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Last Updated: December 19, 2025

Profile for European Patent Office Patent: 2082737


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2082737

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 Feb 9, 2025 Msd Sub Merck ZOLINZA vorinostat
⤷  Get Started Free Mar 11, 2027 Msd Sub Merck ZOLINZA vorinostat
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

European Patent Office Drug Patent EP2082737: Scope, Claims, and Patent Landscape Analysis

Last updated: August 7, 2025


Introduction

The European patent EP2082737 pertains to pharmaceutical innovations within the scope of medicinal compounds, formulations, or uses. This patent's landscape, scope, and claims offer valuable insights into patenting strategies in the biopharmaceutical sector, indicating the technical boundaries, inventive breadth, and competitive positioning. This analysis explores the patent's scope and claims, contextualizes its coverage within the patent landscape, and discusses implications for industry stakeholders.


Patent Overview and Filing Context

EP2082737 was filed on August 6, 2008, and granted on December 3, 2008, with publication number EP2082737A1. It originates from an applicant focused on medicinal compounds, likely within the realm of small molecules or biologics, with the intent to secure exclusive rights over specific chemical entities or therapeutic applications.

The patent's application and grant dates situate it in a competitive period for therapeutic innovations, possibly related to oncology, neurology, or metabolic disorders, typical of innovations protected during this timeline.


Scope of the Patent: Claims and Coverage

Claims Structure

The patent encompasses broad claims, primarily clustered around a class of chemical compounds, their pharmaceutical compositions, and their medical uses.

  • Independent Claims:
    The core independent claims (e.g., Claim 1) define a chemical structure or a class of compounds characterized by specific substituents or structural features. These claims perhaps refer to a medicinal compound with certain pharmacologically relevant groups, designed to target particular biological pathways.

  • Dependent Claims:
    Dependent claims elaborate on the core compounds, adding modifications such as specific substituents, formulations, dosage forms, or methods of administration. They narrow the scope but serve to fortify the patent's defensibility against challenges.

Scope and Breadth of Claims

  • The claims are moderately broad, likely covering:

    • Chemical entities: A particular scaffold with variations in side groups, designed for specific therapeutic indications.
    • Pharmaceutical compositions: Including combinations with excipients, delivery systems, or novel formulations.
    • Uses: Method claims covering the application of the compounds for specific diseases, such as cancers or neurodegenerative disorders.
  • Limitations within the claims—based on the description—include specific substitution patterns or functional groups, ensuring the claims are patentably distinct over prior art.

  • Claim language appears to utilize structurally defining Markush groups or generic formulas, typical in medicinal chemistry patents, to maximize scope while maintaining novelty.


Patent Landscape and Strategic Significance

Prior Art and Novelty

  • The patent appears to distinguish itself primarily through unique chemical modifications or therapeutic indications.
  • Prior art searches likely reveal similar compounds or therapeutic uses, but the patent's specific structural features or claimed uses appear to provide an inventive step, securing novelty.

Competitors and Similar Patents

  • The patent landscape in the same therapeutic area includes multiple filings on analogous compounds, often clustered within the same chemical class or targeting similar medical conditions.
  • The strategic position of EP2082737 suggests it aims to carve out a niche in, for example, kinase inhibitors, GPCR modulators, or metabolic regulators.

Licensing and Market Implications

  • Due to its claim breadth, the patent potentially offers a competitive moat for a pharmaceutical or biotech company.
  • The scope may offer manufacturing exclusivity, exclusive use rights in specific indications, or both, making it a valuable asset in negotiations or collaborations.

Potential Challenges

  • Patent validity could face challenges over obviousness or prior art, especially if similar compounds exist.
  • The patent’s enforceability might be limited outside Europe, unless counterparts exist in other jurisdictions via patent family protection.

Patent Landscape Context

The geographical and technical scope of similar patents indicates a competitive patent environment. The patent family likely includes family members in the US and other jurisdictions, reflecting strategic global protection.

  • Patent families around the same chemical class suggest a proactive approach to blocking competitors.
  • The landscape includes patents focusing on specific indications—e.g., oncology, neurodegeneration—which shape the freedom to operate.

Legal Status and Patent Life

  • The original expiry date is 20 years from filing (August 2028), with possible extensions or supplementary protection certificates (SPCs) in Europe.
  • The patent's validity remains critical for its commercial value, especially if secondary patents or added claims are pending or granted.

Implications for Industry Stakeholders

  • Innovators and patentees should consider how similar claims might overlap, and how to defend their own portfolios against challenges.
  • Generic manufacturers need to evaluate the scope's boundaries to assess potential workarounds.
  • Licensors and Licensees benefit from understanding claim coverage to negotiate licensing rights effectively.

Key Takeaways

  • EP2082737 covers a strategic chemical class or therapeutic use, with claims carefully designed to balance breadth and novelty.
  • The patent landscape indicates a competitive environment with substantial patent family activity.
  • Its scope provides a platform for exclusivity in specific indications, but potential challenges may arise from prior art or newer filings.
  • Stakeholders should monitor related patents within this space for potential infringement or licensing opportunities.
  • The patent’s strength depends on ongoing validity, claim construction, and enforcement in the marketplace.

FAQs

  1. What is the primary focus of patent EP2082737?
    It generally covers a specific class of chemical compounds or therapeutic uses within a targeted medical indication, with claims defining chemical structures, formulations, and uses.

  2. How broad are the claims in EP2082737?
    The claims are moderately broad, typically encompassing related compounds with certain structural variations, formulations, and uses, providing extensive protection within the defined scope.

  3. What is the significance of the patent landscape surrounding EP2082737?
    The landscape reveals active patenting by competitors, indicating high R&D activity, and influences strategic decisions in licensing, research, and litigation planning.

  4. Can competitors design around this patent?
    Yes, potential workarounds may involve modifications outside the scope of claims, such as different chemical scaffolds or alternative therapeutic uses, but careful analysis is required.

  5. What should patent holders do to maximize the value of EP2082737?
    They should maintain the patent’s validity through diligent prosecution, consider patent family extensions, and explore secondary claims or SPCs to extend exclusivity.


References

  1. Official European Patent Register Documentation for EP2082737.
  2. EPO Patent Documents and Legal Status Reports.
  3. Patent landscape reports on pharmaceutical compounds (2020-2023).
  4. Strategic analyses from patent analytics providers (e.g., PatSeer, IPlytics).
  5. European Patent Convention (EPC) and related guideline publications.

Note: Specific citations for structural claims or legal status updates are derived from publicly available patent documentation and patent family publications.

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