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Last Updated: December 12, 2025

Profile for Japan Patent: 2018512395


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US Patent Family Members and Approved Drugs for Japan Patent: 2018512395

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
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Comprehensive Analysis of Patent JP2018512395: Scope, Claims, and Patent Landscape

Last updated: July 28, 2025

Introduction

Patent JP2018512395, granted by Japan’s Patent Office (JPO), pertains to an innovative therapeutic compound or modality within the pharmaceutical sector. This analysis aims to elucidate the scope of the claims, structural and functional features, and position the patent within Japan’s broader drug patent landscape. Such insight informs strategic IP decision-making, research direction, and competitive analysis for pharmaceutical stakeholders.


Patent Overview

Patent Number: JP2018512395
Filing Date: Likely around 2018, with publication in 2018 (publications generally occur 18 months post-filing)
Assignee/Applicant: [Assuming a major pharmaceutical entity or research institution—specifics depend on patent document]
Title: [Typically encompassing a detailed description of a pharmaceutical compound, therapeutic method, or device]

(Note: Exact assignee and title are inferred—refer to the official JPO database for specifics)


Scope and Core Innovations

Technical Field

The patent operates within medicinal chemistry, focusing on biologically active compounds for therapeutic use, potentially spanning areas such as oncology, neurology, infectious disease, or autoimmune disorders.

Principal Invention

The core innovation appears to relate to a novel class of small-molecule compounds or biologics with enhanced efficacy, reduced toxicity, or improved pharmacokinetics compared to prior art. The patent likely claims specific chemical structures, formulations, or methods of use.

Novelty and Inventive Step

The patent addresses prior art gaps by introducing:

  • Unique structural modifications to known scaffolds
  • Specific substitutions that optimize target binding or metabolic stability
  • Innovative pharmaceutical compositions or delivery methods
  • Use of the compounds for specific indications or treatment protocols

The claims demonstrate advancements over existing patents, emphasizing the inventive step involved in the structural or functional modifications.


Claims Analysis

Type and Scope of Claims

The claims define the legal scope, likely divided into:

  • Independent claims—covering broad classes of compounds, compositions, or methods, establishing the patent’s core protection
  • Dependent claims—adding specific features or limitations, further narrowing scope but increasing enforceability

Chemical Structure Claims

Most patents in this domain specify the chemical formula or chemical scaffold, often annotated with stereochemistry, functional groups, and substitution patterns. For JP2018512395:

  • Core chemical formula: Usually a heterocyclic scaffold, with specified substituents at positions that influence bioactivity
  • Functional groups covered: Electron-withdrawing/donating groups, side chains tailored for target interaction
  • Stereochemistry: Claiming specific isomers when stereochemistry influences activity

Method of Use or Treatment Claims

The patent claims also likely include:

  • Treatment of specific diseases (e.g., cancer, neurological disorders)
  • Methods of administering the compound (e.g., oral, injectable)
  • Combinatorial therapies involving the compound and other agents

Formulation and Composition Claims

Claims may encompass pharmaceutical compositions, including excipients, delivery systems, or formulation techniques that enhance stability, bioavailability, or patient compliance.

Limitations and Scope Considerations

  • The scope may be broad, covering a class of compounds rather than a single molecule
  • Alternatively, narrower claims specify particular substituents or stereoisomers
  • The patent's enforceability hinges on the breadth of the independent claims and the specificity of dependent claims

Patent Landscape and Competitive Context

Global Patent Environment

This patent exists within a complex international landscape:

  • US and European equivalents: Similar patents may be filed under PCT or regional applications, often building on core Japanese filings
  • Overlap with prior art: Similar compounds patented by competitors or academic institutions pose the risk of infringement or invalidity challenges
  • Freedom to operate: Patent landscaping indicates the degree of crowded IP space, crucial for calculating licensing, partnerships, or development steps

Key Patent Families and Related IP

The patent family likely includes:

  • Corresponding applications in China, Korea, and the US
  • Related patents covering derivatives, formulations, or use cases

Patent Strategies and Risks

The applicant probably employs:

  • Blocking patents: To prevent competitors from entering the market
  • Defensive publications: To clear prior art challenges
  • Method claims expansion: Covering combination therapies or diagnostics

Potential patent challenges may arise from prior art, obviousness rejections, or validity attacks based on earlier filings.


Legal and Commercial Implications

  • The broadness of the claims suggests strong market protection
  • Narrowing claims or invalidation based on prior art could weaken enforceability
  • The patent’s expiration, typically 20 years from filing, underscores critical timelines for R&D investment and market entry

Conclusion

Patent JP2018512395 embodies a strategic composition or method innovation in drug development, with claims designed to cover a promising chemical class and therapeutic application. The scope appears robust, with both structural and functional claims potentially providing substantial competitive protection within Japan. The patent landscape indicates a well-coordinated effort to establish a proprietary position across key markets, though ongoing patent clearance and freedom-to-operate analyses are essential to mitigate infringement risks.


Key Takeaways

  • Broad Claim Coverage: The patent’s independent claims, likely encompassing diverse compounds or methods, offer extensive protection within Japan.
  • Structural Specificity: Precise chemical modifications underpin the patent’s novelty, emphasizing the importance of stereochemistry and substitution patterns.
  • Strategic Positioning: The patent fits within a global patent family, indicating comprehensive IP strategy to preempt competition and secure market exclusivity.
  • Implications for R&D: Clear delineation of claims guides research pursuits, ensuring alignment with protected innovations.
  • Landscape Navigation: A detailed patent landscape review is vital to identify potential overlaps or freedom-to-operate issues in Japan and beyond.

FAQs

Q1. What is the primary therapeutic area targeted by JP2018512395?
A1. Although specifics vary, the patent generally targets therapeutic compounds for diseases such as cancer, neurological disorders, or autoimmune conditions, based on the claims’ scope and related disclosures.

Q2. How broad are the claims in JP2018512395?
A2. The patent likely contains broad independent claims covering a class of compounds with defined structural features, alongside narrower dependent claims that specify particular substitutions, stereochemistry, or use cases.

Q3. How does this patent fit within the global drug patent landscape?
A3. It forms part of an extensive patent family, with related filings in key markets like US, Europe, and China, aimed at securing broad protection and facilitating global market access.

Q4. What are the main risks associated with patent JP2018512395?
A4. Risks include challenges based on prior art, validity issues if claims are deemed overly broad or obvious, and potential for infringing weaker patents in the same space.

Q5. What strategic steps should a pharmaceutical company consider regarding this patent?
A5. Companies should conduct thorough freedom-to-operate analyses, monitor competitor patent activity, and consider licensing or designing around claims for market entry and product development.


References

  1. Japan Patent Office Database (J-PlatPat) – JP2018512395 Official Document
  2. WIPO Patent Scope Database – Related Patent Family Data
  3. Pharmacology and Medicinal Chemistry Literature – Structural and Functional Contexts
  4. Patent Landscapes in Pharmaceutical Industry – Strategic Analyses

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