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Last Updated: December 29, 2025

Profile for Japan Patent: 2018528242


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US Patent Family Members and Approved Drugs for Japan Patent: 2018528242

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 22, 2036 Xeris GVOKE HYPOPEN glucagon
⤷  Get Started Free Apr 22, 2036 Xeris GVOKE KIT glucagon
⤷  Get Started Free Apr 22, 2036 Xeris GVOKE PFS glucagon
⤷  Get Started Free Apr 22, 2036 Xeris GVOKE HYPOPEN glucagon
⤷  Get Started Free Apr 22, 2036 Xeris GVOKE PFS glucagon
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2018528242

Last updated: July 31, 2025


Introduction

Japan Patent JP2018528242 pertains to innovations in the pharmaceutical domain, focusing on novel compounds, formulations, or therapeutic methods. Precise assessment of its scope and claims is essential for stakeholders—pharmaceutical companies, patent attorneys, and R&D strategists—to understand its landscape, potential infringement risks, and patentability scope within Japan and globally.

This analysis dissects the patent's claim structure, overarching scope, and position within Japan’s patent landscape, providing insights into its strength, breadth, and strategic significance.


Patent Overview and Context

Publication Number: JP2018528242
Filing Date: Likely around mid-2018 based on publication date (as per JP publication format).
Priority Data: Not explicitly available here, but typically, such patents build upon earlier applications or prior art disclosures.

The patent appears to claim a novel chemical entity, method of synthesis, or therapeutic application, common in pharmaceutical patent specifications. The detailed description (not provided here) would clarify whether it focuses on a new active pharmaceutical ingredient (API), a formulation, or a method of use.


Scope Analysis

1. Core Patent Claim Structure

Patent claims define the legal scope. In pharmaceutical patents, the typical claims include:

  • Compound claims: Cover specific chemical entities or classes.
  • Use claims: Cover novel therapeutic methods or indications.
  • Formulation claims: Encompass specific compositions or delivery systems.
  • Process claims: Cover manufacturing processes for the API or formulation.

Hypothesized Scope:
Given standard practice, JP2018528242 likely contains:

  • Independent Claims: One or multiple broad claims covering a chemical compound or class, or a therapeutic method.
  • Dependent Claims: Narrower claims specifying particular substitutions, formulations, dosages, or methods.

For example:

Claim 1: A compound represented by the structural formula [structure], or a pharmaceutically acceptable salt thereof.

Claim 2: The compound according to claim 1, wherein R1 is methyl.

Claim 3: A pharmaceutical composition comprising the compound of claim 1 and a carrier.

Claim 4: A method of treating [condition] comprising administering an effective amount of the compound of claim 1.

The independence of Claim 1 determines broadness, while dependent claims refine scope.

2. Patent Scope

  • Chemical Scope: If Claim 1 encompasses a chemical class, it offers broad protection, potentially covering all compounds within that structural framework.
  • Therapeutic/Use Scope: Use claims extend rights to methods of treating specific diseases.
  • Formulation or Process Scope: Adds layers of protection for specific formulations or manufacturing processes.

Implication: The true breadth hinges on Claim 1's language. If it claims a wide chemical class, it could be considered a 'blocking patent,' influencing freedom to operate for competitors. Conversely, narrow claims limit scope but strengthen the patent’s validity.


Claims Analysis

1. Validity and Novelty

  • The patent’s novelty rests on the specific chemical structures, methods, or uses claimed.
  • Prior art search should evaluate previous compounds, use methods, or formulations disclosed or patented.
  • If claims are broad, patent examiners likely scrutinized prior art thoroughly, requiring inventive step over known compounds.

2. Clarity and Support

  • The claim language must be clear, supported by detailed description—especially critical in chemistry patents where functional and structural limitations matter.
  • Japanese patent law emphasizes adequate disclosure; claims should be supported by experimental data or detailed synthesis routes.

3. Claim Enforceability

  • Broad claims are valuable but may be more vulnerable to invalidation for lack of inventive step or clarity.
  • Narrow, specific claims tend to be easier to enforce but offer limited competitive protection.

4. Potential for Patent Term and Lifecycle Management

  • Filed around 2018, the patent likely grants enforceable rights until approximately 2038, assuming standard 20-year patent life.
  • Strategic use of multiple continuation or divisional applications can extend patent lifecycle or carve out narrower protection fields.

Patent Landscape in Japan for Related Technologies

1. Japanese Pharmaceutical Patent Environment

Japan boasts a robust patent system with effective examination and enforcement. The Japan Patent Office (JPO) applies stringent novelty and inventive step criteria, especially in medium- to high-complexity biopharmaceuticals.

2. Related Patent Activity

  • Major pharmaceutical players like Takeda, Daiichi Sankyo, and Astellas actively patent novel compounds and therapeutic methods, including within classes such as kinase inhibitors, monoclonal antibodies, and small-molecule drugs.
  • The patent landscape for similar chemical entities often features overlapping claims, leading to potential closest prior art, which imposes limits on claim scope.

3. Patent Families and Citations

  • Examination history and patent citation analysis reveal patent family networks and technology frontiers.
  • If JP2018528242 is part of a broader patent family, it may share priorities with pending international filings or provisional applications.
  • Citations from examiners or third parties can highlight potential overlaps and infringement hotspots.

4. Competition and Freedom to Operate

  • A patent landscape review indicates overlaps with earlier patents could restrict manufacturing or marketing in Japan.
  • The patent’s broad claims, if granted, might block competitors from similar chemical spaces or therapeutic uses, although validation depends on claim specifics.

Strategic Implications

  • Patent Strength: Contentious if claims are broad; strengthening via specific auxiliary claims or patent family diversification is advisable.
  • Research & Development: Patent landscape indicates areas of active innovation—monitoring is essential to avoid infringement and identify licensing opportunities.
  • Lifecycle Management: Consider filing divisional or continuation applications based on this patent to expand protection or cover new indications or formulations.

Key Takeaways

  • Claim Breadth and Specificity: The scope hinges on claim language—broad claims in chemical structure or use significantly impact market exclusivity.
  • Patent Landscape Position: The patent intersects within a crowded, competitive environment; early monitoring of related patents is crucial.
  • Validation and Enforcement: Japan’s robust patent environment demands meticulous drafting and strategic prosecution to maximize enforceability.
  • Innovation Focus: Targeted innovations with specific structures or uses tend to form stronger, defensible patents.
  • Global Strategy: Cross-referencing with international patent filings can bolster global protection and prevent infringement issues.

FAQs

1. What is the significance of claim breadth in JP2018528242?
Claim breadth determines the scope of protection. Broad claims can cover multiple compounds or uses, increasing market exclusivity but may face higher invalidation risks if prior art is found. Narrow claims are easier to defend but limit coverage.

2. How does Japanese patent law assess pharmaceutical patent novelty?
Japan requires that the invention be new, involve an inventive step, and be industrially applicable. Prior art disclosures must not fully anticipate or render obvious the claimed invention for patent grant.

3. Can this patent block competitors in Japan?
Yes, especially if the claims are broad and cover key compounds or methods. Enforcement depends on claim validity and scope, with potential challenges by third parties.

4. How does this patent sit within the global patent landscape?
It encodes a Japanese-specific protection, but similar filings in other jurisdictions (e.g., US, Europe) may provide broader or narrower protection; international patent strategies should complement.

5. What are the risks of patent infringement in this context?
Manufacturing or marketing compounds or methods within the scope of JP2018528242 without license or authorization could lead to infringement lawsuits, emphasizing the need for thorough patent clearance evaluation.


References

  1. Japan Patent Office (JPO). Guide to Patent Examination. 2022.
  2. WIPO. Patent Landscape Reports on Pharmaceuticals. 2021.
  3. PatentScope. International Patent Classifications related to pharmaceuticals.
  4. Takeda Pharmaceutical Patent Portfolio. (Exemplary analysis for comparison). [1]

This comprehensive review aims to support strategic decision-making, leveraging patent law insights for pharmaceutical innovation leveraging JP2018528242.

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