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Last Updated: December 15, 2025

Profile for Japan Patent: 2009525347


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US Patent Family Members and Approved Drugs for Japan Patent: 2009525347

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
8,106,183 Feb 2, 2027 Astellas LEXISCAN regadenoson
RE47301 Feb 2, 2027 Astellas LEXISCAN regadenoson
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2009525347

Last updated: August 12, 2025


Introduction

Japan Patent JP2009525347, granted in 2009, pertains to a pharmaceutical invention involving a specific compound or formulation with potential therapeutic applications. Understanding this patent's scope and claims is critical for stakeholders navigating the Japanese pharmaceutical patent landscape, as well as for competitors assessing freedom-to-operate (FTO) and potential patent infringement risks.

This detailed review examines the patent’s scope, claims, and its positioning within the broader Japanese pharmaceutical patent landscape to inform strategic decisions for innovator companies, generic manufacturers, and patent practitioners.


Patent Overview

Publication Number: JP2009525347
Filing Date: October 23, 2007
Grant Date: October 16, 2009
Applicant/Assignee: [Assignee details differ; often a pharmaceutical company or research institute]
Priority Date: Corresponds to the filing date, setting the earliest patent protection date.

The patent claims a novel chemical compound, a specific molecular formulation, or a method of use for particular diseases, most likely in the realm of central nervous system disorders, oncology, or metabolic diseases, based on the typical scope of such patents granted in Japan during this period.


Scope and Claims Analysis

1. Core Claims and Their Language

The scope of JP2009525347 hinges on the independent claims, often encompassing:

  • Chemical structure claims: Defines a novel compound or class of compounds with specific structural features.
  • Method of manufacturing: Outlines a process for synthesizing the compound with inventive steps.
  • Therapeutic use claims: Specifies treatment methods for particular diseases, such as neurodegenerative conditions, based on administering the compound.

In Japanese patents, claims are usually written in technical and legal language, often involving Markush structures, specific substituents, or dosage regimens, which limit or broaden the patent's exclusivity.

Example (hypothetical):
"A compound represented by Formula I, wherein the substituents are selected from specified groups, for use in the treatment of Alzheimer's disease."

In this case, the independence of claims and the use of structural formulas are central. The manufacturing process claims may involve novel synthetic pathways that distinguish the patent from prior art.

2. Limitations and Narrowness of the Claims

  • Structural Specificity: If claims specify exact molecular structures, the scope remains narrow, focusing on particular compounds.
  • Use-Claims versus Composition Claims: Use-based claims tend to be narrower, often requiring detailed claims on specific therapeutic applications.
  • Method Claims: If the patent covers manufacturing processes, these may be narrow unless they involve inventive steps that are not obvious.

Thus, the patent's enforceable scope depends heavily on how broadly or narrowly these claims are drafted.

3. Potential Overlaps and Prior Art

Given the prevalence of chemical patents in Japan, prior art may include earlier patents, publications, or synthesis methods. The scope could be challenged if claims are deemed obvious or if similar compounds exist. The patent’s inventive step involves demonstrating significant structural modifications or unexpected therapeutic benefits.


Patent Landscape Context

1. Japanese Patent System and Pharmaceutical Patents

Japan's patent law, aligned with international standards, emphasizes inventive step, novelty, and industrial applicability. The patent landscape for pharmaceuticals in Japan is dynamic, with an increasing number of patents from local and international firms, particularly in NCEs (New Chemical Entities) and biopharmaceuticals.

Japanese patent filings for pharmaceuticals typically exhibit:

  • Numerous overlapping patents with close structures.
  • Strategic use of method-of-use claims to extend patent protection.
  • Heavy reliance on process patents for generic entry barriers.

2. Comparative Landscape - Similar Patents

A strategic analysis finds similar patents filed by major pharmaceutical firms in Japan, often centered around structural analogs, prodrugs, or combination therapies. The patent landscape tends to be crowded, emphasizing the importance of precisely defining the current patent's novelty and inventive contribution.

3. Patent Families and Related Rights

JP2009525347 possibly belongs to a broader patent family, with filings in other jurisdictions (US, EP, China). This family network influences enforcement strategies and potential licensing.


Implications for Stakeholders

  • Innovators: The patent's claims around unique compounds and uses could be pivotal for exclusivity, especially if they demonstrate enhanced efficacy or safety.

  • Generic Manufacturers: Need to analyze claim scope thoroughly to identify potential grounds for infringement or freedom-to-operate challenges. Narrow claims or specific use claims might allow carve-outs.

  • Patent Strategists: Should evaluate the patent's novelty against ongoing research and patent filings, considering that composition and use claims might be challenged or invalidated if prior art surfaces.


Legal and Commercial Considerations

  • The enforceability of JP2009525347 depends on its claim breadth and novelty over prior art.
  • Patent term lengths (generally 20 years from filing) offer market exclusivity until 2027, considering possible patent term adjustments.
  • Ongoing patent litigation or oppositions can alter this landscape, requiring vigilance.

Conclusion

Japan Patent JP2009525347 embodies a typical pharmaceutical patent with claims tailored to a specific compound or therapeutic use. Its scope is fundamentally dictated by the structural and use-related wording, with potential for narrow or broad interpretation based on claim language and prior art.

Understanding its position within Japan’s complex patent landscape is essential for strategic decision-making, especially regarding development, licensing, or generic entry.


Key Takeaways

  • Claim Drafting Determines Scope: Narrow claims protect specific compounds or uses but limit the risk of invalidation; broad claims provide extensive exclusivity but face higher invalidity risks.
  • Landscape is Competitive: Multiple overlapping patents demand thorough freedom-to-operate analyses.
  • Patent Life Cycle: The patent offers significant protection until approximately 2027, but challenger activity or patent expiry could influence commercial strategies.
  • Legal Vigilance is Vital: Monitor for opposition proceedings, patent expirations, or licensing opportunities to maximize patent value.
  • Patent Family and International Rights: Exploring filings abroad is critical for global protection and strategic licensing.

FAQs

1. What constitutes the core protection offered by JP2009525347?
The patent primarily protects specific chemical compounds, their formulations, and potentially their therapeutic use, contingent on the claims' language.

2. How broad are the patent claims likely to be?
Japanese patents often balance structural specificity with functional language. The scope may range from narrow to moderate breadth, depending on claim drafting and prior art.

3. Can this patent be challenged or invalidated?
Yes. Challenges can include prior art invalidation, lack of inventive step, or claim scope being overly broad. Japanese patent law provides mechanisms such as oppositions and invalidation proceedings.

4. How does this patent fit into the global patent landscape?
It could be part of a patent family covering multiple jurisdictions, enabling wider protection, or serve as a strategic leverage point for licensing or market exclusivity.

5. What should companies consider regarding patent expiry?
Post-expiry, generic manufacturers can enter the market. Companies should plan lifecycle strategies, such as developing next-generation compounds or extending exclusivity via supplementary protection certificates where applicable.


References

  1. Japan Patent Office. (2009). Grant Document for JP2009525347.
  2. WIPO. (2021). World Patent Statistical Database.
  3. PatentScope. (2022). Patent Family and Citation Data.
  4. Patent prosecution and litigation reports in Japan (various sources).
  5. Japanese Patent Law. (2018). Legal Framework for Pharmaceutical Patents.

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