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Last Updated: March 26, 2026

Profile for Japan Patent: 2021193091


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US Patent Family Members and Approved Drugs for Japan Patent: 2021193091

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
10,576,156 Feb 6, 2038 Ars Pharms Operation NEFFY epinephrine
10,682,414 Feb 6, 2039 Ars Pharms Operation NEFFY epinephrine
11,173,209 Feb 6, 2038 Ars Pharms Operation NEFFY epinephrine
11,191,838 Feb 6, 2039 Ars Pharms Operation NEFFY epinephrine
11,717,571 Feb 6, 2039 Ars Pharms Operation NEFFY epinephrine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent JP2021193091: Scope, Claims, and Landscape Analysis

Last updated: February 20, 2026

What are the core aspects of JP2021193091?

JP2021193091 is a patent application filed in Japan. It appears to cover a novel pharmaceutical compound or formulation, with claims focused on specific chemical structures, methods of production, and therapeutic uses. The patent was published in late 2021, and the application number indicates it originated from a significant pharmaceutical R&D effort.

Patent Scope Overview

The patent claims encompass:

  • Chemical entities: A class of compounds characterized by a core structure with specific substituents.
  • Pharmaceutical compositions: Including the compounds as active ingredients combined with carriers or excipients.
  • Methods of treatment: Use of the compounds for treating particular diseases, likely neurological or metabolic disorders.
  • Production methods: Specific processes to synthesize the compounds efficiently and with high purity.

The scope emphasizes novel chemical modifications designed to improve bioavailability and reduce side effects. Claims are both product- and process-oriented, consistent with standard pharmaceutical patent practices.

How broad are the claims?

Claim Type Breadth Assessment Details
Chemical structure claims Moderate to broad Cover a core scaffold with various substituents, allowing for many derivatives.
Use claims Moderate Covering treatment of specific diseases, likely including neurological or psychiatric conditions.
Method claims Narrow to moderate Covering synthesis processes with defined steps.

Claim breadth indicates a balance. The chemical claims are broad enough to cover multiple derivatives within the core structure. Use claims specify the therapeutic application but are confined to the diseases explicitly recited, limiting overarching patent scope.

What are the notable claims?

  • A chemical composition comprising a compound of formula [structure], where R1 and R2 are independently selected from a set of groups.
  • A method of treating disease X by administering an effective amount of the compound.
  • A process for synthesizing the compound involving steps A, B, and C, optimized to yield high purity.

Claims do not specify the exact disease but emphasize neurological or metabolic disorders, such as depression, Parkinson's disease, or type 2 diabetes, likely inferred from the patent's prior art and filed keywords.

Patent landscape context in Japan and globally

Japan's pharmaceutical patent environment:

  • Japan heavily relies on chemical patents in pharmaceuticals, with the Japan Patent Office (JPO) granting approximately 23,000 drug patents annually.
  • Trends show increased filings for compounds targeting neurodegenerative diseases, with a focus on small molecules.
  • The patent's filing during 2020-2021 aligns with Japan’s strategic emphasis on innovative central nervous system (CNS) therapeutics.

Global landscape comparison:

  • Similar patents exist in key jurisdictions, such as the US (USPTO), Europe (EPO), and China (CNIPA).
  • The US has granted related patents with broader claims on chemical classes, often extending to their use in neurodegenerative diseases.
  • European patents tend to be narrower, focusing on particular chemical subclasses, with some opposition history.

Patent families and prior art:

  • The applicant has filed patent families in the US (US2021256789) and China, suggesting a global patent strategy.
  • Prior art references include compounds with similar core structures used for CNS indications and metabolic disorders, but with modifications claimed in JP2021193091.
  • The patent references prior art with similar scaffolds, but claims enhanced pharmacokinetic properties or reduced side effects.

Litigation and licensing landscape

Currently, no known litigations are associated with JP2021193091. However, competitors may compare the claims with existing patented compounds to evaluate freedom-to-operate. Licensing activity or collaborations may develop if the compound proves efficacy in clinical testing.

Innovation and freedom-to-operate considerations

  • The patent claims a specific subclass within a broad chemical class.
  • The territory filing strategy covers Japan, the US, and China, suggesting an intention for regional commercialization.
  • Overlap with existing patents, especially in the US and Europe, requires careful analysis for potential infringement or design-around strategies.

Key Takeaways

  • JP2021193091 claims a targeted chemical class for pharmaceutical use, with moderate claim breadth.
  • Its scope covers compounds, their methods of synthesis, and specific medical uses, primarily centered on CNS or metabolic diseases.
  • The patent strategy aligns with global efforts, particularly in jurisdictions with active neuropharmaceutical development.
  • Competitors will analyze existing patents with similar structures to assess infringement risks or opportunities for design-around.

FAQs

1. Does JP2021193091 cover a specific drug candidate?
The patent appears to claim a class of compounds rather than a single molecule, suggesting it covers multiple derivatives potentially used as drug candidates.

2. What diseases are targeted by this patent?
Likely neurological or metabolic disorders such as depression, Parkinson’s disease, or diabetes, inferred from the claims and prior art.

3. How does the patent compare to similar filings internationally?
It is similar in scope to patents filed in the US and China, but claims are more narrow than some broad chemical class patents granted elsewhere.

4. Can the claims be easily circumvented?
Potentially, by modifying substituents within the scope of the claims or by focusing on different chemical scaffolds not covered in the claims.

5. What is the strategic significance of this patent?
It secures intellectual property rights within Japan, providing a barrier to competitors while supporting global patent filings in alignment with the company’s R&D pipeline.


References

  1. Japan Patent Office (JPO). (2022). Patent application publications. Retrieved from https://www.jpo.go.jp
  2. World Intellectual Property Organization. (2022). Patent landscape reports.
  3. U.S. Patent and Trademark Office. (2022). Patent search database.
  4. European Patent Office. (2022). Patent data and landscape analysis.
  5. China National Intellectual Property Administration. (2022). Patent filings and sectors.

[1] Japan Patent Office. (2022). Patent application publications.
[2] WIPO. (2022). Patent Landscape Reports.
[3] USPTO. (2022). Patent Search Database.
[4] EPO. (2022). European Patent Data.
[5] CNIPA. (2022). Patent Application Analysis.

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