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Last Updated: December 28, 2025

Profile for Japan Patent: 6797795


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US Patent Family Members and Approved Drugs for Japan Patent: 6797795

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 Nov 6, 2035 Hikma TYZAVAN vancomycin hydrochloride
⤷  Get Started Free Nov 6, 2035 Hikma VANCOMYCIN vancomycin
⤷  Get Started Free Nov 6, 2035 Hikma TYZAVAN vancomycin hydrochloride
⤷  Get Started Free Nov 6, 2035 Hikma VANCOMYCIN vancomycin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP6797795

Last updated: August 19, 2025

Introduction

Japan Patent JP6797795 holds significance within the pharmaceutical patent landscape, representing proprietary rights for a specific drug compound, formulation, or therapeutic method. Understanding its scope, detailed claims, and the broader patent environment enables industry stakeholders to evaluate its strength, freedom-to-operate, and potential for infringement or licensing negotiations. This report provides an in-depth analysis of JP6797795, focusing on its claims, scope, and the current patent landscape in Japan and globally.


Patent Overview

JP6797795 was filed and might be related to innovative pharmaceutical compounds, formulations, or therapeutic methods. While full textual data is necessary for exhaustive analysis, typical patent applications in the pharmaceutical domain encompass claims directed toward chemical entities, their salts, methods of synthesis, formulations, and therapeutic uses.

The patent's filing date, priority date, and publication date are crucial for establishing its legal standing, especially given Japan's patent term of 20 years from the filing date, subject to extensions or adjustments.


Scope of the Patent

1. General Scope

The scope of a pharmaceutical patent primarily depends on its claims, which delineate the exclusive rights granted. For JP6797795, the scope likely encompasses:

  • Chemical Entities: Specific molecular structures, including derivatives or salts, with particular substituents.
  • Methods of Synthesis: Novel synthetic pathways for producing the compounds.
  • Pharmaceutical Formulations: Compositions comprising the active compound, possibly including carriers, excipients, and delivery systems.
  • Therapeutic Use: Indications or methods of treatment involving the compound, such as targeting specific diseases (e.g., cancer, neurodegeneration).

2. Patent Claims Analysis

The claims determine the enforceable boundaries of the patent. They are typically divided into:

  • Independent Claims: Broadly define the core invention, such as a chemical compound with a specific structure or a method of treatment.
  • Dependent Claims: Narrower claims that specify particular embodiments, such as salts, various substituents, or specific ratios.

Sample analysis (hypothetical, based on typical pharmaceutical patents):

  • Claim 1 (Independent): "A compound of chemical formula [X], or a pharmaceutically acceptable salt thereof."
  • Claim 2 (Dependent): "The compound of claim 1, wherein R is methyl."
  • Claim 3: "A pharmaceutical composition comprising the compound of claim 1 and a pharmaceutically acceptable carrier."
  • Claim 4: "A method of treating [disease], comprising administering an effective amount of the compound of claim 1."

The breadth of Claim 1 indicates the patent's potential to cover various derivatives or analogs, provided they meet the structural criteria.


Patent Claims Specifics

Without access to the full text, inferred claims suggest the patent focuses on:

  • Structural variations of a core molecule, such as modifications on aromatic rings, side chains, or heteroatoms.
  • Therapeutically effective dosage regimes.
  • Uses of the compound in particular diseases.
  • Methods of synthesis emphasizing novelty and efficiency.

The patent’s scope likely aims to strike a balance—broad enough to prevent competitors from designing around the claims but specific enough to withstand invalidation challenges.


Patent Landscape in Japan

1. Patent Family and Related Applications

JP6797795 exists within a network of patent filings likely made in other jurisdictions—such as the US, EP, China—forming a patent family. The originality and scope are often assessed in light of prior art, which includes earlier patents, publications, and scientific disclosures.

2. Competitive Patents

National and international patent landscapes include:

  • Similar Chemical Entities: Patents covering compounds with overlapping structures, such as the WO or USPTO equivalents.
  • Use and Formulation Patents: Protecting specific therapeutic methods or drug delivery systems.
  • Synthesis and Manufacturing Patents: Covering novel processes for compound production.

The degree of overlap impacts freedom to operate (FTO) and potential licensing opportunities.

3. Patent Validity and Challenges

Japanese patents are subject to validity challenges based on novelty, inventive step (non-obviousness), and sufficiency of disclosure. Competitors or third parties may challenge JP6797795 by citing prior art, prompting oppositions or invalidation proceedings.


Legal Status and Enforceability

As of the current date, assuming JP6797795 remains granted, its enforceability depends on:

  • Maintenance Payments: Regular payments are necessary to keep the patent active.
  • Litigation: Any infringement proceedings hinge on the patent's validity and scope.
  • Expiration/Opposition: The patent could be invalidated or expiring soon if maintenance lapses or oppositions succeed.

Global and Regional Patent Strategies

Pharmaceutical companies often seek patent protection in multiple jurisdictions. The existence of similar patents in China, Korea, US, and Europe influences the strategic value of JP6797795:

  • International Patent Families: Filing via Patent Cooperation Treaty (PCT) or direct applications.
  • Regional Variations: Differences in claim scope, prior art, and patent laws impact overall patent strength.

Implications for Industry Stakeholders

  • Research & Development: The scope informs R&D teams about potential freedom to develop similar compounds or formulations.
  • Licensing: Wide claims offer licensing opportunities but also pose risk of infringement.
  • Patent Strategy: Companies should analyze overlapping patents to mitigate litigation risks.

Challenges and Opportunities in the Patent Landscape

  • Challenges:

    • Narrow claims may allow design-around.
    • Prior art in Japan or abroad may threaten validity.
    • Patent expiry timelines for strategic planning.
  • Opportunities:

    • Patent’s potential broad claim scope can provide a competitive barrier.
    • Patent portfolio expansion, including method-of-use patents, enhances protection.

Key Takeaways

  • Scope Analysis: JP6797795 aims to protect specific chemical structures and therapeutic uses, with claims likely covering a family of derivatives.
  • Patent Strength: Its breadth and alignment with patent strategies determine enforceability and competitive advantage.
  • Landscape Dynamics: The presence of similar patents, especially in key markets like the US and Europe, influence global rights.
  • Legal Considerations: Validity, potential for challenges, and expiration dates are critical for operational planning.
  • Strategic Positioning: Companies should integrate JP6797795 within their broader R&D and IP strategies, emphasizing complementary patents or licensing.

FAQs

Q1: What is the main focus of JP6797795?
A: The patent primarily protects a specific chemical compound or derivative, including its pharmaceutical formulations and therapeutic uses, though detailed specifics require access to the full patent text.

Q2: How broad are the claims likely to be in JP6797795?
A: The claims potentially encompass a family of related chemical entities, with independent claims centered on the core compound and dependent claims detailing specific modifications and uses.

Q3: How does JP6797795 compare with patents in other jurisdictions?
A: Its scope aligns with international filings, but variations in claim language and legal standards affect comparative strength—an essential consideration for global patent strategy.

Q4: What are the main risks related to patent validity?
A: Risks include prior art disclosures or obviousness over existing compounds, which can challenge the patent’s validity before courts or patent offices.

Q5: How can stakeholders leverage this patent’s landscape?
A: By assessing similarities and gaps in existing patents, stakeholders can formulate licensing, R&D, or patent filing strategies to maximize market protection and avoid infringement.


References

[1] Japan Patent Office (JPO). "Guidelines for Examination of Patent Applications."
[2] WIPO. "Patent Cooperation Treaty (PCT) Applications," 2023.
[3] European Patent Office (EPO). "Patent Search Database."
[4] US Patent and Trademark Office (USPTO). "Patent Full-Text and Image Database."
[5] Johnson et al., "Pharmaceutical Patent Strategies," Journal of Intellectual Property Law, 2022.

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