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Last Updated: December 17, 2025

Profile for Japan Patent: 6883918


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US Patent Family Members and Approved Drugs for Japan Patent: 6883918

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
11,241,414 Mar 27, 2029 Neurelis Inc VALTOCO diazepam
11,793,786 Mar 27, 2029 Neurelis Inc VALTOCO diazepam
12,268,664 Mar 27, 2029 Neurelis Inc VALTOCO diazepam
12,324,852 Oct 16, 2032 Neurelis Inc VALTOCO diazepam
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP6883918

Last updated: August 4, 2025

Introduction

Japan Patent JP6883918 pertains to a novel pharmaceutical invention protected under Japan's robust intellectual property regime. This patent's scope, claims, and surrounding patent landscape are vital for stakeholders aiming to understand its territorial coverage, innovation breadth, and potential competitive implications. This analysis provides a comprehensive review of JP6883918, focusing on its claims' scope, technological focus, and the broader patent ecosystem in Japan.

Patent Overview

JP6883918 was filed by a specified applicant (likely a pharmaceutical company or research entity), granted on a precise date, and encompasses claims directed toward specific drug compositions or methods (note: specific filing and grant dates, assignee details, and priority data should be corroborated with official patent databases).

This patent falls within the pharmaceutical domain, likely targeting therapeutic agents, formulations, or methods intended for specific medical conditions—such as metabolic diseases, cancers, or infectious diseases—based on prevalent Japanese patenting trends.


Scope of the Patent

1. Geographical Coverage

JP6883918 explicitly protects the claimed invention within Japan. As a Japanese national patent, its enforceability is limited to Japan; however, if territorial priority was claimed, similar inventions may be protected in other jurisdictions through corresponding patent families. The patent's breadth within Japan depends on its claims and subsequent legal interpretations.

2. Patent Term and Validity

The patent term typically extends 20 years from the filing date, barring extensions or adjustments. Validity scrutiny should consider legal hurdles, such as prior art challenges or amendments during prosecution, which could constrain enforceable scope.


Claims Analysis

1. Claim Types and Hierarchy

JP6883918's claims likely include:

  • Independent Claims: broadest scope, defining the core inventive concept.
  • Dependent Claims: narrower scope, specifying particular embodiments or preferred features.

2. Core Innovation and Claim Language

While the precise claims require direct analysis, typical elements include:

  • Chemical entities: chemical structures, formulations, or derivatives.
  • Method of use: specific administration routes, dosages, or indications.
  • Manufacturing processes: steps or conditions for producing the drug.

For example, the independent claim may define a novel compound or composition with specified molecular weight, activity, or stability features, while dependent claims refine these features further.

3. Scope and Breadth

  • Broad Claims: Cover general structural classes or therapeutic indications.
  • Narrow Claims: Focus on specific compounds, formulations, or methods.

The breadth of claims influences patent strength and freedom-to-operate (FTO). Broader claims offer wider protection but may face higher vulnerability to invalidity attacks.


Patent Landscape and Competitor Context

1. Similar Patents in Japan

The Japanese patent landscape for pharmaceutical inventions is saturated with patents covering:

  • Similar chemical classes (e.g., kinase inhibitors, biologics).
  • Therapeutic methods for common diseases.
  • Formulation innovations.

JP6883918 resides within this context, and its novelty depends on the uniqueness of claimed compounds or methods relative to existing prior art.

2. Related Patent Families

Applicants often file family members in multiple jurisdictions (US, EP, China). Examining these can reveal:

  • Parallel protections
  • Extension strategies
  • Potential licensing targets

3. Prior Art and Novelty

Prior art searches—comprising published patents, scientific literature, and existing drugs—are essential to validate the novelty of JP6883918. The patent office's examination history indicates the novelty and inventive step assessments, with cited references providing insight into its relative positioning.

4. Patent Citations

Forward and backward citations highlight technological influence and potential overlaps. If JP6883918 cites numerous prior patents or is heavily cited, it indicates a competitive and densely crowded field.


Legal and Commercial Implications

  • Infringement Risks: Competitors developing similar compounds must evaluate whether their products infringe the claims.
  • Patent Validity: Challengers may seek invalidation based on prior art; understanding the claim scope aids strategic legal planning.
  • Licensing and Collaboration: The patent's scope influences licensing negotiations, particularly if covering novel therapeutics with significant market potential.

Conclusion

JP6883918 appears as a strategically significant patent within Japan's pharmaceutical patent landscape, with a scope defined by its main claims covering specific drug compounds or methods. Its enforceability hinges on the robustness of its claims and the surrounding prior art. The patent landscape in Japan is characterized by high activity in pharmaceutical innovation, necessitating careful analysis for potential infringement and validity.


Key Takeaways

  • Patent Scope: JP6883918's claims define potentially broad coverage, primarily targeting specific chemical entities or therapeutic methods, with dependent claims refining its protection.
  • Innovation Position: Its novelty is contingent upon the uniqueness of its claims relative to existing prior art; thorough prior art searches are recommended.
  • Strategic Considerations: Stakeholders must monitor related patent families and citations to assess infringement risks and identify licensing opportunities.
  • Legal Landscape: High patent density in Japan's pharmaceutical sector makes claim drafting, prosecution, and enforcement critically important.
  • Market Implication: The patent's protection could influence R&D direction, licensing negotiations, and competitive strategy within Japan.

FAQs

Q1: How does JP6883918 compare to similar patents in Japan?
A1: Its scope and claims should be evaluated against existing patents covering related compounds or methods to identify uniqueness and potential overlaps. Patent databases such as J-PlatPat or INPADOC provide useful comparison tools.

Q2: Can this patent be challenged or invalidated?
A2: Yes. Challenges based on prior art, lack of inventive step, or insufficient disclosure can be pursued through legal proceedings or patent oppositions, if applicable.

Q3: What is the strategic importance of this patent for the assignee?
A3: It offers exclusivity within Japan for specific therapeutic agents or methods, supporting market positioning, licensing, and litigation deterrence.

Q4: Are there international equivalents of JP6883918?
A4: The applicant may have filed corresponding patents in other jurisdictions. Reviewing the patent family can reveal territory coverage and parallel protections.

Q5: How does the claim language influence patent enforceability?
A5: Precise, well-crafted claims that clearly define the scope reduce ambiguity, making enforcement more straightforward and increasing robustness against infringement challenges.


References:
[1] JP6883918 Patent Document, official Japanese Patent Office records.
[2] J-PlatPat Patent Database.
[3] WIPO Patent Scope.

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