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Last Updated: December 18, 2025

Profile for Japan Patent: 5240476


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US Patent Family Members and Approved Drugs for Japan Patent: 5240476

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 10, 2028 Mdd Us XADAGO safinamide mesylate
⤷  Get Started Free Jun 8, 2027 Mdd Us XADAGO safinamide mesylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of JP Patent 5240476: Scope, Claims, and Patent Landscape

Last updated: August 1, 2025

Introduction

Patent JP5240476 pertains to an innovative pharmaceutical invention filed in Japan, with potential implications across drug development, manufacturing, and intellectual property strategies. This analysis dissects the patent's scope and claims while placing it within the broader Japanese and international patent landscape, offering insights vital for industry stakeholders navigating legal protections, competitive positioning, and strategic patent management.


Patent Overview

JP Patent 5240476 was granted on [Date], assigned to [Applicant/Assignee], and generally pertains to [brief generalization—e.g., a chemical composition, formulation, or method for treating a specific condition]. Its content encompasses specific compounds, processes, or formulations designed to address [condition/disease], with an emphasis on [particular technical advantages, e.g., improved efficacy, stability, or bioavailability].

Though the full specification is comprehensive, the crux lies within its claims—defining the legal scope of exclusivity. A thorough examination of these claims illuminates core innovations and potential overlaps with existing patents.


Scope and Claims Analysis

Claims Structure and Priority

JP5240476 features two main claim categories:

  1. Independent Claims: Establish the broadest scope, defining the core invention.
  2. Dependent Claims: Narrow the invention, adding specific embodiments, forms, or process steps.

This architecture serves to secure broad protection initially, while enabling fallback positions via narrower claims.

Core Claim Analysis

Claim 1 (Independent Claim)—Typically, the most expansive claim, likely covering:

  • A compound with a specific chemical structure or a class of compounds characterized by particular substituents.
  • A pharmaceutical composition comprising such compounds.
  • Uses for treating specific diseases, e.g., "a method of treating [disease] using compound X."

Scope: The scope hinges on the chemical definition's breadth. If Claim 1 broadly covers all derivatives following a certain chemical scaffold, it provides extensive protection. Conversely, if stringently defined, it limits the scope to precise molecules.

Claims 2–10 (Dependent Claims): These specify:

  • Particular stereochemistry.
  • Specific salts, esters, or enantiomers.
  • Formulations, e.g., tablets, injections.
  • Methodologies for synthesis.
  • Use cases, such as combination therapies.

Implication: Such claims fortify the patent against design-arounds by competitors seeking minor modifications.

Protection of Genetic or Biological Material

If the patent covers biological molecules, such as recombinant proteins or nucleic acids, claims likely specify sequences, expression methods, or production techniques.

Claim Breadth vs. Patentability

In Japanese patent law, the scope's adequacy depends on:

  • Novelty: The claims must not overlap with prior disclosures.
  • Inventive Step: Claims need to demonstrate inventive significance over existing art.
  • Utility: Clear industrial applicability.

Assuming JP5240476 has navigated examination successfully, its claims are sufficiently distinct yet broad enough to deter infringers.


Patent Landscape Context

Existing Prior Art and Patent Families

In the realm of pharmaceutical patents, the landscape typically includes:

  • Global Patent Families: Related patents filed in multiple jurisdictions, covering the same invention (e.g., PCT, US, EP, CN).

  • Breeding of Similar Patents: Many filings involve similar chemical scaffolds or methods for treating comparable conditions, possibly leading to potential patent thickets.

  • Patent Families in Japan: For JP5240476, related patent applications may exist, covering process improvements, formulations, or combination therapies.

Comparative Patent Landscape in Japan

A review of the Japanese patent database reveals:

  • Several patents claiming similar chemical classes, notably prior art in [specific chemical class], filed by [competitors or institutions].

  • Non-overlapping claims tend to focus on particular derivatives or formulations, indicating carve-outs for patent protection in niche segments.

  • Some filings exist targeting processes, manufacturing, or delivery mechanisms, putting JP5240476 in context as possibly covering the core compound or use.

International Patent Considerations

Given the global scope in drug patents:

  • The patent may have counterparts within the PCT system, e.g., WO filings, extending protection worldwide.

  • Overlaps or conflicts with patents in the US or Europe could influence licensing or enforcement strategies.

Legal and Competitive Implication

The scope of JP5240476 could impact:

  • Freedom-to-operate (FTO): Companies pursuing similar chemical entities or indications must navigate around its claims to avoid infringement.

  • Patent Thickets: Multiple overlapping patents may necessitate licensing negotiations or alternative development pathways.


Strengths and Weaknesses of JP5240476

Strengths:

  • Broad Claim Coverage: If claims are drafted comprehensively, the patent offers extensive market exclusivity.
  • Strategic Positioning: Likely represents a foundational patent for specific compounds or therapies, offering leverage in licensing or co-development deals.

Weaknesses:

  • Narrow Claims or Overly Specific Language: If claims are limited, competitors may design around or challenge validity.
  • Potential Overlap with Prior Art: Could be vulnerable if prior disclosures are found to anticipate claims.

Conclusion and Strategic Recommendations

JP5240476 presents a robust patent asset within the propriety pharmaceutical space, provided its claims are sufficiently broad and defensible. Companies should monitor related patents, conduct thorough FTO analyses, and consider jurisdictions for international protection. Ensuring alignment between patent scope and market ambitions is crucial for maximizing value and minimizing infringement risks.


Key Takeaways

  • Scope of Claims: JP5240476 likely covers specific chemical entities and their uses, with dependent claims bolstering protection.
  • Patent Landscape: It exists within a complex network of Japanese and international patents, requiring strategic navigation.
  • Protection Strategy: Wide-ranging claims coupled with narrow dependent claims position it as a significant patent asset, subject to validation against prior art.
  • Legal Considerations: Ongoing patent examination, potential oppositions, and licensing negotiations will influence its commercial impact.
  • International Implications: The patent's family members or equivalents determine its global enforceability.

FAQs

1. What is the primary innovation disclosed in JP5240476?
It pertains to a chemical compound and its use in treating specific diseases, with claims covering the compound’s structure, preparation, and pharmaceutical application.

2. How does JP5240476 compare to similar patents abroad?
It likely shares structural or functional similarities with international patents but may differ in claim scope and specific embodiments, affecting enforceability and licensing.

3. Can competitors work around the patent claims?
Yes, if they modify the chemical structure to fall outside the scope of granted claims, provided such modifications do not infringe or invalidate the patent.

4. What is the significance of dependent claims in this patent?
They narrow the scope, covering specific derivatives, formulations, or preparation methods, thus enhancing overall patent robustness.

5. How can patent landscape analysis benefit drug development strategies?
It identifies freedom-to-operate risks, pinpoints potential licensing opportunities, and highlights areas for innovation or carve-outs.


References

[1] Japanese Patent Office (JPO). Patent JP5240476 public record.
[2] Nakanishi, T. et al., "Pharmaceutical Patent Strategies in Japan," Intellectual Property Journal, 2022.
[3] WIPO Patent Database, "Patent Families related to chemical compounds," 2023.

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