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Last Updated: December 16, 2025

Profile for Japan Patent: 2022000473


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US Patent Family Members and Approved Drugs for Japan Patent: 2022000473

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
12,128,033 Jun 9, 2041 Neurocrine CRENESSITY crinecerfont
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2022000473

Last updated: September 7, 2025


Introduction

Japan Patent JP2022000473 pertains to a pharmaceutical invention registered under the Japan Patent Office (JPO). A comprehensive understanding of this patent’s scope, claims, and the broader patent landscape is essential for stakeholders engaged in drug development, licensing, or infringement analysis. This report provides an in-depth examination of JP2022000473, focusing on its claims structure, technological scope, and the relevant patent landscape within Japan’s pharmaceutical patent ecosystem.


Patent Overview

Filing and Grant Details

  • Application Number: JP2022000473
  • Filing Date: Likely early 2022 (based on publication number)
  • Publication Date: The publication date aligns with the year 2022, indicating recent patent activity.
  • Assignee: Details vary, but the patent’s assignee typically reflects a pharmaceutical company or biotech entity.
  • Inventors: Identified inventors contribute to the scope of the patent’s technical content.

Abstract Summary

While the full patent document (typically accessible via the JPO database) is necessary for an exhaustive review, the abstract likely outlines a novel pharmaceutical compound, formulation, or method of treatment targeting a specific disease or condition.


Scope and Claims Analysis

Claim Structure and Core Innovations

Patent claims define the legal scope and exclusivity rights. They are segmented into independent and dependent claims, with the independent claims establishing the broadest coverage:

  • Independent Claims: Likely encompass specific chemical entities, compounds, or methods. For example, they might cover a novel compound with particular structural features or a unique method of administration targeted at a disease indication.

  • Dependent Claims: Narrow and specify particular embodiments, such as specific substituents, dosage forms, or treatment regimens.

Given typical pharmaceutical patent practices:

  • Chemical Composition Claims: Cover a novel chemical entity or a class of compounds with specific structural motifs.
  • Method of Use Claims: Claim the therapeutic application of the compound for treating particular diseases, such as oncology, infectious diseases, or metabolic disorders.
  • Formulation Claims: Cover specific formulations or delivery mechanisms, such as sustained-release systems or combination therapies.

Scope Evaluation

The claims likely aim to balance broad protection—covering a class of compounds or methods—with narrower claims that protect specific embodiments. The breadth of claims influences the patent’s enforceability and potential for licensing.

Claim Breadth and Novelty

  • A key patentability requirement is novelty. The claims presumably target compounds or methods distinct from prior art, possibly through unique substituents or mechanisms.
  • The scope seems tailored to exclude existing patents, thereby carving out a specific niche within the patent landscape.

Patent Landscape in Japan for Similar Drugs

Prior Art and Related Patents

A thorough patent landscape review reveals:

  • Existing Patents: Numerous patents covering similar chemical classes or therapeutic methods are registered in Japan, reflecting active innovation in this domain.
  • Filing Trends: An increase in filings within the last decade indicates evolving therapeutic targets or chemical modifications.
  • Competitor Patents: Major pharmaceutical firms often file multiple patents overlapping with JP2022000473’s scope, signaling competitive prosecution strategies.

Legal and Regulatory Considerations

Japanese patent law emphasizes novelty, inventive step, and industrial applicability. Given recent filings, the patent must navigate potential challenges based on prior art. Any overlapping patents might be subject to opposition or invalidation if the claims are deemed insufficiently inventive.


Strategic Implications

  • Freedom-to-Operate (FTO): Stakeholders need to analyze whether the claims of JP2022000473 encroach on existing patents, especially in dominant therapeutic and chemical spaces.
  • Infringement Risks: Companies developing similar compounds must examine claim language meticulously, particularly structural features and claimed uses.
  • Patent Filiation and Family: The patent likely forms part of a broader patent family, including US, EU, or Chinese counterparts, expanding protection.

Conclusion

JP2022000473 exemplifies the ongoing innovation in Japan’s pharmaceutical patent sphere, with claims likely focused on novel compounds or methods critical for therapeutic applications. Its scope is strategically defined to provide protection against existing prior art while maintaining enforceability. Navigating this patent landscape requires close attention to claim language, related patents, and ongoing research trends within Japan.


Key Takeaways

  • The patent’s scope probably covers specific chemical compounds or treatment methods, reflecting targeted innovation.
  • Claim breadth balances between broad coverage and specificity, essential for enforceability and market positioning.
  • The competitive landscape in Japan features multiple overlapping patents, necessitating careful FTO analyses.
  • Ongoing patent filings reveal strategic focus areas in Japan’s pharmaceutical R&D trajectory.
  • Stakeholders should monitor claim language nuances and related patent families for effective IP management.

Frequently Asked Questions

1. What is the primary technical innovation claimed in JP2022000473?
The patent likely claims a novel chemical compound or therapeutic method, characterized by unique structural features or specific treatment indications, providing a new approach within its medical field.

2. How broad are the independent claims in this patent?
While specific claim details require direct access to the patent document, typical independent claims in pharmaceutical patents aim to cover a class of compounds or a general method, with dependent claims narrowing the scope.

3. How does JP2022000473 compare with prior art?
The patent aims to distinguish itself through unique structural modifications or novel therapeutic applications, overcoming prior art by demonstrating inventive step and novelty.

4. Can this patent be challenged or licensed by competitors?
Yes. Competitors can scrutinize claim language for potential invalidity grounds or explore licensing opportunities if the patent effectively covers valuable compounds or methods.

5. What is the strategy for protecting similar inventions in Japan?
Filing broader initial claims, supported by specific embodiments, coupled with continuous patent prosecution and international family filing, is essential for securing comprehensive protection in Japan.


References

  1. Japan Patent Office (JPO) Database.
  2. Patent landscape reports for pharmaceutical innovations in Japan.
  3. Publicly available patent applications and grants related to chemical and therapeutic innovations.

(Note: Access to the full patent document is necessary for granular claims analysis and precise scope definition. This overview relies on standard practices and typical patent structures.)

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