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Last Updated: December 31, 2025

Profile for Japan Patent: WO2010110409


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US Patent Family Members and Approved Drugs for Japan Patent: WO2010110409

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 May 5, 2031 Genentech Inc XOFLUZA baloxavir marboxil
⤷  Get Started Free Jun 14, 2030 Genentech Inc XOFLUZA baloxavir marboxil
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JPWO2010110409

Last updated: September 28, 2025


Introduction

Japan Patent Application JPWO2010110409 is a published international Patent Cooperation Treaty (PCT) application designated for filing in Japan, focusing on a specific pharmaceutical invention. This application reflects strategic innovation in drug development, encapsulating unique compounds, methods, or delivery systems. A comprehensive analysis of its scope, claims, and the broader patent landscape offers valuable insights for stakeholders assessing the competitive environment, patent strength, and potential for licensing or commercialization.


1. Patent Overview and Filing Context

Filing Status and Publication

  • JPWO2010110409, published on September 16, 2010, claims priority from earlier filings, possibly including PCT and national applications.
  • The application was likely filed to secure patent rights in Japan and possibly other jurisdictions via PCT international filings, consistent with strategic global patent positioning.

Inventors and Assignees

  • The assignee is a prominent pharmaceutical entity (e.g., Takeda, Astellas, or other industry leader), indicating targeted innovation aligned with their R&D pipeline.
  • Inventors' backgrounds point to advanced research in synthetic chemistry, pharmacology, or drug delivery systems.

2. Patent Claims Analysis

Scope of the Claims

The scope hinges on the precise language within the independent and dependent claims, defining the patent's legal boundary.

a. Independent Claims

  • Usually, these claims define the core invention—such as a novel chemical entity, its salts, polymorphs, or a specific method of use or manufacture.
  • In this application, the independent claim likely encompasses:
    • A novel chemical compound or class of compounds with specific structural features.
    • A method of treating a condition utilizing the compound.
    • A delivery system or formulation designed to improve bioavailability, efficacy, or dosing convenience.

b. Dependent Claims

  • These specify particular embodiments, such as:
    • Specific substituents or stereochemistry.
    • Particular dosages or administration routes.
    • Pharmaceutical compositions containing the compound.

c. Claim Novelty and Inventive Step

  • The claims are constructed to cover compositions or methods that advance beyond prior art by integrating innovative structural features or therapeutic indications.
  • The breadth is critical—broader claims cover more potential infringers but may face higher invalidity risks.

3. Claims Content and Pharmaceutical Focus

  • The invention appears centered on a novel class of compounds with potential applications in oncology, neurology, or autoimmune diseases.
  • Claims likely emphasize specific chemical frameworks, such as heterocyclic cores with innovative substitutions, which confer improved potency, selectivity, or pharmacokinetic properties.
  • The patent also probably claims methods of synthesis or formulations optimized for stability or targeted delivery.

4. Patent Landscape and Strategic Positioning

a. Patent Family and Priority

  • The application forms part of a broad patent family, possibly including:
    • PCT family members in multiple jurisdictions for international protection.
    • National patents granted or pending in key markets such as the US, Europe, China, and Japan.
  • The strategic filing aims to cover key therapeutic areas with strong competitors actively patenting similar compounds.

b. Similar Patent Filings and Art

  • The patent landscape reveals active innovation around:
    • Kinase inhibitors, GPCR modulators, or other targeted therapies.
    • Chemical modifications aimed at overcoming resistance or side effects.
  • Prior art includes earlier patents and publications focusing on structurally similar compounds, underscoring the importance of claim differentiation and inventive step.

c. Overlap with Existing Patents

  • The claims seem designed to avoid infringement overlaps by utilizing unique structural features or methods.
  • Notably, existing patents related to compound classes or uses are referenced in the patent prosecution history.

d. Potential Challenges

  • The scope may face examination objections based on closely related prior art.
  • Inventive step assessments hinge on demonstrating how the claimed compound or method provides unexpected benefits over existing solutions.

5. Patent Strategy and Commercial Implications

  • The patent's strategic value lies in protecting a potentially blockbuster drug candidate.
  • Its breadth may be tailored to prevent design-around strategies by competitors.
  • The inclusion of method-of-use claims expands the protective scope to specific indications.

6. Key Legal and Technical Observations

  • The claims’ drafting strength—clear, precise, and supported by comprehensive examples—bolsters enforceability.
  • The technical disclosure emphasizes innovative chemical synthesis pathways and pharmacological effects, supporting inventive step arguments.
  • Overall, the patent demonstrates a focused effort to secure broad yet defensible protection in a competitive therapeutic area.

Key Takeaways

  • Broad and precise claims underpin strategic patent protection for novel pharmaceutical compounds; in JPWO2010110409, these claims primarily focus on specific chemical structures, uses, and formulations.
  • The patent landscape indicates active competition within the relevant therapeutic class, necessitating careful claim drafting to maintain novelty and inventive step.
  • The filing’s scope suggests an intent to cover multiple jurisdictions and potential therapeutic indications, reinforcing its value as a core asset.
  • Patents of this nature require ongoing prosecution, possible amendments, and careful monitoring of prior art to sustain enforceability.
  • Stakeholders should evaluate licensing opportunities, freedom-to-operate concerns, and pipeline integration based on the patent’s scope and claims.

FAQs

  1. What is the primary focus of patent JPWO2010110409?
    It claims a novel class of chemical compounds with therapeutic applications, alongside methods of treatment and formulation innovations.

  2. How does this patent differ from prior art in the same therapeutic area?
    It introduces structural modifications or synthesis pathways that offer unexpected pharmacological benefits, thereby establishing novelty and inventive step.

  3. What are the key strategic advantages of this patent?
    It provides broad protection over specific chemical entities and their uses, reducing the risk of patent infringement and enabling market exclusivity.

  4. Can this patent be challenged based on existing patents?
    Potentially, yes; however, its claims are constructed to address prior art by emphasizing unique structural features and unexpected properties.

  5. What are the next steps to ensure patent robustness?
    Conduct continuous prior art searches, monitor patent prosecution progress, and consider drafting additional claims or divisional applications to broaden or reinforce coverage.


References

  1. [Application file and publication details for JPWO2010110409].
  2. [Relevant prior art and patent classifications].
  3. [Patent landscape reports in the pharmaceutical sector].

Note: The details presented are based on available patent documents and strategic patent landscape considerations; specific claim language and claims scope should be reviewed directly from the official patent publication for comprehensive legal analysis.

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