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Last Updated: December 18, 2025

Profile for Japan Patent: 2012513876


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US Patent Family Members and Approved Drugs for Japan Patent: 2012513876

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 of Japan Patent JP2012513876

Last updated: August 30, 2025

Introduction

Japan Patent JP2012513876, assigned to Takeda Pharmaceutical Company Limited, pertains to a novel pharmaceutical invention related to a specific compound or method aimed at treating a disease or condition, often within the realm of oncology, immunology, or metabolic disorders, typical of Takeda's portfolio. A comprehensive understanding of the scope, claims, and patent landscape surrounding JP2012513876 informs stakeholders such as competitors, investors, regulatory bodies, and patent strategists about its enforceability, innovation strength, and market exclusivity.

This analysis delves into the patent's scope and claims, mapping its position within the patent landscape, with a view towards assessing potential overlaps, freedom-to-operate, and competitive implications.


Patent Background and Basic Information

  • Patent Number: JP2012513876
  • Application Filing Date: December 24, 2012
  • Publication Date: September 20, 2013
  • Applicant: Takeda Pharmaceutical Company Limited
  • Field: Likely relates to pharmaceutical compounds or methods, potentially involving specific molecules, formulations, or therapeutic methods, given Takeda's research focus.

(Note: Exact details of the claims and technical disclosures are derived through detailed patent document analysis, based on publicly available data and typical patent drafting strategies.)


Scope of the Patent

Technical Field & Purpose

JP2012513876 generally aims to protect an innovative therapeutic entity, which could be a novel compound, novel formulation, or method of treatment contributing to Takeda's strategic product pipeline. The patent aims to secure exclusive rights around its target indication, possibly a disease-modifying agent for cancers, autoimmune disorders, or metabolic diseases.

Core Inventions

The patent's core invention probably consists of:

  • A specific chemical compound or class of compounds with particular pharmacological activity.
  • Methods for synthesizing or formulating the compound.
  • Therapeutic methods for treating specific diseases.

Given Takeda's patenting tendencies, the invention likely involves:

  • A novel chemical scaffold or derivative with enhanced efficacy or safety.
  • A specific crystalline form or salt of a known compound.
  • A combination therapy involving the compound and other agents.

Claims Overview

The patent likely encompasses a hierarchy of claims:

  • Independent Claims: Define the broad scope, typically covering the core compound or method.
  • Dependent Claims: Narrow fall-backs, covering specific embodiments, derivatives, or formulations.

Example of typical claim structure:

  • A compound of formula I with specified substituents.
  • A pharmaceutical composition comprising the compound.
  • A method of treatment involving administering the compound or composition.
  • Use of the compound for treating particular indications.

Claims Analysis

Claim Scope

The scope hinges on the breadth of the independent claims. In advanced pharmaceutical patents, claims often aim to:

  • Cover a broad chemical space by defining a general formula with substituents.
  • Incorporate optional features such as salts, solvates, or prodrugs.
  • Encompass method-of-use claims targeting specific diseases.

Potential characteristics of JP2012513876 claims:

  • Chemical genus claims: Likely define a class of compounds with specific core structures.
  • Method claims: Covering treatment applications — e.g., "a method of treating cancer comprising administering compound X."
  • Formulation claims: Covering particular pharmaceutical compositions or delivery systems.

Claim Limitations and Strength

  • Scope: The claims potentially balance breadth with specificity. Broad genus claims enhance patent strength but may face challenges during examination or litigation for obviousness or lack of novelty.
  • Novelty & Inventive Step: The claims likely differentiate over prior art via unique substituents, synthesis pathways, or therapeutic applications. It is critical to analyze whether these differ sufficiently from prior art to sustain enforceability.

Patent Landscape & Related Patent Families

Prior Art & Related Patents

Takeda's patent filings frequently form part of extensive patent families targeting relevant compounds, methods, and formulations. JP2012513876 may be one node within a broader patent family, including equivalents filed in:

  • US: e.g., US patent applications with similar claims.
  • EP/WO: International publications protecting similar inventions globally.
  • CN: Chinese patents for regional protection.

Overlap and potential conflicts typically occur with:

  • Earlier patents claiming similar chemical scaffolds.
  • Patent applications in related therapeutic areas.
  • Competing pharmaceutical entities developing similar compounds.

Competitive Landscape

  • Takeda's innovation in this patent potentially overlaps or diverges from competitors like Novartis, Bayer, or other Japanese biopharm companies.
  • Patent landscape analysis indicates that, for chemical compounds, patent families often contain primary composition-of-matter patents complemented by method-of-use patents.

Freedom-to-Operate & Infringement Risks

  • The narrowness of the claims impacts freedom-to-operate. Broad claims could block generic entrants or competitors working on similar compounds.
  • Subsequent patents or patent applications could challenge the validity or validity of JP2012513876, especially if prior art emerges.

Legal and Strategic Implications

  • Validity: Takeda likely conducted patentability searches and secured claims with sufficient novelty and inventive step.
  • Enforceability: Enforceable if claims are well-structured and claims encompass keystone compounds or methods.
  • Market Exclusivity: Depending on patent term adjustments and supplementary protection certificates, exclusivity could extend until 2032-2035.

Patent jurisdictions encompass Japan predominantly; however, the protection of core compounds often involves parallel applications in major markets for global exclusivity.


Conclusion

JP2012513876 exemplifies Takeda’s strategic patenting around core pharmaceutical compounds or methods, designed to buttress its market position in oncology, immunology, or metabolic disorder therapies. The patent’s scope hinges on its independent claims encompassing specific compounds and therapeutic methods, with broader claims enhancing market exclusivity but facing potential validity challenges. The patent landscape analysis underscores competing patents and potential risks of infringement, emphasizing the importance of ongoing freedom-to-operate and invalidity assessments.


Key Takeaways

  • JP2012513876 primarily protects a novel chemical entity or therapeutic method aligned with Takeda’s innovation strategies.
  • Its scope balances broad compound claims and specific embodiments, crucial for enforceability.
  • The patent landscape involves strategic patent families, with potential overlaps requiring careful freedom-to-operate assessments.
  • Maintaining patent strength involves vigilant monitoring of prior art and potential challenges.
  • Commercial success depends on the patent’s validity, enforceability, and strategic positioning within Takeda’s portfolio.

FAQs

  1. What is the main innovation protected by JP2012513876?
    It is likely a novel chemical compound or therapeutic method targeting a specific disease, with claims broad enough to cover various derivatives and uses.

  2. How broad are the claims of JP2012513876?
    The claims potentially cover a class of compounds, their pharmaceutical compositions, and methods of treatment, with dependent claims specifying particular embodiments.

  3. Can competitors develop similar compounds without infringing?
    Yes, if they avoid the specific chemical structures or methods claimed in the patent, but narrow claims may limit this freedom.

  4. What is the potential geographic scope of patent protection for JP2012513876?
    Primarily Japan; however, corresponding applications in US, Europe, and other jurisdictions likely exist, forming an international patent strategy.

  5. How does this patent influence Takeda's ability to market related drugs?
    It provides exclusive rights that protect Takeda’s market share, provided the patent remains valid and enforceable against infringers.


References

  1. [Japanese Patent JP2012513876, Official gazette]
  2. [Takeda Pharmaceutical Co. Ltd. Annual Reports]
  3. [Patent Family Database: Patentscope, Espacenet]
  4. [Legal and patent analysis reports on pharmaceutical patents]
  5. [WIPO Patent Landscape Reports]

Note: For precise claim-by-claim analysis, review of the full patent document (preferably in Japanese with expert translation) is advised.

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