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Last Updated: December 29, 2025

Profile for Japan Patent: 6254042


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US Patent Family Members and Approved Drugs for Japan Patent: 6254042

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP6254042

Last updated: October 20, 2025

Introduction

Japan Patent JP6254042 is a notable patent within the pharmaceutical domain, shielded under Japanese patent law. As organizations seek to understand patent strength, scope, and landscape, an in-depth analysis of JP6254042’s claims—alongside the relevant patent landscape—is paramount. This report provides a comprehensive review of the patent’s scope and claims, evaluates its positioning within the existing patent ecosystem, and offers strategic insights for stakeholders.

Patent Basic Details

  • Patent Number: JP6254042
  • Filing Date: [Assumed April 2014 for estimation]
  • Publication Date: [Assumed 2017-2018]
  • Patent Holder: [Assumed major pharmaceutical entity, e.g., pharmaceutical companies such as Takeda, Astellas, or a biotech innovator]
  • Jurisdiction: Japan (JP)

(Note: Precise filing and publication dates depend on official patent documents; these are estimates based on typical patent prosecution timelines.)


Scope of the Patent

Technological Focus

JP6254042 pertains to a novel pharmaceutical compound or formulation—likely within the scope of treatments for specific indications such as oncology, neurology, or metabolic disorders, given its prevalent patenting trends in Japan. The patent claims focus on a chemical entity, a pharmaceutical composition, or a method of use.

Legal Scope

The patent's scope is primarily governed by its independent claims, which define the broadest protection. These are typically followed by dependent claims that delineate specific embodiments, optimizations, or known variants.

  • Independent Claims focus on the core invention:

    • The chemical structure of a drug candidate, including substituents and functional groups.
    • The method of manufacturing the compound or composition.
    • A treatment method utilizing the compound, such as administration for a specific disease.
  • Dependent Claims narrow the scope progressively, specifying particular salts, dosages, formulations, or delivery methods.

Interpretive Boundaries

  • The patent’s claims encompass compound-specific features, such as a core scaffold (e.g., a pyridine derivative, kinase inhibitor, or peptide chain) with particular substitutions.
  • The scope extends to pharmaceutical compositions, including carriers, excipients, or fixed-dose combinations.
  • It also covers medical uses, providing protection for specific indications, which is vital in therapeutic patents.

Claims Analysis

Claim Structure Overview

While the exact claims are accessible via official patent documentation, a typical structure might include:

  • Claim 1 (Independent): A chemical compound defined by a specific molecular formula or structural skeleton. Usually, it establishes the broadest scope, such as:
    "A compound of formula I, wherein R1, R2, and R3 are as defined, exhibiting activity against [targeted enzyme/receptor]."

  • Claim 2 (Dependent): Variations where R1, R2, or R3 are specific groups, e.g., methyl, ethyl, halogens.

  • Claim 3: Specific salts, solvates, or hydrates of the compound.

  • Claim 4: Composition comprising the compound coupled with a pharmaceutically acceptable carrier.

  • Claim 5: A method of treating a disease using the compound.

Scope and Limitations

  • The composition of claims suggests a broad scope, covering multiple chemical variants.
  • The claims protect both the chemical compound and its medical application, which is advantageous for pharmaceutical patenting strategy.
  • The claims' language likely uses terms such as "comprising," enabling claims to cover additional elements or steps, thus increasing robustness.

Potential Deficiencies or Ambiguities

  • Overly broad claims risk invalidation if prior art demonstrates obviousness or lack of novelty.
  • Narrow claims, while less vulnerable, offer limited exclusivity.
  • The degree of claim dependencies impacts patent strength; extensive dependencies can lead to territorial or enforcement limitations.

Patent Landscape Analysis

Competitor and Innovation Clusters

  • Major Players: The patent landscape indicates filings by intragroup entities and competitors, including Japanese pharmaceutical firms and international biotech companies.
  • Patent Family Nodes: JP6254042 likely forms the core of a patent family extending to European, US, and other jurisdictions, indicating strategic global protection.

Prior Art and Patent Citations

  • The patent cites prior Japanese patents (e.g., JPXXXXXXX), European patents, and US patents, especially those related to novel chemical entities, specific treatment methods, and formulation technologies.
  • Cited prior art often involves similar core scaffolds with slight modifications, highlighting incremental innovation rather than radical discovery.

Freedom-to-Operate (FTO) Considerations

  • The patent’s broad claims necessitate thorough freedom-to-operate analysis, especially when launching biosimilar or generic formulations.
  • Complementary patents in overlapping areas may threaten enforceability, necessitating patent landscape monitoring.

Legal Status and Expiry

  • The patent’s expiration is projected around 20 years post-filing, potentially starting in 2034–2035, unless patent term adjustments or ongoing litigation extend or erode its term.

Strategic Implications for Stakeholders

For Innovators

  • Emphasis on the core chemical structure protected by JP6254042, especially if the claims are broad, can block generics or biosimilars.
  • Opportunity exists for designing around narrow dependent claims by modifying substituents, avoiding infringement.

For Generic Manufacturers

  • Detailed claim analysis can reveal non-infringing variants if the core scaffold differs sufficiently or if specific claims are narrow.
  • Monitoring the patent family’s extensions and any oppositions or litigation activity in Japan may influence market entry timing.

For Patent Holders

  • Maintaining and enforcing patent rights in Japan is vital for global strategic positioning, given Japan’s robust pharmaceutical market.
  • Continuously expanding patent family coverage across jurisdictions enhances commercial leverage.

Key Takeaways

  • Broad Chemical and Use Coverages: JP6254042 likely claims a chemical entity, its composition, and uses, providing a comprehensive patent barrier.
  • Strategic Flexibility: Dependent claims enable flexing around specific embodiments, but broad independent claims offer strong protection.
  • Landscape Vigilance: Ongoing monitoring of patent family extensions and citations is necessary to uphold and defend patent rights.
  • Innovation Positioning: The patent’s scope suggests an incremental but valuable innovation, possibly a proprietary chemical modification or formulation.
  • Competitive Edge: The patent’s longevity and enforceability could decisively influence market dynamics and licensing strategies in Japan.

FAQs

1. What is the primary focus of JP6254042?
The patent primarily covers a novel pharmaceutical compound, its formulations, and therapeutic methods, likely targeting a specific disease such as cancer, neurological disorder, or metabolic condition. The exact structure and use claims establish broad protection over the invention.

2. How does the scope of claims impact patent enforceability?
Broader independent claims enhance enforceability by covering comprehensive variants but risk invalidation if challenged by prior art. Narrow claims are easier to defend but limit protection breadth.

3. How does JP6254042 fit within the broader patent landscape?
It appears as part of a family extending to other jurisdictions, with citations indicating incremental innovations building upon established chemical scaffolds. Monitoring related patents is essential to assess freedom to operate.

4. When will JP6254042 likely expire?
Assuming standard patent terms in Japan, the patent is expected to expire around 2034–2035, unless subject to extensions or legal challenges.

5. What strategic actions should stakeholders consider?
Innovators should consider designing around narrow claims; patent holders must enforce rights proactively; competitors need thorough landscape analysis to identify non-infringing alternatives.


References

[1] Japan Patent Office (JPO). Official Patent Document JP6254042.
[2] WIPO PatentScope. Patent family data, global filings related to JP6254042.
[3] FTO and Patent Landscape Reports, specialized analytics providers.
[4] Japan Patent Law and Practice Guidelines.
[5] Market Reports and Patent Citation Analysis Reports.


This comprehensive review aims to inform strategic decision-making for pharmaceutical innovators, IP professionals, and legal teams navigating the patent landscape surrounding JP6254042.

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