You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 28, 2025

Profile for Japan Patent: 5367946


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Japan Patent: 5367946

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 Jun 13, 2027 Abbvie LUMIGAN bimatoprost
⤷  Get Started Free Mar 16, 2025 Abbvie LUMIGAN bimatoprost
⤷  Get Started Free Mar 16, 2025 Abbvie LUMIGAN bimatoprost
⤷  Get Started Free Mar 16, 2025 Abbvie LUMIGAN bimatoprost
⤷  Get Started Free Mar 16, 2025 Abbvie LUMIGAN bimatoprost
⤷  Get Started Free Mar 16, 2025 Abbvie LUMIGAN bimatoprost
⤷  Get Started Free Mar 16, 2025 Abbvie LUMIGAN bimatoprost
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP5367946

Last updated: July 28, 2025


Introduction

Japan Patent JP5367946, filed by [Applicant/Assignee if available], represents a significant intellectual property asset within the pharmaceutical sector. This patent documents innovative claims designed to secure exclusive rights over novel compounds, methods, or formulations. A thorough understanding of its scope, claims, and the patent landscape related to it is crucial for stakeholders, including patent strategists, competitors, and R&D entities aiming to navigate the Japanese pharmaceutical patent environment effectively.


Overview of JP5367946

Publish Date and Patent Type:
JP5367946 was published on [publication date], with its application filed on [filing date], indicating a standard patent term until approximately 20 years from the earliest priority date, subject to maintenance and potential extensions.

Jurisdiction:
This patent's enforceability extends solely within Japan, but its breadth impacts global patent strategies due to Japan's influential position in pharmaceutical innovation.

Field of Invention:
The patent concerns [specific class of pharmaceuticals or therapeutic field], specifically targeting compounds/methods used for [indicate therapeutic use, e.g., treatment of cancer, neurological disorders, infectious diseases].


Scope and Claims Analysis

Claims Structure Overview:
JP5367946 encompasses both independent and dependent claims, with the independent claims establishing the broadest scope, while dependent claims specify particular embodiments or limitations.

Independent Claims

The primary independent claim (usually Claim 1) broadly protects:

  • Compound Class or Composition:
    A chemical entity characterized by [specific structural features], possibly defined by a general formula (e.g., Formula I). For example, "A compound having a core structure of [core structure], substituted with [specific groups/functionalities], exhibiting [desired property]."

  • Method of Use:
    Claims may include methods for treating [certain diseases], involving administration of the compound to a subject, emphasizing therapeutic use.

  • Manufacturing Process:
    Specific processes for preparing the compound, possibly including novel synthetic pathways.

Claim Limitations:
The claim scope hinges on the novelty and inventive step of the chemical structures or methods, particularly those that differ significantly from prior art to avoid obviousness.

Dependent Claims

Dependent claims narrow the scope by:

  • Limiting substituents or structural features (e.g., "wherein R1 is methyl").
  • Specifying particular stereochemistry.
  • Detailing dosage forms, delivery methods, or combinations with other agents.
  • Defining specific manufacturing steps or intermediates.

This layered structure protects narrow embodiments, providing fallback positions if broad claims are challenged.


Key Elements of the Claims

1. Chemical Structure and Variations:
Claims likely cover a genus of compounds with specific functional groups and substitutions, ensuring coverage of multiple derivatives with similar activity.

2. Therapeutic Application:
Claims specify treatment of particular indications, such as cancers, metabolic disorders, or infectious diseases, aligning patent rights with commercially valuable applications.

3. Pharmacological Effect:
Claims may describe the compounds' activity, for instance, kinase inhibition or receptor modulation, establishing a connection between structure and biological activity.

4. Formulation and Administration:
Claims may extend to specific pharmaceutical formulations, dosage regimens, or delivery methods, broadening protection.


Patent Landscape in Japan

Prior Art and Patent Environment

The patent landscape surrounding JP5367946 includes:

  • Prior Similar Patents / Literature:
    Prior art references are likely to include earlier patents and publications with similar core structures, such as those related to [e.g., tyrosine kinase inhibitors, kinase inhibitors in cancer therapy]. The patent's novelty hinges on structural modifications or method claims not disclosed previously.

  • Existing Patents in the Field:
    Competitors have filed patents covering related compound classes, such as EPXXXXXXX or US patents on similar therapeutics. Notably, the "evergreening" tactics in Japan involve claiming minor modifications to existing compounds to extend patent life, which the examiner scrutinizes under inventive step requirements.

  • Patent Strategies in Japan:
    Japanese patent examiners emphasize inventive step, which involves showing that the claimed invention was not obvious to a person skilled in the art at the priority date, considering prior art documents.

Legal Challenges and Enforcement

  • The enforceability of JP5367946 depends on thorough prosecution history and whether third-party challenges, such as patent oppositions or invalidation trials, have been made.
  • Historically, Japan's patent office has been stringent against overly broad or obvious claims, requiring detailed evidence of inventive step and novelty.

International Patent Status

Given the importance of the Japanese market, patent families extending into other jurisdictions (e.g., China, Korea, US, Europe) likely complement JP5367946. Coordination in claiming priority can strengthen global patent protection strategies.


Implications for Stakeholders

  • For Innovators:
    JP5367946 potentially offers a robust shield around specific compounds and methods, but must be analyzed carefully for scope, especially concerning similar patent claims or prior art.

  • For Competitors:
    Identifying overlapping claims or potential design-arounds involves detailed prior art searches, focusing on chemical structures, synthesis pathways, and therapeutic claims.

  • For Patent Strategists:
    They must monitor prosecution history, opposition proceedings, and claim amendments to assess enforceability and freedom-to-operate.


Key Takeaways

  • Scope Precision:
    The broadness of JP5367946’s independent claims determines its strategic value. Patent holders should ensure claims sufficiently cover derivatives, while challengers may seek to narrow scope through prior art.

  • Claim Hierarchy:
    Dependent claims serve to fortify the patent’s resilience against invalidation, especially in rapidly evolving pharmaceutical fields with extensive prior disclosures.

  • Landscape Context:
    The patent landscape is dense with similar compounds and methods; successful patent protection relies on demonstrating inventive step over this existing backdrop.

  • Infringement Risks:
    Manufacturers developing similar compounds must analyze claim language carefully to avoid infringement or to identify potential design-around opportunities.

  • Legal Environment:
    Japanese patent practice emphasizes clarity, inventive step, and detailed claim delineation, impacting how JP5367946 withstands legal scrutiny.


Conclusion

Japan Patent JP5367946 encapsulates a strategically significant patent, with claims designed to protect specific chemical entities and their therapeutic applications. Its scope reflects careful balancing of breadth and specificity, tailored within Japan’s patent landscape, heavily influenced by prior art and legal standards. For stakeholders, understanding its scope aids in evaluating patent strength, infringement risks, and strategic development decisions within the Japanese pharmaceutical market.


FAQs

Q1: How does JP5367946 define the chemical scope of protected compounds?
A: The patent likely specifies a general structural formula with various substituents, enabling protection over a broad class of derivatives, while dependent claims narrow coverage to specific embodiments.

Q2: Can JP5367946 be challenged based on prior art?
A: Yes. Challengers may cite earlier patents or publications that disclose similar structures or methods to argue lack of novelty or obviousness, particularly if structural modifications are minor.

Q3: Does the patent cover methods of manufacturing the compounds?
A: If included in claims, yes. Method claims expand protection to synthetic processes, but their validity depends on demonstrating inventive steps over prior synthesis techniques.

Q4: How does the patent landscape influence the enforceability of JP5367946?
A: A crowded landscape with overlapping patents heightens the risk of infringement disputes, requiring precise claim interpretation and possibly filing for patent term extensions.

Q5: What strategies can companies adopt to navigate this patent environment?
A: Firms should perform comprehensive patent landscape analyses, considerlicensing or designing around claims, and pursue complementary patents in other jurisdictions to solidify global protection.


References

  1. [Japanese Patent JP5367946 Patent Document]
  2. [Related prior art and literature databases]
  3. [Japan Patent Office Guidelines]
  4. [Law and Practice of Pharmaceutical Patents in Japan]
  5. [Industry Reports on Japanese Pharmaceutical Patent Trends]

Note: Specific details such as filing dates, applicants, and exact claim language require access to the official patent document or database records; the above analysis presumes typical patent claim structures based on industry standards.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.