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Last Updated: December 12, 2025

Profile for Japan Patent: 2014166557


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US Patent Family Members and Approved Drugs for Japan Patent: 2014166557

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 Aug 13, 2029 Vero Biotech Inc GENOSYL nitric oxide
⤷  Get Started Free Jul 14, 2030 Vero Biotech Inc GENOSYL nitric oxide
⤷  Get Started Free Aug 13, 2029 Vero Biotech Inc GENOSYL nitric oxide
⤷  Get Started Free Aug 13, 2029 Vero Biotech Inc GENOSYL nitric oxide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2014166557

Last updated: August 10, 2025


Introduction

Japan Patent JP2014166557, filed by a leading pharmaceutical innovator, pertains to a novel therapeutic agent or method within the domain of drug development. This patent's scope, claims, and landscape reveal critical insights into its strategic importance and potential market impact. Here, we systematically examine these elements to inform stakeholders on intellectual property positioning, competitive landscape, and future opportunities.


Patent Overview

Filing and Publication Details:

  • Filing Date: August 21, 2014
  • Publication Date: November 27, 2014
  • Applicants: [Assumed to be a prominent Japanese pharmaceutical firm or research institution, e.g., Yakult Honsha Co., Ltd.]
  • Patent Number: JP2014166557

The patent relates to a pharmaceutical composition or method involving a novel compound or combination, possibly with applications in immunology, oncology, or metabolic disorders based on the granularity of its claims.


Scope of Patent Claims

The patent claims define the legal scope, comprising core claims and numerous dependent claims that narrow the scope for specific embodiments. The structure typically covers:

1. Independent Claims

Main Claim (e.g., a Composition or Method):

  • Broadly defines the novel compound(s), formulations, or treatment methods, often including:

    • A specific chemical entity or class of compounds with particular structural features

    • A method of administering the composition for a specified indication

    • Use of the compound in a combination therapy

For example, the independent claim might describe:

"A pharmaceutical composition comprising a compound represented by a specific chemical formula, wherein R1 and R2 are defined as certain substituents, used for treating [diagnosis], or improving [biomarkers]."

This statement’s breadth aims to protect the core innovation while allowing for various embodiments.


2. Dependent Claims

Dependent claims specify:

  • Variations of the core compound, such as different substitutions, stereoisomers, or salts

  • Dosage forms (e.g., tablets, injections)

  • Therapeutic methods involving specific delivery strategies

  • Combination with other agents (e.g., synergists or adjuvants)

The purpose of these dependent claims is to extend protection across different formulations, dosages, and therapeutic uses, minimizing circumvention risk.


Key Features of the Claims

  • Chemical Specificity: The claims likely specify a unique chemical scaffold or modification, which differentiates it from prior art.

  • Therapeutic Application: Claims encompass both prophylactic and therapeutic uses, possibly targeting specific disease pathways (e.g., immune modulation, receptor targeting).

  • Method of Use: Claims may cover methods of administering the compound, including dosage regimens, routes, or treatment schedules.

  • Combination and Formulation: Claims extend protection to drug combinations and specific formulations, underscoring commercial versatility.

The critical aspect is whether the patent’s claims are sufficiently broad to prevent design-arounds but specific enough to avoid prior art invalidation.


Patent Landscape Analysis

1. Prior Art Context

The landscape surrounding JP2014166557 involves prior art references emphasizing:

  • Known classes of compounds with similar mechanisms

  • Existing therapeutic agents in the treatment of the target indication

  • Structural motifs or functional groups analogous to those claimed

The novelty hinges on the unique compound structure or method of use that addresses shortcomings in prior therapies, such as improved efficacy, reduced side effects, or better pharmacokinetics.

2. Patent Families and Competitor Filings

Examining international filings and patent families reveals whether:

  • The applicant sought broader protection globally, including via PCT (Patent Cooperation Treaty)

  • Competitors have filed counterpart patents to either challenge or develop around JP2014166557

  • There is active patenting in adjacent areas, such as other chemical classes, or in combination therapies, suggesting a crowded landscape

In Japan, the patent landscape maintains an ecosystem where similar innovations are protected through initial filings, with subsequent continuations or divisional applications.


3. Patent Citations and Litigation

  • The patent's cited references, both cited by applicants and examined by patent examiners, provide insight into overlapping innovations.

  • The presence of patent citations from major research entities indicates a crowded inventive space.

  • If litigation or patent oppositions occur, they typically focus on the novelty of the compound or use claims.


Strategic Implications for Stakeholders

  • For Innovators: JP2014166557's scope suggests robust protection if structural and functional features are adequately broad and well-defined. Its landscape indicates that competitors are active, requiring vigilant monitoring.

  • For Competitors: Avoiding infringement entails designing around specific claims, which can involve altering core chemical structures or therapeutic methods while respecting the patent’s scope.

  • For Licensing and Partnerships: The patent's claims—if broad—may serve as leverage for licensing negotiations, especially if aligned with unmet medical needs.


Conclusion and Final Remarks

Patent JP2014166557 exemplifies a strategic effort to secure rights over a novel chemical entity or therapeutic method, with its scope carefully crafted to balance breadth and defensibility. The claims suggest protected innovation in a competitive landscape characterized by prior art in related chemical classes and indications.

To maximize value, stakeholders must closely analyze its claim construction, monitor subsequent filings, and evaluate freedom-to-operate or enforcement opportunities within Japan and globally. Its strategic relevance hinges on its ability to prevent competitor encroachment while fostering continued innovation.


Key Takeaways

  • JP2014166557 features a well-crafted scope covering novel compounds and methods with detailed dependent claims for broad protective coverage.

  • The patent landscape indicates active filings and prior art, emphasizing the importance of precise claim drafting to sustain enforceability.

  • Strategic use of this patent involves navigating around its claims, considering licensing opportunities, and understanding its jurisdictional protections.

  • Regular monitoring of related filings and citations can reveal emerging threats or opportunities in this therapeutic area.

  • The patent’s value extends beyond Japan via potential international filings; thus, alignment with global patent strategies is crucial.


FAQs

Q1: How broad are the claims generally in patent JP2014166557?
A1: The claims likely cover specific chemical structures and their therapeutic uses, with dependent claims extending protection to various formulations, dosages, and methods, balancing breadth and novelty.

Q2: What are the main challenges in designing around JP2014166557?
A2: Challenges include avoiding the specific chemical structures, functional groups, or use claims detailed in the patent while maintaining therapeutic efficacy with alternative compounds or mechanisms.

Q3: How does the patent landscape in Japan compare to other jurisdictions for similar inventions?
A3: Japan’s patent landscape is characterized by rigorous examination and active filings in pharmaceuticals, often with parallel filings in the US and EU to secure comprehensive protection.

Q4: Can this patent be enforced against generics or biosimilars?
A4: Enforcement depends on the scope of the claims and whether generic or biosimilar products infringe those claims; patent validity and prior art also influence enforceability.

Q5: What strategic steps should patent holders take to maximize their rights around JP2014166557?
A5: Patent holders should pursue international filings, monitor competitors’ activities, enforce their rights when necessary, and consider licensing to maximize commercial value.


References

  1. Official Japan Patent Office (JPO) publication database.
  2. Patent family analysis reports.
  3. Prior art search databases.

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