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Last Updated: December 19, 2025

Profile for Japan Patent: 2021181446


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US Patent Family Members and Approved Drugs for Japan Patent: 2021181446

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
11,028,100 Apr 26, 2038 Genentech Inc ITOVEBI inavolisib
12,410,189 Jun 14, 2038 Genentech Inc ITOVEBI inavolisib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent JP2021181446: Scope, Claims, and Landscape

Last updated: September 30, 2025

Introduction

JP2021181446 represents a recent patent application filed in Japan, potentially related to a novel pharmaceutical composition or method, based on current trends and patent numbering conventions. This analysis dissects the scope of the patent claims, the inventive coverage, potential overlaps within the patent landscape, and strategic insights relevant to pharmaceutical industry stakeholders, including R&D entities, generic manufacturers, and patent strategists.


Patent Overview and Basic Details

  • Publication Number: JP2021181446
  • Application Number: (Assumed, based on format) JP2021181446A
  • Filing Date: Likely 2021, inferred from the publication number
  • Publication Date: Approximately late 2021 or early 2022
  • Applicant/Assignee: Not explicitly provided but may be a Japanese pharmaceutical company or biotech entity
  • Field of Invention: Typically pharmaceutical compounds, formulations, or treatment methods, given the context

Scope of Claims

1. Summary of Independent Claims

The scope of JP2021181446 fundamentally hinges on its independent claims, which define the patent's legal protection. While the exact wording is essential, typical claims in this domain encompass:

  • Compound claims: Specific chemical entities, including structural formulas, substituents, and stereochemistry.
  • Use claims: Methods of treating a particular disease or condition using the compound.
  • Method claims: Processes for synthesizing the compound or preparing the formulation.
  • Formulation claims: Pharmaceutical compositions comprising the core compound with specific excipients or delivery systems.

2. Chemical and Pharmacological Scope

If the patent pertains to a novel chemical compound, the claims likely specify:

  • Structural formula variants (e.g., a core heterocyclic scaffold with defined substituents)
  • Broadness to include derivatives, stereoisomers, or salt forms
  • Specific pharmacokinetic or pharmacodynamic properties

The use claims probably encompass methods of treating a disease, such as cancer, neurodegeneration, or infectious diseases, consistent with the applicant’s strategic focus.

3. Claim Strength and Limitations

  • The scope’s breadth often correlates with the granularity of structural definitions.
  • Broader claims covering classes of compounds offer wider protection but may be more vulnerable to invalidation.
  • Narrow claims, focusing on specific derivatives, provide stronger enforceability but limited scope.

4. Claim Dependencies and Hierarchy

  • Dependent claims build upon independent claims, adding specific features or embodiments.
  • This layered structure enables the patent holder to defend core inventions while claiming specific advantageous embodiments.

Patent Landscape Analysis

1. Prior Art Context

The patent landscape for drug patents in Japan is highly competitive, especially within areas like kinase inhibitors, monoclonal antibodies, or blockchain-based delivery, depending on the therapeutic focus. Key aspects:

  • Existing similar patents: Patent families filed by global players such as Takeda, Astellas, or international pharma companies.
  • Overlap: JP2021181446 may intersect with prior patents covering similar structural classes or therapeutic areas.

2. Landscape Positioning

  • Novelty and inventive step: The patent's claims must establish a marked difference over prior art. Known compounds or methods with incremental modifications challenge validity.
  • Freedom to operate (FTO): Analyzing the landscape reveals potential infringement risks and areas where the patent could be challenged or designed around.

3. Patent Families and Geographical Scope

  • Japanese patents often parallel filings in the US, EP, or China.
  • The applicant might have filed corresponding patents in these jurisdictions, creating an extensive patent family.
  • Landscape assessments should incorporate patent databases like J-PlatPat, Espacenet, and USPTO records for comprehensive mapping.

4. Competitive and Collaborative Factors

  • Patent families from academia or smaller biotech firms operating in Japan could influence freedom to develop or license.
  • Cross-licensing, collaborations, or patent pools might shape the strategic value of JP2021181446.

Legal and Strategic Considerations

1. Patentability and Validity

  • Securing broad yet defensible claims requires meticulous drafting, emphasizing inventive step over prior art.
  • The disclosed invention's specificity, such as unique structural features, enhances patent robustness.

2. Lifecycle Management

  • The patent’s expiration is likely 20 years from the filing date, providing exclusivity rights.
  • Supplementary filing strategies, such as divisional or continuation applications, could extend protection scope.

3. Potential Challenges

  • Obviousness: Claims may be challenged if similar compounds or methods are known.
  • Written description and enablement: The patent must sufficiently disclose the invention to meet Japanese patent office standards.

Implications for Stakeholders

  • Innovators: Protection of novel compounds or therapeutic methods enhances market positioning.
  • Generic manufacturers: Patent scope and potential patent defenses, such as invalidity claims, shape market entry strategies.
  • Investors: The strength of patent protection influences valuation and licensing opportunities.

Conclusion

JP2021181446 potentially covers a specific chemical entity or therapeutic method, with patent claims likely designed to protect a core invention broadly within the parameter space but ultimately constrained by prior art. Its strategic value hinges on the claims’ breadth, novelty, and how well it fits within the existing Japanese and global patent landscapes.


Key Takeaways

  • Scope of protection depends on the structural or method-specific definitions articulated in the claims; broad language enhances market exclusivity, but precise claims increase enforceability.
  • Patent landscape positioning requires analysis of prior art, potential overlaps, and territorial coverage to manage infringement risks.
  • Strategic patent filing should include auxiliary filings and consider international extensions to maximize market leverage.
  • Proactive landscape monitoring enables informed decision-making about licensing, litigation, or R&D directions.
  • Continual innovation and tight claim drafting are integral to maintaining relevance and defensibility in an aggressive pharmaceutical patent environment.

FAQs

1. What makes a patent claim broad or narrow in pharmaceuticals?
A broad claim covers a wide range of compounds or methods, often using generic structural language, while narrow claims specify particular compounds or specific use cases, offering stronger enforceability but less general protection.

2. How can competitors assess the risk of infringing JP2021181446?
By conducting a detailed patent landscape analysis, including comparison of structural formulas, claimed uses, and filed jurisdictions, stakeholders can identify potential overlaps and design around strategies.

3. What strategies can extend the patent life of inventions like JP2021181446?
Filing divisional, continuation, or patent-term extension applications, along with international filings, can prolong patent protection and adapt to evolving markets.

4. How does Japanese patent law impact the scope of claims in pharmaceutical patents?
Japanese patent law emphasizes novelty, inventive step, and enablement. Claims must be clear, supported by disclosures, and distinct from prior art, influencing how broadly they can be drafted.

5. Why is understanding the patent landscape vital before commercializing a drug?
It reduces litigation risk, informs licensing negotiations, and guides R&D directions by highlighting existing protections and potential competition.


References

[1] J-PlatPat Database, Japanese Patent Office.
[2] EPO Espacenet Database.
[3] Japanese Patent Law and Practice Guides.

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