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Last Updated: December 29, 2025

Profile for Japan Patent: 6437119


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US Patent Family Members and Approved Drugs for Japan Patent: 6437119

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
10,220,023 Dec 10, 2035 Vanda Pharms Inc PONVORY ponesimod
12,336,980 Dec 10, 2035 Vanda Pharms Inc PONVORY ponesimod
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP6437119

Last updated: August 9, 2025


Introduction

Japan Patent JP6437119 pertains to a pharmaceutical invention designed to enhance therapeutic efficacy, stability, or administration of a specific drug. As part of an ongoing effort to understand the competitive patent landscape within the Japanese pharmaceutical sector, a comprehensive review of JP6437119—its scope, claims, and patent environment—is essential. This analysis aims to elucidate the patent's intellectual property boundaries, its strategic importance, and its positioning relative to existing patents within Japan's robust pharmaceutical patent landscape.


Patent Overview

Publication Details:

  • Patent Publication Number: JP6437119
  • Application Filing Date: The specific date requires access to the patent database (assumed pre-2014 based on publication number convention)
  • Grant Date: The patent was granted in Japan, securing exclusive rights in Japan’s pharmaceutical market.

Assignee and Inventors:

  • Assignee information and inventor details provide insight into the strategic corporate or institutional interests—often key to understanding patent strength and potential infringement risks.

Title and Abstract:

  • The title likely references a pharmaceutical composition or method of treatment involving the specific drug, which can range from chemical compounds, formulations, or therapeutic methods.

Scope of the Patent

Legal Scope and Breadth Analysis:
The scope of JP6437119 is primarily determined by its claims. The claims delineate the legal boundaries indicating what is protected and what is not.

  • Independent Claims:
    These usually define the core invention, likely covering a specific pharmaceutical composition, method of preparation, or method of administration.
  • Dependent Claims:
    These narrow the scope, detailing specific embodiments, concentrations, nPl formulations, or treatment protocols.

Scope Considerations:

  • Chemical Composition Claims:
    If the patent covers a novel chemical entity, the claims may include specific structures, substitutions, or stereochemistry.
  • Method Claims:
    Covering particular treatment protocols or administration methods.
  • Formulation Claims:
    Including excipients, carriers, or delivery systems that enhance stability or bioavailability.

Limitations:

  • The scope is influenced by prior art; claims must demonstrate novelty and inventive step beyond existing patents or publications.
  • The claims' breadth may be constrained by the description and experimental data provided in the patent specification.

Claims Analysis

Claim Structure and Focus:
Claims in JP6437119 likely encompass:

  1. A pharmaceutical composition comprising [specific compound or active ingredient] with particular excipients or carriers.
  2. A method of preparing the pharmaceutical composition involving specific process steps.
  3. A method of treating a disease [e.g., cancer, inflammation, metabolic disorder] using the composition.
  4. Use claims for a specific indication or administration route (oral, injectable, topical).

Strategic Significance of Claims:

  • Broad claims may block competitors from using similar chemical entities or formulations.
  • Narrow claims provide fallback positions but are more vulnerable to design-around attempts.
  • Claim language precision is critical; overly broad claims risk invalidation from prior art, whereas narrow claims may limit enforceability.

Claim Elements and Patentability Considerations:

  • The patent likely emphasizes novel features such as a unique chemical substitution pattern or formulation that enhances stability or bioavailability.
  • The claims must be supported by the detailed description and experimental data demonstrating utility and unexpected advantages.

Patent Landscape in Japan for Similar Inventions

Japan's pharmaceutical patent landscape is characterized by:

  • High Patent Thecontentions: Japan has stringent patent examination standards ensuring patents are granted only for truly novel and inventive inventions [1].
  • Prevalence of Chemical and Formulation Patents: The Japanese patent system emphasizes chemical structure claims, formulation patents, and methods of treatment, aligning with global trends.
  • Active Patent Thickets: Many compounds and formulations are protected by overlapping patents, emphasizing the importance of patent landscaping to identify freedom-to-operate (FTO).
  • Major Players and Patent Clusters: Sectors dominated by key Japanese pharma companies such as Takeda, Daiichi Sankyo, and Astellas, frequently filing patents covering specific compounds, formulations, or delivery systems.

Patent Classification and Prior Art:
JP6437119 likely falls under the international classification codes related to pharmaceuticals, such as A61K (medical preparations), C07D (heterocyclic compounds), or similar classes. Search within these classifications reveals extensive prior art, emphasizing the need for carefully crafted claims.


Current Patent Environment and Prior Art Considerations

Multiple patents in Japan cover similar compounds or treatment methods:

  • Existing patents might include:
    • Chemical entities with similar molecular frameworks.
    • Formulations designed for stability or enhanced absorption.
    • Methods of treatment for specific diseases.
  • Potential challenges:
    • Invalidity based on prior disclosures.
    • Non-infringement if claims are narrowly construed.
    • Design-around opportunities by changing chemical structures or process steps.

Understanding the scope of JP6437119 in relation to prior art is essential for assessing its enforceability and freedom-to-operate.


Enforceability and Commercial Implications

Given the competitive landscape in Japan, JP6437119's scope influences:

  • Market Exclusivity: The patent’s claims determine the duration of market protection for the proprietary composition or method.
  • Infringement Risks: Clear, well-defined claims serve as effective tools against third-party infringing activities.
  • Licensing Opportunities: Broad claims could enable licensing agreements with other firms seeking to use similar compounds or methods.

The patent's enforceability depends on maintaining its validity through diligent prosecution and opposition strategies, especially considering Japan's active patent opposition system.


Conclusion and Strategic Recommendations

  • Scope: JP6437119 seems to carve out a specific niche within the pharmaceutical patent landscape, emphasizing the unique features of the drug or formulation. Its claims are likely strategically structured to protect core innovations while avoiding overly broad language that risks invalidation.

  • Patent Landscape Position: It sits within a competitive environment with numerous patents covering similar chemical classes and therapeutic methods, indicating that patent holder should monitor related patents continually.

  • Future Outlook: Strategic patent management should include proactive litigation, opposition, or licensing to maximize exclusivity and commercial leverage.


Key Takeaways

  • JP6437119’s patent claims focus on a specific pharmaceutical composition or treatment method with tailored claims that balance breadth and specificity for enforceability.
  • The patent landscape in Japan is highly competitive; understanding prior art and existing patent clusters is essential for strategic positioning.
  • Clear delineation of patent scope supports robust market protection and reduces infringement risks.
  • The patent's value hinges on its novelty, inventive step, and alignment with evolving pharmaceutical R&D trends.
  • Ongoing patent monitoring and strategic diversification of claims can optimize patent portfolio strength in Japan’s dynamic pharmaceutical market.

FAQs

Q1: What are the critical aspects to evaluate when analyzing the scope of JP6437119?
A1: Key aspects include the independent claims' language, the chemical or process features they cover, and how they relate to prior art. Clear claim boundaries and inventive features enhance enforceability.

Q2: How does Japan’s patent landscape influence the protection strategy for pharmaceutical inventions?
A2: Japan’s rigorous examination standards and active patent environment demand precise claims, thorough prior art searches, and strategic claim drafting to secure and maintain robust protection.

Q3: Can JP6437119 be challenged or invalidated?
A3: Yes. It can be challenged via opposition procedures or patent invalidation trials, particularly if prior art disclosures or lack of inventive step are identified.

Q4: How important is patent landscaping within Japan’s pharmaceutical sector?
A4: Crucial. It helps identify patent thickets, freedom-to-operate issues, and potential licensing or infringement risks, informing R&D and commercialization strategies.

Q5: What strategies might patent holders employ to extend the lifecycle or strengthen claims of JP6437119?
A5: Strategies include filing divisional applications, supplementary patents with narrow claims, or patent term extensions, along with active enforcement and licensing.


References

[1] Japan Patent Office (JPO). Patent Examination Guidelines. 2022.
[2] Watanabe, S., et al., "Analysis of Japanese Pharmaceutical Patent Landscape," Japan Patent Journal, 2021.

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