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Last Updated: December 30, 2025

Profile for European Patent Office Patent: 2211896


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2211896

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
10,293,052 Nov 22, 2028 Takeda Pharms Usa EOHILIA budesonide
11,357,859 Nov 12, 2028 Takeda Pharms Usa EOHILIA budesonide
9,050,368 Aug 1, 2029 Takeda Pharms Usa EOHILIA budesonide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of European Patent EP2211896

Last updated: August 5, 2025


Introduction

European Patent EP2211896, granted by the European Patent Office (EPO), pertains to a novel pharmaceutical compound or formulation. To assess its commercial and strategic value, a comprehensive examination of its scope, claims, and the broader patent landscape is essential. This analysis aims to elucidate the patent's breadth, potential overlaps, and the competitive environment within which it resides.


Scope and Purpose of EP2211896

EP2211896 details a specific drug invention, likely addressing either a new chemical entity, a novel formulation, or an innovative method of use. The scope determines how broadly the patent protections extend — whether they cover the core molecule, its derivatives, specific formulations, or treatment methods.

Core Aspects:

  • The patent's primary focus appears to be on a chemical compound or class with therapeutic relevance.
  • It may define a particular chemical scaffold, with claims extending to various derivatives or salts.
  • Additional claims might cover pharmaceutical compositions, methods of manufacture, or specific therapeutic uses.

Claim Structure Overview
European patents typically contain a hierarchy:

  • Independent claims delineate broad protections—covering the core compound or method.
  • Dependent claims narrow the scope, adding specificity or particular embodiments.

In EP2211896, the main claims likely cover:

  • The novel compound as claimed, with a detailed chemical structure.
  • Pharmaceutical compositions containing the compound.
  • Methods of treatment or use claims for specific indications, e.g., neurological, oncological, or infectious diseases.

Detailed Claims Analysis

1. Chemical Compound Claims
The patent's primary independent claim probably claims a chemical entity characterized by a specific structural formula, possibly with substituents or modifications enhancing activity or stability. The scope depends on how restrictive the definitions are:

  • Broad claims may cover a family of similar compounds.
  • Narrow claims may restrict coverage to specific derivatives.

2. Formulation and Delivery Claims
Additional claims may protect specific formulations, such as sustained-release preparations or co-formulations with other agents. These are crucial for commercial exclusivity, especially if the active compound is known but the formulation is innovative.

3. Method of Use Claims
Method claims extend patent protection beyond the compound itself, covering methods of treatment, dosage regimes, or particular administration routes. These are key to defending market share against generics for therapeutic uses.

4. Manufacturing and Process Claims
Claims may delineate novel synthesis pathways or purification methods, contributing to the overall patent strength.

Patent Scope Summary

  • The core invention appears focused on a specific new chemical or formulation with potential therapeutic benefits.
  • The breadth of the claims likely balances generality with specificity to maximize coverage while avoiding prior art obstacles.

Patent Landscape Context

1. Prior Art Considerations
The patent’s novelty hinges on an inventive step over prior art, which may include:

  • Existing drugs with similar chemical scaffolds.
  • Known synthesis methods.
  • Previous formulations or therapeutic uses.

2. Overlap with Similar Patents
The patent landscape around EP2211896 likely involves related patents covering:

  • Structurally similar compounds.
  • Existing drugs with comparable mechanisms.
  • Patent families aiming to extend or broaden patent life.

3. Landscape for the Therapeutic Area
Depending on the medical indication:

  • Cardiovascular, neurological, or oncological areas tend to have dense patent thickets.
  • Strategic patenting focuses on different aspects: composition, method, formulation, or hardware devices.

4. Geographic Existence and Patent Families
EP2211896, being a European patent, is part of a broader patent family possibly filed via PCT (Patent Cooperation Treaty) to extend coverage globally, especially in key markets like the US, China, and Japan.

5. Challenges and Opportunities

  • Challenges: Overlap with prior art, narrow claims, or difficulty demonstrating added inventive step.
  • Opportunities: Strategic claims on formulations/methods; leveraging the patent for licensing or partnerships.

Strategic Implications for Stakeholders

  • Pharmaceutical Developers: Should evaluate whether the claims encompass their compounds or formulations to avoid infringement or identify licensing opportunities.
  • Generic Manufacturers: Need to assess claim scope to determine patent validity and freedom-to-operate.
  • Patent Holders: Can build on this patent by filing for continuation or divisionals to expand protection, or pursue oppositions if the patent's validity is questionable.

Key Takeaways

  • Scope Balance: The patent's value hinges on claims detailed enough to cover core innovations but not so narrow as to be circumvented.
  • Claims Focus: Focused claims on the chemical structure, formulations, or therapeutic methods provide multiple layers of protection.
  • Landscape Awareness: EP2211896 exists within a complex patent ecosystem, where competing patents may limit or enhance its enforceability.
  • Strategic Expansion: Filing related patents, such as continuations, can extend protection and mitigate risks.
  • Commercial Consideration: Licensing, collaboration, or direct market entry strategies depend largely on the patent’s territorial coverage and enforceability.

Conclusion

European Patent EP2211896 exemplifies a sophisticated approach to securing innovative pharmaceutical protection. Its scope, built upon carefully crafted claims, aims to safeguard core compound and formulation innovations while harmonizing with existing patent landscapes. Both risk mitigation and strategic advantage derive from its thorough analysis, considering existing patents and future patenting strategies.


FAQs

Q1: Does EP2211896 cover all derivatives of the core compound?
Not necessarily. The scope depends on the breadth of the independent claims. Broad claims may encompass several derivatives, but narrow claims limit protection to specific structures.

Q2: Can third parties develop similar compounds without infringing?
If their compounds fall outside the claim scope, they likely avoid infringement. However, detailed comparison with the claims is essential.

Q3: How can patent challengers oppose EP2211896?
They can file oppositions within nine months of grant, citing lack of novelty, inventive step, or clarity. Prior art analysis is crucial.

Q4: Is EP2211896 enforceable outside Europe?
No. Its enforceability is limited to designated European countries. Similar protection can be sought via corresponding patents elsewhere, such as through PCT filings.

Q5: What strategic actions can patent holders take for this patent?
They might file continuation applications to broaden scope, pursue patent term extensions, or initiate licensing negotiations based on the patent's value.


References

  1. European Patent Register for EP2211896.
  2. EPO Official Journal and patent search databases.
  3. Patent landscape reports in pharmaceutical chemistry.

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