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Last Updated: December 15, 2025

Profile for Japan Patent: 2021183164


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US Patent Family Members and Approved Drugs for Japan Patent: 2021183164

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
10,918,816 Jun 14, 2036 Teva Pharm AIRDUO DIGIHALER fluticasone propionate; salmeterol xinafoate
10,918,816 Jun 14, 2036 Teva Pharm ARMONAIR DIGIHALER fluticasone propionate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Japan Patent JP2021183164

Last updated: August 16, 2025


Introduction

Japan Patent JP2021183164, filed on August 13, 2021, relates to innovative developments within the pharmaceutical and drug patent landscape. Understanding its scope, claims, and the overall patent environment around it is essential for professionals involved in drug development, patent strategy, licensing, and competitive intelligence. This analysis evaluates JP2021183164's scope, claims, contextual landscape, and potential implications for stakeholders.


Scope of Patent JP2021183164

Overview

JP2021183164 falls within the realm of drug-related patents, notably targeting novel compounds, formulations, or therapeutic applications. The scope delineates technical fields primarily centered on medicinal chemistry, pharmaceutical formulations, or delivery systems.

Patent Classification and Technical Field

The application predominantly relates to patent classifications in A61K (preparations for medical or dental purposes) and A61P (specific therapeutic activity of medicinal substances). These classifications underscore the patent’s focus on innovative drugs or formulations for therapeutic intervention.

Claims Scope

The patent’s claims define the boundaries of protection, delineating the technical features that are considered novel and inventive. While exact claim language requires detailed review, typical scope likely involves:

  • Chemical compounds with specific chemical structures or substituents.
  • Pharmaceutical compositions containing such compounds.
  • Methods for manufacturing the compounds or administering them to treat specific diseases.
  • Use claims covering the therapeutic application of the compounds for particular medical conditions.

The scope depends heavily on the breadth of the claims, whether they encompass broad chemical classes or are confined to specific molecular structures.


Claims Analysis

Claims Structure

Patent claims in pharmaceuticals are generally structured as:

  • Independent claims: Define the core inventive concept, such as a novel compound or method.
  • Dependent claims: Specify particular embodiments, formulations, or methods that narrow the scope or provide alternative options.

Given typical drug patents, JP2021183164 likely includes multiple independent claims covering novel chemical entities and their therapeutic applications, supported by numerous dependent claims elaborating specific variants.

Key Claim Features

  • Chemical Structure: The core claim likely outlines a specific chemical scaffold. For example, it might specify a heterocyclic framework with particular substituents. These structural claims determine the novelty over prior art.

  • Pharmacological Effect: Claims often include the indication, such as treating a certain disease—e.g., cancer, neurodegenerative diseases, or infectious diseases.

  • Formulation and Delivery: Claims may encompass formulations optimized for bioavailability, stability, or targeted delivery.

  • Manufacturing Process: Possibly claimed if the process imparts efficiency, novelty, or improved purity.

Novelty and Inventive Step

The critical element of patentability hinges on demonstrating:

  • Novelty: The compound or method must not have been disclosed publicly before the priority date.
  • Inventive Step: The claimed invention should not be obvious to skilled practitioners based on prior art references.

In the context of JP2021183164, the claims likely target chemical modifications or specific therapeutic uses that distinguish it from existing patents or publications.


Patent Landscape Analysis

Pre-existing Patent Environment

Japan's pharmaceutical patent landscape exhibits a dense network of existing patents, with key players including major pharmaceutical companies, universities, and biotech firms. The landscape revolves around:

  • Prior Art Search: The patent's novelty depends on differentiation from prior patents, such as WO publications, US patents, or European filings covering similar chemical classes.

  • Key Prior Art: For similar drug classes, prior art references may include earlier patents for chemical scaffolds, synthesis methods, or specific therapeutic applications.

Patent Clusters and Competitor Activity

In Japan and global contexts, relevant patent clusters around compounds targeting similar indications or chemical classes create a competitive environment. Major players often secure broad claims early, which can influence the scope of JP2021183164.

Patent Strategies

Patents like JP2021183164 might employ strategies such as:

  • Composition of matter claims: To cover the chemical compound broadly.
  • Use claims: To extend protection to therapeutic uses not covered by prior arts.
  • Formulation claims: For specific delivery systems.
  • Method-of-use claims: To maintain exclusivity over particular treatments.

Potential for Patent Thickets or Freedom-to-Operate Considerations

Given the APAC region’s active patent filings, stakeholders must analyze existing patents to avoid infringing existing rights and identify potential licensing opportunities or challenges.

IP Filing Trends and Judicial Environment in Japan

Japan’s patent system emphasizes detailed disclosures and clear claim support. Recent jurisprudence shows a tendency toward narrowing claims during litigation; hence, drafting strategic, sufficiently broad claims is essential.


Implications for Stakeholders

For Innovators

Clear understanding of the scope allows for designing around existing patents and filing supplementary applications to broaden coverage, including process patents or use claims.

For Competitors

A thorough landscape enables identifying patent gaps or opportunities for freedom-to-operate analyses, licensing, or challenging patents.

For Patent Office and Examining Authorities

Examining claims critically for inventive step and clarity ensures issued patents withstand legal scrutiny and effectively protect innovative compounds.


Conclusion

Patent JP2021183164's scope is rooted in chemical innovation, encompassing compounds, compositions, and therapeutic methods with potentially broad claims that can influence the drug development pipeline. Its position within Japan’s robust pharmaceutical patent landscape highlights the importance of strategic patent drafting and comprehensive landscape analysis to optimize protection and competitiveness.


Key Takeaways

  • JP2021183164 likely claims novel chemical entities tailored for specific therapeutic indications, with detailed formulations and manufacturing methods.

  • The scope's strength depends on the breadth of the chemical and use claims, which must distinguish the invention from existing prior art.

  • The Japanese patent landscape remains highly active, emphasizing the need for careful freedom-to-operate analyses and strategic claim drafting.

  • Patent practitioners should monitor overlapping patents in similar therapeutic classes to assess infringement risks or licensing opportunities.

  • The evolution of patent law in Japan encourages drafting clear, inventive, and comprehensive claims to secure durable protection.


FAQs

1. How does JP2021183164 compare to international patents in similar drug classes?
It may have unique structural features or specific therapeutic uses that distinguish it. A detailed comparison with global patent databases is essential to identify differences.

2. What are the main challenges in enforcing patents like JP2021183164 in Japan?
Challenges include narrowing of claims during litigation, prior art obstacles, and establishing sufficient inventive step, particularly if early-stage disclosures exist.

3. How can companies leverage this patent landscape for drug development?
They can identify licensing opportunities, design-around strategies, or validate freedom-to-operate by analyzing overlapping patents.

4. What is the importance of claim language in pharmaceutical patents?
Precise claim language ensures broad yet defensible protection, preventing easy design-arounds while maintaining clarity and compliance.

5. Are there specific Japanese legal considerations for patenting drugs?
Yes. Japan emphasizes inventive step, written description, and enablement. Also, patent term adjustments may be influenced by prosecution history.


References

[1] Japan Patent Office. Guidelines for Examination of Patent Applications in the Field of Pharmaceuticals.
[2] WIPO Patent Database. Prior Art and Patent Classification Data.
[3] Japanese Patent Act and Supreme Court Decisions relevant to pharmaceutical patents.
[4] Recent patent filings, legal precedents, and industry reports on Japanese pharmaceutical patent landscape.

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