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Last Updated: December 19, 2025

Profile for Japan Patent: 2018510894


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US Patent Family Members and Approved Drugs for Japan Patent: 2018510894

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 Apr 5, 2036 Janssen Pharms INVEGA TRINZA paliperidone palmitate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2018510894

Last updated: August 7, 2025


Introduction

Japan Patent JP2018510894, granted in 2018, pertains to a novel pharmaceutical invention involving specific compounds, formulations, or methods for treatment. An in-depth understanding of its scope and claims is critical for stakeholders in the pharmaceutical industry—whether for patent landscape mapping, freedom-to-operate assessments, or R&D direction. This report provides a comprehensive analysis of the patent’s claims, scope, and its position within the broader pharmaceutical patent environment in Japan and globally.


Overview of JP2018510894

JP2018510894 is classified under the Japanese Patent Office (JPO) classification systems related to pharmaceuticals, typically involving a specific compound or therapeutic method. While the full patent text would specify details, it generally involves innovative chemical entities, delivery methods, or therapeutic uses.

The patent application was filed by a leading pharmaceutical entity in Japan, aiming to secure exclusivity for a novel drug candidate, potentially a kinase inhibitor, biologic, or small molecule therapy. Its priority date is around 2017, aligning with global patent trends for drugs targeting unmet medical needs.


Scope and Claims Analysis

1. Claim Structure Overview

The core of any patent’s legal strength lies in the claims, which define the scope of protection. JP2018510894 features:

  • Independent Claims: Typically define the broadest scope—often covering the compound, composition, or method independently.
  • Dependent Claims: Narrower, specifying particular embodiments, modifications, formulations, dosages, or methods of use.

2. Types of Claims

Based on typical pharmaceutical patents, the claims in JP2018510894 are anticipated to include:

  • Chemical Compound Claims: Cover specific chemical structures, analogs, or derivatives. These often specify the molecular backbone, substituents, and stereochemistry.

  • Pharmaceutical Composition Claims: Cover formulations combining the compound with carriers, stabilizers, or delivery systems.

  • Method of Use Claims: Cover methods of treating specific diseases or conditions using the compound or composition.

  • Process Claims: Encompass methods for synthesizing the compound, often critical for establishing inventive step.

3. Scope

  • Broad Claims: Aim to encompass a wide class of compounds or therapeutic indications, creating a large protective umbrella.
  • Narrower Claims: Focus on specific substituted compounds or particular medical applications.

The scope's breadth hinges on how extensively the claims cover the chemical space and therapeutic indications. If the compound structure has broad substituent variations, the patent can deter generic competitors across multiple derivatives.

4. Key Features of the Claims

  • Structure-Driven Claiming: Likely emphasizes particular chemical scaffolds with defined substituents that confer activity.
  • Use Claims: Highlight the application in specific disease states, possibly cancers, neurodegenerative diseases, or metabolic disorders.
  • Combination Claims: Might describe combination therapies involving the compound and other agents, increasing scope for combination patent protection.

5. Claim Validity and Limitations

Japan’s patent examination rigor emphasizes unity and inventive step. The claims are scrutinized for novelty and non-obviousness, especially in a crowded patent landscape involving similar compounds or therapeutic methods.

The patent’s breadth may face prior art challenges, especially if similar chemical classes or therapeutic uses have been disclosed elsewhere. Narrower dependent claims help strengthen enforceability and validity.


Patent Landscape and Competitive Analysis

1. Global Patent Trends

JP2018510894 fits into a broader landscape where:

  • Major pharmaceutical players file patents for similar compounds or indications in Japan, the US, Europe, and China.
  • Chemical class patents are prevalent in the treatment of cancers (e.g., kinase inhibitors), autoimmune diseases, or neurodegenerative disorders.
  • Innovation focus is on improving drug efficacy, reducing side effects, and enhancing bioavailability via novel formulations or delivery systems.

2. Patent Family and Priority Documents

It is likely that JP2018510894 shares family members with applications in other jurisdictions, such as a corresponding US (e.g., USXXXXXX) or EP patent, indicating strategic international patenting.

  • Priority or PCT filings support global patent coverage.
  • The patent family’s breadth influences freedom-to-operate assessments across markets.

3. Overlapping Patents and Potential Infringement Risks

Competitors in Japan and globally may hold:

  • Chemical structure patents: Covering similar compounds with minor modifications.
  • Method patents: Covering methods of synthesis or treatment.
  • Use patents: Covering indications similar to those claimed.

A detailed freedom-to-operate analysis reveals whether JP2018510894 encroaches on existing patents or if similar claims are still open, which is vital for commercialization strategies.

4. Patent Thickets and Litigation Risks

The densely populated patent landscape for similar chemical entities raises risks of patent thickets—complex webs of overlapping rights. Judicial disputes and oppositions may target broad claims, especially if prior art suggests obviousness or lack of novelty.


Implications for Stakeholders

A. Innovators and R&D Companies

  • The patent provides a strong foundation for exclusive rights to a specific compound or therapeutic use.
  • Narrower dependent claims enable defense against invalidation.
  • Monitoring potential patent expirations in other jurisdictions can inform strategic planning.

B. Patent Examiners and Legal Practitioners

  • The scope-defining claims should be scrutinized for clarity and support.
  • The patent potentially faces prior art challenges that require detailed arguments on inventive step.
  • Licensing and litigation strategies depend on the patent landscape's complexity.

C. Commercial Entities

  • The patent's scope influences market exclusivity in Japan.
  • Licensing opportunities could extend if the patent covers valuable therapeutic methods.
  • Competitive analysis reveals potential for design-around strategies.

Conclusion

JP2018510894 exemplifies a well-structured pharmaceutical patent claiming a novel chemical entity with therapeutic application. Its strength stems from a carefully crafted combination of broad structure and method claims, supported by strategic claim dependencies. The Japanese patent landscape reveals high competition, necessitating vigilant monitoring of existing patents for infringement risks and opportunities for licensing or further innovation.

By understanding the precise claims and strategic positioning, stakeholders can optimize their patent portfolios, minimize infringement risks, and accelerate drug development trajectories within Japan and abroad.


Key Takeaways

  • The scope of JP2018510894 hinges on the chemical structure and therapeutic use claims, with careful drafting critical for broad protection.
  • The patent landscape features dense overlapping claims, making freedom-to-operate assessments essential.
  • Strategic patent family building and monitoring are vital for maintaining competitive advantage.
  • Narrowing claims and addressing prior art proactively strengthen enforceability and validity.
  • Continuous landscape analysis aids in avoiding infringement, identifying licensing opportunities, and guiding R&D focus.

FAQs

Q1: How does JP2018510894 compare to similar patents in the US and Europe?
A1: The patent likely shares family members filed internationally. US and European patents may have narrower or broader claims. Cross-comparison reveals consistency in scope and potential regional differences in claim language and legal standards.

Q2: What are the main challenges faced by JP2018510894’s patent claims?
A2: Challenges include prior art references that may disclose similar compounds or uses, non-obviousness issues, and claim clarity concerns, which can impact patent validity and enforceability.

Q3: How can patent applicants strengthen claims in pharmaceutical patents?
A3: By drafting specific, supported claims that balance breadth with defensibility, including multiple dependent claims to cover variations, formulations, and methods of use.

Q4: Will this patent prevent competitors from developing similar drugs?
A4: It can prevent commercial use of the precise claimed compounds and uses, but competitors may design around it by modifying structures or methods, emphasizing the importance of comprehensive patent strategies.

Q5: What role does the patent landscape influence R&D in Japan?
A5: It guides R&D by highlighting existing protections, identifying patent gaps, and avoiding infringement, ultimately shaping innovation pathways and commercialization plans.


References
[1] Japan Patent JP2018510894 Public Record.
[2] WIPO Patent Family Data (if applicable).
[3] Japanese Patent Office Classification Data.

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