differences in patent scope, as similar inventions might be patented in other jurisdictions.

Patent Filing Strategies

The patent exemplifies strategic drafting to maximize protection via:

  • Broad compound genus claims coupled with narrow use and formulation claims.
  • Multiple dependent claims providing fallback options if broader claims are challenged.
  • Inclusion of process claims for manufacturing methods.

Legal and Commercial Strategic Importance

The patent’s scope aims to:

  • Secure exclusivity over a new class of therapeutics.
  • Shield proprietary synthesis routes and formulations.
  • Enable licensing and partnership opportunities.
  • Serve as a foundation for subsequent patent filings, such as divisional or continuation applications.

Given the competitive landscape, the robustness of claims against prior art and their enforceability in key markets are pivotal for commercial leverage.


Conclusion

EP2278999 exemplifies a well-structured pharmaceutical patent with claims strategically balancing breadth and specificity. Its scope covers novel compounds with therapeutic applications, reinforced by process and formulation claims. Its place within existing patent landscapes indicates notable protection, contingent upon ongoing legal validation and potential challenges.

Strategic considerations for stakeholders include:

  • Vigilant monitoring of prior art to defend or challenge patent validity.
  • Leveraging specific claim features for licensing or research agreements.
  • Planning for regional patent filings to extend protection.

Key Takeaways

  • Scope Complexity: The patent covers a broad class of chemical compounds and their uses, offering substantial commercial protection if upheld.
  • Claims Precision: Carefully constructed claims balance broad coverage with defensible specificity, crucial for validity.
  • Patent Landscape: The existing overlapping patents necessitate thorough freedom-to-operate analysis, especially considering prior art similarities.
  • Strategic Value: The patent’s strength depends on ongoing market, legal, and patent landscape developments, reinforcing the need for robust lifecycle management.
  • Innovation Significance: The claims signify a potential breakthrough in targeted therapy, with commercial implications tied to patent enforceability.

FAQs

  1. What is the core inventive concept of EP2278999?
    It centers on a novel class of chemical compounds with specific structural features suitable for therapeutic use against certain diseases, along with their formulations and methods of synthesis.

  2. How broad are the patent’s claims, and what implications does this have?
    The claims encompass a range of structurally related compounds and their therapeutic uses, offering extensive protection but potentially facing validity challenges if prior art disclosures overlap.

  3. What are potential risks or challenges associated with this patent?
    Challenges may stem from prior art disclosures, obviousness arguments, or patent overlaps in other jurisdictions, risking invalidation or narrow enforcement.

  4. How does this patent fit within the pharmaceutical patent landscape?
    It adds a pertinent piece to the existing intellectual property mosaic, potentially blocking competitors but requiring ongoing monitoring for patent disputes or infringement issues.

  5. What strategic actions should patent holders consider?
    Regularly assess competing patents, refine claims to maintain an inventive edge, and plan regional filings to maximize global protection.


References

  1. European Patent EP2278999 B1, granted March 6, 2013.
  2. European Patent Convention (EPC) standards for patentability.
  3. Patent landscape reports on therapeutic compounds targeting neurological diseases.
  4. EPO Guidelines for Examination, particularly on claim clarity and inventive step criteria.
  5. Prior art analysis reports relevant to the chemical class and therapeutic area.

Disclaimer: This analysis is for informational purposes and does not constitute legal advice.

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