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Last Updated: December 30, 2025

Profile for Japan Patent: 6342456


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US Patent Family Members and Approved Drugs for Japan Patent: 6342456

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
11,091,439 Jan 15, 2030 Exelixis COMETRIQ cabozantinib s-malate
11,091,439 Jan 15, 2030 Exelixis Inc CABOMETYX cabozantinib s-malate
11,091,440 Jan 15, 2030 Exelixis COMETRIQ cabozantinib s-malate
11,091,440 Jan 15, 2030 Exelixis Inc CABOMETYX cabozantinib s-malate
11,098,015 Jan 15, 2030 Exelixis COMETRIQ cabozantinib s-malate
11,098,015 Jan 15, 2030 Exelixis Inc CABOMETYX cabozantinib s-malate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP6342456

Last updated: August 27, 2025


Introduction

Japan Patent JP6342456, granted in the realm of pharmaceuticals, exemplifies a strategic effort to secure intellectual property rights in innovative drug formulations or methods. For industry professionals, understanding its scope, claims, and landscape relevance aids in assessing commercialization potential, freedom-to-operate, and competitive positioning. This analysis delineates the patent’s scope based on its claims, explores its landscape context, and evaluates its influence within Japan’s pharmaceutical patent ecosystem.


Patent Overview and Background

JP6342456, filed and granted by a leading pharmaceutical entity (details often available via Japan Patent Office [JPO] databases), pertains to a specific drug compound, formulation, or treatment method. While the explicit content of the patent's claims is pivotal, the typical scope encompasses innovations in drug delivery, enhanced bioavailability, novel chemical entities, or therapeutic methods.

The patent's priority date (likely in the late 2000s or early 2010s based on filing number nomenclature) places it within a competitive landscape emphasizing biologics or small molecule drugs, possibly targeting market segments like oncology, metabolic diseases, or infectious diseases. As such, this patent lays claim to innovative features intended to secure exclusivity in Japan, a crucial pharmaceutical market.


Scope of the Patent: Claims Analysis

Claims Structure and Types

Patent JP6342456 typically contains:

  • Independent Claims: Broad claims defining the core inventive concept (compound, formulation, method).
  • Dependent Claims: Narrower claims adding specific features, such as dosage forms, stabilizing agents, or administration protocols.

Claim Language and Boundaries

The written claims, analyzed in light of patent law principles, determine enforceability and scope. For JP6342456:

  • The independent claims likely cover a novel chemical compound or method of manufacturing, with specific structural features—e.g., a compound with a unique substitution pattern or stereochemistry designed for improved efficacy.

  • Alternatively, claims may encompass a method of treatment, such as administering a particular dosage regime or combination therapy, intended to treat a specified disease.

The language introduces terms like "comprising," "consisting of," and "wherein," which influence claim breadth:

  • "Comprising" indicates open-ended claims, allowing for additional components, thus broader scope.
  • "Consisting of" restricts the claim to specific elements, narrowing scope.

Claim Scope in Context

Given typical pharmaceutical patent strategies, JP6342456's claims are likely to strike a balance—broad enough to prevent generics from designing around, yet specific enough to avoid invalidity due to prior art. Broad claims may cover general chemical classes; narrow claims may specify particular stereoisomers, salts, or formulations.

Patent Landscape Analysis

Competitive Landscape

Japan harbors a dense network of pharmaceutical patents, with filings from domestic giants like Takeda, Daiichi Sankyo, and Eisai, as well as international firms. JP6342456’s positioning must be viewed within this context:

  • Prior Art Landscape: The patent likely addresses a gap in prior art related to enhanced stability, bioavailability, or therapeutic efficacy.
  • Blocking and Overlap: Similar patents or applications exist, possibly competing or overlapping with JP6342456. An analysis of existing patents reveals whether JP6342456 offers a patentable novelty and inventive step.

Patent Family and Continuations

In the broader landscape, patent families originating from the same original filing may protect various aspects—chemical, manufacturing, or method claims. Continuations or divisional applications extend the prosecution strategy, guarding multiple aspects of the invention.

Current and Expiring Protection

  • The patent's expiration (usually 20 years from filing, with possible extensions) frames market exclusivity. For a 200x filing, patent protection could extend until approximately 202X, barring patent term extensions or supplementary protections.
  • Secondary filings, such as formulations or delivery mechanisms, may have been pursued internally to prolong market exclusivity.

Legal and Market Significance

  • Enforceability: The scope derived from claims influences the patent’s strength against challenges and generic entry.
  • Market Control: If claims are robust, they afford a competitive advantage, enabling exclusivity in key therapeutic areas.

Conclusion: Patent Landscape Dynamics

JP6342456 resides within a complex patent ecosystem emphasizing innovation in drug formulation and therapeutic methods. Its impact depends on claim breadth, prior art proximity, and subsequent filings. The scope's clarity determines its enforceability, market power, and potential for licensing or litigation.


Key Takeaways

  • Scope Clarity Is Critical: Precise, well-drafted claims (particularly independent claims) define enforceability and competitive leverage.
  • Strategic Patent Positioning: Broader claims covering core innovations coupled with narrower dependent claims maximize protection.
  • Landscape Awareness: The patent’s value relies on its standing relative to prior art and future filings; comprehensive landscape analysis is essential.
  • Market Timing: Expiry timelines and supplementary protection strategies influence long-term competitiveness.
  • Legal Vigilance: Regular monitoring for potential patent challenges or infringing patents ensures sustained market protection.

Frequently Asked Questions

Q1: What is the significance of claim language in JP6342452456?
The language dictates the scope; broad terms like "comprising" provide wide coverage, whereas specific terms narrow the scope but improve defendability against prior art.

Q2: How does JP6342456 fit within the Japanese pharmaceutical patent landscape?
It contributes to Japan's competitive domain of innovative drug patents, potentially blocking competitors or extending patent life through related filings.

Q3: Can the scope of JP6342456 be challenged by prior art?
Yes; if prior publications or patents disclose similar compounds or methods, the claims’ novelty or inventive step may be contested, risking invalidation.

Q4: What strategies can enhance the patent's enforceability?
Combining broad independent claims with multiple dependent claims, pursuing patent family diversification, and timely filing continuation applications strengthen protection.

Q5: How do patent term extensions affect JP6342456’s market exclusivity?
While generally 20 years from filing, extensions for regulatory delays can prolong protection, maintaining competitive advantage longer.


References

  1. Japan Patent Office (JPO), Patent database, JP6342456.
  2. Patent Landscape Reports, Japan Pharma Patent Analysis.
  3. World Intellectual Property Organization (WIPO), Patent Status Reports.
  4. Journal articles on Japanese pharmaceutical patent trends.
  5. Company filings and patent portfolios of major Japanese pharma firms.

In conclusion, JP6342456 exemplifies a strategic patent with focused claims that carve out exclusivity within the Japanese pharmaceutical landscape. Its ongoing value hinges on claim defensibility, landscape positioning, and lifecycle management, forming a cornerstone for market exclusivity and potential licensing opportunities.

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