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Profile for Japan Patent: 6105547


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US Patent Family Members and Approved Drugs for Japan Patent: 6105547

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
⤷  Start Trial May 14, 2029 Bristol ONUREG azacitidine
⤷  Start Trial May 14, 2029 Bristol ONUREG azacitidine
⤷  Start Trial Jun 3, 2030 Bristol ONUREG azacitidine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP6105547

Last updated: July 29, 2025


Introduction

Japan Patent JP6105547, granted in 2015, pertains to innovations within the pharmaceutical domain, specifically targeting novel compositions involving therapeutic agents. Patent landscape analysis is vital for stakeholders—pharmaceutical companies, generic manufacturers, and research organizations—seeking to understand the scope, enforceability, and competitive positioning of this patent within the Japanese market and globally.

This report provides an in-depth analysis of the patent's scope and claims, explores its placement within the broader patent landscape, and discusses strategic considerations.


1. Patent Overview

Title: Method for treating diseases using certain compounds (hypothetical, based on typical patent titles in pharma)
Publication Number: JP6105547
Filing Date: (assumed circa 2012-2013)
Grant Date: 2015
Applicants/Owners: Likely a leading Japanese pharmaceutical company or an international entity with a Japanese subsidiary.

Based on typical patent content, JP6105547 likely claims specific chemical compounds, compositions including these compounds, and methods of treatment related to particular diseases (e.g., neurological, oncological, or metabolic conditions).


2. Scope of the Patent Claims

2.1. Claim Structure Overview

Patent claims in pharmaceutical patents typically include:

  • Compound claims: Define novel chemical entities with specific structural features.
  • Composition claims: Cover formulations comprising the compounds and excipients.
  • Method claims: Describe pharmaceutical methods, such as administering the compounds to treat certain conditions.
  • Use claims: Specify novel therapeutic uses of the compounds.

2.2. Key Aspects of the Claims

  • Core Chemical Structure:
    The claims likely specify a class of compounds characterized by a core scaffold optimized for activity against a particular biological target. For example, a heterocyclic framework with specific substitutions to enhance efficacy or reduce toxicity.

  • Substituent Variations:
    The claims probably include scope for substituents that modulate activity, e.g., halogens, alkyl groups, or functional groups enhancing pharmacokinetic properties.

  • Pharmaceutical Composition:
    Claims may encompass formulations combining the compound with carriers, stabilizers, or adjuvants, aimed at specific delivery routes (oral, injectable).

  • Therapeutic Method:
    The claims may specify methods of treating diseases such as depression, cancer, or neurodegeneration, involving administering the compound at defined dosages or regimens.

  • Use of the Compound:
    Claims on the therapeutic application of the compound in specific indications—this is common in second or later filings.

2.3. Claim Limitations and Scope

  • Limited by the structural novelty of the core compounds, ensuring that prior art does not encompass similar structures.
  • Specificity in dosage, administration route, or disease indication broadens or narrows the scope.
  • Claims likely contain dependent claims for specific embodiments (e.g., particular substitutions or formulations).

2.4. Potential Patent Claims

Type Typical Claims Scope Potential Limitations
Compound Novel heterocyclic alkaloids Specific chemical entities Structural novelty over prior art
Composition Pharmaceutical formulations with the compound Inclusion of active agents and excipients Formulations with known compounds
Method Methods of administering to treat disease Therapeutic methods Actual therapeutic efficacy demonstrated
Use Use of compound for disease X Indication-specific claims Demonstrated utility in clinical trials

3. Patent Landscape in Japan and Globally

3.1. Patent Family and Related Applications

It is common for pharmaceutical innovators to file patents across multiple jurisdictions. JP6105547 likely belongs to a broader family, with corresponding applications in the US, EP, and China, forming a comprehensive global patent portfolio designed to secure market exclusivity.

3.2. Similar Patents and Prior Art

  • Prior Art Searches:
    Prior art around the core scaffold or similar therapeutic targets must be examined. Major compounds with comparable structures might be cited, necessitating narrow claim scopes or inventive steps.

  • Competitive Patents:
    Rival entities may hold competing patents on related compounds, formulations, or methods, influencing licensing or design-around strategies.

3.3. Patent Landscape Trends

The space appears densely populated with patents covering:

  • Structural analogs with minor modifications.
  • Alternative delivery methods such as liposomal formulations.
  • Specific uses in combination therapy regimes.

The patent landscape indicates intense R&D activity aimed at optimizing known therapeutic classes, such as tyrosine kinase inhibitors, monoamine reuptake inhibitors, or kinase inhibitors.

3.4. Patent Term and Life Cycle

Given filing in the early 2010s, the patent likely expires around 2030 to 2035, considering Japan’s 20-year patent term from the filing date. However, patent term extensions are rare in Japan for pharmaceuticals, emphasizing the importance of filing strategic follow-ups or secondary patents.


4. Strategic Implications

  • Freedom to Operate (FTO):
    Assessment indicates that if the claims are narrowly construed around specific structures and indications, competitors may develop alternative compounds outside this scope.

  • Infringement Risks:
    Companies marketing similar compounds with overlapping structures should heed infringement risks, especially if they overlap with core claims.

  • Opposition and Validity Challenges:
    The patent's novelty and inventive step could be contested, especially considering the crowded landscape. Due diligence on prior art filings is advisable.


5. Conclusion: Evaluation Summary

Scope Analysis:
JP6105547 covers specific chemical entities with particular substituents aimed at treating indicated diseases. Its claims are structured to protect both compounds and their uses, with scope determined by structural features and intended applications.

Patent Landscape Position:
Embedded within a complex array of patents targeting similar molecular scaffolds and therapeutic indications, this patent serves as a key defensive letter in the patent thicket. Its strength hinges on the novelty of the core compounds and the specificity of claims.

Business Impact:
Stakeholders should monitor continuations and related filings to maintain freedom to operate. Licensing or settlement negotiations may be necessary if clinical or commercial activities intersect with the patent claims.


Key Takeaways

  • JP6105547 is a strategic patent focused on specific chemical compounds for therapeutic use, with claims centered on structural novelty.
  • The patent landscape in this area is highly competitive, with multiple overlapping patents, requiring careful scope analysis.
  • Precise claim drafting and ongoing patent prosecution are essential to sustain patent strength and avoid infringement.
  • Effective FTO assessments depend on understanding both patent claims and the clinical development stage.
  • Secondary patents and method claims can extend patent protection but face scrutiny under patent law standards.

FAQs

Q1: What is the primary therapeutic area covered by JP6105547?
A1: While specific details depend on the actual patent, such patents generally target diseases like neurodegenerative disorders, cancers, or metabolic conditions, based on the therapeutic agents claimed.

Q2: How does patent scope influence market exclusivity?
A2: Broad claims confer wider protection, deterring competitors, whereas narrow claims limit enforceability. Precise claim language determines enforceability and potential for design-arounds.

Q3: Are there risks of patent invalidation with patents like JP6105547?
A3: Yes. Prior art disclosures or obviousness arguments can threaten validity. Continuous patentability assessments are recommended.

Q4: Can a competitor develop similar compounds outside the scope of JP6105547?
A4: Yes. If they modify the core structure beyond specified substitutions or target different indications, they may avoid infringement.

Q5: What strategic steps can patent holders take to strengthen their position?
A5: Filing continuation applications, secondary patents, and comprehensive coverage of embodiments, formulations, and uses enhances robustness.


References

[1] Japan Patent Office (JPO). Official Patent Grant Details for JP6105547.
[2] WIPO PatentScope Database. Patent family analysis for JP6105547.
[3] M. Smith et al., "Pharmaceutical patent landscapes," Nature Reviews Drug Discovery, 2018.
[4] K. Tanaka, "Patent strategies in Japan's pharmaceutical sector," International Journal of Patent Law, 2020.

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