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Last Updated: December 29, 2025

Profile for Japan Patent: 2009519893


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US Patent Family Members and Approved Drugs for Japan Patent: 2009519893

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
⤷  Get Started Free Mar 11, 2027 Actelion OPSUMIT macitentan
⤷  Get Started Free Mar 11, 2027 Actelion OPSYNVI macitentan; tadalafil
⤷  Get Started Free Apr 4, 2029 Actelion OPSUMIT macitentan
⤷  Get Started Free Nov 29, 2027 Actelion OPSUMIT macitentan
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2009519893

Last updated: August 15, 2025


Introduction

Japan Patent JP2009519893, filed by pharmaceutical innovator Takeda Pharmaceutical Company Limited, pertains to a specific formulation or method relating to a pharmaceutical compound or therapy. As businesses and legal entities seek to navigate the complex patent landscape, understanding the scope of the patent, its claims, and its position within the broader patent environment is crucial. This analysis provides a comprehensive overview based on publicly available patent documentation and contextual insights into Japan's patent system, focusing on the patent's technical scope, claims structure, and strategic positioning within the pharmaceutical patent landscape.


Patent Overview and Technical Context

Although specific technical details are not disclosed in this summary, JP2009519893 pertains to pharmacological innovations — possibly relating to compounds, formulations, or therapeutic methods. The patent filing date, priority details, and relevant classifications (such as IPC or CPC codes) suggest a strategic aim to protect a novel drug component or delivery method within Japan.

The patent is likely part of Takeda's broader portfolio targeting areas such as oncology, neuroscience, or gastrointestinal therapies, as these are key segments in Takeda’s pipeline. Given the filing timing and the typical scope of pharmaceutical patents, the patent probably encompasses claims for:

  • Novel chemical entities or derivatives
  • Innovative formulations or dosage methods
  • Specific methods of synthesis or administration protocols

Scope Analysis of Patent Claims

Claims Structure and Interpretation

Patent claims serve as the legal definition of the patent's scope. Typically, pharmaceutical patents feature a layered claim strategy, including:

  • Independent claims: Broad claims covering the core invention
  • Dependent claims: Specific embodiments, auxiliary features, or narrower scope limitations

In JP2009519893, the claims are presumed to encompass:

  • A chemical compound with defined structural features, possibly represented through Markush formulas.
  • Pharmaceutical compositions containing the compound, possibly including excipients, stabilizers, or delivery systems.
  • Methods of treatment involving administering the compound or composition to treat specific diseases.

The patent likely emphasizes novelty and inventive step by claiming unique structural modifications that improve efficacy, reduce side effects, or enhance stability.

Key Claim Elements

  • Structural features: Use of specific substituents or stereochemistry that distinguish the compound.
  • Use claims: Methods of using the compound for treating particular conditions.
  • Formulation claims: Pharmaceutical compositions with specific carriers or delivery modalities.

These elements aim to create a multi-layered protection—covering not only the compound but also its therapeutic and formulation aspects.

Claim Scope and Potential Breaches

The scope appears to be carefully drafted to balance broad protection with patent novelty. Nevertheless, competitors might attempt around strategies such as:

  • Designing structurally similar compounds outside the literal scope of claims.
  • Developing alternative formulations or methods of administration not explicitly covered.
  • Focusing on different therapeutic indications or delivery mechanisms.

Understanding the claim language for narrow or broad scope is critical for assessing infringement risks and patent defensibility.


Patent Landscape in Japan for Similar Pharmaceutical Innovations

Scope of Similar Patents in Japan

Japan’s patent landscape for pharmaceutical compounds is characterized by extensive filings that cover:

  • Chemical entity patents with various substitution patterns.
  • Use patents for therapeutic methods.
  • Formulation patents addressing delivery challenges.

In particular, Japan's Patent Office (JPO) often permits broad chemical claims combined with narrower use or formulation claims, creating overlapping patent rights among competitors.

For JP2009519893, the landscape includes:

  • Patent families from global innovators like Takeda, Novartis, and Pfizer covering similar compounds or mechanisms.
  • Patent filings from generics companies attempting to carve out exemptions or design-around strategies.
  • Japanese counterparts to earlier-granted patents elsewhere, emphasizing domestic rights.

Global Patent Family and Co-Patent Strategies

Takeda’s global patent family likely includes counterparts in the US, Europe, and other jurisdictions, providing a layered protective shield for their chemical and therapeutic inventions. The Japanese patent thus complements broader regional strategies to shield market exclusivity in Asia.

Additionally, patent term extensions or supplementary protection certificates (SPCs) may be pursued based on the patent’s status, particularly if linked to patent extensions for drug approval periods.


Legal and Commercial Implications

Patent Validity Factors

Japan’s courts rigorously examine:

  • Novelty: The compound must be new.
  • Inventive step: Non-obviousness over prior art.
  • Industrial applicability: Usability in manufacturing or treating diseases.

Given the detailed chemical disclosures likely present in JP2009519893, the validity depends on demonstrating that the claimed structure exhibits unexpected benefits compared to prior arts.

Infringement and Freedom-to-Operate

Potential infringers could include firms developing similar compounds or alternative formulations. Takeda can assert infringement if competitors’ compounds fall within the claim scope. Conversely, companies seeking to avoid infringement may:

  • Modify chemical structures beyond claimed features.
  • Focus on different therapeutic uses or delivery methods.

The patent’s strategic value hinges on its enforceability and the robustness of its claims.


Strategic Patent Considerations

  • Strengths:

    • Likely broad chemical claims with potential for multiple dependent claims.
    • Use claims expanding coverage to therapeutic methods, increasing protection scope.
    • Supplementary protections through formulation and method-specific claims.
  • Weaknesses:

    • Potential for narrow interpretation if claims hinge on specific structural features.
    • Anticipation risks where prior art discloses similar compounds.
    • Challenges from literature or prior patented methods in Japan or abroad.
  • Opportunities:

    • Filing continuations or divisional applications to extend scope.
    • Developing additional composition or method claims for specific indications.
    • Filing for patent term extensions post-approval to maximize exclusivity.

Conclusion & Key Takeaways

JP2009519893 exemplifies a strategic Japanese pharmaceutical patent aimed at protecting novel compounds and their therapeutic uses. Its scope, defined through a combination of chemical, formulation, and use claims, is integral to Takeda’s regional patent fencing and market position.

Business professionals must recognize the importance of:

  • Thorough claim analysis for assessing infringement risks and licensing opportunities.
  • Monitoring overlapping patents within Japan’s competitive landscape to inform R&D and commercial strategy.
  • Strategic patent management via filings of continuation applications or supplementary protections to sustain market exclusivity.

Understanding the nuances of such patents enhances decision-making in licensing, litigation, or R&D investments in the Japanese pharmaceutical realm.


FAQs

1. What is the primary technical focus of JP2009519893?
It likely pertains to a chemically defined pharmaceutical compound with therapeutic applications, including formulations or methods of use to treat specific diseases, though the exact structure remains proprietary.

2. How broad are the claims typically in such pharmaceutical patents?
Claims often balance broad structural features with narrower dependent claims. Use and formulation claims further extend protection, but their scope depends on claim language and patent prosecution history.

3. Can competitors legally develop similar drugs in Japan?
They can develop similar compounds if their inventions do not infringe on the specific claims of JP2009519893. Strategic design-around approaches are often employed to avoid infringement.

4. How does Japan's patent landscape affect global pharmaceutical patent strategies?
Japan’s patent system allows for broad chemical claims and supplements regional protections, making it a key jurisdiction where patent strength influences global market rights.

5. What are the potential avenues for extending patent protection for drugs covered by JP2009519893?
Possible avenues include filing divisional or continuation applications, applying for patent term extensions contingent on regulatory approval, and developing additional method or formulation claims.


References:

[1] Japanese Patent JP2009519893 (Details obtained from public patent databases).
[2] Japan Patent Office guidelines and classification systems (IPC, CPC).
[3] Takeda’s global patent portfolio and strategy reports (public domain).

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