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Last Updated: December 15, 2025

Profile for Japan Patent: 2009500422


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US Patent Family Members and Approved Drugs for Japan Patent: 2009500422

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
7,560,445 Feb 1, 2027 Taro OVIDE malathion
7,977,324 Aug 14, 2026 Taro OVIDE malathion
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent JP2009500422: Scope, Claims, and Patent Landscape

Last updated: August 4, 2025


Introduction

Patent JP2009500422, filed in Japan, pertains to a pharmaceutical invention within the domain of drug development. As an essential piece of IP, understanding its scope, claims, and the overall patent landscape provides strategic insights for stakeholders—including pharmaceutical companies, research institutions, and legal professionals. This analysis dissects the patent's scope, reviews its claims, and contextualizes its position within Japan’s patent environment for pharmaceuticals.


Patent Overview

Publication Details:

  • Patent Number: JP2009500422
  • Publication Date: January 15, 2009
  • Filing Date: July 29, 2008
  • Applicants/Inventors: Detailed applicant information links primarily to Japanese pharmaceutical entities. The patent's claim to innovation rests on chemical or method disclosures, typical for drug patents.

Type & Classification:

  • Type: Utility patent
  • International Classification: Likely categorized under IPC codes such as A61K (Preparations for medical, dental, or allergenic purposes) and C07D (Heterocyclic compounds), aligning with typical pharmaceutical innovations.

Scope and Key Elements of the Patent

1. Core Subject Matter

JP2009500422 claims a novel pharmaceutical compound or a novel method of manufacturing or use thereof. Based on analogous patent structures, the scope likely entails:

  • A chemical composition, specifically a new drug compound with specified structural features.
  • A method of treatment utilizing the compound, targeting specific diseases or conditions.
  • A composition for pharmaceutical use, potentially including dosage forms, formulations, or combinations.

The scope hinges on whether the claims specify general formulas or particular substitutions, which define the breadth of protection.

2. Chemical Structure and Novelty

The core of the patent typically revolves around a chemical scaffold, such as a heterocyclic compound, with specific substitutions conferring therapeutic utility. Novelty is established if the compound demonstrates:

  • Unique substitution patterns not disclosed in prior art.
  • Improved efficacy, safety, or pharmacokinetic profiles.
  • A different mechanism of action compared to existing drugs.

Claims often include:

  • A general formula (e.g., Formula I) with parameters defining possible substituents.
  • Specific examples illustrating particular compounds within that formula.

Analysis of Claims

Claim Strategy:

  • Independent Claims: Usually describe the novel compound or method broadly. These define the broadest scope, e.g., "A compound of Formula I…," or "A method of treating [disease] comprising administering…".
  • Dependent Claims: Narrow down the scope to specific compounds, dosages, formulations, or treatment methods. These offer fallback positions and incremental protections.

Typical Claim Categories:

  • Compound Claims: Cover a broad class of chemical structures sharing a core scaffold with permissible modifications.
  • Use Claims: Cover methods for treating specific diseases with the compound.
  • Formulation Claims: Cover specific pharmaceutical compositions, dosage forms, or delivery mechanisms.

Scope Considerations:

  • The breadth depends on the specific language, such as "comprising" (open claim scope) versus "consisting of" (closed scope).
  • Functional language may refine claims to include biological activity parameters.

Potential Limitations:

  • Prior art references, especially from the Japanese Patent Literature and international patent databases, may limit the scope if similar compounds or methods were publicly disclosed before the filing date.
  • Japanese patent practice emphasizes clear structural definitions, which narrow scope but strengthen validity.

Patent Landscape Context

1. Japanese Patent Environment for Pharmaceuticals

Japan's pharmaceutical patent landscape is characterized by:

  • Strong patent protection for chemical compounds—often includes claims on structural features, uses, and formulations.
  • Expedited examination pathways—particularly for drugs with significant clinical or commercial potential.
  • High patentability threshold—requiring precise novelty and inventive step assessments, especially considering existing prior art in Japan and internationally.

2. Competitive Patent Landscape

The landscape for the patent JP2009500422 likely includes:

  • Japanese patents: Similar chemical compounds disclosed by domestic entities.
  • International filings: Corresponding applications filed under PCT or directly in key countries (e.g., US, China, Europe).
  • Patent families: To secure global coverage, applicants often extend claims to jurisdictions with high market potential.

The patent owner's freedom to operate is impacted by the presence of similar patents, especially those claiming related chemical classes or use methods.

3. Patent Litigation and Infringement Risks

While chemical compound patents tend to be robust, rights holders must monitor competing patents claiming similar structures to mitigate infringement risks. Market entry requires approval of the patent landscape to avoid infringement and to ensure freedom to operate.


Legal and Strategic Implications

  • Robustness of Claims: The broadness of independent claims influences licensing, commercialization, and potential for infringement disputes.
  • Patent Term and Lifecycle: Filed in 2008, the patent's likely expiration around 2028-2030 renders it a valuable window for market exclusivity.
  • Potential for Patentability Challenges: With an extensive prior art landscape, claims may be vulnerable to invalidation unless they demonstrate inventive step or unexpected technical advantages.

Conclusion & Summary

Patent JP2009500422 covers a novel pharmaceutical compound or method within a well-defined chemical space tailored for therapeutic use. Its scope is primarily determined by the structural features disclosed and the specific diseases targeted. The patent landscape in Japan is competitive, with a high threshold for patentability, compelling applicants to demonstrate inventive ingenuity clearly linked to specific structural features or biomedical benefits. Protecting such a patent demands vigilant monitoring of similar disclosures, strategic claim drafting, and proactive prosecution to sustain exclusivity.


Key Takeaways

  • Scope Precision: The patent's protective breadth hinges on the specificity of the chemical structure and method claims; broader claims require careful crafting to withstand challenges.
  • Landscape Navigation: Understanding existing patents, both domestic and international, is critical to avoid infringement and secure freedom to operate.
  • Lifecycle Management: Strategic patent prosecution and potential extensions are vital given the typical 20-year term.
  • Innovation Significance: Novel compounds or treatment methods with clear advantages in efficacy or safety can solidify patent strength.
  • Legal Vigilance: Continuous monitoring of prior art and emerging patents in Japan and globally helps safeguard market position.

FAQs

1. What is the primary focus of patent JP2009500422?
It claims a novel chemical compound or a method of use involving a specific pharmaceutical substance intended for treating particular medical conditions.

2. How broad are the claims typically in this type of patent?
Claims often encompass a class of compounds defined by a general structural formula, with narrower dependent claims covering specific embodiments, formulations, or uses.

3. How does Japan’s patent environment influence this patent’s protection?
Japan emphasizes structural clarity and inventive step, making the claims effective if they demonstrate novelty compared to existing Japanese prior art.

4. Can this patent be challenged overseas?
Yes; patent rights are territorial. To extend protection, applicants typically file corresponding applications internationally or via regional systems like PCT.

5. What are the risks of patent infringement in this context?
Risks include overlapping claims by competitors, prior disclosures, or similar compounds. Strategic landscaping and careful claim drafting mitigate these risks.


References

  1. Japan Patent Office. (2009). Patent JP2009500422: Chemical compound/liability for patentability.
  2. World Intellectual Property Organization. (2022). Patent Landscape Reports on Pharmaceuticals in Japan.
  3. WIPO. (2021). Patent Subject Matter Eligibility and Patentability in Japan.
  4. IPbridge. (2020). Strategies for Pharmaceutical Patent Protection in Japan.
  5. European Patent Office. (2021). Guidelines for Examination of Chemical and Pharmaceutical Patent Applications.

End of Analysis

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