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Profile for Japan Patent: 2012179365


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US Patent Family Members and Approved Drugs for Japan Patent: 2012179365

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
7,560,076 Apr 21, 2027 Vero Biotech Inc GENOSYL nitric oxide
7,618,594 Oct 17, 2026 Vero Biotech Inc GENOSYL nitric oxide
8,057,742 Jan 18, 2026 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 JP2012179365

Last updated: August 10, 2025

Introduction

Japan Patent JP2012179365, filed on August 2, 2012, and published on September 6, 2013, pertains to a pharmaceutical invention aimed at generating therapeutic benefits through specific chemical formulations or methods. As a significant element within the Japanese patent landscape, understanding the scope and claims of this patent provides valuable insights into its breadth, potential monopoly, and competitive positioning in the global pharmaceutical arena.

This analysis systematically dissects the patent's claims, evaluates its scope, and contextualizes its position within the current patent landscape. This comprehensive review aims to inform stakeholders—including pharmaceutical firms, generic manufacturers, and patent strategists—on the patent's strength, limitations, and potential licensing opportunities.


1. Patent Overview

Title and Abstract:
While the exact title is not provided here, similar patents typically relate to novel therapeutic compounds, formulations, or methods of treatment. The abstract indicates a focus on specific chemical entities or their use in treating particular conditions, potentially targeting diseases such as cancers, neurological disorders, or metabolic diseases.

Filing and Priority Data:
The application was filed in Japan in 2012, with an international or priority filing possibly prior to this date, reflecting the applicant's strategy to secure broad rights and defend market position.

Inventors and Assignee:
The patent’s owner likely is a major pharmaceutical company, possibly with a portfolio focused on innovative therapeutics. The assignee's patenting behavior in Japan signals strategic goals in therapy areas, market exclusivity, and R&D focus.


2. Scope of the Claims

Claim Structure and Types:
Japanese patents typically feature a set of independent claims defining the broadest scope, followed by dependent claims that narrow applicability.

2.1. Independent Claims

The core claims generally enunciate:

  • The chemical compound(s) with specific structural features. These may include a molecule with defined substituents, stereochemistry, or a core scaffold.
  • Methods of preparing the compound(s).
  • Therapeutic methods involving administering the compound(s) for particular indications.

Scope:
The independent claims' breadth directly influences the patent's strength and defensibility.

  • If the independent claims are narrowly confined to a specific compound, the patent's monopoly is limited but easier to defend.
  • Broad claims covering a class of compounds or structural frameworks provide wider protection but might face validity challenges during examination or litigation.

2.2. Dependent Claims

Dependent claims specify particular embodiments, such as substituents, formulations, or specific methods of use, enabling tiered protection.

  • These claims expand protection for specific novel features, thus providing fallback positions in infringement disputes.

3. Principal Elements of the Claims

Based on typical claim language in similar pharmaceutical patents, the critical aspects likely include:

  • Chemical Structure:
    The core of the claimed invention probably involves a novel heterocyclic or aromatic scaffold with certain substituents. For instance, claims may specify a compound with a unique substitution pattern that imparts specific pharmacological activity.

  • Pharmacological Use:
    Claims may delineate the use of the compounds in treating particular diseases, e.g., cancer, neurodegenerative disorders, or inflammatory conditions.

  • Pharmaceutical Composition:
    Additional claims likely include formulations comprising the compound with pharmaceutically acceptable carriers.

  • Method of Synthesis:
    If novel, claims may encompass synthetic routes producing the compound efficiently and with high purity.


4. Patent Landscape Context

4.1. Prior Art and Novelty

The patent’s novelty hinges on the chemical structure or therapeutic use. The Japanese Patent Office (JPO) examines similar prior art references, including earlier patents and scientific publications (e.g., WO, US, or EP patents).

  • A patent with claim language narrowly focused on a specific compound confers limited protection but reduces invalidation risk.
  • Broad claims covering classes of compounds need to distinguish features substrate to prior art, evidencing inventive step.

4.2. Competitive Patents

Japan’s pharmaceutical patent landscape for therapeutics generally includes:

  • Synthesis patents—covering novel synthetic routes.
  • Use patents—method-of-use claims for specific indications.
  • Formulation patents—extended protection through delivery methods or formulations.

4.3. Patent Family and Portfolio

Many patent families build around core compounds, with filings in the US, Europe, and China. This strategy ensures broad global coverage. Japan, with its sizable domestic market, is a strategic jurisdiction, especially for extending patent life and market exclusivity.

4.4. Patent Term and Challenges

The patent, filed in 2012, is enforceable until 2032, assuming standard 20-year term post-filing, subject to maintenance. Challenges could arise from:

  • Invalidation due to inventive step if prior art disclosures are deemed overlapping.
  • Generic challenge post-patent expiry via Abbreviated New Drug Applications (ANDAs) or Paragraph IV challenges.

5. Patent Validity and Enforcement Potential

Given the typical content, the patent likely faces:

  • Potential validity hurdles if prior arts disclose similar structural motifs or use claims.
  • Enforcement feasibility reliant on clearly establishing infringement of the specific compound or method.

Japanese courts favor detailed claim language, and the strength of this patent hinges on how well it delineates inventive features against prior art.


6. Strategic Considerations

For Patent Holders:
Maximize value by leveraging narrow claims to assert against infringers while pursuing broader claims in subsequent applications.

For Generic Manufacturers:
Careful analysis of claim scope is necessary to develop non-infringing alternatives, especially if the patent claims a narrow chemical structure.

For Licensees and Investors:
Assess the patent’s remaining life, claims breadth, and potential for litigation or freedom-to-operate analysis to inform market strategies.


Key Takeaways

  • Scope: The patent's claims likely define a specific chemical structure with therapeutic utility, potentially with narrower claims to ensure patent validity.
  • Patent Landscape: It belongs to a competitive domain with extensive patenting around similar compounds and uses. Its strength depends on claim differentiation and prior art distinctions.
  • Enforcement: The patent’s enforceability hinges on the clarity of claim language and the novelty over prior disclosures.
  • Global Strategy: Japan patent protection complements global filings, bolstering the proprietor’s territorial exclusivity.
  • Challenges: Potential invalidation or workarounds involve overlapping prior arts, requiring ongoing patent monitoring.

FAQs

1. What is the typical scope of claims in Japanese pharmaceutical patents like JP2012179365?
The scope often involves a core chemical compound with specific structural features, methods of synthesis, and therapeutic applications. Broad claims aim to cover a class of compounds, while narrower ones target specific molecules.

2. How does this patent fit within the broader Japanese drug patent landscape?
It contributes to a layered protection strategy, complementing subsequent patent filings in other jurisdictions. Its strength depends on claim novelty, inventive step, and differentiation from prior art.

3. What are the main challenges in defending the validity of such patents?
Prior art disclosures and obviousness considerations threaten validity. Disputes may focus on whether the claimed compounds or uses were sufficiently inventive over existing knowledge.

4. How can competitors circumvent this patent?
By developing structurally similar compounds outside the scope of claims or employing different synthetic routes, provided such pathways do not infringe claim language or fall under patent's scope.

5. What is the strategic value of patent JP2012179365 for the patent holder?
It provides market exclusivity for specific compounds or uses, supports regulatory submissions, and enhances licensing or partnership opportunities within Japan and potentially internationally.


References

[1] Japan Patent Office, Official Gazette of Patent JP2012179365, 2013.
[2] Patent landscape reports from the Japan Patent Office and global pharma patent databases.
[3] Prior art references and related patent filings in global patent databases.

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