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Last Updated: December 18, 2025

Profile for Japan Patent: 2009510171


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US Patent Family Members and Approved Drugs for Japan Patent: 2009510171

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
7,465,800 Apr 27, 2027 Bristol Myers Squibb REVLIMID lenalidomide
8,198,262 Dec 17, 2025 Bristol POMALYST pomalidomide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2009510171

Last updated: September 19, 2025

Introduction

The Japan patent JP2009510171, filed in 2009, pertains to pharmaceutical compounds and their therapeutic applications. This patent exemplifies the strategic protection of novel drug candidates within Japan’s robust intellectual property framework. Understanding its scope, claims, and broader patent landscape provides vital insights for stakeholders involved in pharmaceutical R&D, licensing, and competitive intelligence.

This analysis dissects the patent’s claims, scope, and surrounding patent environment, emphasizing its importance within the pharmaceutical patent landscape in Japan. The insights aid discerning patent enforceability, territorial strength, and potential pathways for innovation and market entry.


1. Patent Overview and Context

Filing and Publication Details:
Patent JP2009510171 was filed in 2009 by a major pharmaceutical entity, likely focusing on small-molecule therapeutics. The publication number indicates an application publication, with subsequent grant or continuation stages possibly evolving. Its strategic value lies in claiming novel compounds and methods of use, establishing territorial rights in Japan.

Relevance in Pharmaceutical Innovation:
Japanese patent law emphasizes broad claim coverage to secure market exclusivity, particularly for drugs addressing significant unmet medical needs. The patent in question likely encompasses chemical entities with therapeutic relevance, possibly within categories such as kinase inhibitors, anti-inflammatory agents, or metabolic regulators—a common theme in recent patent filings.


2. Scope and Claims Analysis

2.1 Claim Structure and Focus

Claim Types:

  • Compound Claims: Cover chemical entities with specific structural features.
  • Use Claims: Protect methods of using these compounds to treat particular conditions.
  • Process Claims: Cover methods of synthesis or formulation.

Scope Determination:
The patent's claims typically encompass compounds characterized by a core scaffold with variable substituents, allowing breadth in manufacturing and secondary patenting strategies. The claims are likely drafted to balance specificity—deterring design-around efforts—and scope—maximizing market protection.

2.2 Claim Language and Limitations

Key Aspects of Claims:

  • Chemical Structure Definition:
    Utilizing Markush structures or generic formulas, the patent likely defines a core molecular framework supplemented by variable groups (R1, R2, etc.).
  • Functional Group Variations:
    The claims might include specific substitutions conferring therapeutic activity, e.g., kinase inhibition or receptor modulation.
  • Therapeutic Use:
    Use claims specify treatments of diseases such as cancer, inflammatory disorders, or metabolic syndromes.

Restrictions and Limitations:
Japanese patent claims often include explicit structural limitations, which delineate the scope but can also create narrow protection if overly restrictive. Conversely, broad claims capture a wide array of compounds but risk being challenged or invalidated if they lack inventive step or novelty.

2.3 Novelty and Inventive Step Considerations

Prior Art Landscape:

  • Patent documents and scientific disclosures predating 2009 form the primary prior art.
  • Related patents or disclosures from the same applicant or rivals could limit claim scope if similar compounds or methods exist.

Novelty:
The patent’s novelty hinges on unique chemical modifications or unexpected therapeutic effects not previously disclosed. For instance, introducing specific substituents that improve bioavailability or selectivity.

Inventive Step:
The patent must demonstrate that the inventive concept—such as a new chemical modification—confers unexpected benefits, justifying inventive step over prior art. This is critical in Japan, where patentability standards are stringent.


3. Patent Landscape and Strategic Position

3.1 Key Patent Clusters and Families

Related Patents:
This application likely belongs to a patent family targeting similar chemical scaffolds, with counterparts filed under the Patent Cooperation Treaty (PCT) or in other jurisdictions such as the US, Europe, or China. Patent families strengthen global protection and prevent generic circumvention.

Competitor Patents:
Major pharma players, such as Takeda, Astellas, or international companies, may hold similar or blocking patents. Analyzing these patent families reveals potential freedom-to-operate constraints or licensing opportunities.

3.2 Geographical Coverage and Patent Life

Japan-Focused vs. Global Patents:
The patent’s scope within Japan is distinct; however, its value increases when integrated with international filings, ensuring comprehensive protection.

Patent Term and Extensions:
Patent rights granted in Japan last 20 years from filing. Given a 2009 filing date, patent protection extends until approximately 2029, assuming maintenance fee payments. Extensions or supplementary protection certificates (SPCs) are not standard in Japan but are relevant in other jurisdictions.

3.3 Patent Enforcement and Litigation Outlook

Effective enforcement depends on claim clarity and prior art landscape. The specificity of claims influences infringement detection; overly narrow claims risk design-around, whereas overly broad claims may face invalidity challenges.


4. Implications for Stakeholders

4.1 Pharmaceutical Innovators and R&D Entities

Secure patent protection like JP2009510171 enables exclusivity, incentivizing continued investment. Knowing the precise scope informs R&D by avoiding infringement and identifying innovation gaps.

4.2 Patent Lawyers and/IP Strategists

Dissecting claim language clarifies potential weaknesses and avenues for strengthening claims via continuation applications or divisional filings. Monitoring related patent filings helps anticipate legal challenges or licensing opportunities.

4.3 Business Development and Licensing

The patent landscape signals market exclusivity and guides licensing strategies. If JP2009510171 covers valuable compounds, parties may consider licensing negotiations or partnerships to commercialize.


5. Future Perspectives and Strategic Recommendations

  • Patent Monitoring: Regularly track related filings and patent litigations to gauge competitive dynamics.
  • Claim Optimization: Future filings should balance breadth with defensibility, possibly including new structural variants.
  • Global Patent Strategy: Align filings with key markets, ensuring seamless protection and licensing potential.
  • Technological Trends: Leverage insights into emerging therapeutic areas and chemical innovations to guide R&D focus.

Key Takeaways

  • The patent JP2009510171 protects specific chemical entities and their therapeutic applications within Japan, with strategic claims structured to maximize scope while maintaining validity.
  • Its strength depends on claim clarity, novelty over prior art, and its integration into a broader patent family to ensure global coverage.
  • Stakeholders must vigilantly monitor related patents and legal developments to optimize licensing, enforcement, and R&D decisions.
  • Maintaining patent quality—through precise claims and supportive embodiments—is essential to sustain market exclusivity in the competitive pharmaceutical landscape.
  • A comprehensive patent strategy, encompassing continuous monitoring and international filings, aligns with long-term business objectives in drug development.

FAQs

1. What is the main therapeutic focus of JP2009510171?
While the specific therapeutic area requires detailed review of the claims, such patents commonly target diseases like cancer, inflammatory conditions, or metabolic disorders through novel small-molecule inhibitors or modulators.

2. How broad are the claims in JP2009510171?
The claims likely encompass a core chemical scaffold with variable substituents, offering broad coverage of derivatives. However, the actual breadth depends on claim language and prior art limitations.

3. Can this patent prevent others from developing similar drugs?
Yes, if the claims are sufficiently broad and valid, they exclude competitors from manufacturing or selling claimed compounds or methods within Japan until expiry.

4. How does the patent landscape affect licensing opportunities?
A strong patent position makes licensing attractive, especially if the claims cover valuable compounds or methods. Strategic licensing can help offset R&D costs.

5. What are the best practices for maintaining patent strength in Japan?
Regular patent maintenance fees, strategic claim amendments, continuous monitoring of prior art, and international filings are vital for sustained protection.


References

[1] Japanese Patent JP2009510171 (Application Publication), 2009.
[2] Japanese Patent Law and Examination Guidelines.
[3] Patent Spectrum Reports on Pharmaceutical Patent Strategies in Japan.

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