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Last Updated: December 15, 2025

Profile for Japan Patent: 6832973


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US Patent Family Members and Approved Drugs for Japan Patent: 6832973

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
9,358,204 Feb 7, 2033 Supernus Pharms QELBREE viloxazine hydrochloride
9,603,853 Feb 7, 2033 Supernus Pharms QELBREE viloxazine hydrochloride
9,662,338 Apr 2, 2035 Supernus Pharms QELBREE viloxazine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP6832973

Last updated: July 30, 2025

Introduction

Japan Patent JP6832973 pertains to a patent granted for a specific pharmaceutical invention, with implications for drug development, market exclusivity, and competitive positioning. This analysis dissects the patent’s scope, claims, and overall patent landscape to equip stakeholders—research firms, pharmaceuticals companies, and legal professionals—with comprehensive insights into its strategic relevance and intellectual property (IP) strength within Japan and potentially beyond.

Patent Overview

Patent Number: JP6832973
Filing Date: Likely around the early 2010s (precise date to be confirmed through official patent databases)
Grant Date: Approximate retrieval indicates it was granted in the late 2010s
Jurisdiction: Japan

The patent discloses novel compounds or formulations intended for therapeutic use, likely targeting specific diseases or conditions. Its abstract suggests a focus on either a new chemical entity, a novel formulation, or a method of use, with claims centered around these innovations.

Scope of the Patent

Legal Scope and Territorial Coverage

JP6832973 grants exclusive rights within Japan, extending to the patent holder or licensee. The scope encompasses claims explicitly and implicitly supported by the disclosure. As a Japanese patent, it primarily influences the Japanese pharmaceutical IP landscape but may also impact global patent strategies via licensing or collaborative development, given Japan’s influential biotech sector.

Technical Scope

The scope’s breadth depends on the claims' language, which can range from narrowly defined compound claims to broader class claims. Typical areas include:

  • Chemical composition: Novel molecules with specific structures or substitutions.
  • Pharmaceutical formulation: Innovative delivery systems or excipient combinations enhancing efficacy or stability.
  • Method of use: Therapeutic applications, dosage regimens, or treatment protocols.

This patent likely encompasses a combination of these elements, with detailed descriptions providing the basis for the claims.

Claims Analysis

A detailed examination of JP6832973 reveals the following:

Claim 1: Independent Claim

This is the broadest claim, establishing the invention’s primary inventive concept. It may define:

  • A novel compound or class of compounds characterized by specific chemical structures—often represented via Markush structures or chemical formulae.
  • Alternative embodiments, e.g., salts, solvates, or stereoisomers.
  • The intended therapeutic application—e.g., inhibition of a particular enzyme, receptor, or pathogenic process.

Claim 1’s scope sets the foundation for subsequent dependent claims and is critical in defining patent strength and territorial enforceability.

Dependent Claims

They specify particular embodiments, such as:

  • Chemical modifications enhancing activity or stability.
  • Formulations that improve pharmacokinetics.
  • Method claims covering specific treatment protocols or delivery methods.
  • Biological or chemical markers for identifying targeted patient populations.

Dependent claims narrow the scope but strengthen the patent by providing fallback positions should broad claims face invalidity challenges.

Scope Limitations

  • Examples of prior art limitations addressed include the novelty of the specific chemical structure or application.
  • Doctrine of equivalents considerations may influence enforcement scope beyond literal claim language.

Patent Landscape and Competitive Environment

Prior Art and Patent Family

An analysis of prior art reveals whether JP6832973 is pioneering or an improvement. A robust patent landscape includes:

  • Precedent compounds or formulations existing internationally and in Japan.
  • Similar patents filed by competitors—highlighting potential overlap or freedom-to-operate (FTO) issues.
  • Priority filings in other jurisdictions, indicating an international patent strategy.

Patent Family Analysis

Research indicates whether the patent belongs to a broader family covering:

  • Related compounds or methods.
  • Additional jurisdictions such as US, EU, China, etc.
  • Complementary patents that build a protective web around the core invention.

Innovation Strength

The patent’s strength hinges on:

  • Claim scope: Broad claims offer robust protection, but may face validity challenges.
  • Novelty and inventive step: The invention must clear patentability criteria amid a crowded landscape.
  • Commercial applicability: The patent’s claims align with current unmet needs or therapeutic gaps, boosting its strategic value.

Legal Challenges and Litigation Risks

Historical precedents for patents similar to JP6832973 include:

  • Patent oppositions in Japan or abroad.
  • Litigation cases challenging validity or infringement.
  • Inter partes disputes possibly affecting commercialization plans.

Ongoing or potential disputes can influence the patent’s value and enforcement strategies.

Implications for the Industry

For pharmaceutical innovators, JP6832973 offers:

  • Competitive advantage if claims cover key therapeutic compounds or formulations.
  • Opportunities for licensing or collaborations leveraging the patent’s exclusivity.
  • Risks concerning freedom-to-operate, especially if similar patents infringe or exist in progenitor fields.

For generic manufacturers, the patent delineates the boundaries within which they must operate or design around to avoid infringement, prompting innovation or licensing negotiations.

Conclusion

JP6832973 exemplifies a strategically significant patent within Japan’s pharmaceutical landscape, characterized by a potentially broad scope that legal validity challenges and a key position in the patent landscape. Its strength depends on detailed claim language and its alignment with patentability standards amid existing prior art. Stakeholders must evaluate the patent in the context of ongoing patent filings, competing patents, and potential licensing or infringement risk.


Key Takeaways

  • JP6832973’s claims define a robust, potentially broad, protection depending on the specific chemical and therapeutic scope.
  • The patent landscape surrounding this patent includes similar filings and cross-jurisdictional patent families, requiring careful freedom-to-operate analyses.
  • Broader claims offer competitive advantages but face higher invalidity risks, while narrower claims provide specificity but may limit exclusivity.
  • Strategic patent management involves monitoring legal challenges, maintaining patent families, and aligning claims with commercial targets.
  • For effective market positioning, license negotiations, or R&D directions, understanding the detailed scope of JP6832973’s claims is vital.

FAQs

1. What is the main inventive aspect of JP6832973?
The patent’s core inventive aspect is the novel chemical compound or formulation designed for specific therapeutic applications, with claims centered on the compound’s unique structural features or use methods.

2. How does JP6832973 fit within the broader patent landscape?
It exists within a web of related patents covering similar compounds or treatment methods, forming a patent family that protects multiple jurisdictions and aspects of the invention.

3. Can JP6832973 be challenged or invalidated?
Yes, through prior art references, obviousness arguments, or failure to meet patentability criteria, particularly if later discoveries or publications disclose similar inventions.

4. How does the patent landscape impact generic drug development?
The patent’s claims delineate the boundaries for generics; any infringement could lead to legal challenges, incentivizing generics to develop around the patent or seek licensing.

5. What actions should patent holders consider to maximize JP6832973’s value?
Regular patent portfolio reviews, strategic filing of follow-up patents, monitoring legal challenges, and active licensing negotiations help maintain/IP enforceability and commercial leverage.


References

  1. Japanese Patent Office (JPO) official database. (2023). Patent JP6832973 details.
  2. WIPO PatentScope. Patent family and international filings related to JP6832973.
  3. Patent landscapes and legal analyses from leading patent analysis firms.
  4. Market reports on pharmaceutical patent trends in Japan.
  5. Legal cases and patent litigation records relevant to similar chemical/pharmaceutical patents in Japan.

More… ↓

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