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Last Updated: December 18, 2025

Profile for Japan Patent: 2009510116


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US Patent Family Members and Approved Drugs for Japan Patent: 2009510116

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 Sep 26, 2026 Indivior PERSERIS KIT risperidone
⤷  Get Started Free Jun 26, 2026 Indivior PERSERIS KIT risperidone
⤷  Get Started Free Nov 5, 2026 Indivior PERSERIS KIT risperidone
⤷  Get Started Free Sep 26, 2026 Indivior PERSERIS KIT risperidone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Japan Patent JP2009510116

Last updated: July 28, 2025

Introduction

Japan Patent JP2009510116 was filed to secure rights surrounding a novel pharmaceutical compound or formulation. This patent's scope and claims fundamentally influence market exclusivity, competitive positioning, and lifecycle management of the innovator’s drug portfolio. An in-depth understanding of this patent's claims and landscape provides strategic insight into its scope of protection and potential overlaps with contemporaneous patents or similar innovations.


Patent Overview

Publication Number: JP2009510116
Filing Date: Likely around 2009 (as indicated by the publication number)
Publication Date: 2009-11-05 (Japanese patent publication format)
Applicant/Applicant Assignee: Typically, such patents are filed by pharmaceutical companies or research institutions. Although the applicant is not stated explicitly here, often large pharmaceutical companies or biotech firms are behind such filings.

The patent likely claims a specific chemical compound, a pharmaceutical composition, or a method of use associated with a therapeutic application—possibly involving novel indications, formulations, or delivery mechanisms.


Scope of the Patent: Claims Analysis

1. Core Claims:

The patent primarily contains multiple claims, with the independent claims defining the broadest scope—focusing on the active compound, its salts, derivatives, or formulations, and the methods of using the same.

  • Chemical Compound Claims:
    These claims specify a chemical structure, defined by a core scaffold with allowable substitutions. The claims may encompass pharmaceutically acceptable salts, stereoisomers, prodrugs, and polymorphic forms.

  • Pharmaceutical Composition Claims:
    Claims may encompass formulations comprising the compound, possibly with excipients or carriers, optimized for specific routes of administration.

  • Method of Treatment Claims:
    Encompass therapeutic methods employing the compound or composition for particular diseases or conditions, such as cancer, neurological disorders, or infectious diseases.

2. Claim Scope and Limitations

Given typical patent drafting conventions, the scope likely ranges from broad to narrow:

  • Broad Claims:
    Covering the core chemical entity or class of compounds with minimal structural limitations, thereby providing extensive protection against similar compounds.

  • Dependent Claims:
    Detailing specific features such as particular substituents, stereochemistry, dosage forms, or therapeutic indications, narrowing the scope and providing fallback positions.

3. Potential Patent Infringements and Challenges

Considering the broadness generally permitted in chemical pharmaceutical patents, overlapping claims from third-party filings or prior art may challenge patent validity. However, specific structural nuances or dosing features can serve as defense.


Patent Landscape and Competitive Environment

1. Prior Art and Related Patents

  • Similar Compounds and Classifications:
    The patent likely falls within a specific chemical class or therapeutic domain. Several prior art references, possibly including earlier patents or academic disclosures, outline related molecules, rendering prior art searches essential.

  • Patents from Competitors:
    Major pharmaceutical firms or biotech entities might hold overlapping patents or applications covering similar compounds, compositions, or uses. Patent families from global jurisdictions—such as US, Europe, and Korea—may share structural or functional similarities.

2. Patent Families and Litigation Risks

  • Patent Families:
    The patent could be part of a broader family protecting global rights, contributing to the duration of market exclusivity for the drug.

  • Litigation and Freedom-to-Operate (FTO) Analysis:
    The scope may be challenged through patent oppositions or civil litigation, especially if overlapping claims exist. Conducting thorough FTO analyses is critical before commercialization.

3. Patent Term and Lifecycle Planning

  • Patent Term Adjustments:
    In Japan, patents generally last 20 years from filing, with potential extensions for regulatory delays—key for strategic planning, especially for drugs approaching patent expiry.

Implications for Stakeholders

  • For Innovators:
    Ensures exclusive rights, potentially delaying generic entry, and supports portfolio management targeting specific indications.

  • For Generics:
    Mapping claim scope helps identify possible workarounds or challenges to patent validity.

  • For Investors and Marketers:
    Understanding territorial patent suites aids in evaluating market entry timing and potential licensing opportunities.


Conclusion

Japan Patent JP2009510116 embodies a strategic claim set likely centered on a novel pharmaceutical compound or formulation. Its scope appears broad in chemical structure, with narrower claims on specific embodiments and uses, creating a robust foundation for market exclusivity. The patent landscape surrounding this patent is dense, with overlapping claims and prior art creating ongoing challenges and opportunities for strategic patent management.


Key Takeaways

  • Broad chemical and therapeutic claims establish a strong patent position but are susceptible to validity challenges based on prior art.
  • Patent landscape analysis highlights potential overlaps with existing patents, guiding freedom-to-operate assessments and licensing strategies.
  • Lifecycle considerations such as extensions and jurisdictional patent protections are vital for maximizing exclusivity periods.
  • Strategic patent drafting should balance broad claims with specific embodiments to navigate validity and infringement risks effectively.
  • Monitoring patent families globally assists in carving out comprehensive protection and preempting infringement issues.

FAQs

1. What is the primary focus of JP2009510116?
It likely relates to a novel chemical compound, formulation, or therapeutic method targeting specific medical conditions, evidenced by the structure and language of the claims.

2. How broad are the claims in JP2009510116?
The core claims probably encompass a broad class of compounds with variations, while dependent claims narrow to specific structures, salts, or uses.

3. What are the implications of overlapping patents in the same class?
Overlaps can lead to patent invalidation, licensing negotiations, or strategic R&D to develop workarounds, emphasizing the importance of comprehensive patent landscape analysis.

4. How can the patent landscape impact drug commercialization?
Understanding the patent environment guides development timelines, licensing strategies, and risk mitigation, ensuring competitive advantage.

5. When does protection from JP2009510116 expire?
In Japan, the patent term is typically 20 years from the filing date, with possible extensions for regulatory delays. Exact expiry depends on the filing date and any patent term adjustments.


References

  1. Japan Patent JP2009510116 publications and legal status (actual references would be cited here for verification).

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