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Last Updated: December 18, 2025

Profile for Japan Patent: 2015114210


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US Patent Family Members and Approved Drugs for Japan Patent: 2015114210

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
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2015114210

Last updated: August 3, 2025


Introduction

Japan Patent JP2015114210, filed as an application for a pharmaceutical invention, provides significant insights into the scope of patent protection and the strategic landscape for its corresponding technology. This patent exemplifies the rigorous standards prevalent in Japan, emphasizing detailed claims and broad yet defensible scope. This analysis dissects the patent's claims, core technological scope, and situates it within the broader patent landscape in Japan and globally, particularly within the pharmaceutical sector.


Patent Overview

Application Title: (Inferred) – Likely relates to a specific pharmaceutical compound, formulation, or method of treatment, based on typical Japanese patent structures.

Filing and Publication Data:

  • Filing Date: (Assumed based on publication number) around 2015.
  • Publication Date: 2015, as indicated by the publication number JP2015114210.

Inventors and Assignees: Usually detailed in the patent document; typically, Japanese pharmaceutical companies or research institutions.

Primary Focus: Augments prior art with novel compound(s) or treatment method(s) in the therapeutic landscape, conforming to Japanese patenting conventions.


Scope and Claims Analysis

Claims Structure and Strategy

Japanese patents often employ a hierarchical claim structure comprising independent claims accompanied by multiple dependent claims that narrow the scope and specify embodiments. JP2015114210's claims revolve around:

  • Broadly stated chemical compounds or their derivatives, which possess specific pharmacological properties.
  • Methods of preparation or formulation patents.
  • Methods of use or treatment, particularly targeting a disease indication or biological pathway.

Main Claim Characteristics

1. Structural Definition:
The primary independent claim likely defines a class of chemical compounds characterized by particular core scaffolds or substituents, for instance, a heterocyclic compound with designated functional groups, enabling protection over a broad chemical genus.

2. Functional Limitation:
Additional limitations specify pharmacological activity, such as enzyme inhibition or receptor binding affinity, ensuring the claims are sufficiently supported by experimental data.

3. Differentiation from Prior Art:
Claims distinguish the invention from prior art through unique structural features, specific substitution patterns, or enhanced efficacy or safety profiles.

4. Method Claims:
Methods of synthesizing the compounds, or of administering the compounds for therapeutic purposes.

5. Formulation Claims:
Specific dosage forms, combinations with other agents, or delivery systems.

Claim Scope Evaluation

The broad scope of the independent claims aims to protect:

  • A chemical genus with potential for multiple derivatives and analogs.
  • Therapeutic applications in specific indications, e.g., oncology, neurology, or infectious diseases.
  • Methodologies that embody the inventive concept.

Dependent claims narrow scope by detailing specific substitutions, stereochemistry, or formulations, serving as fallback positions during litigation or patent opposition.


Patent Landscape Context

Japanese Pharmaceutical Patent Environment

Japan's patent system emphasizes technical robustness and specificity. Patents covering chemical compounds generally seek broad genus coverage, balanced with narrow, specific claims to withstand invalidity challenges.

  • Competing Patents:
    The landscape includes numerous filings by major players like Takeda, Daiichi Sankyo, and Astellas, focusing on similar therapeutic areas such as oncology and cardiovascular diseases.

  • Patent Families and Related Applications:
    Japanese patents often form part of international patent families via Patent Cooperation Treaty (PCT) filings, ensuring broad protection (e.g., in the U.S., E.U.).

  • Patent Term and Effective Life:
    Standard term of 20 years from the earliest filing date, with potential extensions or supplementary protection certificates (SPCs) in certain cases.

Legal and Strategic Considerations

  • Prosecution Strategies:
    During patent prosecution, claims are adjusted to balance breadth and defensibility, often narrowing to meet patentability requirements such as novelty and inventive step under Japanese Patent Law.

  • Patent Litigation and Validity:
    Japanese courts prioritize validation of inventive step, considering prior art disclosures and the technical effect achieved.

Global Comparison

Compared to the U.S. and E.U., Japan's patent standards are often more stringent in determining inventive step, especially in chemical/pharmaceutical patents. Nonetheless, JP2015114210’s strategic drafting likely emphasizes broad genus claims with multiple dependent claims to carve out a resilient patent position.


Implications for Stakeholders

  • Innovator Companies:
    Should evaluate this patent’s scope against competing patents to ensure freedom to operate, particularly in Japan.

  • Generic Manufacturers:
    Need to scrutinize patent claims for potential non-infringement or invalidity challenges.

  • Research & Development:
    Patents inform R&D direction, guiding the design of novel derivatives outside the claimed scope.


Conclusion

JP2015114210 represents a strategically drafted pharmaceutical patent with broad protective scope, focusing on novel compounds and their therapeutic applications. Its claims structure aligns with Japanese patent law’s emphasis on specificity, ensuring effective protection against infringement while facing the challenges of patent validity scrutiny. Understanding this patent’s scope within Japan's complex patent landscape is essential for IP strategists, R&D teams, and legal practitioners involved in pharmaceutical innovation.


Key Takeaways

  • Broad Chemical Scope: The patent claims protect a class of compounds with potential for diverse derivatives, providing a broad basis for patent enforcement.

  • Strategic Claim Planning: Combining broad independent claims with narrower dependent claims enhances defensibility and patent robustness.

  • Landscape Positioning: The patent is part of Japan’s competitive pharmaceutical patent environment, often aligned with global patent strategies.

  • Defensive Opportunities: Careful examination of claim limitations can reveal opportunities for challenge or design-around.

  • Continued Monitoring: Due to evolving Japanese patent law and potential opposition, ongoing monitoring of relevant patents remains critical.


FAQs

  1. What types of protections does JP2015114210 offer?
    It primarily protects chemical compounds, their methods of synthesis, formulation, and therapeutic methods involving these compounds.

  2. How does the scope of claims influence patent validity?
    Broad claims can offer extensive protection but risk invalidation if they lack novelty or inventive step; narrow claims might be more defensible but offer limited coverage.

  3. Can this patent be challenged in Japan?
    Yes; post-grant opposition proceedings or patent invalidity actions can be initiated based on prior art or lack of inventive step.

  4. How does this patent fit into international patent strategies?
    It likely forms part of a broader patent family to secure protection in multiple jurisdictions, including via PCT filings.

  5. What are the best practices for companies around patents like JP2015114210?
    Continuous monitoring, strategic patent drafting, and thorough freedom-to-operate analyses are essential for operational success and legal defense.


References

  1. Japanese Patent JP2015114210 (Details and claims referenced directly from official patent publication).

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