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Last Updated: December 31, 2025

Profile for Japan Patent: 2018030873


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US Patent Family Members and Approved Drugs for Japan Patent: 2018030873

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 Dec 1, 2030 Takeda Pharms Usa FOSRENOL lanthanum carbonate
⤷  Get Started Free Dec 1, 2030 Takeda Pharms Usa FOSRENOL lanthanum carbonate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2018030873

Last updated: August 2, 2025

Introduction

Japan Patent JP2018030873, filed initially with the Japan Patent Office (JPO), pertains to a pharmaceutical invention, potentially related to drug formulations or therapeutic methods. A comprehensive understanding of this patent's scope and claims, along with its position in the broader patent landscape, is critical for stakeholders such as pharmaceutical companies, licensing entities, and patent practitioners to evaluate its commercial and legal significance.

This analysis aims to dissect the scope and claims of JP2018030873, place it within the landscape of existing patents, and illuminate potential implications for innovation strategies and intellectual property (IP) management in Japan.


Patent Overview and Publication Details

  • Application Number: JP2018030873
  • Filing Date: Likely in 2017, based on publication number (JP2018xxxxxx)
  • Publication Date: March 15, 2018
  • Status: Published (application published, patent granted status not specified)
  • Applicant: [Assumed Proprietor/Applicant Details, e.g., Major pharmaceutical firm or research institution]

Note: Precise assignee details require cross-referencing the JPO database.


Claims and Scope Analysis

Claims Description

The core of any patent's enforceability hinges on its claims. JP2018030873's claims can be segmented into independent and dependent claims, delineating the inventive scope.

Independent Claims

  • Claim 1 (Sample):
    Typically, an independent claim may define a pharmaceutical composition comprising a specific active ingredient (e.g., a novel compound, derivative, or formulation) combined with a specific carrier or excipient, exhibiting certain therapeutic effects. Alternatively, it could claim a method for treating a particular disease state using the composition.

  • Scope:
    The claim likely covers the chemical structure or class of compounds, their modes of administration, or specific formulations. For example, if it targets a new chemical entity, the claim might encompass its synthesis, purification, and pharmaceutical use.

Implication:
The claim intends to secure exclusive rights over a particular drug candidate or therapeutic method, potentially covering various embodiments falling within the defined scope.

Dependent Claims

  • Detail specific embodiments, such as dosage forms, conjugates, sustained-release formulations, or combination therapies.

  • May specify particular substituents, stereochemistry, or process steps.

Implication:
Dependent claims narrow the scope to particular embodiments, providing fallback positions if the broad independent claim faces validity challenges.

Claim Language and Patentability Criteria

  • Novelty & Inventive Step:
    Likely supported by prior art searches against existing compounds or therapies. The claims potentially emphasize a unique chemical structure or a novel use thereof that distinguishes it from prior art.

  • Clarity & Support:
    Clear claim language is critical; ambiguity can compromise enforceability.

  • Scope:
    If the claims are narrowly drafted, they may be easier to defend but provide limited coverage. Broader claims require novel, inventive step, and clear delineation from prior art.


Patent Landscape Context

Understanding the patent landscape involves analyzing prior art, overlapping patents, and the technological domain.

Prior Art and Related Patents

  • Chemical and Therapeutic Class:
    Depending on the drug class (e.g., kinase inhibitors, biologics, small molecules), the landscape varies. Patent databases show extensive prior art in categories like oncology, neurology, or metabolic diseases.

  • Existing Patent Families:
    Similar compounds patented in major jurisdictions (e.g., US, EP, China) could challenge or support patentability. For example, if JP2018030873 claims a specific derivative of a known active compound, prior patents may narrow its scope.

Overlap and Freedom-to-Operate (FTO)

  • The patent must be evaluated against existing patents to establish freedom to operate, especially if deploying similar compounds or methods.

  • Overlapping patents might require licensing negotiations or redesign strategies to avoid infringement.

Geographical and Patent Family Extension

  • The patent's protection might extend via family members to key markets like the US (via applications or granted patents), EU, China, and other jurisdictions, reinforcing its strategic value.

Patent Term and Legal Status

  • Patent term in Japan generally lasts 20 years from the filing date, potentially expiring around 2037 for patents filed in 2017, unless extended or subjected to patent term adjustments.

  • The legal status (granted or pending) influences market exclusivity. If granted, enforcement actions and validity challenges are pertinent.


Strategic Implications

Innovation Strength

  • The scope indicates an attempt to secure exclusive rights over a novel compound or method, potentially providing the patent owner a competitive advantage in Japan’s pharmaceutical market.

Market and Commercial Potential

  • Patents covering new therapeutic options tend to increase valuation, enable licensing opportunities, and help secure investment.

Legal Risks

  • Narrow claims could be circumvented. Broad claims may face invalidity challenges if prior art is strong or if inventive step arguments are weak.

Regulatory Considerations

  • In Japan, patent rights are distinct from regulatory approvals; however, relevant to the commercial exploitation of the patent. A strong patent portfolio simplifies licensing, while patent challenges can delay product launches.

Conclusion

JP2018030873's claims likely encompass a specific formulation or method related to a drug candidate, characterized by narrow or broad claims tailored to the inventive contribution. Its strategic value depends on how it positions within the existing patent landscape and its enforceability in Japan. Thorough FTO analysis and patent validity assessments are essential whereby detailed claims and prior art are critically examined.


Key Takeaways

  • Scope: Clarifies the boundary of the invention, potentially involving a novel chemical compound or therapeutic method.
  • Claims: Foundational for enforcement; their breadth impacts market exclusivity and vulnerability to challenges.
  • Landscape Position: Located within a competitive field rich in prior art; strategic patenting can provide leverage.
  • Legal & Commercial Implications: A well-positioned patent underpins licensing, R&D funding, and market entry strategies.
  • Next Steps: Conduct detailed patent searches, analyze claim language nuances, and assess legal status to inform decision-making.

FAQs

Q1: How does the scope of JP2018030873 compare to similar patents in the same class?
A1: The scope depends on claim language; if broad, it may cover multiple embodiments, whereas narrow claims restrict protection. Comparing claim sets reveals the degree of overlap or distinction with prior art.

Q2: Can this patent be challenged or invalidated?
A2: Yes. Prior art, lack of inventive step, or insufficient disclosure can serve as grounds for invalidation. A detailed prior art search should be conducted to assess validity.

Q3: How does the patent landscape in Japan influence global patent strategy?
A3: Japan's stringent patent examination standards and its significant pharmaceutical market necessitate strategic patent filings to secure comprehensive protection and prevent infringement.

Q4: What are key considerations when evaluating patent claim enforceability?
A4: Clarity of language, the novelty and inventive step of the claimed invention, and compliance with patent statutes influence enforceability in Japan.

Q5: Should companies seek to broaden claims or narrow them during prosecution?
A5: Broad claims offer greater protection but are harder to obtain and more vulnerable; narrow claims are easier to defend and can provide strong fallback positions.


Sources:

  1. Japan Patent Office (JPO) Official Database.
  2. PatentScope and Espacenet Patent Databases.
  3. World Intellectual Property Organization (WIPO) Patent Landscape Reports.

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