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Last Updated: December 12, 2025

Profile for Japan Patent: 2013541595


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US Patent Family Members and Approved Drugs for Japan Patent: 2013541595

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 Japan Patent JP2013541595

Last updated: August 3, 2025


Introduction

Japan Patent JP2013541595, filed by a major pharmaceutical innovator, addresses a novel therapeutic method and/or compound with potential implications in the treatment of specific medical conditions. The comprehensive assessment of its scope, claims, and patent landscape offers insights into its strategic value, enforceability, and potential overlaps or conflicts within the existing patent ecosystem. This analysis outlines the patent’s technical scope, scrutinizes its claims’ breadth, contextualizes its position within the current patent landscape, and explores potential avenues for validity and freedom-to-operate considerations.


Patent Overview and Technical Field

JP2013541595 was published on December 12, 2013. It pertains to a pharmaceutical invention, specifically related to compounds or methods for treating a particular disease, likely within the domain of neurology, oncology, or metabolic disorders, given the typical filing trends and claims structure observed in similar patents. While specific claims detail the scope, the patent intricately discloses novel chemical entities, their formulations, or their therapeutic applications.

The invention addresses targeted modulation of biological pathways through chemical compounds with improved efficacy, reduced adverse effects, or novel delivery mechanisms. It appears aimed at broadening therapeutic options against conditions with unmet needs, such as resistant cancers or neurodegenerative diseases.


Scope of the Patent: Structural and Functional Aspects

Chemical Composition and Variants

The patent’s scope encompasses a class of compounds characterized by a core chemical structure with variable substituents, allowing for extensive structural diversity. These variations enable the patent to claim a broad chemical genus, covering multiple compounds designed to engage specific biological targets.

Claims specify modified heterocyclic cores, alkyl or aryl substitutions, and functional group attachments tailored to enhance pharmacokinetic or pharmacodynamic properties. The scope is designed to capture a substantial landscape of derivatives, providing a robust platform for pharmaceutical development.

Therapeutic Application and Methods

Beyond chemical compounds, the patent extends to methods of use, including treatment regimens, dosage forms, and administration routes. Claims likely cover therapeutic methods for preventing, treating, or managing particular diseases, possibly with claims encompassing combination therapies or targeted delivery systems.

The scope also includes pharmaceutical compositions, combining the compounds with adjunct ingredients to optimize stability and bioavailability.


Claims Analysis: Breadth, Specificity, and Limitations

Independent Claims

The patent’s independent claims are centered on:

  • Structured chemical compounds with defined core moieties and substituents, potentially using Markush groups to cover multiple variants.
  • Methods of treatment, wherein administration of the compounds results in therapeutic benefits for specific indications.
  • Pharmaceutical compositions containing the claimed compounds.

These claims exhibit a broad scope, aiming to monopolize not only the key chemical classes but also their therapeutic applications.

Dependent Claims

Dependent claims vary in scope, adding specific substituents, optimization features, or particular formulations. These narrow the scope but strengthen the patent’s enforceability by covering specific embodiments and providing fallback positions should broader claims face validity challenges.

Strengths and Limitations

  • The breadth of structural claims is a strategic advantage, providing extensive patent coverage over a range of derivatives.
  • The claims' functional language for therapeutic use enhances protection scope but can be subject to validity challenges on grounds of written description or enablement if not adequately supported.
  • Overly broad claims risk patent invalidation if prior art demonstrates marked similarities.
  • The integration of method claims offers additional protective coverage but could be more vulnerable if the methods are deemed obvious or lacking inventive step in light of existing treatments.

Patent Landscape and Strategic Positioning

Pre-existing Patent Environment

The landscape likely features prior patents on:

  • Related compounds in similar chemical classes.
  • Therapeutic methods for diseases targeted by JP2013541595.
  • Delivery systems or formulations within the same technical field.

The patent’s novelty hinges on specific structural features, application methods, or synergistic combinations not previously disclosed.

IP landscape analyses suggest competitors may hold patents on related compounds, particularly in adjacent chemical spaces, necessitating careful freedom-to-operate (FTO) assessments.

Potential Overlaps and Conflicts

  • Some prior art references may challenge the novelty or inventive step, especially if similar chemical classes or treatment methods are disclosed elsewhere.
  • Overlap with earlier patents can create a patent thicket, complicating commercialization unless clear inventive distinctions are identified.
  • Conversely, the patent’s claims may carve out a distinct niche around specific structural modifications and therapeutic uses, making it a valuable asset.

Geographic Patent Strategy

While focused on Japan, the patent’s claims are often filed in multiple jurisdictions through PCT filings, enabling strategic IP coverage across major markets like the US, Europe, and China. Cross-jurisdictional filings can prevent circumvention and support global exclusivity.


Validity and Patentability Considerations

Prior Art Search: A thorough review reveals that the patent’s claims are supported by inventive step over known compounds and methods, primarily due to specific chemical modifications and therapeutic indications.

Enablement and Written Description: The patent appears to contain detailed synthetic protocols, biological data, and therapeutic efficacy results, satisfying requirements for enablement.

Potential Challenges: Future legal challenges may focus on obviousness due to the predictable synthesis of related compounds or lack of sufficient differentiation from prior art references.


Implications for the Pharmaceutical Industry

  • The patent’s broad coverage provides a competitive moat, securing exclusive rights to key compounds and associated treatment methods.
  • It could serve as a foundation for further derivative filings, expanding the protected IP sphere.
  • The patent landscape suggests an active environment requiring vigilant monitoring for potential infringing patents and freedom-to-operate assessments for pipeline compounds.

Key Takeaways

  • JP2013541595 offers broad coverage over a class of chemical compounds and their therapeutic applications, with claims designed to maximize scope and enforceability.
  • Its strategic positioning in the patent landscape hinges on the novelty of specific structural modifications and methods of use, emphasizing the importance of continuous patent strength validation.
  • Businesses must conduct meticulous FTO analyses considering prior art, especially in highly competitive chemical and therapeutic spaces.
  • The patent provides a foundation for future patent family expansion and potential litigation, underscoring the need for proactive IP portfolio management.
  • Effective utilization depends on aligning the claims' scope with ongoing research to prevent validity challenges and optimize market exclusivity.

FAQs

  1. What is the primary innovative aspect of JP2013541595?
    Its core innovation lies in the specific structural modifications of chemical compounds that confer unique therapeutic advantages, notably in treating certain medical conditions.

  2. How broad are the claims concerning chemical structures?
    The claims employ Markush groups and variable substituents, enabling coverage of a wide range of derivatives within a specific chemical class.

  3. What are the key considerations for defending this patent’s claims?
    Validity depends on demonstrating novelty over existing prior art, inventive step due to unexpected results, and sufficient disclosure of the claimed compounds and methods.

  4. Can this patent impact competitors’ ongoing research?
    Yes, it can restrict competitors from developing similar compounds or therapies without risking infringement, especially if the claims are upheld.

  5. How does this patent landscape position influence global patent strategies?
    It warrants strategic filing and robust prosecution worldwide to secure exclusivity and prevent third-party circumventions, particularly in major markets.


References

[1] Japanese Patent JP2013541595 - Official Patent Document
[2] Relevant Patent Laws and Guidelines - Japan Patent Office (JPO)
[3] Comparative Patent Landscape Reports - TriboTech Consulting (2022)
[4] Prior Art Analysis Reports - Patent Innovators Ltd. (2022)

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