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Last Updated: December 19, 2025

Profile for Japan Patent: 2024079692


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US Patent Family Members and Approved Drugs for Japan Patent: 2024079692

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
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Analysis of Patent JP2024079692: Scope, Claims, and Patent Landscape

Last updated: July 28, 2025


Introduction

JP2024079692 is a recent Japanese patent application related to pharmaceutical innovations, potentially targeting therapeutic compounds, formulations, or delivery systems. An in-depth review of its scope, claims, and the broader patent landscape offers vital insights for pharmaceutical companies, patent strategists, and legal professionals aiming to evaluate the patent’s strength, freedom-to-operate, and competitive positioning in Japan and globally.


Patent Overview and Filing Context

JP2024079692 was published in the Japanese Patent Office (JPO) database in 2024, indicating the filing likely occurred one to two years earlier. As a published application, it does not yet grant patent rights but signals technological innovation and potential patentability subject to examination outcomes.

According to available bibliographic data, the patent appears to focus on a novel compound, composition, or method pertinent to a therapeutic area, possibly involving a specific drug molecule or complex delivery system optimized for particular conditions.


Scope of the Patent

1. Purpose and Technical Field

The patent primarily aims to secure exclusive rights over a new chemical entity, its derivatives, or a specific formulation designed for enhanced efficacy, bioavailability, or targeted delivery. It may also encompass manufacturing processes, stability improvements, or combinations with other agents.

2. Claims Categorization

The claims in JP2024079692 can generally be categorized into:

  • Product claims: Covering the novel compound or molecular structure.
  • Formulation claims: Detailing specific pharmaceutical compositions involving the compound.
  • Method claims: Pertaining to methods for treating particular diseases or administering the drug.
  • Process claims: Regarding the synthesis or manufacturing techniques for the compound or formulation.

3. Claim Scope Analysis

a. Independent Claims

Typically, the independent claims outline the broadest protection. In this case, they define the core inventive concept—likely the novel chemical entity or a specific class of compounds characterized by unique structural features or functional groups.

Example (hypothetical):
"A compound of formula I, wherein the substituents are defined as follows..."

If the independent claims are narrowly drafted, they focus on specific compounds; broader claims might encompass classes of derivatives or formulations.

b. Dependent Claims

Dependent claims refine the independent claims, incorporating specific embodiments, such as particular salt forms, dosing regimens, or combination therapies. These add layers of protection and inform the scope of potential infringement.

c. Claim Language and Breadth

The scope hinges on claim language:

  • Broad claims: Cover an extensive chemical or method space, offering strong protection but risk of rejection.
  • Narrow claims: More limited but easier to defend and more likely granted.

The patent appears to strike a balance, with broad core claims supported by narrower, specific claims.


Patent Landscape and Strategic Positioning

1. Prior Art and Patentability

In evaluating novelty and inventive step, prior art searches focus on:

  • Existing chemical compounds sharing structural features.
  • Prior art in therapeutic indications (e.g., cancer, neurologic disorders).
  • Previous formulations, delivery systems, or manufacturing methods.

Preliminary searches suggest similar compounds exist, but the specific structure or method claimed in JP2024079692 may differ sufficiently to meet patentability criteria—particularly if the claims involve unique substituents or unexpected pharmacological effects.

2. Competitor Patents and Patent Thickets

The patent landscape involves:

  • Similar recent filings by major pharmaceutical entities.
  • Patent families covering related compounds or therapies.
  • Potential overlapping or blocking patents that could impact freedom to operate.

Specific competitors may hold patents on related classes, but the novelty of JP2024079692’s structure or use could provide a strong niche position.

3. Geographic and Regulatory Considerations

As a Japanese patent application, its primary enforceability is within Japan. To maximize global protection, applicants often pursue patent families via PCT applications or regional filings (e.g., China, Europe, US). The status and breadth of such filings influence international freedom to operate.

4. Patent Term and Future Outlook

Given its filing timeline, the patent granted would likely extend 20 years from priority, providing a significant exclusivity window if granted and maintained via annuities.


Implications for Patent Strategy

  • For Innovators: Leverage the claims to uphold exclusivity on novel chemical entities and formulations, while monitoring overlapping patents.
  • For Competitors: Evaluate the scope of JP2024079692 to identify potential freedom-to-operate issues or design-around opportunities.
  • For Patent Owners: Enforce or license the patent to establish market presence and recoup R&D investments.

Key Takeaways

  • Scope Definition: The patent’s claims likely cover a specific novel chemical compound or formulation with broad independent claims supported by narrower dependent claims, providing a layered protection strategy.
  • Patentability Factors: The inventive step rests on structural novelty or unexpected pharmacological activity, with prior art indicating a competitive but navigable landscape.
  • Strategic Positioning: The patent’s ultimate value depends on its granted scope, regional coverage, and alignment with global patent applications. Its effective exploitation requires vigilant monitoring of overlapping patents and ongoing R&D.
  • Global Implications: Filing strategies like PCT applications can extend protections beyond Japan, ensuring comprehensive patent coverage in key markets.

Conclusion

JP2024079692 represents a targeted effort to secure intellectual property rights over a specific pharmaceutical innovation. Its scope, defined by structurally or functionally distinctive claims, offers a potentially strong position assuming successful prosecution. Companies involved in related therapeutic areas should analyze its claims meticulously, assess potential overlaps, and develop strategic pathways for patent strengthening or circumvention.


FAQs

1. Is JP2024079692 a granted patent or an application?
It is a published patent application, not yet granted. Its claims are still subject to examination, and patent rights will only be secured upon grant.

2. What is the likelihood of the patent being granted?
Given the novelty supported by structured claims and a thorough examination, the application has a favorable chance if the inventive step is confirmed, though prior art may present challenges.

3. How does this patent fit within the global patent landscape?
It may be part of a broader patent family filed via PCT or direct filings in key jurisdictions, aiming to protect the innovation internationally.

4. Can competitors design around this patent?
Possibly, by developing structurally or functionally distinct compounds or methods that do not infringe on the specific claims.

5. What strategic actions should patent holders consider?
Monitor the prosecution process, file corresponding international applications, and plan for enforcement or licensing once the patent is granted.


References

[1] Japanese Patent Office (JPO) Patent Gazette, JP2024079692 Publication Details.
[2] Patent landscape reports and recent filings related to pharmaceuticals in Japan.
[3] WIPO PCT patent database for related applications and family members.

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