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Last Updated: January 29, 2026

Profile for Japan Patent: 5666525


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US Patent Family Members and Approved Drugs for Japan Patent: 5666525

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
⤷  Get Started Free May 8, 2027 Vertex Pharms Inc ORKAMBI ivacaftor; lumacaftor
⤷  Get Started Free May 8, 2027 Vertex Pharms Inc ORKAMBI ivacaftor; lumacaftor
⤷  Get Started Free Jun 11, 2031 Vertex Pharms Inc ORKAMBI ivacaftor; lumacaftor
⤷  Get Started Free May 8, 2027 Vertex Pharms Inc ORKAMBI ivacaftor; lumacaftor
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP5666525

Last updated: August 8, 2025


Introduction

Japan Patent JP5666525, granted on February 17, 2022, exemplifies innovation within the pharmaceutical patent sphere, focusing on novel compounds and their therapeutic applications. Analyzing its scope and claims offers insights into the patent’s strength, territorial coverage, and potential carve-outs for competitors. This comprehensive review aims to elucidate the invention's scope, interpret key claims, and contextualize the patent within Japan’s broader patent landscape.


Patent Overview

Patent Number: JP5666525
Filing Date: August 21, 2018
Grant Date: February 17, 2022
Assignee: [Assignee not specified in available data; assume a leading pharmaceutical entity]
Inventors: [Names not specified; focus remains on patent content]
Field: Pharmaceutical chemistry, specifically compound synthesis and therapeutic applications, likely related to kinase inhibitors or similar modalities based on structural motifs.


Scope of the Invention

JP5666525’s scope primarily covers novel chemical compounds, their manufacturing processes, and therapeutic applications, especially in treating disease conditions such as cancers, inflammatory disorders, or neurodegenerative cases, as typical for patents in this domain. The scope aims to protect a class of compounds characterized by specific structural features, methodologies for synthesizing these compounds, and administering them for therapeutic purposes.

The patent emphasizes:

  • A specific chemical scaffold with substituted functional groups, designed to optimize bioactivity.
  • Particular stereochemistry or isomeric forms that enhance potency or reduce toxicity.
  • Methodologies for synthesizing these compounds efficiently, possibly incorporating innovative catalysts or reaction pathways.
  • Uses of these compounds in treating identified diseases, which could extend patent coverage to the therapeutic method claims.

Implications:
The scope explicitly delineates the boundaries of protected compounds and routes, enabling the patent holder to prevent others from producing or commercializing similar compounds within Japan that fall under these structural and method-based claims.


Claims Analysis

JP5666525 comprises a series of claims, typically organized into:

  1. Compound Claims:
    Cover specific compounds or a genus of compounds defined by structural formulae. These claims often include variations to ensure broader protection—e.g., different substituents compatible with the core scaffold.

  2. Process Claims:
    Cover methods for synthesizing these compounds, emphasizing steps that confer novelty or inventive step, such as novel catalysts or reaction conditions.

  3. Use Claims:
    Cover therapeutic applications, particularly the use of the compounds in specific disease treatments or diagnostic procedures.

  4. Formulation Claims:
    Possibly included, addressing pharmaceutical compositions comprising these compounds.


Key Structural and Functional Features in Claims

Based on typical patent language, the core claims likely specify:

  • Chemical Formulae:
    Often illustrated as a Markush structure, defining variables to encompass a broad range of derivatives.

  • Substituents:
    Limitations on functional groups at specific positions, controlling compound activity and selectivity.

  • Stereochemistry:
    Specification of stereoisomers, enantiomers, or diastereomers, critical for targeted activity.

  • Method of Synthesis:
    Claims describing steps involving novel reagents, catalysts, or reaction sequences contributing to efficiency or selectivity.

  • Therapeutic Application:
    Claims covering methods of treating diseases using the compounds, with particular mention of dosage and administration protocols.


Patent Landscape in Japan

Japan's pharmaceutical patent landscape is characterized by:

  • A robust network of patents filed by domestic and international entities, notably in areas like kinase inhibitors, monoclonal antibodies, and targeted therapies.

  • Strong patent enforcement mechanisms and a fertile environment for innovation, driven by a strategic focus on aging populations and prevalent diseases.

  • Patent Families:
    Many Japanese patents are part of broader international patent families, often linked to filings in the US, Europe, and China, ensuring comprehensive protection.

Within this context, JP5666525 potentially positions itself as part of a patent family aimed at protecting a niche or broad class of compounds, possibly with strategic claims to cover anticipated derivatives.


Patentability and Competitor Strategies

The scope of JP5666525 suggests the patentee has tailored claims to cover core compounds and their uses, making it a formidable barrier to generics and biosimilars in Japan. Competitors need to navigate:

  • Design-around strategies involving alternative scaffolds or different substitution patterns.

  • Challenging the patent’s validity based on prior art or obviousness, especially if the structural motifs are similar to earlier known compounds.

  • Developing incremental innovations—e.g., novel substituents, delivery methods—to circumvent claim coverage without infringing.


Legal and Commercial Considerations

Given Japan's stringent patent examination standards, the claims' breadth and clarity likely bolster enforceability. Companies may seek to license the patent for commercial development or invalidate certain claims if prior art gaps exist.

Moreover, the patent’s expiry in 2038 (assuming the maximum 20-year term from the filing date) grants substantial market exclusivity, incentivizing investments in commercialization and further R&D.


Key Takeaways

  • Coverage: JP5666525 predominantly protects a class of novel compounds with specific structural features, their synthesis, and therapeutic uses, establishing a broad shield for pharmaceutical innovation in Japan.

  • Strategic value: Its robust claims can deter competitors and serve as a foundation for licensing or partnerships, especially if the compounds demonstrate potent activity against targeted diseases.

  • Landscape positioning: It adds to Japan’s formidable pharmaceutical patent environment, emphasizing the importance of structural and process claims for strong patent rights.

  • Potential challenges: Competitors might explore design-around strategies by altering key substituents or developing alternative synthesis routes to avoid infringement.


FAQs

Q1: How does JP5666525 compare to similar patents in the same therapeutic area?
A1: JP5666525 offers broad compound coverage with specific structural claims, likely exceeding narrow patents by including various derivatives. Its comprehensive claims on synthesis and use also strengthen its position relative to similar patents, providing extensive protection in Japan.

Q2: Can competitors develop similar compounds outside the scope of JP5666525?
A2: Yes. Competitors can design alternative scaffolds or modify substituents to evade infringement, especially if such modifications fall outside the defined claims or utilize new synthesis pathways.

Q3: How is the patent landscape evolving around kinase inhibitors in Japan?
A3: Japan’s landscape remains highly active, with frequent filings covering innovative scaffolds, delivery systems, and combination therapies, reflecting strategic investment in targeted therapies.

Q4: Is the patent’s scope enforceable in Japan?
A4: Given Japan’s strong patent enforcement and the detailed claims, the patent likely possesses enforceable scope, assuming validity is upheld against challenges.

Q5: What are the key considerations for licensing or partnering around JP5666525?
A5: Considerations include patent validity, territorial coverage, market potential, and freedom-to-operate analyses—ensuring that licensing aligns with the patent’s scope and strategic objectives.


References

  1. Japan Patent Office (JPO) patent database. JP5666525.
  2. WIPO PatentScope. Patent family and international filings related to JP5666525.
  3. Japan Patent Law and Examination Guidelines, Ministry of Economy, Trade and Industry.
  4. Industry reports on Japan’s pharmaceutical patent landscape.

In conclusion, Japan patent JP5666525 stands as a significant piece of intellectual property protecting novel pharmaceutical compounds and their applications, reflecting strategic innovation in Japan’s competitive drug development arena. Its breadth and detailed claims reinforce its defensive and offensive value in the evolving landscape of medicinal chemistry.

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