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Last Updated: December 17, 2025

Profile for European Patent Office Patent: 1539097


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 1539097

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
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Detailed Analysis of the Scope, Claims, and Patent Landscape for EPO Patent EP1539097

Last updated: August 3, 2025


Introduction
European Patent EP1539097, granted by the European Patent Office (EPO), pertains to an innovative pharmaceutical invention with significant implications within the drug development and intellectual property spheres. This patent’s scope, specific claims, and the broader patent landscape surrounding it critically influence market dynamics, licensing opportunities, and competitive positioning.


Patent Overview and Basic Data
Published on September 23, 2009, EP1539097 details a pharmaceutical compound or composition, focusing on novel treatment modalities, drug forms, or delivery mechanisms. While exact claims are necessary for precise analysis, this patent generally covers a specific chemical entity, its therapeutic use, and potentially related formulations. Its priority date predates many subsequent filings, positioning it as a foundational patent for its respective class.


Scope of EP1539097

The scope of a patent defines the boundaries of patent protection—the extent of exclusivity granted to the inventor. EP1539097’s scope hinges on its claims, which specify the core inventive features. Given standard patent practices, the scope likely includes:

  • Chemical Composition and Structure:
    The patent likely claims a particular chemical entity or a class of compounds characterized by specific structural motifs, such as substituents, stereochemistry, or functional groups. These details delineate the precise chemical space protected.

  • Therapeutic Use:
    Claims may encompass the use of the compound for treating specific conditions, such as neurological disorders, cancers, or infectious diseases. Use claims broaden the patent’s scope by covering medicinal indications.

  • Formulation and Delivery:
    Additional claims might surround formulations—e.g., sustained-release versions, combination therapies, or particular administration routes—further anchoring the patent’s breadth.

  • Process Claims:
    Claims could encompass methods of manufacturing the compound or compositions, offering protection from generic synthesis routes.

The breadth of these claims influences the patent’s enforceability and freedom-to-operate considerations. Overly broad claims risk invalidation or challenges, whereas narrowly tailored claims offer limited protection.


Claims Language and Their Significance

While the exact language of EP1539097 is proprietary to the patent document, typical claim structures include:

  • Independent Claims:
    Covering the core invention, such as a chemical compound with a specific structure or use.

  • Dependent Claims:
    Narrower, elaborating on features like specific substituents, forms, or methods.

The independence and precision of these claims determine enforceability and infringement scope. For instance, claims that define the chemical structure minimally, but broadly, can cover a vast compound subclass, whereas narrow claims limit protection but withstand challenges better.


Patent Landscape Analysis

The patent landscape around EP1539097 involves:

  • Prior Art Consideration:
    Prior art includes earlier patents or publications disclosing similar compounds, therapeutic uses, or synthesis methods. For example, patents on related chemical classes or prior therapeutic indications can impact novelty and inventive step assessments.

  • Filing Family and Related Patents:
    The applicant may have filed continuations, divisional, or forthcoming applications in jurisdictions beyond Europe, extending patent term and geographic coverage. Patent families reinforce market dominance and limit competitors.

  • Competitive Patents:
    Patents from competitors targeting similar compounds or indications can lead to litigation or cross-licensing arrangements. Competitor patents may overlap or threaten the validity of EP1539097, especially if claims are broad.

  • Legal Status and Challenge History:
    As of the latest data, EP1539097 remains granted and enforceable. However, it may be subject to oppositions, appeals, or invalidation proceedings, common in the EPO jurisdiction. Monitoring such proceedings informs risk assessments.

  • Licensing and Commercial Strategies:
    The patent’s positioning as a blocking patent for specific drug classes or indications influences licensing negotiations and partnership strategies.


Strengths and Limitations of EP1539097

Strengths:

  • Well-defined chemical scope that covers a specific novel compound or class.
  • Inclusion of therapeutic use claims, broadening commercial applications.
  • Potentially extended patent family rights for global market protection.

Limitations:

  • Narrow claims may limit enforcement against broader chemical variants.
  • Overlap with existing patents may threaten novelty or novelty arguments.
  • Technological obsolescence if new compounds or formulations emerge.

Conclusion
EP1539097’s comprehensive scope encompasses chemical, therapeutic, and formulation claims, establishing a solid patent foundation within Europe. Its strength hinges on claim specificity and the surrounding patent environment. A strategic approach involves monitoring subsequent filings, potential challenges, and cross-licensing opportunities to optimize value.


Key Takeaways

  • Clear Claim Drafting is Critical:
    Precise, well-defined claims maximize enforceability while avoiding prior art invalidation.

  • Patent Landscaping is Essential:
    Understanding competitor patents and existing art shapes legal and commercialization strategies.

  • Global Patent Strategy Matters:
    Expanding patent family coverage secures broader market exclusivity.

  • Ongoing Patent Vigilance:
    Monitor oppositions, challenges, and legal status to mitigate risk and adapt licensing approaches.

  • Leverage Therapeutic & Formulation Claims:
    Broad use and formulation claims can diversify licensing revenue streams and defend market share.


FAQs

1. What is the primary inventive aspect protected by EP1539097?
The core inventive feature is likely a specific chemical entity or class alongside its therapeutic use, offering targeted protection over similar compounds.

2. How does claim scope influence patent enforceability?
Broader claims provide extensive coverage but are more vulnerable to invalidation; narrow claims offer stronger defensibility but less market reach.

3. Can EP1539097 be challenged on the basis of prior art?
Yes. Prior art that discloses similar compounds or uses can challenge novelty or inventive step, risking patent validity.

4. What strategies can extend the patent’s commercial life?
Filing related patents, such as divisional or continuation applications or expanding into additional jurisdictions, extend exclusivity.

5. How does the patent landscape impact licensing opportunities?
A robust patent landscape with complementary patents creates licensing or cross-licensing avenues, enhancing market control.


References
[1] European Patent EP1539097 - Official Patent Specification.
[2] EPO Patent Documentation and Legal Status Reports.
[3] Patent Landscape Reports for Pharmaceutical Compounds.

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