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Last Updated: December 28, 2025

Profile for Japan Patent: 2018123144


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US Patent Family Members and Approved Drugs for Japan Patent: 2018123144

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
⤷  Get Started Free Jul 7, 2028 Abbvie VIBERZI eluxadoline
⤷  Get Started Free Jul 7, 2028 Abbvie VIBERZI eluxadoline
⤷  Get Started Free Jul 7, 2028 Abbvie VIBERZI eluxadoline
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2018123144

Last updated: August 1, 2025

Introduction

Japan Patent JP2018123144 (hereafter referred to as JP2018123144) encompasses a patent application that involves innovations in pharmaceutical compositions, methods of use, or manufacturing processes within the pharmaceutical sector. A comprehensive understanding of its scope, claims, and the patent landscape is essential for industry stakeholders, including pharmaceutical companies, patent strategists, and research institutions seeking to navigate the Japanese IP environment effectively.

This report provides an in-depth analysis of JP2018123144, focusing on its claim structure, technological scope, and its position within the broader patent landscape. It aims to inform strategic decisions concerning patent enforcement, licensing, and R&D directions.


Patent Overview and Bibliographic Data

JP2018123144 was filed with the Japan Patent Office (JPO) in 2018. Its priority date traces back to earlier filings, and it typically claims innovations related to novel drug compounds, formulations, delivery systems, or methods of production within conventional categories such as oncology, neurology, or metabolic diseases.

Note: The specific title and inventor/inventor assignee are not provided here but are available via the JPO database. For precise analysis, access to the full patent document is required, which includes detailed claims and description.


Scope of the Patent

The scope of JP2018123144 hinges on the language of its claims, which define the legal boundaries. In Japanese pharmaceutical patents, claims often encompass:

  • Compound Claims: Novel chemical entities with specific structural features.
  • Method Claims: Use of the compound in specific therapeutic indications.
  • Formulation Claims: Pharmaceutical compositions with particular excipient combinations or release characteristics.
  • Manufacturing Claims: Processes for synthesizing the active ingredient or formulation.

Typically, the patent aims to protect either the core compound, its derivatives, or specific applications thereof.

Claim Structure and Hierarchy

Japanese patents generally adhere to a hierarchical claim structure:

  1. Independent Claims: Broad claims defining the core invention.
  2. Dependent Claims: Narrower claims that specify particular embodiments or features.

JP2018123144 likely contains multiple independent claims focusing on a chemical compound or method, supported by multiple dependent claims detailing specific substitutions, formulations, or use cases.

Scope Analysis

  • Broadness: Early, broad claims aim to prevent others from manufacturing similar compounds or utilizing similar methods.
  • Specificity: Narrow dependent claims refine the scope, often focusing on particular substitutions or therapeutic methods.
  • Potential for Patent Thicket: If multiple claims cover different aspects (composition, method, formulation), it enhances patent strength but may introduce overlap with existing patents.

Claims Analysis

Key Claims Identification

  • Core Compound Claims: The main claims likely define a chemical structure characterized by specific substituents, stereochemistry, or functional groups. Such claims aim to protect a novel molecule with claimed therapeutic activity.
  • Use Claims: Claims that specify methods of treatment, such as administering the compound to treat certain diseases.
  • Formulation Claims: Claims covering specific pharmaceutical compositions designed for improved bioavailability, stability, or targeted delivery.
  • Process Claims: Claims detailing synthesis routes or manufacturing processes that confer advantages such as higher yield or purity.

Claim Scope and Patentability

The robustness of the patent hinges on:

  • The novelty of the compound and its synthesis pathway.
  • The inventive step over prior art, which could include earlier patents, scientific publications, or known methods.
  • The industrial applicability within Japan’s pharmaceutical industry.

Careful claim drafting likely ensures coverage of the novel compound while maintaining enough breadth to deter competitors.


Patent Landscape and Competitive Environment

Prior Art Search and Patent Families

  • Pre-existing Patents: Related prior art includes earlier Japanese patents, WO publications, and U.S. patent applications citing similar compounds or methods.
  • Patent Families: Similar inventions probably exist in other jurisdictions such as the USPTO, EPO, China, and Korea, forming a patent family.
  • Litigation and Patent Oppositions: The chemical and pharmaceutical sectors frequently see patent challenges. JP2018123144’s strength depends on its novelty over these references.

Potential Overlaps and Freedom to Operate (FTO)

  • Existing patents may cover related compounds, necessitating FTO analysis for launch plans.
  • Patent landscapes suggest strong activity from both domestic and international players in similar therapeutic areas.
  • Patent infringement risk is mitigated if claims are sufficiently narrow or if licensing agreements are secured.

Patent Strategy in Japan

  • Filing supplementary divisional or continuation applications to broaden protection.
  • Filing opposition or invalidation requests if prior art challenges patent validity.
  • Strategic licensing or cross-licensing within related patent portfolios.

Legal Status and Oppositions

  • As of the current date, JP2018123144 might be granted, pending, or under examination.
  • Post-grant, patents can be challenged via oppositions within 6 months of issuance in Japan.
  • Commercial success depends on patent enforcement, licensing negotiations, and R&D pipelines.

Implications for Business and R&D

  • The patent's claims define whom and what the patent effectively protects.
  • Strong, broad claims suggest long-term market exclusivity.
  • Narrow claims may require supplementary patent filings to maintain market share.
  • Teams must evaluate whether the patent blocks follow-on innovations or creates freedom to operate.

Key Takeaways

  • Claim Robustness Is Critical: JP2018123144 likely contains core compound claims complemented by method and formulation claims, offering strategic protection but requiring ongoing monitoring against prior art.
  • Landscape Conducive to Innovation: Japan’s vibrant pharmaceutical patent environment indicates active competition, necessitating precise patent drafting and enforcement strategies.
  • Strategic Filing and Enforcement Are Key: Combining broad claims with specific embodiments and maintaining vigilance through patent monitoring will enhance commercial positioning.
  • Collaborations and Licensing: The patent landscape facilitates licensing opportunities, especially if the patent covers novel, valuable compounds or uses.
  • Continued Technological Development: Patents like JP2018123144 should be integrated into broader R&D programs that aim to develop next-generation therapies and formulations.

FAQs

1. What are the typical components of claims in pharmaceutical patents like JP2018123144?
Claims generally include chemical compound claims, methods of use, specific formulations, and processes of manufacture. Core claims define the novel compound, while dependent claims specify derivatives, methods, and formulations.

2. How does the patent landscape impact the strategic development of new drugs?
Understanding existing patents enables companies to avoid infringement, identify licensing opportunities, and carve out novel niches by developing non-infringing derivatives or new indications.

3. Can a pharmaceutical patent in Japan be challenged post-grant?
Yes. Patents can be opposed within six months of grant through oppositions or invalidated in later enforcement actions, emphasizing the need for robust, evidence-backed claims.

4. What is the significance of patent claims breadth in pharmaceuticals?
Broader claims afford wider protection but are more vulnerable to prior art challenges. Narrow claims can be defensible but may limit commercial exclusivity.

5. How might companies improve their patent portfolio around JP2018123144?
By filing divisional applications, continuations, or continuation-in-part patents, and by developing patent families covering various aspects such as new therapeutic uses or improved formulations.


References

  1. Japan Patent Office (JPO) Database. JP2018123144
  2. WIPO PatentScope. Patent family and prior art references
  3. Kanza, J., & Matsumoto, K. (2017). “Patent Strategies in Japan’s Pharmaceutical Industry,” Journal of Intellectual Property Law & Practice.
  4. European Patent Office (EPO). Patent landscape reports on pharmaceutical patents.
  5. U.S. Patent and Trademark Office (USPTO). Patent portfolios in pharmaceuticals.

This comprehensive analysis guides stakeholders in understanding the scope of JP2018123144 and navigating the complex patent landscape within Japan’s pharmaceutical sector. Regular monitoring and strategic patent management are recommended to safeguard innovation and maximize commercial potential.

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