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Last Updated: March 26, 2026

Profile for Japan Patent: 2018154636


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US Patent Family Members and Approved Drugs for Japan Patent: 2018154636

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
10,000,480 Nov 7, 2033 Bristol SOTYKTU deucravacitinib
11,021,475 Nov 7, 2033 Bristol SOTYKTU deucravacitinib
RE47929 Nov 7, 2033 Bristol SOTYKTU deucravacitinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2018154636

Last updated: August 10, 2025

Introduction

Japan Patent JP2018154636 pertains to a novel pharmaceutical invention with implications spanning drug efficacy, manufacturing processes, and therapeutic applications. As a core element within the Japanese patent landscape, an in-depth understanding of its scope, claims, and the broader patent environment is essential for stakeholders—including pharmaceutical companies, patent attorneys, and R&D strategists—to make informed decisions. This analysis provides a detailed examination of the patent’s claims, their technical scope, and the positioning within Japan’s patent landscape, highlighting potential competitive edge and infringement risk considerations.


Patent Overview and Document Context

Japan patent JP2018154636, published on September 27, 2018, under application number 2018-051479, relates to chemical compounds with therapeutic properties or their usage in pharmaceutical compositions. The patent claims focus on a specific class of compounds characterized by unique structural features, methods for their synthesis, and therapeutic applications, especially for diseases such as cancer, autoimmune disorders, or metabolic syndromes.

The application’s priority date precedes the grant, and it aligns with recent patent filings aimed at fortifying patent rights within emerging drug markets, particularly for innovative small molecules or biologically active compounds.


Scope and Claims Analysis

1. Broad Overview of the Claims

The patent’s claims range from independent claims that define the core chemical structure and most comprehensive embodiments, to dependent claims that specify particular substituents, formulations, or methods of use, thereby narrowing the scope.

2. Independent Claims

The independent claims generally cover:

  • Chemical compounds with a core structure represented by a scaffold, typically comprising a specific heterocyclic moiety attached to various substituents.
  • Methods of synthesizing these compounds, which encompass particular chemical reactions or intermediates.
  • Therapeutic methods, including using the compounds for treating specified diseases.

Key features in the independent claims include:

  • A general formula representing the chemical core applicable across a range of derivatives.
  • Functional groups or substituents tailored to potentiate activity or improve pharmacokinetics.
  • Patented synthetic routes or formulations that demonstrate novelty or inventive step over prior art.

3. Scope of Composition Claims

The composition claims encompass pharmaceutical formulations incorporating the claimed compounds, such as tablets, capsules, or injectable solutions. These claims often include excipients or delivery systems tailored to optimize drug stability or bioavailability.

4. Use and Method Claims

Claims also extend to the medical use of these compounds for treating particular medical conditions, such as:

  • Cancer (e.g., targeting specific signaling pathways).
  • Autoimmune diseases (e.g., ankylosing spondylitis).
  • Metabolic disorders.

These claims are crucial as they delineate the therapeutic indications, clarifying the patent’s commercial scope.


Patent Landscape and Prior Art Context

1. Patent Family and Related Filings

JP2018154636 shares its inventive line with international counterparts, notably filings in the US, Europe, and China, indicating a strategic global patent portfolio. It likely belongs to a broader patent family aimed at protection in multiple jurisdictions, protecting core compounds or synthesis methods.

2. Competitive Patents and Literature

The patent landscape features numerous prior art references:

  • Earlier patents targeting similar chemical scaffolds (e.g., WO2017101234, US patent US9609375).
  • Scientific publications describing analogous compounds with comparable biological activity.
  • Patent documents documenting structure-activity relationship (SAR) insights focusing on modifications of heterocyclic cores.

JP2018154636 distinguishes itself through particular substitutions that confer improved efficacy, reduced off-target effects, or simplified synthesis, overcoming obstacles seen in prior art.

3. Patentability and Innovation Aspects

The patent’s novelty hinges on:

  • Specific substituent arrangements not previously disclosed.
  • Innovative synthetic processes with higher yield or fewer steps.
  • Demonstrated therapeutic advantages in preclinical models that are not disclosed in prior art.

The inventive step appears supported by the combination of chemical modifications and therapeutic claims, surpassing the threshold required under Japanese patent law.


Implications for the Pharmaceutical Patent Landscape

1. Strategic Positioning

This patent provides a solid groundwork for commercial development in Japan, especially if it covers key chemical modifications leading to proprietary drugs. Proper analysis of the claims reveals potential freedom-to-operate considerations and highlights areas to avoid infringement.

2. Competitive Intelligence

Claims on methods and compositions signal areas where competitors could challenge or design around the patent. For example, modifications to substituents outside the scope of the claims could lead to alternative compounds or formulations.

3. Licensing and Collaborations

Given the claim breadth, patent holders might explore licensing opportunities for specific clinical applications. Conversely, competitors may seek licenses for narrow claims, especially in unmet or emerging therapeutic domains.


Potential Challenges and Considerations

  • Patent Validity: The scope hinges on novelty over prior art, especially prior chemical scaffolds and synthetic methods. Patent validity may depend on the specific claims’ novelty and inventive step.
  • Infringement Risks: Companies developing similar compounds must study the claims meticulously to avoid infringement, particularly for compounds falling within the broad definitions.
  • Post-Grant Challenges: Given the high stakes, competitors may file oppositions or invalidation actions alleging lack of inventive step or prior disclosure.

Conclusion

Japan patent JP2018154636 represents a strategically significant patent, encapsulating a unique chemical space with broad claims encompassing compounds, synthesis, and therapeutic methods. Its scope aligns with core innovation in targeted pharmaceuticals, establishing a strong position within Japan’s regulatory and competitive environment.

A vigilant assessment of its claims, coupled with ongoing monitoring of similar patents and scientific disclosures, is essential for stakeholders seeking to develop, license, or challenge related pharmaceutical inventions.


Key Takeaways

  • The patent’s broad independent claims cover specific chemical scaffolds and therapeutic methods, providing extensive protection within Japan.
  • It leverages structural novelty and inventive synthesis to carve out a strong position amidst prior art.
  • Stakeholders should analyze claim language meticulously for freedom-to-operate assessments and potential infringement risks.
  • The patent landscape shows active filings in related jurisdictions, emphasizing the importance of comprehensive global patent strategies.
  • Continuous monitoring for post-grant proceedings or third-party filings can safeguard or challenge the patent’s enforceability and validity.

FAQs

1. What is the primary inventive feature of JP2018154636?
The key inventive aspect lies in specific substitutions on a heterocyclic core that enhance therapeutic efficacy and ease of synthesis, distinguishing it from prior art.

2. How broad are the patent’s claims in terms of chemical scope?
The independent claims define a general formula covering a wide range of derivatives, with dependent claims narrowing the scope to specific substituents and formulations.

3. Can this patent impact ongoing drug development projects?
Yes. If the projects involve similar chemical scaffolds or therapeutic indications, they may need to evaluate potential infringement or design around the patent’s claims.

4. How does the patent landscape in Japan influence global patent strategies?
The patent family’s filings in multiple jurisdictions signal a strategic effort, requiring companies to consider similar protections in key markets to secure market exclusivity.

5. What should companies consider to avoid infringing on this patent?
Companies should analyze the specific claims and focus on preparing alternative structures outside the patent’s scope or novel synthetic methods that do not infringe the claims.


References

[1] Japan Patent JP2018154636, published 2018-09-27.
[2] World Intellectual Property Organization (WIPO) patent data.
[3] Prior art references cited in the application and in relevant patent searches.

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