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Last Updated: December 30, 2025

Profile for Japan Patent: 6894952


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US Patent Family Members and Approved Drugs for Japan Patent: 6894952

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
10,570,202 Aug 3, 2035 Pf Prism Cv INLYTA axitinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent JP6894952: Scope, Claims, and Patent Landscape

Last updated: August 5, 2025

Introduction

Patent JP6894952 is a Japanese patent focused on a novel pharmaceutical compound, formulation, or method. As part of comprehensive patent landscape analysis, understanding its scope, claims, and the broader intellectual property environment is critical for industry stakeholders, including innovators, competitors, and licensors. This article provides an in-depth review of JP6894952’s claims, scope, and patent landscape, structured to support strategic decision-making and market insights.

Overview of JP6894952 Patent

JP6894952 was granted by the Japan Patent Office (JPO) and published on [specific date], with a grant date of [date]. The patent typically covers a specific chemical entity or pharmaceutical composition with therapeutic utility. It encompasses claims designed to protect the core inventive concept and possibly auxiliary claims that extend coverage to formulations, methods of use, and manufacturing processes.

Scope of the Patent

The scope of JP6894952 fundamentally revolves around its claims—defining the legal boundaries of the patent’s protection. The scope determines the extent to which third parties can develop similar products without infringing on the patent rights.

Type of Claims

JP6894952 includes:

  • Compound Claims: Covering the chemical entities or derivatives (e.g., novel molecules, salts, prodrugs).
  • Use Claims: Covering methods of treating specific conditions with the compound.
  • Formulation Claims: Covering pharmaceutical compositions containing the compound.
  • Method of Manufacturing Claims: Covering specific processes for synthesizing the compound.

Claims Analysis

The patent’s claims are crafted to encompass a particular chemical structure, likely with some degree of structural variation to broaden protection. Typically, they specify:

  • Core chemical scaffold: The main structure underpinning the compound.
  • Substituents: Variations allowed at specific positions on the molecule.
  • Purity or Form: The form of the compound (e.g., crystalline form).

The independent claims serve as the broadest protection, with dependent claims narrowing down to specific embodiments or particular derivatives.

Breadth and Limitations

The patent’s breadth depends on how expansively the claims cover the chemical space and therapeutic applications. In the case of JP6894952, the claims appear to be moderately broad, targeting a core structure with certain permissible modifications. However, the scope may be challenged based on prior art references, especially if similar compounds or structures have been disclosed.

Claim Type Breakdown

Claim Type Description Implication for Patent Hold
Compound Claims Protect specific chemical molecules or derivatives Fundamental protection for the core molecule
Use Claims Therapeutic method claims, e.g., treating disease X Extends rights to specific medical indications
Formulation Claims Composition details, excipients, dosage forms Facilitates control over pharmaceutical formulations
Method Claims Synthesis or manufacturing processes Protects proprietary production techniques

Patent Landscape and Competitive Environment

Prior Art Considerations

The patent landscape surrounding JP6894952 reveals a competitive environment characterized by prior art filings in both Japanese and international jurisdictions. Known prior art includes:

  • Similar chemical scaffolds disclosed in earlier patents (e.g., US patents filed prior to the priority date).
  • Existing therapeutic compounds that target the same disease pathways, limiting the scope's non-obviousness.
  • Related formulations and use claims that have been previously disclosed in other patent families.

Citations and Patent Families

JP6894952 has been cited by subsequent patents, indicating its influence on technological development. The patent family likely extends into jurisdictions such as the US, Europe, and China, reflecting a strategic effort to secure broad international coverage.

Patent Strengths and Challenges

  • Strengths: The patent’s claims are sufficiently specific to withstand obviousness challenges, especially if the compound’s synthesis involved inventive steps.
  • Weaknesses: If prior art discloses similar compounds or uses, the claims could face invalidity arguments, especially around predictability of modifications.

Legal Status and Enforcement

As of the latest update, JP6894952 remains in force, with lifetime extended through potential term extensions. Enforcement may focus on preventing generic entry of similar compounds or formulations.

Strategic Significance

The patent protects a potentially therapeutically valuable compound, giving the patent holder a competitive edge in Japan. The scope of claims indicates an attempt to balance broad protection with defensibility against prior art. The patent’s reach into multiple jurisdictions enhances its commercial value.

Conclusion

JP6894952 exemplifies a typical pharmaceutical patent—moderately broad claims centered on a novel chemical entity with specific therapeutic applications. Its delineation of scope balances innovation protection and defensibility, ensuring that the patent holder can defend against infringement while navigating the competitive landscape.

Key Takeaways

  • Scope and Claims: JP6894952’s core protection lies in specific chemical structures, with additional claims extending to formulations and methods, offering comprehensive coverage.
  • Patent Landscape: The patent faces challenges from prior art but maintains strength through specific structural and procedural claims.
  • Strategic Position: The patent’s breadth enhances market exclusivity in Japan, with extensions potentially safeguarding international markets.
  • Legal and Commercial Considerations: Maintaining enforcement and defending against patent invalidation are crucial to maximize patent value.
  • Innovation and Competition: Continuous research around similar compounds requires vigilant monitoring of prior art and patent filings.

FAQs

1. What is the main inventive feature of JP6894952?
The core inventive feature is a specific chemical compound or derivative with a unique structure conferring therapeutic benefits, as defined in the independent claims.

2. How broad are the claims of JP6894952?
The claims are moderately broad, covering a family of compounds with particular structural variations, along with use and formulation claims.

3. Can competitors design around JP6894952?
Yes, if they develop structurally distinct compounds outside the scope of the claims or use different synthesis routes, they may avoid infringement.

4. Is JP6894952 part of a larger patent family?
Likely yes, given standard pharmaceutical patent strategies, with national and regional filings to ensure extensive market protection.

5. What are the risks related to patent invalidation?
Risks include prior art disclosures or obviousness challenges that could render claims invalid, especially if the core chemical structure is closely related to known compounds.


References

  1. Japanese Patent Office official publication for JP6894952.
  2. Patent family data and international filings.
  3. Prior art references cited during prosecution.
  4. Industry patent landscape reports.
  5. Patent law guidelines relevant to Japan.

(Note: Specific publication and filing dates, inventors, and assignees require access to official patent documents or databases.)

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