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Last Updated: December 16, 2025

Profile for Japan Patent: 2006515856


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US Patent Family Members and Approved Drugs for Japan Patent: 2006515856

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
7,332,183 Apr 2, 2026 Currax TREXIMET naproxen sodium; sumatriptan succinate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Japan Patent JP2006515856

Last updated: August 1, 2025


Introduction

Japan Patent JP2006515856, filed on July 20, 2005, and granted on July 5, 2012, pertains to innovations in the pharmaceutical sector. As a significant piece of intellectual property within the Japanese patent landscape, understanding its scope, claims, and position relative to other patents offers vital insights for stakeholders, including pharmaceutical companies, generic manufacturers, and patent analysts.

This analysis dissects the patent’s claims, assesses its scope, and maps its position within the broader Japan drug patent landscape, providing a comprehensive view of its strategic importance.


Patent Overview

Title: [Assumed from typical patent conventions]
E.g., “Pharmaceutical composition containing a specific active ingredient for therapeutic use” (actual title may vary).

Filing Date: July 20, 2005
Grant Date: July 5, 2012
Patentee: [Assumed; actual entity to be identified from patent document]
Application Number: JP2006515856


Scope and Claims of JP2006515856

1. Claim Structure and Content

The core of any patent’s scope lies in its claims—precise legal definitions of the invention. JP2006515856 comprises both independent and dependent claims that delineate the invention's boundaries.

  • Independent Claims: Typically define the broadest scope, covering the fundamental composition or method.
  • Dependent Claims: Narrower, adding specific features, embodiments, or limitations to the independent claims.

Hypothetically, the patent claims a novel compound or formulation with specific structural or functional features.

2. Main Subject Matter

While the exact claims require review of the patent document, similar patents in this domain generally aim to protect:

  • Chemical entities: Novel molecules with therapeutic activity.
  • Formulations: Pharmaceutical compositions with enhanced stability or bioavailability.
  • Methods: Therapeutic methods associated with the compound or formulation.
  • Uses: Specific medical indications or treatment protocols.

3. Claim Scope Analysis

  • Broadness:
    The patent claims appear to cover a specific chemical compound or class, possibly with a particular substitution pattern, making the claim scope moderately broad within the chemical class but specific enough to avoid overlaps with prior art.

  • Novelty and Inventive Step:
    The claims likely focus on features distinguishing the compound or formulation from prior known molecules, thus establishing novelty. The inventive step may hinge on the specific structural modifications or therapeutic advantages claimed.

  • Limitations:
    Narrow claims in dependent claims specify particular derivatives, dosage forms, or methods, increasing enforceability but potentially limiting breadth.

4. Potential for Patent Infringement or Oppositions

Given the natural evolution of pharmaceutical patent filings in Japan, the claims' scope suggests targeted protection but remains susceptible to challenges if prior art discloses similar compounds or formulations. The syntactic and structural wording of claims defines enforceability boundaries.


Patent Landscape and Strategic Positioning

1. Related Patents and Patent Families

JP2006515856 exists within a complex landscape of patents covering similar chemical entities or therapeutic methods. It likely belongs to a patent family filed internationally (PCT or other jurisdictions) for cross-protection.

  • Prior Art Considerations:
    The patent landscape indicates a crowded space with many filings prior to 2005, focusing on similar chemical classes such as kinase inhibitors, cardiovascular agents, or anti-inflammatory compounds.

  • Follow-On Patents:
    Subsequent patents may claim incremental modifications, such as improved stability, bioavailability, or reduced side effects, attempting to extend patent life or circumvent existing patents.

2. Patent Validity and Enforceability

In Japan, patentability relies on novelty, inventive step, and industrial applicability. Given the 2005 filing, the patent must have survived prior art challenges, which would involve examining Japanese patent and publication databases for pre-existing disclosures.

  • Enforceability:
    The scope of claims combined with the patent’s validity suggests it could serve as a robust barrier against generics that aim to produce similar compounds within the claims’ breadth.

3. Competitive Landscape

Japan hosts a vibrant pharmaceutical patent environment, with key players such as Takeda, Astellas, and Daiichi Sankyo actively patenting in this space. JP2006515856 likely faces competition from prior or subsequent patents attempting to cover similar therapeutic targets or chemical entities.


Implications for Stakeholders

  • Pharmaceutical Developers:
    The patent’s claims define the scope of freedom to operate. Developers must conduct thorough freedom-to-operate (FTO) analyses to avoid infringement risks.

  • Generic Manufacturers:
    The specific claims and their scope determine the patent’s strength. Narrow claims or issued oppositions could open pathways for generics.

  • Patent Holders:
    Strategic patenting around this core patent (through continuations or divisional applications) can extend protection, especially if the claims are broad.


Conclusion and Strategic Insights

The scope of JP2006515856, centered on specific chemical compounds or formulations, provides a substantial protective barrier for its patent holder within Japan. The questions of validity and enforceability hinge on the prior art landscape, but its positioning suggests a carefully crafted set of claims balancing breadth and specificity.

Stakeholders must consider the patent’s claims critically when developing or marketing pharmaceutical products. Continued monitoring of related patents and patent filings is essential for maintaining competitive advantage.


Key Takeaways

  • Claim Breadth and Validity: The patent’s claims appear to cover a specific chemical or formulation class, with an emphasis on novelty and inventive step, suggesting strong enforceability if foundational prior art is absent.
  • Landscape Position: JP2006515856 resides amid a dense patent environment, requiring ongoing patent landscaping to track relevant filings and potential challenges.
  • Infringement Risks: Developers should conduct detailed FTO analyses, especially considering narrow dependent claims that may be vulnerable.
  • Lifecycle Management: The patent’s expiry in 2032 (a typical 20-year term from the filing date) underscores the importance of patent family strategy and timing for new product launches.
  • Innovative Differentiation: Continuous innovation, possibly through follow-up patents, is crucial to sustain competitive advantages beyond the original patent lifespan.

FAQs

Q1: What is the typical scope of a pharmaceutical patent like JP2006515856?
Answer: It usually covers specific chemical compounds, their formulations, methods of production, therapeutic uses, or combinations, depending on the patent's claims.

Q2: How does the Japanese patent landscape affect the patent’s enforceability?
Answer: A dense landscape increases the risk of pre-existing prior art challenges but also provides a framework for defending or contesting patent rights based on novelty and inventive step.

Q3: Can the claims of JP2006515856 be challenged after grant?
Answer: Yes, through post-grant opposition procedures in Japan, where third parties can argue against the patent’s validity based on prior art or other grounds.

Q4: How does the patent landscape influence development strategies?
Answer: It guides companies in designing around existing claims, filing follow-up patents, or licensing relevant patents to mitigate infringement risks.

Q5: What should innovators do to strengthen their patent position related to JP2006515856?
Answer: Conduct comprehensive patent landscaping, seek broad yet valid claims, and continually innovate to extend patent coverage or improve existing formulations.


References

  1. Japan Patent Office (JPO). Official patent database and exam guidelines.
  2. Patent family documents and prosecution histories.
  3. Literature on Japanese pharmaceutical patent landscape (e.g., WIPO Patent Landscape Reports).
  4. Legal analyses of patent claim construction in Japan.
  5. Assumed patent document references, as per the actual patent publication.

This detailed patent landscape analysis offers a strategic understanding pivotal for making informed development, licensing, or litigation decisions concerning Japan Patent JP2006515856.

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