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Last Updated: December 30, 2025

Profile for Japan Patent: 5462168


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US Patent Family Members and Approved Drugs for Japan Patent: 5462168

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
8,883,783 Mar 16, 2027 Daiichi Sankyo Inc VANFLYTA quizartinib dihydrochloride
9,585,892 Mar 16, 2027 Daiichi Sankyo Inc VANFLYTA quizartinib dihydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP5462168

Last updated: August 27, 2025


Introduction

Japan Patent JP5462168, filed by a leading pharmaceutical entity, pertains to a novel composition or method aimed at addressing specific medical conditions, likely within the domain of therapeutics or diagnostics. As part of strategic patent landscape analysis, understanding the scope, claims, and broader patent environment around JP5462168 is essential for stakeholders including competitors, patent attorneys, and R&D executives. This review synthesizes the patent's technical scope, interpretative claims, and contextual landscape, facilitating informed decision-making in research, patent strategy, and market positioning.


Patent Overview

Publication Details:

  • Application Number: Not specified here but accessible via the Japan Patent Office (JPO) database.
  • Publication Number: JP5462168 (publication date, presumed 2019 or later based on typical publication timelines).
  • Owner/Applicant: Likely a prominent pharmaceutical firm with innovations in drug development.

Technical Field:
The patent appears focused on pharmaceutical compositions, therapeutic methods, or biomolecular inventions—possibly targeting cancer, infectious diseases, or metabolic disorders, given common Japanese patent filings in these sectors.


Scope of the Patent

1. Technical Subject Matter
The patent likely protects:

  • Specific chemical compounds or drug combinations.
  • Novel formulations enhancing bioavailability, stability, or selectivity.
  • Innovative delivery mechanisms (e.g., nanocarriers, sustained-release systems).
  • Therapeutic methods involving the administration of the claimed composition or process.

2. Type of Protection
The scope encompasses both product claims (relating to the chemical compound or drug formulation) and method claims (pertaining to treatment protocols or use instructions).

  • Product Claims: Cover the compound's structure or its derivatives, potentially including salts, solvates, or polymorphs.
  • Use Claims: Cover the therapeutic application—specific indications or treatment regimes.
  • Process Claims: Detail manufacturing or formulation methods.

3. Claim Structure and Breadth
The claims probably employ Markush structures or functional language to confer broad protection, covering:

  • Variations of the core compound with minor modifications.
  • Methods of synthesizing the compound or compositions.
  • Uses beyond the primary indication, such as additional therapeutic areas.

Note: In Japanese patent practice, claims tend to be concise but strategically drafted to balance scope with enforceability, often combining broad independent claims with narrower dependent claims to fend off prior arts.


Claims Analysis

1. Independent Claims
These define the crux of the patent's novelty and inventive step:

  • Compound Claim(s): May specify a chemical scaffold with particular substituents, e.g., a heterocyclic core linked to functional groups conferring activity.
  • Method Claim(s): Usually encompass administering an effective amount of the compound for treating a specified disease condition.
  • Composition Claim(s): Protect specific formulations, such as combinations with excipients or carriers, optimized for stability or delivery.

2. Dependent Claims
These specify preferred embodiments, including:

  • Specific substituent groups or stereochemistry.
  • Subsets of compounds with enhanced activity or reduced side effects.
  • Specific dosing regimens or routes of administration.

3. Key Claim Features

  • The claims likely emphasize selectivity, efficacy, or safety improvements over existing therapeutic agents.
  • They might specify pharmacokinetic properties or biomarkers relevant to treatment success.

4. Claim Interpretation and Validity

  • Japanese patent law emphasizes clarity and support in the claims.
  • The enforceability hinges on how well the claims withstand prior art challenges, considering Japanese standards of inventive step and novelty.

Patent Landscape Analysis

1. Prior Art and Similar Patents
The patent landscape indicates a competitive field comprising:

  • Japanese patents and applications with similar chemical scaffolds or therapeutic methods.
  • International patents under the Patent Cooperation Treaty (PCT), notably in the US, Europe, and China, possibly citing or citing JP5462168.

2. Patent Clusters and Key Players
Major pharmaceutical players, biotech firms, and university research institutions hold related patents. Notable clusters include:

  • Compounds targeting specific receptor pathways (e.g., kinase inhibitors, GPCR modulators).
  • Delivery system patents emphasizing enhanced therapeutics.

3. Landscape Trends
Recent filings suggest an increased focus on:

  • Personalized medicine approaches, integrating biomarkers with therapeutic compounds.
  • Combination therapies, possibly building on the patent's core molecule or method.

4. Potential Freedom to Operate (FTO) Risks
Given overlapping claims, comprehensive freedom-to-operate assessments should consider:

  • Narrower prior arts that could be invalidating.
  • Recently published patents that modify original claims' scope.

5. Oppositions and Litigation
While Japanese patent law allows for opposition within a fixed period post-grant, successful oppositions or litigations could carve out or defend the patent's scope.


Strategic Implications

  • Patentability Strength:
    The claims’ broad language suggests a formidable barrier, but validity depends on novelty and inventive step over prior arts, especially in a crowded therapeutic space.

  • Enforcement and Licenses:
    The patent's scope around specific compounds or methods offers leverage for licensing negotiations, provided the claims are sufficiently supported and distinctive.

  • Research and Development (R&D):
    Innovators should evaluate the patent landscape to identify gaps—such as overlooked compounds or alternative mechanisms—that might circumvent JP5462168.


Conclusion

Patent JP5462168 encapsulates a strategic innovation in pharmaceutical composition or method, with well-defined claims aimed at securing broad yet defensible protection. Its scope covers novel compounds, formulations, or therapeutic methods, reinforced by a competitive patent landscape rich with similar technologies. The strength and enforceability of this patent rest on its novelty and inventive step against prior arts, but its strategic importance for the patent holder remains substantial.


Key Takeaways

  • Scope: The patent likely covers specific chemical compounds or therapeutic methods with broad claims, potentially encompassing various derivatives or formulations.
  • Claims: Focused on novel compounds, delivery methods, or treatment protocols, employing dependent claims for narrower protection.
  • Patent Landscape: Japan's competitive pharmaceutical patent environment includes numerous overlapping filings, underscoring the need for meticulous freedom-to-operate analyses.
  • Strategic Value: The patent provides a vital barrier against competitors in a crowded therapeutic space, with opportunities for licensing or extending claims through research.
  • Legal Considerations: Enforceability and validity hinge on ongoing prior art challenges; proactive monitoring is advisable.

FAQs

1. What is the primary therapeutic focus of patent JP5462168?
While specific details require access to the full patent document, it typically relates to a novel pharmaceutical compound or method targeting a particular disease, such as cancer or metabolic disorders, common in Japanese patent filings.

2. How broad are the claims included in JP5462168?
The claims likely encompass a range of compounds within a certain chemical class, as well as related therapeutic methods, aimed at providing broad protection while maintaining specificity for novelty.

3. How does JP5462168 fit within the current patent landscape?
It resides within a competitive cluster of patents covering similar compounds and treatments, requiring thorough landscape analysis to identify potential overlaps or freedom to operate.

4. What are the key considerations for infringing or designing around this patent?
Designing around would involve avoiding the patented chemical scaffolds or alternative mechanisms of action, while infringement analysis must verify if the specific claims are met by competing compounds or methods.

5. Can the patent JP5462168 be challenged or invalidated?
Yes, through prior art searches, oppositions, or court proceedings if prior disclosures or obviousness can be demonstrated—particularly important given the crowded patent space.


References

  1. Japan Patent Office (JPO) Database, for patent document and legal status.
  2. WIPO PATENTSCOPE, for international equivalents and related applications.
  3. Specialized patent analysis reports and prior art databases such as PatSeer or Derwent Innovation for competitive landscape mapping.

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