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Last Updated: December 28, 2025

Profile for Japan Patent: 2024071399


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US Patent Family Members and Approved Drugs for Japan Patent: 2024071399

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 29, 2041 Abbvie QULIPTA atogepant
⤷  Get Started Free Jun 6, 2039 Abbvie QULIPTA atogepant
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Patent Analysis of Japan Patent JP2024071399

Last updated: September 24, 2025

Introduction

Japan’s pharmaceutical patent landscape continues to evolve, driven by innovations aimed at addressing unmet medical needs and enhancing therapeutic efficacy. Patent JP2024071399, filed and published recently, exemplifies this dynamic environment. A detailed examination of its scope, claims, and broader patent landscape provides essential insights for stakeholders—researchers, patent strategists, and pharma companies—interested in this technology’s commercialization potential.


Overview of Patent JP2024071399

Filing and Publication Details:

  • Filing Date: Likely around mid-2024 (exact date not specified here)
  • Publication Number: JP2024071399
  • Application Type: Patent Application (publicly available document post-publication)
  • Application Status: Pending or granted (pending status needs verification via official JPO databases)

Technological Focus:
Patents of this nature generally involve novel compounds, pharmaceutical formulations, or therapeutic methods. While the detailed claims are necessary for precise delineation, preliminary indications suggest a focus on small-molecule drugs, biologics, or drug delivery systems relevant to specific disease indications.


Scope and Claims Analysis

1. Claim Structure and Hierarchy

A typical Japanese patent comprises multiple claims, beginning with independent claims that define the broadest scope, followed by dependent claims that specify particular embodiments or optional features.

Expected composition for JP2024071399:

  • Independent Claims: Likely to define a novel compound, pharmaceutical composition, or method of treatment.
  • Dependent Claims: Narrow to specific variants—e.g., formulation specifics, dosage forms, or targeting particular patient populations.

2. Scope of Claims

Without the full text, an assumed analysis indicates the patent’s scope might include:

  • Chemical Entities or Compounds: Novel molecules with unique structures or modifications that improve efficacy, stability, or safety.
  • Method of Use: Treatment methods involving the compound for specific diseases or conditions, such as cancers, neurological disorders, or infectious diseases.
  • Formulation Techniques: Novel drug delivery systems, sustained-release formulations, or combination therapies.

The breadth of claims determines the patent's enforceability and commercial relevance. Broad claims covering a class of compounds or general methods provide wider protection, while narrow claims focus on specific compounds or methods.

3. Patentability and Novelty Considerations

The patent’s claims must demonstrate a clear novelty and inventive step relative to prior art:

  • Prior Art Landscape:

    • International patents and publications, especially from major pharmaceutical developers.
    • Existing compounds with similar structures or functions.
    • Previous therapeutic methods or formulations designed for similar indications.
  • Innovative Features:

    • Structural modifications that confer additional benefits.
    • Innovative delivery mechanisms enhancing bioavailability.
    • Specific therapeutic combinations that demonstrate synergistic effects.

Potential inventive step arguments:
A notable leap beyond existing knowledge—such as a novel chemical modification leading to reduced toxicity or improved therapeutic index—would strengthen patent robustness.

4. Patent Validity and Enforcement Challenges

The enforceability of JP2024071399 hinges on the uniqueness and non-obviousness of the claims. Prior art searches are essential for identifying overlaps and potential challenges. Additionally, as Japan’s patent office (JPO) emphasizes clarity and support, claims must precisely define the scope and technical features.


Patent Landscape Context

1. International Patent Filing Strategy

Patent applicants often seek protection via PCT processes or direct national filings in major markets like the US, EU, and China. For a Japanese patent, it’s crucial to evaluate whether:

  • JP2024071399 corresponds to a European, US, or PCT application.
  • Similar patents exist in global jurisdictions, influencing potential freedom-to-operate.

Comparative landscape:

  • Patents similar in structure or claims might be inquired into for patent thickets or freedom-to-operate strategies.
  • Major players such as Pharma Co. A and B hold extensive patent portfolios covering related compounds or methods.

2. Competitive Analysis

  • Patent Families: Similar patents that form part of a broader patent family protect related embodiments, increasing defense robustness.
  • Litigation and Licensing: Patent JP2024071399 may be subject to licensing or infringement disputes, especially if overlapping with existing patents.
  • Market Impact: Valid and broad patents can provide exclusivity for 20 years from filing, fostering market advantages.

3. Patent Trends in the Relevant Field

  • The Japanese pharmaceutical sector leans heavily into oncology, neurology, and infectious diseases.
  • Recent filings indicate a focus on innovative small molecules and delivery systems designed to improve patient compliance and treatment outcomes.
  • Patent filings are increasingly incorporating biologics, personalized medicine, and combination therapies.

Implications for Stakeholders

Pharmaceutical Companies:

  • Identifying the scope of JP2024071399 informs licensing opportunities and R&D direction.
  • Monitoring competitors’ patent claims helps avoid infringement and identify areas for innovation.

Legal & Patent Strategists:

  • Validity assessments require thorough prior art searches.
  • Developing workarounds or designing around broad claims could secure competitive advantages.

Researchers:

  • Understanding claim scope guides translational efforts, focusing on novel features that can extend or improve upon the patented technology.

Conclusion: Strategic Considerations

  • Scope Clarity: Broad independent claims that cover a wide class of compounds or therapeutic methods confer competitive strength but are more scrutinized in validity assessments.
  • Patent Position: The strength hinges on the novelty, inventive step, and clarity of claims compared to prior art.
  • Landscape Dynamics: The Japanese patent environment emphasizes specific structural features and methods, but global patents may offer additional layers of protection or challenges.

Key Takeaways

  • JP2024071399 likely claims a novel chemical compound, formulation, or therapeutic method, with the scope determined chiefly by the independent claims’ breadth.
  • Thorough prior art analysis is required to evaluate patent strength and freedom-to-operate.
  • The patent landscape is populated by competing patents, underscoring the importance of strategic filing, licensing, and potential enforcement actions.
  • Global patent comparability will shape the commercial viability and licensing opportunities for the patent.
  • Ongoing monitoring of subsequent prosecution, patent grants, or challenges is critical for leveraging this patent in strategic decision-making.

FAQs

Q1. How does the scope of claims in JP2024071399 influence its market exclusivity?
The broader the independent claims, the wider the protection, potentially covering entire classes of compounds or methods, thereby extending market exclusivity. Narrow claims limit protection but may be easier to defend and validate.

Q2. What factors determine the patentability of the claims in this patent?
Novelty, inventive step (non-obviousness), and industrial applicability. Thorough prior art searches are crucial to establish these criteria.

Q3. How does this patent compare with international patent filings?
It depends on whether equivalent applications exist in major jurisdictions. Parallel filings or PCT applications can extend protection globally.

Q4. Can existing patents challenge the validity of JP2024071399?
Yes. Validity challenges can be based on prior art, obviousness, or lack of inventive step, potentially leading to patent revocation or narrowing.

Q5. What strategic steps should stakeholders take regarding this patent?
Conduct comprehensive prior art searches, monitor patent prosecution status, explore licensing opportunities, and consider designing around broad claims for competitive advantage.


References
[1] Japan Patent Office (JPO). Patent databases and official publications.
[2] WIPO. Patent Insight Reports.
[3] Patent scope analysis tools (e.g., Patentscope, Espacenet).

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