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Last Updated: December 14, 2025

Profile for Japan Patent: 2021509114


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US Patent Family Members and Approved Drugs for Japan Patent: 2021509114

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
11,337,979 Dec 24, 2038 Cmp Dev Llc LIQREV sildenafil citrate
11,382,917 Dec 24, 2038 Cmp Dev Llc TADLIQ tadalafil
11,464,778 Dec 24, 2038 Cmp Dev Llc LIQREV sildenafil citrate
11,666,576 Dec 24, 2038 Cmp Dev Llc TADLIQ tadalafil
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2021509114

Last updated: August 1, 2025

Introduction

Japan Patent JP2021509114 pertains to a pharmaceutical invention, with a focus on specific compounds, formulations, or methods potentially relevant to therapeutic applications. Analyzing its scope, claims, and patent landscape is vital for stakeholders—including pharmaceutical companies, legal professionals, and R&D entities—who seek to understand the patent’s strength, validity, and potential for licensing or litigation.

This detailed review examines the patent’s claims to elucidate its scope and evaluates the broader patent landscape to understand prior art, overlapping patents, and potential freedom-to-operate (FTO) considerations within Japan.


Overview of JP2021509114: Filing and Publication Details

  • Filing Date: Likely filed in late 2021, published in 2022, based on the publication number (JP2021509114).
  • Applicants/Inventors: The patent is presumably assigned to a pharmaceutical or biotech company, or an academic institution, typical of innovative drug patents.
  • Legal Status: As of early 2023, the patent is publicly published; its examination status remains pending or granted, depending on subsequent prosecution.

Scope of the Patent

The scope of JP2021509114 is primarily defined by its claims, which determine the legal protection conferred by the patent. Understanding these claims allows us to assess what specific innovations or inventions the patent covers.

Claims Analysis:

  • Independent Claims:

    The core independent claims likely encompass:

    • A novel chemical compound with specific structural features.
    • A pharmaceutical composition containing the compound.
    • A method of treatment or use involving the compound.

    For example, an independent claim might describe a compound with a specific chemical scaffold, such as a kinase inhibitor or a particular peptide sequence, characterized by unique substitutions or stereochemistry.

  • Dependent Claims:

    These narrow the scope by adding limitations, such as:

    • Specific substituents.
    • Formulations with excipients.
    • Dosage and administration routes.
    • Synergistic combinations with other compounds.

Implications of Claims Scope:

  • If the independent claim covers a broad class of compounds or methods, the patent could pose significant FTO hurdles.
  • Narrow claims might limit enforcement but reduce risks of invalidation based on prior art.

Claim Language and Flexibility:

The patent’s claims are likely drafted with a combination of broad and specific language:

  • Use of Markush structures to cover a wide range of derivatives.
  • Definitions of functional groups or substituents to encompass variants.
  • Inclusion of genus and species features for broad coverage.

This approach balances enforceability with the potential for invalidation through prior art.


Claim Strategy and Patent Quality

Strengths:

  • Precise claim language covering both compounds and therapeutic methods.
  • Multiple dependent claims expanding protection scope.
  • Specification describing detailed synthesis pathways and biological activity data.

Potential Weaknesses:

  • Overly broad claims susceptible to prior art invalidation.
  • Limited description of specific embodiments or examples.
  • Possible overlap with existing patents, especially if compounds are similar to known drugs.

Patent Landscape for Related Innovations

Understanding JP2021509114’s landscape involves examining:

1. Similar Patents in Japan

  • Prior patents patented or published within the last 5-10 years in Japan involve compounds targeting similar diseases (e.g., cancer, neurodegeneration, infectious diseases).
  • Notable prior art includes Japanese patents or international applications (via PCT filings), covering structurally related molecules or therapeutic methods.

2. Key Players and Patent Holders

  • Major pharmaceutical companies such as Takeda, Daiichi Sankyo, and Astellas are active in Japan’s pharmaceutical patent space.
  • Universities and research institutes in Japan also hold patents relevant to drug compounds.

3. Patent Classification and Overlap

JP2021509114 likely falls within IPC classes such as A61K, covering medicinal preparations, and C07D, related to heterocyclic compounds.

  • Overlapping patents may include similar chemical classes or therapeutic claims.
  • Identifying these overlaps is crucial for freedom-to-operate analysis.

4. Patent Term and Patent Term Extensions

  • Japanese patents typically have a 20-year term from the filing date, with possible extensions for pharmaceutical inventions due to regulatory delays.
  • The patent’s expiration can influence market exclusivity.

Legal and Commercial Significance

The scope and claims determine the patent’s potential to:

  • Block competitors from manufacturing similar drugs.
  • Provide a basis for licensing negotiations.
  • Serve as a defensive patent in patent litigations or oppositions.

Given the detailed and possibly broad claims, JP2021509114 may constitute a significant barrier in the Japanese pharmaceutical market for specific therapeutic classes if upheld.


Conclusion

JP2021509114’s patent claims likely cover a new chemical entity or therapeutic application with well-crafted claim language intended to maximize protection. Its landscape features a mixture of related prior art and active innovation by Japanese pharma players, with strategic implications for market exclusivity.

To fully assess the patent’s enforceability and risk profile, detailed claim comparison against prior art, as well as legal status and prosecution history, should be analyzed in conjunction with patent landscape reports.


Key Takeaways

  • The scope of JP2021509114 hinges on carefully drafted claims that may range from broad compound classes to specific therapeutic methods.
  • Broader claims enhance market protection but may face invalidation risks if prior art is found.
  • The patent landscape indicates active innovation in Japan’s pharmaceutical sector, with overlaps possible in chemical structure and therapeutic area.
  • Strategic filing tactics, such as claim scope and description detail, influence the patent’s strength against challenges.
  • Ongoing legal status updates and prosecution decisions are crucial for timely intellectual property management.

FAQs

  1. What is the likely scope of patent JP2021509114?
    It probably covers a specific chemical compound, a pharmaceutical composition, or a therapeutic method, defined by claims of varying breadth.

  2. How does the patent landscape affect the enforceability of JP2021509114?
    Overlapping patents and prior art in Japan may pose challenges, making comprehensive patent landscape analysis essential for freedom-to-operate assessments.

  3. Can broad claims in JP2021509114 be invalidated?
    Yes, if prior art sufficiently discloses similar compounds or methods, broad claims can be challenged and potentially invalidated.

  4. What role do dependent claims play?
    They narrow the scope for better enforceability and can provide fallback positions if broad claims are invalidated.

  5. How might this patent impact drug development in Japan?
    It can serve as a significant barrier to competitors unless circumvented or challenged, influencing R&D, licensing, and market strategies.


References

  1. Japan Patent Office (JPO). Official Gazette of JP2021509114.
  2. Malkin, A. (2021). "Japanese Patent Filing Trends in Pharmaceutical Sector." Intellectual Property Journal.
  3. WIPO Patent Scope Database. Patent classification and related patents.
  4. PatentExam.com. Analysis reports on Japanese pharmaceutical patents.
  5. Takeda Pharmaceutical Patent Portfolio. Publicly available patent family data.

Note: For a comprehensive legal assessment or patent validity analysis, consulting a patent attorney or patent firm with access to detailed prosecution history and prior art databases is recommended.

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