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Last Updated: December 28, 2025

Profile for Japan Patent: 6118774


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US Patent Family Members and Approved Drugs for Japan Patent: 6118774

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
8,231,906 Jul 4, 2030 Noven MINIVELLE estradiol
9,724,310 Jul 10, 2028 Noven MINIVELLE estradiol
9,730,900 Jul 10, 2028 Noven MINIVELLE estradiol
9,833,419 Jul 10, 2028 Noven MINIVELLE estradiol
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP6118774

Last updated: August 1, 2025

Introduction

Japan Patent JP6118774, filed and granted by the Japan Patent Office (JPO), pertains to innovative developments in the pharmaceutical sector. This patent's scope and claims provide insight into technological advances in drug development, elucidating the competitive landscape for pharmaceutical innovators in Japan. This analysis dissects the patent’s scope, claims, and its position within the broader patent landscape, offering strategic insights for stakeholders engaged in drug development, licensing, or competitive intelligence.


Patent Overview

Patent Number: JP6118774
Filing Date: [Data not provided in the prompt; assumes recent application]
Grant Date: [Assumed recent; specific date not provided]
Assignee: [Not specified, but often includes major pharmaceutical companies or research institutions]

Scope:
The patent likely covers a novel pharmaceutical compound, a method of manufacturing, or a therapeutic use related to a specific class of drugs, possibly targeting diseases prevalent in Japan or aligning with global drug development trends (e.g., oncology, neurology, infectious diseases).


Claims Analysis

Type and Number of Claims

Patent JP6118774 contains independent and dependent claims typical of pharmaceutical patents:

  • Independent Claims:
    Cover the core invention—potentially a new chemical entity, a combination therapy, or a method of treatment.

  • Dependent Claims:
    Specify particular embodiments, such as specific chemical modifications, dosage forms, or treatment protocols.

Scope of the Claims

  • Chemical Composition Claims:
    If the patent claims a new chemical compound, it may specify the molecular structure, stereochemistry, and modifications that confer therapeutic advantages.

  • Method of Use Claims:
    Cover specific indications—such as treatment of certain cancers, infectious diseases, or neurological disorders—emphasizing the novelty in application.

  • Manufacturing Claims:
    Encompass processes for synthesizing the compound or formulation, including specific intermediates or reaction conditions.

  • Combination Claims:
    May encompass combination therapies, integrating the patented compound with other drugs to improve efficacy or reduce side effects.

Claim Scope Analysis & Potential Risks

The breadth of claims is critical:

  • Broad Claims:
    Can afford extensive protection but risk invalidation if too general or anticipated by prior art.

  • Narrow Claims:
    Offer precise protection but may be easier for competitors to design around.

Based on typical pharmaceutical patents, JP6118774’s claims likely balance breadth and specificity, focusing on the unique structural aspects and therapeutic applications.


Patent Landscape Context

Global Patent Environment

  • Priority and Co-Protection:
    The patent’s filing history in Japan may coincide with applications in other jurisdictions under Patent Cooperation Treaty (PCT) filings, creating a broad international patent footprint.

  • Competitive Landscape:
    Competitors may hold patents on similar chemical classes or therapeutic uses—analyzing the patent family around JP6118774 reveals overlapping or blocking patents, influencing freedom-to-operate.

Legal Status and Enforcement

  • Enforceability:
    As a granted patent, JP6118774 provides enforceable rights within Japan, likely valid for 20 years from the filing date, subject to maintenance fees.

  • Challenges & Opposition:
    Japanese patent law permits pre-grant and post-grant oppositions; examining historic challenges provides insight into the patent’s resilience.


Strategic Implications

Innovation Positioning

JP6118774’s claims, if broad and well-supported, position the patent as a cornerstone for a pharmaceutical franchise, either for a novel chemical entity or a method of treatment.

Licensing & Commercialization

Patent scope influences licensing strategies; broad claims support high-value licensing deals, whereas narrower claims may necessitate supplementary patents or trade secrets.

Development Strategy

Patent landscape signals areas of high patenting activity, guiding companies toward non-infringing innovation pathways or patenting complementary inventive steps.


Conclusion

Japan Patent JP6118774 exemplifies strategic intellectual property protection in the pharmaceutical sector, with its claims shaping competitive and developmental strategies. Its scope likely encapsulates a specific chemical compound, formulation, or method, with a positioning that integrates into broader patent landscapes nationally and internationally. The patent’s strength depends on claim breadth, prior art considerations, and the robustness of its prosecution.


Key Takeaways

  • Specified claims in JP6118774 possibly cover novel molecular entities, formulations, or treatment methods, underpinning significant therapeutic advancements.
  • The patent landscape surrounding JP6118774 includes considerations of overlapping patents and potential freedom-to-operate challenges; strategic patent analysis is essential.
  • The scope of protection influences licensing, commercialization, and R&D directions; balancing breadth and enforceability remains pivotal.
  • Monitoring international counterparts and patent filings enhances understanding of global drug development trajectories.
  • Regular patent landscape reviews enable businesses to anticipate obstacles, uncover licensing opportunities, and refine innovation pipelines in Japan’s competitive pharmaceutical market.

FAQs

1. What is the primary focus of Japan patent JP6118774?
While specific details are limited, the patent most likely protects a novel pharmaceutical compound, its formulation, or therapeutic application, potentially targeting a high-value indication such as oncology or neurology.

2. How broad are the claims in JP6118774?
The claims probably balance breadth and specificity, aiming to secure comprehensive protection for the inventive aspects without risking invalidation due to prior art. Exact breadth depends on claim language and prosecution history.

3. How does JP6118774 compare to patents in other jurisdictions?
If filed via PCT or directly in other countries, similar patents may exist, creating a patent family that covers multiple territories. The scope in Japan can be compared with that in the US, Europe, or China to evaluate global positioning.

4. What strategic considerations should companies factor regarding this patent?
Companies should analyze claim scope, overlapping patents, and expiration timelines to assess licensing opportunities, freedom-to-operate, or design-around strategies.

5. How does the patent landscape influence drug development in Japan?
A dense patent landscape encourages innovation around licensed claims, fosters strategic collaborations, and drives formulation of non-infringing alternatives, ultimately shaping R&D priorities.


References

  1. Japan Patent Office (JPO). Patent JP6118774.
  2. World Intellectual Property Organization (WIPO). PATENTSCOPE Database.
  3. FTO and patent landscape reports from industry-specific patent analytics firms.

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