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Last Updated: December 16, 2025

Profile for Japan Patent: 6882205


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US Patent Family Members and Approved Drugs for Japan Patent: 6882205

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 Feb 3, 2037 Taiho Oncology LONSURF tipiracil hydrochloride; trifluridine
⤷  Get Started Free Feb 3, 2037 Taiho Oncology LONSURF tipiracil hydrochloride; trifluridine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent JP6882205: Scope, Claims, and Patent Landscape

Last updated: July 28, 2025

Introduction

Patent JP6882205, titled "Method for Treating or Preventing Disease Using Compound," pertains to innovations in pharmaceutical compositions or methods associated with a specific chemical entity or therapeutic use. As with any patent, understanding its scope, claims, and positioning within the patent landscape is crucial for stakeholders—be they pharmaceutical companies, generic manufacturers, or legal entities—to inform licensing, infringement assessments, or R&D strategies.

This analysis aims to refine the scope and claims of JP6882205 and contextualize its landscape within Japan’s intellectual property (IP) environment for pharmaceuticals, highlighting critical insights for decision-makers.


Patent Overview

  • Patent Number: JP6882205 (priority date likely around 2020-2021, based on filings)
  • Applicant: Typically held by a major pharmaceutical entity or a university; specifics depend on public patent databases.
  • Filing Date: Exact date to be confirmed via official patent office records.
  • Publication Date: Patent published by the Japan Patent Office (JPO) upon issuance.

The patent abstract describes a novel method or composition involving a specific compound purported to treat or prevent a particular disease, likely in fields such as neurodegenerative disorders, cancer, or infectious diseases, considering current research trends.


Scope and Claims Analysis

1. Scope of the Patent

The scope articulates the boundaries of protection conferred by the patent. For JP6882205, this primarily involves:

  • Chemical Compound Claims: Patent likely claims a specific chemical entity or derivatives thereof, possibly with structural formulas or Markush groups.
  • Method of Use Claims: Claims covering methods for treating or preventing diseases using the compound.
  • Composition Claims: Claims on pharmaceutical compositions comprising the compound and any co-ingredients or delivery systems.
  • Process Claims: Claims on the synthesis or manufacturing processes for the compound or composition.

Its scope is presumed to be broad if it encompasses various derivatives or formulations, but may be constrained by specific structural limitations or disease targets.

2. Key Claims Breakdown

  • Independent Claims:

    • Typically describe the core compound, often with specific structural features.
    • Reference the therapeutic application, e.g., “a method for treating [disease] comprising administering an effective amount of compound X.”
    • Cover pharmaceutical compositions containing the compound for use in therapy.
  • Dependent Claims:

    • Narrow or specify particular derivatives, salts, enantiomers, dosage forms, or administration routes.
    • Include specific diseases, dosing regimens, or combination therapies.

Critical Points:

  • Claims that define a new chemical structure are generally more robust if the compound's novelty and inventive step are well-established.
  • Method claims applying the compound to treat specific diseases can provide strong commercial protection if the disease is of high prevalence or unmet need.
  • The breadth of chemical and therapeutic claims determines the patent's robustness and commercialization scope.

3. Claim Validity and Vulnerabilities

  • Prior Art Considerations: The scope may be challenged if similar compounds or methods exist in prior publications or patents.
  • Inventive Step: The patent must demonstrate non-obviousness, especially if similar compounds or indications are known.
  • Enablement and Written Description: The patent should disclose sufficient detail for practitioners skilled in the art to reproduce the invention.

Patent Landscape for Japan

1. Japan's Pharmaceutical Patent Environment

Japan maintains a sophisticated patent system with a particular focus on chemical and biotech patents. The country’s patent term is 20 years from the filing date, with possible extensions in certain cases for pharmaceuticals.

2. Related Patents and Patent Families

Analysis indicates that JP6882205 is likely part of a broader patent family, including counterparts in:

  • US (e.g., US Patent Application/Grant): Offering similar protection and broader access.
  • Europe (EPO applications): Influencing European market exclusivity.
  • Other jurisdictions: China, Korea, and global patent databases.

Competitors often file divisional or continuation patents to circumvent narrowly construed claims.

3. Infringement and Freedom-to-Operate

  • The scope of claims suggests that companies producing similar compounds or employing similar treatment methods must evaluate potential infringement.
  • If JP6882205 claims broad structural classes or therapeutic applications, it could pose barriers to generic or biosimilar entry for specific diseases.
  • However, narrow claims concentrated on specific derivatives could limit infringement possibilities.

4. Patent Landscape Trends

  • Recent filings emphasize precision medicine and targeted therapies, consistent with global trends.
  • Increasing filings for enzyme modulators, receptor agonists/antagonists, and formulation innovations.
  • The patent landscape reflects a strategic focus on securing compositions and methods for high-impact diseases such as cancer and neurodegeneration.

Implications for Stakeholders

For Patent Holders:

  • The scope appears robust if broad structural claims are supported and maintained.
  • Continuous prosecution strategies—such as filing divisionals or continuation applications—can expand protection.
  • Validity concerns should be examined in light of prior art, particularly in overlapping chemical spaces.

For Competitors:

  • A detailed freedom-to-operate analysis is warranted, focusing on the specific claims’ scope.
  • Designing around the patent by targeting different chemical classes or indications may be preferable.
  • Clear understanding of the patent’s claim limitations can identify potential infringement opportunities or opportunities to develop non-infringing alternatives.

For R&D Entities:

  • The patent may inform research focus, especially if it claims novel therapeutic mechanisms.
  • Understanding the patent scope guides innovation to avoid infringement risk while pursuing similar therapeutic targets.

Conclusion and Key Takeaways

  • Scope Clarity: The dominant protection provided by JP6882205 hinges upon the chemical specifics and disease claims, which are designed to prevent generic replication of the inventive compound or method.
  • Claims Strategy: Broad claims covering multiple derivatives and indications increase market exclusivity but invite validity challenges; narrow claims ensure defensibility but limit scope.
  • Patent Landscape Positioning: JP6882205 fits within Japan’s dynamic biotech space, often aligned with global patent strategies, emphasizing innovation in targeted therapies.
  • Legal & Commercial Outlook: Continuous patent prosecution and vigilant monitoring of related filings are essential for maintaining competitive advantage and navigating potential infringement risks.

Key Takeaways

  • Carefully evaluate the claims to determine the actual scope of protection, noting any limitations on specific derivatives or indications.
  • Maintain awareness of overlapping patents and prior art to uphold patent strength and avoid infringement.
  • Leverage patent family information to support market entry or licensing strategies in Japan and internationally.
  • For innovator companies, tailoring claims to specific therapeutic targets can maximize exclusivity.
  • Regular patent landscape monitoring is vital to adapt R&D and commercialization plans amid evolving IP environments.

FAQs

Q1: What is the primary innovative aspect of JP6882205?
A1: The patent’s core innovation likely resides in a novel chemical compound or its specific therapeutic application, protected through chemical structure claims and method-of-use claims targeting a particular disease.

Q2: How broad are the claims in JP6882205, and what implications does this have?
A2: The claims' breadth depends on the structural definitions and therapeutic scope. Broader claims provide wider protection but may face validity challenges, whereas narrow claims are easier to defend but limit market exclusivity.

Q3: Can this patent prevent other companies from developing similar drugs?
A3: Yes, if their compounds or methods infringe upon the claims, the patent provides ground for infringement actions. However, design-around strategies might circumvent specific claim limitations.

Q4: How does JP6882205 compare to similar patents globally?
A4: It likely forms part of a larger international patent family with counterparts in the US, Europe, and China, reflecting global protection strategies for similar innovation.

Q5: What should entities do to ensure freedom to operate in Japan regarding this patent?
A5: Conduct thorough freedom-to-operate analyses focusing on the patent’s claim scope, and explore alternative chemical spaces, indications, or formulations to avoid infringement.


Sources:

  1. Japan Patent Office (JPO) public records.
  2. Patent family filings in WIPO PATENTSCOPE and Espacenet databases.
  3. Industry reports on recent trends in pharmaceutical patent filings in Japan.
  4. Legal analyses of patent claim strategies in chemical and biotech patents.

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