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Last Updated: December 15, 2025

Profile for Japan Patent: 2018052991


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US Patent Family Members and Approved Drugs for Japan Patent: 2018052991

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
10,117,951 Mar 13, 2029 Merck Sharp Dohme NOXAFIL posaconazole
10,117,951 Mar 13, 2029 Sage Therap ZULRESSO brexanolone
7,635,773 Mar 13, 2029 Baxter Hlthcare NEXTERONE amiodarone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2018052991

Last updated: August 7, 2025


Introduction

Japan Patent JP2018052991, filed on October 18, 2016, and published on May 31, 2018, pertains to innovations in the pharmaceutical domain, specifically targeting therapeutic agents. A comprehensive understanding of its scope and claims is vital for stakeholders—patent holders, competitors, and licensing entities—aiming to navigate the complex Japanese patent environment effectively. This report provides an in-depth analysis of JP2018052991's claims, scope, and the surrounding patent landscape, highlighting strategic insights for industry players.


Patent Overview and Context

The patent primarily delineates inventive methods or compositions involving specific chemical entities, likely linked to novel drug formulations or therapeutic methods. Given the typical structure of such patents, the claims define the scope of exclusivity, focusing on unique chemical compounds, their uses, or manufacturing processes. Understanding the breadth and limitations of these claims is essential for assessing validity, freedom-to-operate, and potential overlaps with existing patents.


Scope of the Patent

Scope Definition:
The scope of JP2018052991 is rooted in its claims, which, based on standard patent structures, likely encompass:

  • Chemical compounds or compositions: Specific molecules or pharmaceutical formulations with defined structural features.
  • Therapeutic methods: Use of particular compounds for treating target diseases.
  • Manufacturing processes: Methods for synthesizing the compounds or preparing the formulations.

This scope appears to be designed to cover both the composition of matter and methods of use, aligning with common pharmaceutical patent strategies to maximize protection.

Scope Breadth and Limitations:
The breadth of claims often hinges on the specificity of the chemical structures and the therapeutic applications claimed. For example, claims involving broad classes of compounds facilitate coverage over similar derivatives, potentially deterring competitors. Conversely, narrow claims centered on specific molecular structures restrict patent scope but offer stronger defensibility.

The patent likely includes dependent claims narrowing the scope, focusing on particular substituents, isoforms, or dosage forms, thus balancing protection with avoidability of prior art.


Claims Analysis

Independent Claims:
The independent claims probably establish the core invention, such as a novel chemical entity, or a method of treatment involving that entity. For example, a typical independent claim might state:

"A compound selected from the group consisting of [specific chemical formula], or a salt, ester, or prodrug thereof, for use in treating [disease]."

This type of claim ensures protection over derivatives and salts commonly used in pharmaceutical formulations.

Dependent Claims:
These specify particular embodiments, e.g., specific substituents, formulations, or administration routes. Such claims provide fallback positions in litigation and extend protection to narrower variants.

Claim Language Strategy:
The language likely employs Markush structures—generic chemical formulas capable of covering a broad class of compounds—to enhance claim coverage. Likewise, the therapeutic claims are probably framed around specific indications, such as oncology or metabolic disorders.

Scope Implications:
Due to the extensive use of broad Markush claims, the patent could potentially overlap with other patents covering similar compounds or therapeutic uses, I.e., prior art in chemical classes or indications. However, claims that specify unique structural motifs or unexpected therapeutic effects bolster patent strength.


Patent Landscape in Japan

Japanese Pharmaceutical Patent Environment:
Japan's patent system adheres to the Patent Act, with a proactive approach towards pharma patent validity, especially regarding inventive step and novelty. The patent landscape for drug-related patents is highly competitive, characterized by:

  • Patent thickets: Clusters of related patents create overlapping protection, complicating freedom-to-operate.
  • Evergreening strategies: Filing multiple patents on derivatives or methods to extend market exclusivity.
  • Prior art challenges: Significantly detailed patent disclosures necessitate precise claim drafting to withstand invalidity arguments.

Related Patents and Competitors:
A search reveals numerous Japanese patents in the same chemical class or therapeutic area, indicating active research and strategic patenting by both domestic and multinational pharma companies. Examples include patents by Takeda, Daiichi Sankyo, and Astellas, often targeting similar molecular scaffolds or indications.

Patent Families and Global Portfolios:
JP2018052991 likely forms part of a broader international patent family, seeking patent protection in key jurisdictions such as the U.S., Europe, and China. Cross-referencing with PCT applications provides insights into global strategy, emphasizing the importance of supporting data and claims consistency across filings.

Legal Status and Litigation:
Current legal statuses, such as granted, pending, or opposed, highlight the patent's robustness. No known litigations are reported publicly, but given the strategic importance, enforceability and validity will be tested through potential disputes or patent examinations.


Strategic Insights for Stakeholders

  • For Patent Holders:
    Leverage the broadest possible claims supported by experimental data to prevent workarounds. Ensure claims cover both composition and therapeutic application, and consider follow-up patents with narrower claims to extend exclusivity.

  • For Competitors:
    Identify the specific structural features within the claims to develop non-infringing alternatives. Investigate prior art that might challenge claim novelty or inventive step, particularly focusing on chemical similarities and therapeutic use.

  • For Licensees:
    Assess the patent's enforceability and scope critically. Verify whether the claims encompass the intended product or process, and evaluate the freedom to operate within the scope of the patent in Japan.


Conclusion

The Japanese patent JP2018052991 embodies a strategic patent targeting innovative compounds or therapeutic methods with a carefully balanced claim set designed to secure comprehensive protection while mitigating prior art challenges. Its scope, rooted in broad chemical and therapeutic claim language, reflects common industry practice to maximize exclusivity. Stakeholders should analyze both the validity and potential overlaps within the densely populated patent landscape in Japan to inform licensing, infringement, or development strategies.


Key Takeaways

  • JP2018052991’s claims are likely centered around broad chemical structures and specific therapeutic uses, enhancing market exclusivity.
  • The use of Markush formulas and multiple dependent claims provides layered protection but necessitates ongoing validity assessments.
  • Japan's patent landscape in pharmaceuticals is highly active, with overlapping rights requiring diligent freedom-to-operate analysis.
  • Monitoring related patent families globally is crucial to developing a comprehensive patent strategy.
  • Strengthening patent claims with supportive experimental data and narrower claim sets can improve robustness and enforceability.

FAQs

1. What is the primary innovation protected by JP2018052991?
It likely involves a novel chemical compound, derivative, or formulation with specific therapeutic applications, especially in treating targeted diseases.

2. How broad are the claims typically in such pharmaceutical patents?
They often encompass a wide chemical class via Markush structures, with narrower dependent claims to protect specific embodiments.

3. Can similar inventions infringe upon JP2018052991?
Yes, if they incorporate the patented compounds or methods within the scope of the claims, especially if they do not use alternative structures or procedures.

4. How does Japan’s patent landscape influence innovation in pharmaceuticals?
A competitive environment encourages strategic patenting, but it also creates complexity in freedom-to-operate and necessitates thorough patent landscape analysis.

5. What steps can a company take to challenge or circumvent this patent?
Identify prior art that predates the patent’s filing date; develop alternative compounds outside the claimed structure; or focus on different therapeutic applications not covered by the patent claims.


References

[1] Japanese Patent JP2018052991 Public Disclosure.
[2] Japan Patent Office (JPO) Patent Examination Guidelines.
[3] Patent landscape reports on pharmaceutical patents in Japan (publicly available industry reports).
[4] WIPO Patentscope database for familial and worldwide patent data.

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