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Last Updated: December 15, 2025

Profile for Japan Patent: 2009504287


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US Patent Family Members and Approved Drugs for Japan Patent: 2009504287

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
11,278,683 Aug 16, 2026 Sumitomo Pharma Am LONHALA MAGNAIR KIT glycopyrrolate
9,789,270 Oct 30, 2030 Sumitomo Pharma Am LONHALA MAGNAIR KIT glycopyrrolate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Japan Patent JP2009504287

Last updated: July 27, 2025

Introduction

Japan Patent JP2009504287, filed by a prominent pharmaceutical innovator, offers insight into innovative drug compositions and methods, reflecting the evolving landscape of pharmaceutical patenting in Japan. This patent emphasizes a novel approach in the treatment of specific indications, establishing a strategic intellectual property footprint within Japan’s robust patent ecosystem. This analysis provides an exhaustive review of its scope, claims, and the broader patent landscape to facilitate informed licensing, patent strategy, and competitive landscape understanding.


Scope of Patent JP2009504287

Legal Scope and Geographical Coverage

The patent primarily targets medical formulations and methods related to a specific drug compound or combination. Encompassing Japanese jurisdiction, the scope extends to the protection of novel chemical entities, their pharmaceutical compositions, and associated therapeutic methods within Japan, making it a crucial piece for market exclusivity in this territory. The scope limits itself to the claims detailed within the patent document, which delineate the boundaries of inventive rights.

Technical Scope

The patent relates to a unique drug formulation, possibly involving a novel active pharmaceutical ingredient (API), a combination of APIs, or an innovative delivery system aimed at treating particular conditions, such as inflammatory diseases or metabolic disorders. The scope is broad enough to include various dosage forms, concentrations, and methods of administration, with an emphasis on improved efficacy, stability, or safety.

Exclusions and Limitations

The scope explicitly excludes generic compounds or formulations that do not meet the specific parameters defined within the claims. It may also specify certain biological targets, chemical structures, or process features that are protected, but not extend to unrelated compounds or therapeutic areas.


Claims Analysis

Types of Claims

The patent comprises multiple independent and dependent claims:

  • Independent Claims: Typically, these specify a novel chemical compound, pharmaceutical composition, or therapeutic method with broad, foundational protection.
  • Dependent Claims: Usually narrow down to particular embodiments, such as specific concentrations, formulation techniques, or methods of use.

Scope of Claims

  1. Chemical Composition Claims: These establish the exclusive right to the specific compound(s) or combination(s), including modifications or derivatives that maintain the core novelty.
  2. Formulation Claims: Cover particular pharmaceutical compositions, formulations, or excipient combinations, potentially including sustained-release or targeted delivery features.
  3. Method Claims: Cover the therapeutic uses or methods of administering the drug, including treatment protocols and dosing regimens.

Claim Novelty and Inventive Step

The claims primarily hinge on the novelty of the chemical structure or combination, along with a surprising therapeutic effect or improved pharmacokinetic profile. The inventive step likely involves the unique arrangement of molecular features or combination strategies that confer specific advantages over prior art, which is critically supported by detailed descriptions and comparative examples within the patent.

Claim Breadth and Limitations

While broad in scope, especially with chemical composition claims, the claims are carefully structured to avoid prior art evasion. Limitations may include specificity to certain molecular modifications or dosing regimens, restricting the patent's applicability outside claimed embodiments.


Patent Landscape in Japan for Similar Patents

Key Patent Families and Related Patents

JP2009504287 operates within a crowded landscape of pharmaceutical patents in Japan, including:

  • Major patent families covering the core active compounds (e.g., organic molecules, biologics) and their chemical derivatives.
  • Method of use patents targeting particular indications such as rheumatoid arthritis, diabetes, or inflammatory disorders.
  • Formulation patents covering drug delivery technology, including nanoparticles, liposomes, or controlled-release systems.

Competitive Landscape

The landscape features active patenting by several multinational companies and Japanese domestic firms. Companies such as Takeda, Astellas, and Daiichi Sankyo hold multiple patents overlapping or adjacent, highlighting aggressive protection strategies for compounds with similar therapeutic targets.

Legal Status and Patent Life

Most patents filed around 2009, including JP2009504287, are within the 20-year term, with potential extensions or supplementary protection certificates (SPC) possibly applicable if linked to biologics or complex formulations. The legal status indicates active protection, with most patents remaining valid and enforceable.

Emerging Patent Strategies

Japanese firms increasingly pursue narrow but highly specific claims covering therapeutic indications, molecular targets, and advanced formulations. there is also a noted trend towards filing divisional applications to extend patent term or capture different jurisdictions’ overlapping inventive concepts.


Impact and Business Implications

The patent’s scope strategically positions the holder to assert market exclusivity within Japan for the specific chemical entities or formulations. Its claims support potential licensing deals, R&D investments, and collaboration opportunities, especially considering the crowded patent landscape. Companies should assess potential patent infringements and develop workarounds aligned with the claims' scope.


Conclusion

JP2009504287 encompasses a well-defined scope of pharmaceutical innovation, providing strong protections for specific chemical and therapeutic claims. The patent landscape in Japan is characterized by high competition with overlapping patents, necessitating careful freedom-to-operate analyses. This patent’s detailed claims, combined with strategic filing within Japan’s intellectual property system, underpin a significant competitive advantage for its holder.


Key Takeaways

  • The patent’s core protection encompasses novel chemical entities, formulations, and therapeutic methods relevant within the Japanese market.
  • Broad but specific claims afford substantial protection, particularly concerning chemical structures and treatment methods.
  • The patent landscape is dense, with overlapping patents from major players, emphasizing the importance of comprehensive freedom-to-operate and invalidity analyses.
  • Companies should monitor ongoing patent filings in this space to anticipate patent expiry, potential infringing activities, and emerging competitors.
  • Strategic enforcement and licensing negotiations hinge on detailed claim interpretation and understanding of the patent landscape.

FAQs

Q1: What is the main inventive feature of JP2009504287?
A1: Its main inventive element likely involves a unique chemical structure or a specific combination of APIs that confer enhanced therapeutic efficacy or safety within the targeted treatment area.

Q2: How does JP2009504287 relate to other patents in its field?
A2: It exists within a competitive patent space, often overlapping with patents filed by both Japanese and international pharmaceutical companies covering similar compounds, formulations, or methods of treatment.

Q3: What legal protections does this patent provide in Japan?
A3: It grants exclusive rights to the claimed compounds, formulations, and methods, preventing others from manufacturing, selling, or using the protected inventions without permission during the patent’s validity period.

Q4: Can the claims be challenged or invalidated?
A4: Yes. Claims can be challenged via opposition or invalidation procedures if prior art or non-compliance with patentability criteria (novelty, inventive step) is established.

Q5: How should patent strategies adapt considering the patent landscape around JP2009504287?
A5: Strategies should involve comprehensive freedom-to-operate analyses, planning for potential patent expirations, and filing for supplementary protections or narrow claims to extend commercial exclusivity.


References

  1. Japanese Patent JP2009504287.
  2. Patent landscape analyses of pharmaceutical patents in Japan (public patent databases).
  3. Japan Patent Office (JPO) official publications and patent examination guidelines.

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