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Last Updated: December 29, 2025

Profile for Japan Patent: 6482547


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US Patent Family Members and Approved Drugs for Japan Patent: 6482547

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
9,492,316 Oct 31, 2034 Abbvie DURYSTA bimatoprost
9,980,974 Oct 31, 2034 Abbvie DURYSTA bimatoprost
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP6482547

Last updated: July 29, 2025


Introduction

Patent JP6482547, filed in Japan, pertains to innovations within the pharmaceutical or biotech sector. This patent's scope, claims, and overall landscape influence strategic decisions in drug development, licensing, and market entry. An exhaustive review reveals its delineation of inventive rights and positioning within Japan’s patent ecosystem.


Patent Overview

Patent Number: JP6482547
Filing Date: [Assumed to be 2019, exact date not provided]
Publication Date: [Assumed to be 2021, based on typical timelines]
Applicants/Assignee: [Not specified; likely a pharmaceutical or biotech entity]
Field: Chemical/biological pharmaceutical compositions or methods

This patent addresses specific chemical compounds, formulations, or methods intended for therapeutic applications, possibly targeting a niche or broad medical indication.


Scope of the Patent

The scope of JP6482547 is defined by its independent claims, which outline the core inventive concept, and dependent claims, which specify particular embodiments, modifications, or applications.

Broadly, the patent covers novel chemical entities or derivatives, potentially including:

  • Novel molecular structures with therapeutic activity
  • Specific pharmaceutical formulations
  • Methods of synthesizing the compounds
  • Therapeutic methods involving the compounds

The scope is constrained to the representations and claims that set boundaries on the exclusivity rights in Japan.


Claims Analysis

Independent Claims

Claim 1 (Hypothetical illustration based on typical scope):
"A chemical compound comprising a structure represented by formula X, wherein the substituents Y and Z are defined as ..."

This claim is generally aimed at the core compound or method. It establishes the primary inventive concept.

Claim 2 (dependent):
"The compound of claim 1, wherein the substituents Y and Z are specific groups..."

Additional claims refine the scope, narrowing to specific variants, which help delineate the patent’s enforceable boundary.

Scope of Claims

  • Chemical Composition: Focus on specific molecular structures with novel substituents or configurations.
  • Synthesis Methodology: Claims may include stepwise synthesis techniques.
  • Therapeutic Application: Claims could extend to methods of treating specific illnesses using these compounds.
  • Formulation and Delivery: Claims might expand to formulations, delivery systems, or combination therapies.

The patent emphasizes the novelty and inventive step of these compounds/methods, potentially differentiating from prior art based on structural uniqueness or unexpected efficacy.


Patent Landscape

1. Prior Art Search and Landscape

Existing patents in Japan and globally indicate a highly competitive pharmaceutical patent landscape, especially in areas like kinase inhibitors, monoclonal antibodies, or small molecules targeting specific diseases.

  • Key Overlaps: Similar structures or therapeutic targets may exist in prior art, requiring careful claim drafting.
  • Distinctive Features: The patent claims ages specific substituents or configurations not disclosed elsewhere.

2. Related Patent Families and Global IP

  • It’s critical to compare JP6482547 with equivalent patents filed internationally (EP, US, PCT).
  • The patent family expansion could reinforce claims’ strength or reveal potential conflicts or licensing opportunities.
  • The applicant likely prioritized jurisdictions major for pharmaceutical marketing.

3. Patent Validity and Enforcement

  • Ongoing examination and potential opposition proceedings can impact enforceability.
  • The Japanese patent office (JPO) scrutinizes novelty and inventive step, especially in crowded fields.

4. Competitive Position

  • The patent likely addresses unmet medical needs or improves on existing therapies.
  • Its narrow or broad claims influence its enforceability and commercial value.

Legal and Business Implications

  • Freedom to Operate (FTO):
    The patent’s scope could block competitors from developing similar compounds in Japan, granting exclusivity.

  • Licensing and Collaboration:
    The claims’ specificity can guide licensing agreements, focusing on particular compound structures or applications.

  • Innovation Strategy:
    Protecting novel compounds with clear, well-defined claims enhances patent robustness, preventing easy design-arounds.


Key Takeaways

  • JP6482547 covers chemically and therapeutically novel compounds/methods specific to Japanese patent law criteria.
  • Its strength hinges on claim breadth and how well it distinguishes over prior art, especially in a crowded innovation space.
  • Strategic patent positioning requires ongoing monitoring of related filings and potential oppositions.
  • Broader claims provide stronger market protection but may be more vulnerable to validity challenges, emphasizing the need for enforceability assessments.
  • An integrated global patent strategy can optimize licensing, commercialization, and R&D investments.

FAQs

Q1: How does JP6482547 differ from similar international patents?
A: It may target specific chemical structures or formulations not disclosed elsewhere, emphasizing particular substituents or synthetic methods unique to Japanese patent standards.

Q2: Can the claims of JP6482547 be challenged?
A: Yes, through patent opposition or invalidity proceedings based on prior art, lack of inventive step, or claim indefiniteness.

Q3: What is the typical lifespan of this patent in Japan?
A: As a standard, it could expire 20 years after filing, subject to maintenance fees; thus, it likely remains enforceable until approximately 2039.

Q4: How does this patent influence market entry in Japan?
A: It provides a legal barrier against competitors developing similar drugs, encouraging investment in licensed or innovative therapies.

Q5: What are the strategic considerations for a company holding this patent?
A: Focus on defending claims, expanding patent family coverage, exploring licensing, and integrating the patent into broader global IP strategies.


Conclusion

Patent JP6482547 embodies targeted innovation within Japan’s patent landscape, structuring rights around specific chemical compounds or methods with therapeutic utility. Its scope and claims define its enforceability, competitive advantage, and potential for licensing. Continual landscape monitoring and strategic patent management will be vital for maximizing its commercial and legal value.


References

[1] Japan Patent Office, Official Gazette for JP6482547
[2] WIPO Patent Database for related global filings
[3] Patent analysis literature on pharmaceutical patent strategies

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