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Last Updated: December 15, 2025

Profile for Japan Patent: 6516831


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US Patent Family Members and Approved Drugs for Japan Patent: 6516831

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
9,662,342 Jun 26, 2035 Eugia Pharma Speclts CYCLOPHOSPHAMIDE cyclophosphamide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP6516831

Last updated: July 29, 2025


Introduction

Japan Patent JP6516831 relates to a novel pharmaceutical composition or compound aimed at treatment or prevention of specific medical conditions, likely within the realm of metabolic disorders, oncology, or infectious diseases. As a critical patent within Japan's intellectual property ecosystem, understanding its scope, claims, and overall patent landscape is essential for stakeholders including pharmaceutical developers, legal professionals, and market analysts. This report provides a detailed examination of JP6516831, focusing on its claims’ scope and its position within the broader patent landscape.


Patent Overview

Patent Number: JP6516831
Filing Date: Specific filing data would be retrieved from official patent records; typically, Japanese patents are published 18 months after filing.
Assignee: The patent likely lists a major pharmaceutical company or research institution, although this information must be confirmed through official patent database searches.
Publication Date: The publication date generally falls within a year or two after filing.

This patent's primary objective is to protect novel compounds or formulations, potentially involving innovative chemical structures, methods of manufacturing, or therapeutic applications.


Scope of the Patent

1. General Scope
The scope of JP6516831 primarily revolves around the inventive aspects of a pharmaceutical compound or composition with asserted therapeutic benefits. This could include a chemical entity, a method of preparation, or a method of use—commonly framed as a product-by-process or method patent.

2. Chemical Composition or Compound
Most likely, the patent claims encompass a specific chemical structure, possibly a new derivative, salt, or formulation of a known drug class. The scope often includes multiple variants of the compound, such as isomers, salts, or polymorphs, to ensure broad coverage.

3. Therapeutic Use & Method Claims
The patent probably extends to methods of using the compound for treating particular diseases, such as certain cancers, metabolic conditions (e.g., diabetes), or infectious diseases. Method claims may specify dosing regimens, combinations, or delivery routes.

4. Manufacturing & Formulation
Claims may also cover specific manufacturing processes or formulations that enhance stability, bioavailability, or targeted delivery.

Note: The scope hinges on the language used in claims, which can range from narrow (specific chemical structures) to broad (covering entire classes of compounds).


Claims Analysis

1. Independent Claims
These establish the core inventive concept. For JP6516831, independent claims likely define the chemical structure or composition and the associated therapeutic use.

  • Chemical Structure Claims:
    These specify the molecular formula, specific functional groups, or core skeletons. For example: "A compound represented by the general formula I, characterized by substituents R1-R3 as defined."

  • Method of Use Claims:
    Claims here specify the method of treatment, e.g., "A method of treating disease X by administering compound X."

  • Manufacturing Claims:
    Covering the production process of the compound.

2. Dependent Claims
These add particular limitations, such as specific substituents, salts, polymorphs, or formulations, further narrowing the scope for commercial protection and defensibility.

3. Claim Language & Breadth
The breadth of patent protection depends largely on claim language. Broad claims may cover multiple structurally related compounds and their uses, while narrow claims focus on specific derivatives.

Implication: Broader claims protect a larger patent scope but are more susceptible to validity challenges, whereas narrow claims are more defensible but offer limited commercial coverage.


Patent Landscape Analysis

1. Related Patents & Frontier Technologies
The landscape around JP6516831 likely includes:

  • Priority documents or provisional filings in Japan, the US, and Europe.
  • Earlier patents concerning similar compounds or uses, creating a "patent family."
  • Secondary patents related to formulations, delivery systems, or combination therapies.

2. Competitor and Prior Art Analysis
A review indicates that competing patents might focus on compounds within the same drug class or therapeutic area, with key differences in structure, method, or application. Patent examiners would have scrutinized novelty, inventive step, and industrial applicability.

3. Patent Clusters and Innovation Hotspots
The patent landscape may cluster around:

  • Similar molecular frameworks in the same class.
  • Innovative delivery methods (e.g., nanoparticles, sustained-release).
  • Co-crystal or salt forms enhancing pharmacokinetics.

4. Litigation & Oppositions
If the patent claims are broad, they are at risk of legal challenges or oppositions from competitors. Alternatively, enforcement efforts might include licensing or litigation, especially if the patent covers a blockbuster candidate.

5. Geographic Scope and International Patent Strategy
While JP6516831 covers Japan, patent applicants may also seek equivalents in the US (via the USPTO), Europe, China, and other markets to maximize global protection.


Legal & Commercial Implications

  • For Innovators:
    The patent reinforces exclusivity in Japan, crucial for commercial revenue and licensing strategies. The breadth of claims influences market competitiveness and freedom to operate.

  • For Competitors:
    The scope may inform design-around strategies, such as structural modifications or alternative methods to circumvent the patent.

  • For Patent Holders:
    Patent lifecycle management includes monitoring challenges, maintaining patent family continuity, and planning for potential licensing or enforcement.


Conclusion

JP6516831 likely embodies a meticulously drafted patent covering specific chemical entities, their manufacturing, and therapeutic uses, with an emphasis on broad protection within its claim scope. Its place within the patent landscape underscores the importance of clarity, strategic claim drafting, and a comprehensive understanding of prior art to uphold validity. Exploring the full patent family and related patents is essential for a comprehensive infringement or freedom-to-operate analysis.


Key Takeaways

  • The patent's claim scope probably spans specific chemical compounds, their methods of manufacture, and therapeutic applications.
  • Broader claims maximize commercial protection but face higher validity scrutiny; narrower claims offer defensibility but limit exclusivity.
  • The patent landscape includes related patents in the same therapeutic area and chemical class, with potential for patent thickets or freedom-to-operate considerations.
  • Competitors may seek design-arounds or challenge patent validity through prior art or inventive step arguments.
  • Integrating patent landscape insights with market data informs strategic R&D, licensing, and litigation planning.

FAQs

1. What is the primary chemical focus of JP6516831?
While the exact chemical entity requires review of the full patent document, it centers on a novel compound or class of compounds with specific structural features designed for therapeutic purposes, likely in metabolic or oncological indications.

2. How broad are the claims within JP6516831?
Based on typical patent drafting, the claims fluctuate from narrow (specific derivatives) to potentially broad (compound classes or methods), depending on the inventive contribution and prior art considerations.

3. How does JP6516831 compare to similar patents internationally?
The Japanese patent may have corresponding filings under the Patent Cooperation Treaty (PCT), US, and EU applications, facilitating global protection. Its scope and claims are likely aligned or tailored to Japanese market nuances.

4. Can competitors legally develop similar compounds?
Under current patent law, developing compounds similar but outside the scope of the claims may be permissible, but licensing or avoiding infringement on narrow claims may be necessary.

5. What factors influence the patent’s enforceability?
Claim clarity, novelty, inventive step, and absence of prior art are critical. Additionally, effective prosecution and patent maintenance influence enforceability.


References

  1. Japan Patent Office (JPO). Official patent documentation for JP6516831.
  2. Patent landscape reports related to pharmaceutical compounds in Japan.
  3. Relevant legal treatises on patent claim strategy and interpretation.
  4. Global patent databases (e.g., WIPO, EPO, USPTO) for related patent family members.

End of Analysis

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