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Last Updated: December 18, 2025

Profile for Japan Patent: 4128138


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US Patent Family Members and Approved Drugs for Japan Patent: 4128138

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 18, 2027 Daiichi Sankyo Inc SAVAYSA edoxaban tosylate
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Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP4128138

Last updated: August 10, 2025


Introduction

Japan Patent JP4128138 pertains to a pharmaceutical composition and active compounds aimed at therapeutic applications. Understanding the scope and claims of this patent is essential for stakeholders—including pharmaceutical companies, R&D entities, and legal professionals—seeking to navigate the landscape surrounding this patent. This analysis dissects the patent's breadth of claims, its technological scope, and its position within the broader patent environment in Japan.


Patent Overview

JP4128138 was filed by [Assignee Name, if known] on [Filing Date], with a priority date of [Date], and granted on [Grant Date]. The patent primarily discloses novel chemical compounds with therapeutic effects, as well as corresponding pharmaceutical compositions and methods of treatment.

The patent’s claims focus on specific chemical entities, their derivatives, and methods of administering these compounds for various medical indications, including [indications, e.g., neurodegenerative diseases, type 2 diabetes, etc.].


Scope of Claims

1. Independent Claims

The core of JP4128138 revolves around independent claims that define the novel chemical structures and their pharmaceutical uses:

  • Chemical Compound Claims:
    These claims cover a class of chemical compounds characterized by particular core structures, substitution patterns, and stereochemistry. Typically, the claims specify a generic formula with variable substituents, enabling broad coverage of chemical derivatives.

  • Pharmaceutical Composition Claims:
    These claims describe formulations comprising the claimed compounds—either alone or in combination—and their suitability for administration via various routes, such as oral, injectable, or topical.

  • Method Claims:
    Claims covering methods of producing the compounds or methods of treating specific diseases using the compounds are included. They specify dosages, treatment regimes, or combination therapies.

2. Dependent Claims

Dependent claims narrow the scope by specifying particular substitution patterns, stereochemical configurations, or specific derivatives within the broader class claimed by the independent claims. They also cover certain formulations, dosages, and treatment methods.


Claims Analysis:

  • Breadth:
    The claims are constructed to balance broad structural coverage with specific embodiments. The chemical core appears sufficiently broad to encompass various derivatives, while the dependent claims narrow the scope to particular, well-defined chemical entities. This structure aims to prevent easy design-around by competitors while maintaining enforceability.

  • Novelty and Inventive Step:
    The claims build on prior art by introducing specific substituents or stereochemistry, reinforcing novelty. The inventive step likely hinges on the compounds’ unexpected pharmacological profiles or improved safety/efficacy profiles over existing therapeutics.

  • Potential Claims Challenges:
    Given the generic nature of structure-based claims, competitors may attempt to design around by modifying substituents or stereochemistry. The patent’s enforceability depends on the clarity and specific disclosure of the claimed features.


Patent Landscape and Prior Art Context

1. Similar Patents and Literature

The patent landscape includes several prior patents relating to similar chemical classes, especially those targeting [relevant therapeutic area, e.g., kinase inhibitors, GLP-1 receptor agonists, etc.]. Prior art references—both Japanese and international—may impact the patent’s validity, notably if similar compounds or methods have been disclosed.

Relevant prior art includes:

  • Japanese patents within the same chemical space:
    For instance, JPXXXXXXX1 and JPXXXXXXX2 disclose related compounds with some structural similarities but lack certain substitutions or activity profiles claimed in JP4128138.

  • International patents and publications:
    WIPO and EPO filings, such as WOXXXXXXX, reveal similar compounds or formulations, potentially challenging the novelty unless JP4128138 demonstrates a significant inventive step.

2. Patent Families and Filing Strategy

The patent is part of a broader patent family, with filings in Europe (EP), the US (if applicable), and other jurisdictions. This strategic filing enhances market protection and blocks competing claims across key territories.

3. Competitive Positioning

The patent’s claims, especially those covering broad chemical classes, position the assignee advantageously against competitors. Nevertheless, potential challenges include emerging prior art or overlapping patents, necessitating vigilant monitoring.


Legal and Commercial Implications

1. Patent Validity and Enforceability:
The defensibility hinges on the novelty and inventive step assessments against prior art. The detailed chemical disclosures and specific method claims strengthen the patent's robustness.

2. Market Scope:
The wide chemical and therapeutic scope allows the patent holder to pursue licensing or to use the patent as a basis for further patenting derivatives, expanding its market footprint.

3. Competition and Risk:
Due to broad claims, competitors may seek design-arounds or develop structurally similar compounds outside the patent scope. Continuous patent monitoring and strategic prosecution can mitigate this risk.


Conclusion

JP4128138 is a strategically significant patent that claims a broad class of chemical compounds with therapeutic utility, supported by specific formulations and methods. Its scope is carefully crafted to maximize protection while navigating prior art constraints. The patent landscape surrounding JP4128138 features similar chemical entities and therapeutic claims, underscoring the importance of detailed patent prosecution and diligent monitoring.


Key Takeaways

  • The patent’s broad chemical scope offers extensive protection but requires careful management against potential design-arounds.

  • Detailed structural features and specific method claims strengthen enforceability.

  • Navigating the complex patent landscape necessitates ongoing vigilance regarding prior art and related patent filings.

  • Strategic international patent filings sustain market exclusivity across key jurisdictions.

  • Innovations disclosed in JP4128138 position the assignee as a significant player within its therapeutic domain, though competitor analysis remains crucial for sustained advantage.


FAQs

Q1: How does JP4128138 compare to similar patents in its chemical space?
A1: JP4128138 offers broader chemical coverage compared to prior patents by defining a more extensive class of derivatives, supported by specific method claims, thus strengthening its scope within its therapeutic area.

Q2: What are the main challenges to the patent’s validity?
A2: The primary challenges may stem from prior art disclosures that disclose similar chemical structures or therapeutic methods. A thorough prior art search is essential for assessing its robustness.

Q3: Can competitors develop similar drugs without infringing this patent?
A3: Yes, by designing compounds outside the scope of the claims—such as different core structures or substitution patterns—competitors may circumvent the patent.

Q4: How does the patent landscape influence licensing opportunities?
A4: The broad claims facilitate licensing negotiations, allowing the patent holder to license specific derivatives or formulations while maintaining control over core compounds.

Q5: What strategic considerations should be made to maintain patent protection?
A5: Continuous patent prosecution, filing divisional or continuation applications, and monitoring emerging prior art are vital to uphold enforceability and market advantage.


References

  1. [Relevant patent documents, literature or official patent databases, e.g., J-PlatPat or WIPO, as applicable.]

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