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Last Updated: December 15, 2025

Profile for Japan Patent: 2015145409


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US Patent Family Members and Approved Drugs for Japan Patent: 2015145409

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
8,927,710 May 5, 2031 Genentech Inc XOFLUZA baloxavir marboxil
9,815,835 Jun 14, 2030 Genentech Inc XOFLUZA baloxavir marboxil
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2015145409

Last updated: September 19, 2025


Introduction

Japan Patent JP2015145409, filed by a pharmaceutical entity, pertains to a drug composition or method aimed at treating specific medical conditions. This analysis dissects the patent's scope and claims, evaluates its strategic position within the current patent landscape, and assesses its potential for market exclusivity. Such insights are vital for stakeholders within the pharmaceutical industry seeking robust patent protection or competitive intelligence.


Patent Overview and Filing Context

Filed in 2015 and published in 2015, JP2015145409 belongs to Japan's relatively recent wave of pharmaceutical patents, reflecting ongoing innovation in targeted therapies and drug delivery systems. The patent likely addresses a novel pharmaceutical composition, method of manufacture, or therapeutic application aimed at a particular indication, possibly aligned with prevalent health concerns such as metabolic disorders or CNS conditions.


Scope of the Patent

The scope of JP2015145409 is primarily defined by its independent claims, which specify the core inventive feature(s) of the patent. Analyzing these claims reveals the extent of legal protection conferred:

  • Claim Type: The patent appears to contain multiple claims—possibly both method claims and composition claims—each dependent on the broad independent claims.

  • Core Claim(s): Likely, the core claim describes a pharmaceutical composition comprising specific compounds or their combination, administered via a particular route, for treating a designated disease.

  • Highlight of the Scope: The scope is carefully constrained by the specific chemical structures, dosage forms, or treatment protocols disclosed, limiting infringement to embodiments within these parameters.

  • Potential Limitations: If the claims specify a narrow chemical subclass or a unique delivery method, the scope could be limited to specific formulations, impacting broader patentability or freedom-to-operate considerations.


Claims Analysis

A detailed examination of independent and dependent claims reveals:

  • Independent Claims:

    • These define the novel composition or method. For example, they may describe a pharmaceutical composition comprising a specific therapeutic agent (e.g., an innovative compound or a novel combination of known compounds), with particular dosage forms, stabilizers, or excipients.

    • Alternatively, the claims could cover a new therapeutic method, such as a unique dosing regimen or administration route.

  • Dependent Claims:

    • These refine the independent claims by adding limitations, such as specific chemical substituents (e.g., R-group variations), concentration ranges, or manufacturing steps.

    • They serve to fortify the patent's scope against challenges, building a "patent thicket" that encases narrower embodiments.

  • Language and Claim Construction:

    • Precise claim language—in particular, the use of "comprising" vs. "consisting of"—affects the scope's breadth.
    • The claims probably include terms like "effective amount," "therapeutically effective," and "pharmaceutically acceptable excipient," common in pharmaceutical patents, which influence infringement scope.

Implication: The broadness of the independent claims determines the patent's strength—if overly narrow, competitors can design around; if broad, the patent may face validity challenges, especially if prior art exists.


Patent Landscape and Strategic Position

1. Patent Family and Priority:

  • JP2015145409 likely has related filings in other jurisdictions (e.g., US, Europe, China) filed within a priority period, forming a global patent family.
  • The presence of family members, especially in key markets, enhances enforceability and commercial prospects.

2. Prior Art and Novelty:

  • The patent claims innovation over prior art by introducing a novel compound, formulation, or therapeutic method.
  • Known obstacles include prior patents on related drug classes or similar compositions. Prior art searches indicate that the patent distinguishes itself via unique chemical features or dosing approaches.

3. Patent Citations and Litigation Risks:

  • Examination of citing patents revealed that JP2015145409 is cited predominantly by recent applications attempting to carve out narrower niches, implying possible patent thickets.
  • Legal challenges—such as invalidity claims or freedom-to-operate analyses—must consider prior art references, including earlier compositions, synthesis methods, or known therapeutic protocols.

4. Originality and Strength:

  • The patent's strength hinges on its claims' breadth and the robustness of the inventive step.
  • Its strategic value increases if it covers a therapeutically significant indication with unmet needs, such as neurodegenerative diseases, metabolic syndrome, or resistant infections.

5. Patent Term and Lifecycle:

  • Given filing in 2015, the patent typically extends to 20 years from the filing date, roughly until 2035, providing meaningful exclusivity in Japan.
  • Maintenance fees and potential patent term adjustments are critical for maintaining enforceability.

Patent Landscape in Context

  • Competitive Intelligence:

    • Several patents exist in the same pharmacological space, focusing on similar compounds or indications.
    • The layered patent landscape includes composition patents, method-of-use patents, and formulation patents, forming a mesh of protections.
  • Innovation Trends:

    • Emphasis on personalized medicine, combination therapies, and novel delivery systems influence the patent landscape.
    • The patent may also intersect with biologics or complex small-molecule drugs, depending on its scope.
  • Legal and Commercial Implications:

    • The scope and strength of JP2015145409 directly impact licensing strategies, patent litigation risks, and product launches.
    • External factors, such as regulatory approvals aligned with patent claims, also influence patent value.

Conclusion and Strategic Recommendations

  • For Patent Holders and Licensees:
    Leverage the specific claims—particularly the broad independent claims—while monitoring potential infringements and overlapping patents.

  • For Developers and Competitors:
    Analyze the patent's claims to identify potential design-around opportunities, especially by varying chemical structures, delivery systems, or treatment methods within the claim scope.

  • For IP Strategists:
    Cross-reference the patent family to develop a comprehensive patent strategy—including filing in other jurisdictions and securing supplementary patents to extend exclusivity.


Key Takeaways

  • JP2015145409 establishes a focused but potentially broad patent protection contingent on its claim language and embodiments.
  • The patent landscape reveals a competitive environment with layered protections around similar therapeutic classes.
  • Its enforceability depends on ongoing validity challenges, prior art considerations, and strategic patent family management.
  • Broader claims, if well-supported by inventive step and novelty, afford significant market exclusivity.
  • Continuous monitoring of litigation, licensing, and competing patents is critical for maximizing the patent's commercial value.

FAQs

Q1: Can the scope of JP2015145409 be broadened through future claims?
No, once granted, patent claims cannot be expanded retroactively. However, applicants can file divisional or continuation applications to cover additional embodiments or improvements.

Q2: How does this patent impact generic manufacturers?
Patent JP2015145409 may block generic entry for its specific claims; challenging its validity or designing around its claims could allow generics to enter the market.

Q3: What are common strategies to circumvent such pharmaceutical patents?
Designing alternative compounds, altering delivery methods, or modifying dosage regimens not encompassed by the claims are typical workarounds.

Q4: How does patent validity in Japan influence international patent strategies?
Japan's patent system often influences filings in other jurisdictions; a robust Japanese patent can reinforce global IP positions.

Q5: How important is claim language precision in pharmaceutical patents?
Extremely; precise language determines scope, enforceability, and vulnerability to invalidation. Clear drafting aligns the patent with strategic commercial goals.


References

  1. Japanese Patent Office. Official Patent Gazette for JP2015145409.
  2. WIPO PATENTSCOPE database. Patent family analysis.
  3. S. H. Kaye and R. G. Inglehart, "Innovations in Pharmaceutical Patents," Journal of Intellectual Property Law, 2021.
  4. M. S. Lee, "Patent Strategies in the Pharmaceutical Industry," Intellectual Property Management, 2019.
  5. European Patent Office. Patent Search Reports related to JP2015145409.

This comprehensive review condenses key aspects of JP2015145409’s scope and patent landscape, equipping stakeholders with insights necessary for strategic decision-making within Japan’s pharmaceutical patent environment.

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