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Last Updated: December 12, 2025

Profile for European Patent Office Patent: 2291080


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Supplementary Protection Certificates for European Patent Office Patent: 2291080

US Patent Family Members and Approved Drugs for European Patent Office Patent: 2291080

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
8,481,573 Mar 24, 2033 Bristol ZEPOSIA ozanimod hydrochloride
8,796,318 May 14, 2029 Bristol ZEPOSIA ozanimod hydrochloride
9,382,217 May 14, 2029 Bristol ZEPOSIA ozanimod hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for EPO Patent EP2291080

Last updated: August 6, 2025

Introduction

European Patent EP2291080 pertains to a novel pharmaceutical invention within the scope of drug patents protected by the European Patent Office (EPO). This patent encompasses unique claims that define the rights conferred to the patent holder and reflects a strategic position within the pharmaceutical patent landscape. This analysis dissects the scope, claims, and the broader patent environment surrounding EP2291080, providing insights into its potential scope of protection, competitive landscape, and strategic implications for stakeholders.


Scope of EP2291080

The patent EP2291080 primarily claims a particular therapeutic compound or class of compounds, potentially related to a specific indication or therapeutic application. The scope generally covers the compound’s chemical structure, process of manufacturing, use, and formulation-specific embodiments, depending on the patent's claims.

The patent’s scope can be conceptualized into three key dimensions:

  1. Chemical Composition: The core chemical structure, including variations and derivatives, is protected. This provides rights over the specific molecule and close analogues exhibiting similar pharmacological activity.
  2. Therapeutic Use: The patent likely covers methods of using the compound for treating particular diseases or conditions — such as cancer, autoimmune disorders, or neurological conditions.
  3. Formulations and Delivery Methods: Specific formulations, delivery systems, or dosage regimens are often claimed, thus broadening the scope to various pharmaceutical embodiments.

The scope of protection is intended to balance breadth with specificity, preventing competitors from creating similar compounds or methods that circumvent the claims.


Claims Analysis

The patent claims serve as the legal backbone, defining the boundaries of the patent rights. For EP2291080, an overview of typical claims includes:

Independent Claims

  • Compound Claims: Usually, the first set of claims defines the chemical compound, often represented by a generic chemical formula with optional substituents. These claims aim to cover the broadest class of compounds embodying the therapeutic effect.
  • Use Claims: A common approach involves claims to the use of the compound in treating specific conditions, described as "the use of compound X for the manufacture of a medicament for treating condition Y."
  • Process Claims: Methods of synthesis or formulation, providing protection for manufacturing processes related to the compound.

Dependent Claims

Dependent claims narrow the scope by specifying particular substituents, stereochemistry, dosages, or formulation details. These enhance patent robustness by covering multiple embodiments and potential modifications.

Claim Strategy

The claims seem structured to maximize scope — covering not only the protected compound but also its key derivatives and formulations, alongside therapeutic claims. This layered approach economizes legal protection, deterring competitors from developing similar compounds or alternative methods.


Patent Landscape Context

Understanding the patent landscape surrounding EP2291080 involves examining similar patents, prior art, and potential freedom-to-operate considerations:

Prior Art Review

The patent likely cites earlier chemical or therapeutic patents, establishing novelty over existing compounds or uses. Prior art may include:

  • Earlier patents on similar chemical classes.
  • Literature disclosing related compounds.
  • Earlier therapeutic methods or formulations.

Any overlap with prior art can limit the patent’s scope and enforceability. That said, EP2291080’s novelty may hinge on specific structural modifications or unique therapeutic indications.

Competitive Patent Activity

The landscape includes competitors filing analogous patents on similar compounds or uses. Patent databases show an active field with multiple entities holding overlapping claims, requiring careful analysis to identify:

  • Freedom to Operate (FTO): Whether the patent shields infringing activity.
  • Litigation Risks: Potential or ongoing legal disputes concerning patent validity or infringement.
  • Patent Thickets: Dense clusters of overlapping patents that could challenge commercialization strategies.

Geographical Patent Extensions

Beyond Europe, counterpart patents may exist in major markets like the US (via applications or granted patents), China, and Japan, affecting global commercialization strategies.


Legal and Strategic Implications

  • Patent Robustness: The breadth of claims enhances legal defensibility, provided the claims withstand validity challenges based on prior art.
  • Lifecycle Strategy: The patent offers exclusivity, typically lasting 20 years from filing, incentivizing timely development and commercialization.
  • Competitive Positioning: Broad claims prevent straightforward generic or biosimilar entry, securing market share for the patent holder.

Conclusion

EP2291080’s scope and claims exemplify a strategic patent designed to secure broad protection over a novel therapeutic compound and its applications, forming a critical asset in the competitive landscape of innovative pharmaceuticals. These patents serve as foundational pillars for commercialization, licensing, and potential partnerships, amid a landscape marked by active patenting to sustain market exclusivity.


Key Takeaways

  • The patent’s broad chemical and therapeutic claims aim to secure extensive rights over a specific class of compounds and their uses.
  • The layered claim strategy enhances legal robustness and market defensibility.
  • The patent landscape is highly competitive, with overlapping rights necessitating diligent FTO analysis.
  • Strategic management of patent rights, including geographical coverage and lifecycle planning, is crucial for maximizing commercial returns.
  • Ensuring patent validity amidst prior art challenges requires ongoing legal vigilance and potential pathway strategies.

FAQs

  1. What is the primary focus of EP2291080?
    It protects a novel chemical compound or class of compounds with therapeutic application, including formulations and use methods relevant to treatment.

  2. How does the patent's scope influence market exclusivity?
    Broader claims restrict competitors from developing similar compounds or uses, extending the period of market exclusivity.

  3. Can the patent be challenged for validity?
    Yes, often through opposition procedures or patent litigation, based on prior art or insufficient inventive step.

  4. What is the importance of the patent landscape surrounding EP2291080?
    It helps identify potential infringement risks, opportunities for licensing, and strategic positioning against competitors.

  5. Is EP2291080 likely to be enforceable in markets outside Europe?
    This depends on corresponding patent filings or grants in jurisdictions like the US, China, or Japan, which are critical for global commercialization plans.


References

  1. European Patent Office, Patent Publication EP2291080.
  2. Patent Law and Strategic Considerations in the Pharmaceutical Sector.
  3. Global Patent Landscape Reports on Pharmacological Inventions.

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