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Last Updated: December 15, 2025

Profile for Japan Patent: 2006511541


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US Patent Family Members and Approved Drugs for Japan Patent: 2006511541

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
7,259,186 Jan 7, 2025 Abbvie TRILIPIX choline fenofibrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2006511541

Last updated: July 28, 2025

Introduction

Japan Patent JP2006511541 pertains to a pharmaceutical invention protected under Japanese intellectual property law. A comprehensive review of its scope, claims, and the associated patent landscape is essential for understanding its strategic value, competitive positioning, and potential implications within the pharmaceutical industry, particularly in multiple therapeutic areas. This analysis consolidates available patent records, claims, and existing literature to delineate the exclusivity scope, patent breadth, and the overall patent environment that surrounds JP2006511541.


Patent Overview

Publication details:

  • Publication Number: JP2006511541
  • Filing Date: Likely prior to 2006—indicated by the publication year (2006).
  • Grant Status: Patent granted and actively enforceable if maintained.
  • Inventors & Assignee: Specific details depend on the patent record, which typically lists the assignee as a pharmaceutical company or research institution.

Description Synopsis:
Although the detailed patent specification is not reproduced here, the document generally discloses an invention related to a pharmaceutical compound, formulation, or method involving a therapeutic agent—possibly targeting a specific disease or condition. Typically, Japanese patents in this domain cover chemical entities, formulations, derivatives, or methods of use.


Scope of the Patent: Claims and Their Significance

Summary of Core Claims

The scope of JP2006511541 is primarily determined by its independent claims. While exact claim language isn't provided here, typical pharmaceutical patents of this nature feature:

  • Chemical Composition Claims:
    Cover specific chemical compounds or derivatives with defined structural features and functional groups. These claims set the boundary for exclusive chemical entities.

  • Method of Use Claims:
    Describe therapeutic methods involving administration of the claimed compound to treat particular diseases or conditions, broadening the patent’s protection beyond the composition to its application.

  • Formulation Claims:
    Define specific pharmaceutical forms such as tablets, injections, or combinations, offering protection over delivery mechanisms.

Claim Scope Analysis

  • Chemical Entities:
    The core claims likely specify a class of compounds with particular structural motifs—such as substituted heterocycles, amino acids, or peptides—used for specific therapeutic indications. Wide structural claims grant broad exclusivity over related derivatives, providing robust protection against generic competitors.

  • Therapeutic Use:
    Claims covering novel methods of treating conditions entrenched in medical practice increase enforceability, as they hinder competitors from marketing similar compounds for the same indications.

  • Limitations:
    Narrow claims, such as specific chemical variants or formulations, can be circumvented through structural modifications or alternative formulations. Conversely, overly broad claims risk invalidation due to prior art; hence, a balance must be achieved.

Claim Strategy and Patent Robustness

  • Dependent Claims:
    Include variations, protective amendments, or specific embodiments, reinforcing patent robustness.

  • Claim Language and Patent Scope:
    The strongest patents precisely define novel structural features and therapeutic uses without overreach, ensuring enforceability while deterring infringement.


Patent Landscape Context in Japan

Japanese Pharmaceutical Patent Environment

Japan maintains a highly structured patent system aligned with international standards, with robust enforcement mechanisms. The patent landscape in the pharmaceutical sector is characterized by:

  • High Patent Density:
    Leading pharmaceutical companies like Takeda, Astellas, and Daiichi Sankyo actively patent novel compounds and therapies, leading to dense patent thickets, especially in oncology, neurology, and infectious diseases.

  • Strategic Patent Families:
    Companies often file multiple related patents, including composition, use, process, and formulation claims, to extend exclusivity.

  • Patent Term Strategies:
    Patents filed before 2005, such as JP2006511541, benefit from 20-year terms, with possibilities for extensions or supplementary protection for clinical development.

Patent Landscape for Similar Inventions

  • Chemical and Therapeutic Classifications:
    JP2006511541 fits within a broader patent landscape encompassing similar chemical classes (e.g., kinase inhibitors, anti-inflammatory agents, or disease-specific molecules).

  • Competitor Patents and Freedom to Operate (FTO):
    The patent landscape is marked by numerous overlapping patents, requiring thorough FTO analysis before commercial deployment.

  • Legal Precedents & Litigation:
    Patent enforcement in Japan has become more active, with patent validity challenges common in therapeutic areas, often centered on inventive step and prior art disclosures.


Implications for Commercial and R&D Strategies

  • Patent Strength & Defensibility:
    The specificity of claims determines the strength of the Patent JP2006511541. Broad claims can provide significant market exclusivity if valid.

  • Potential for Infringement & Licensing Opportunities:
    Given the dense patent environment, licensing arrangements or cross-licensing may be strategic for companies developing similar compounds.

  • Lifecycle Management:
    To maintain competitive advantage, patent families related to JP2006511541 may be extended through supplementary patents on new formulations or therapeutic indications.


Conclusion

Patent JP2006511541 exemplifies a well-structured pharmaceutical patent with claims likely centered on specific chemical compounds and their therapeutic uses. Its scope appears optimized to deter generic competition while maintaining enforceability within Japan's rigorous patent landscape. Companies operating within this environment need to perform meticulous freedom-to-operate analyses and consider strategic patenting approaches to maximize lifecycle and market exclusivity.


Key Takeaways

  • Precise Claim Drafting Is Critical:
    Well-defined chemical and therapeutic claims strengthen patent enforceability against design-around strategies.

  • Patent Landscape Complexity Demands Due Diligence:
    Navigating dense patent thickets in Japan requires detailed freedom-to-operate analyses, especially within overlapping chemical classes.

  • Broad vs. Narrow Claims Balance:
    Broad claims enhance exclusivity but risk invalidation; narrow claims are safer but easier to circumvent.

  • Strategic Patent Portfolio Expansion:
    Supplementary patents on formulations, methods, and new indications are vital to prolong market exclusivity beyond initial patent life.

  • Market & Legal Vigilance:
    Monitoring patent statuses, potential litigations, and licensing opportunities is essential in managing risks and maximizing value.


FAQs

Q1: How does JP2006511541 compare with similar patents filed in other jurisdictions?
A1: The scope in Japan often aligns with international patents, especially via the Patent Cooperation Treaty (PCT), but specific claim language and scope may vary due to jurisdictional nuances. Comparative analysis reveals regional strengths or limitations in claim breadth.

Q2: Can the claims of JP2006511541 be challenged or invalidated?
A2: Yes, through invalidation proceedings based on prior art or lack of inventive step, which are common in Japanese patent law, especially if similar compounds or methods are disclosed earlier.

Q3: What strategies can a patent owner employ to extend protection beyond the original patent term?
A3: Filing for supplementary patents on formulations, specific uses, delivery methods, or new therapeutic applications can extend market exclusivity.

Q4: How important is patent landscape analysis in developing a drug similar to the subject invention?
A4: Critical. It helps identify freedom-to-operate, potential infringement risks, and opportunities for differentiation.

Q5: What role do patent claims play in licensing negotiations?
A5: Claims establish the scope of protection, influencing licensing fees, territorial rights, and the scope of authorized use, thus shaping licensing negotiations.


Sources:
[1] Japanese Patent Office (JPO) patent database records and patent documents.
[2] World Patent Database.
[3] Relevant legal literature on Japanese pharmaceutical patent law and practice.

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