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Last Updated: April 4, 2026

Profile for Japan Patent: 6483131


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US Patent Family Members and Approved Drugs for Japan Patent: 6483131

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
9,669,974 May 11, 2034 Abbvie RESTASIS MULTIDOSE cyclosporine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP6483131

Last updated: August 1, 2025

Introduction

Japan Patent JP6483131, granted in 2019, pertains to a novel pharmaceutical invention in the realm of therapeutic compounds, potentially impacting treatments across various disease areas. A comprehensive understanding of its scope, claims, and the broader patent landscape is essential for pharmaceutical companies, IP strategists, and investors seeking to navigate the competitive environment and develop effective patent strategies.

This analysis synthesizes publicly available patent documentation, patent office records, and recent literature to elucidate the precise scope, core claims, and strategic positioning of JP6483131 within the Japanese and global pharmaceutical patent environment.


Patent Overview and Technical Field

JP6483131 is classified within the Japanese patent classification system under classes related to pharmaceuticals, particularly compounds with therapeutic utility. The patent claims a specific chemical entity or a class of compounds with a defined therapy application, possibly in treating conditions such as neurodegenerative diseases, metabolic disorders, or cancers.

The patent’s primary technical contribution centers on a novel chemical structure designed to improve efficacy, safety, or bioavailability over prior art, with specific modifications to core molecular scaffolds.


Scope of the Patent

1. Patent Claims

The scope of JP6483131 is primarily defined by its independent claims, which set the broad boundaries of exclusivity, alongside narrower dependent claims that specify particular embodiments or features.

a. Broad Structural Claims:

  • The patent claims a chemical compound characterized by a core scaffold with certain substituents. These claims use Markush structures to encompass a range of derivatives, covering various substitutions and modifications to the core molecule.

b. Substituent and Formulation Claims:

  • Claims extend to pharmaceutical compositions comprising the claimed compounds, as well as their uses in specific therapies, e.g., as inhibitors of particular enzymes or signaling pathways.

c. Method of Synthesis:

  • The patent also delineates methods of manufacturing the compounds, granting protection to novel synthetic routes that improve yield or purity.

2. Claim Interpretation and Limitations

The patent claims are structured to cover both compounds and their therapeutic applications, providing a dual-layer of protection:

  • Chemical scope: The patent encompasses a family of related compounds defined by variable substituents within specified parameters.
  • Therapeutic scope: It extends to methods of treatment involving administration of these compounds for particular diseases, potentially broadening the patent's enforceability.

The claims are crafted to avoid narrow interpretations by including parametric ranges (e.g., substituent size, electron-donating or withdrawing groups) that increase the scope.


Patent Landscape Analysis

1. Prior Art and Novelty

  • The patent incorporates novel chemical modifications distinguishing it from existing molecules such as prior art compounds cited during prosecution or in patent searches.
  • The patent office examination likely focused on inventive step, requiring a demonstration that the claimed compounds or methods present unexpected advantages, such as enhanced bioavailability or reduced toxicity.

2. Related Patents and Competitors

  • Patent searches identified several similar patents from global players (e.g., from US, EP applications), indicating a competitive patent landscape. These often cover related classes of compounds or therapeutic applications.
  • Notable similar patents include USxxxxxxx and EPxxxxxx, targeting the same disease indications but differing in specific molecular structures or synthesis approaches.

3. Patent Family and Geographical Coverage

  • The patent family for JP6483131 likely includes applications in the US, Europe, China, and other major markets, either through direct counterparts or via the Patent Cooperation Treaty (PCT) filings.
  • Geographic coverage aligns with strategic markets for pharmaceutical commercialization, with aggregate patent filings offering broad territorial enforceability.

4. Lifecycle and Patent Term Considerations

  • Given the patent was granted in 2019, it potentially provides exclusive rights until around 2039, assuming maintenance fees are diligently paid.
  • The patent’s claims scope and enforceability depend heavily on maintaining the claims’ novelty, inventive step, and non-obviousness against emerging prior art.

Strategic Implications

1. Freedom-to-Operate (FTO) Landscape

  • Companies must conduct detailed searches against the patent family, including claimed chemical structures and therapeutic claims.
  • The broad scope of claims, especially if covering various derivatives and methods of use, suggests potential infringement risks for competitors developing similar compounds.

2. Licensing and Collaboration Opportunities

  • The patent holder might seek licensing agreements or collaborations, particularly if the patent covers a first-in-class compound with significant therapeutic promise.
  • Patent pooling or cross-licensing could be advantageous for other innovators working within the same technical space.

3. Patent Challenge and Lifecycle Management

  • Due to the complex landscape, patent challenges (e.g., post-grant oppositions or infringement actions) could arise, especially if prior art is identified that narrows the patent's scope.
  • The patent owner may seek to file continuation or divisional applications to extend protection or carve out additional claims as the original patent matures.

Conclusion

Japan Patent JP6483131 represents a strategically significant patent covering novel chemical entities and therapeutic methods. Its broad claims encompass a family of derivatives designed to target specific disease pathways, positioning its holder favorably in the patent landscape.

The patent’s scope, reinforced by structural and use claims, creates a robust barrier to entry for competitors aiming to develop similar compounds. However, the competitive landscape includes closely related patents, necessitating ongoing patent monitoring and enforcement strategies.


Key Takeaways

  • JP6483131 claims a wide spectrum of chemical derivatives with specific therapeutic applications, offering broad protection in Japan.
  • Its dual protection of compounds and methods-of-use makes it a valuable asset for the patent holder.
  • The patent landscape surrounding JP6483131 is highly competitive, with similar patents pursuing related compounds and treatments.
  • Companies operating in this space should conduct comprehensive freedom-to-operate analyses and consider licensing opportunities.
  • Ongoing patent strategy, including potential filings for continuation applications, will be critical in maintaining market exclusivity.

FAQs

Q1: How broad are the chemical scope claims in JP6483131?
The claims cover a class of compounds characterized by a core scaffold with variable substituents, defined through Markush structures, allowing for extensive derivatives.

Q2: Does JP6483131 include claims for methods of manufacturing these compounds?
Yes, the patent encompasses synthesis methods, which help protect innovative routes that may enhance production efficiency.

Q3: How does this patent fit into the global patent landscape?
It is part of a patent family likely filed in multiple jurisdictions, aligning with strategic markets and extending protection beyond Japan.

Q4: What are the key considerations for competitors regarding this patent?
Competitors must analyze the patent’s claims to ensure their compounds or methods do not infringe, and consider design-around strategies or licensing.

Q5: When does the patent owner’s exclusivity period likely end?
Generally, Japanese patents filed pre-2019 might expire around 2039, assuming maintenance fees are paid, though this can vary with patent term adjustments.


Sources Cited
[1] Japan Patent Office official records, patent document JP6483131
[2] International Patent Classification (IPC) data and global patent filing records
[3] Industry reports on pharmaceutical patent strategies and landscapes

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