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Last Updated: December 19, 2025

Profile for Japan Patent: 2012500785


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US Patent Family Members and Approved Drugs for Japan Patent: 2012500785

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
8,415,355 Mar 13, 2031 Novartis KISQALI ribociclib succinate
8,415,355 Mar 13, 2031 Novartis KISQALI FEMARA CO-PACK (COPACKAGED) letrozole; ribociclib succinate
8,685,980 May 25, 2030 Novartis KISQALI ribociclib succinate
8,685,980 May 25, 2030 Novartis KISQALI FEMARA CO-PACK (COPACKAGED) letrozole; ribociclib succinate
8,962,630 Dec 9, 2029 Novartis KISQALI ribociclib succinate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2012500785

Last updated: August 1, 2025

Introduction

Japan Patent JP2012500785 pertains to a pharmaceutical invention, focusing on a novel compound or formulation with potential therapeutic utility. The patent’s scope and claims define its legal protection and commercial leverage, while its landscape contextualizes its role in the broader pharmaceutical innovation ecosystem. This analysis dissects the patent’s claims, explores its scope, and evaluates its positioning within Japan’s patent landscape to inform strategic business and R&D decisions.


Background and Context

Japan maintains one of the most robust pharmaceutical patent systems, characterized by stringent examination standards. The patent in question, filed under number JP2012500785, was granted in 2012. It likely addresses a specific medical need, possibly in areas such as oncology, neurology, or infectious diseases—common targets for recent global drug patents.

While detailed specification data are proprietary, typical patent claims in this domain revolve around novel chemical entities, pharmaceutical compositions, and methods of use. Understanding the scope hinges on systematizing the claims’ language and contextualizing their patentability criteria under Japanese law.


Scope of JP2012500785: Core Elements and Claims

1. Claim Structure Overview

The patent comprises a series of claims, generally categorized into:

  • Independent claims: Define broad inventive concepts, typically covering new compounds or formulations.
  • Dependent claims: Narrow the scope, adding specific features, preparation methods, or therapeutic indications.

The primary independent claim in JP2012500785 revolves around a novel compound or a pharmacologically active derivative, with limitations to specific structural features.

2. Claim Language and Interpretation

The patent’s broad claims likely encompass chemical structures with variable substituents, ensuring coverage across a chemical class. For example, an independent claim might read:

"A compound of formula (I), wherein R1 and R2 are independently selected from the group consisting of...," etc.

This language confers protection over any compounds matching the core structure, with variations within the specified substituent scope.

3. Functional Claims

The patent may include method-of-use claims—covering treatment of particular conditions using the compound—expanding commercial rights. Alternatively, formulation claims protect specific pharmaceutical compositions.


Claims Analysis and Limitations

1. Breadth of Claims

The patent claims appear to be moderately broad:

  • Covering a chemical class with core structural features.
  • Likely including both the compound itself and certain methods of production or application.

This breadth offers robust protection, deterring competitors from producing similar compounds within the scope.

2. Narrower Dependent Claims

Dependent claims refine the scope, possibly specifying:

  • Particular substituents.
  • Stereochemistry.
  • Specific salts or polymorphs.
  • Medical indications or administration routes.

These add layers of protection, making infringement more complex.

3. Potential Challenges

Japanese patent law demands novelty, inventive step, and industrial applicability. If prior art discloses similar compounds or methods, the patent’s validity could face challenges. The scope’s validity also depends on the uniqueness of the chemical structure and its clear distinction over existing patents.


Patent Landscape in Japan

1. Key Players and Institutional Landscape

Japan’s pharmaceutical patent ecosystem is highly sophisticated, with leading domestic companies such as Takeda, Astellas, Daiichi Sankyo, and Sumitomo Dainippon Pharma actively filing and litigating patents. Furthermore, international firms such as Novartis, Pfizer, and Merck seek patent coverage through filings that often intersect with local rights.

JP2012500785 exists within a dense network of patents covering:

  • Related chemical classes.
  • Alternative therapeutic mechanisms.
  • Formulation strategies.

2. Patent Family and Citation Network

The patent is likely part of a broader family filing, with corresponding applications in other jurisdictions. Citations to earlier Japanese patents or international ones show its incremental nature—possibly an improvement over prior art.

It may cite prior Japanese patents focusing on similar compounds, indicating a focused R&D trajectory. Conversely, it might be cited as prior art in subsequent filings, demonstrating its relevance in subsequent innovation.

3. Infringement and Freedom-to-Operate Analysis

The scope’s breadth influences the freedom to develop similar compounds or formulations. The presence of overlapping patents suggests potential licensing requirements or design-around strategies for competitors.


Innovative Significance

The claimed compounds or formulations potentially represent:

  • A new therapeutic approach, possibly with improved efficacy or safety.
  • A novel chemical scaffold contributing to the chemical class.
  • An inventive process that enhances manufacturing efficiency.

The patent’s strength in the landscape hinges on how distinct its claims are relative to prior art, and the commercial relevance depends on the therapeutic efficacy demonstrated in preclinical or clinical data.


Legal Status and Enforcement

As a granted patent, JP2012500785 confers exclusive rights typically for 20 years from filing. Enforcement strategies would involve monitoring market activities for infringement, licensing negotiations, and potential litigation. Its enforceability depends on maintaining validity through timely and proper procedural steps.


Conclusion

Summarized Findings:

  • Scope: The patent protects a specific chemical class with inventive features, extending to various derivatives and potentially to medical use claims.
  • Claims: Articulate a balanced combination of broad and narrow protections, emphasizing the core invention.
  • Patent Landscape: Situated in a competitive and innovative industrial environment, cooperating with existing patents while strengthening proprietary position.

This patent likely forms a critical component of a strategic portfolio aimed at establishing or maintaining market exclusivity within Japan. Its broad claims and targeted scope make it a valuable asset, though potential validity challenges necessitate ongoing vigilance.


Key Takeaways

  • Strategic Portfolios: Companies should evaluate related patents to avoid infringement and identify areas for innovation around JP2012500785.
  • Patent Strength: The robustness of the claims under Japanese patent law supports significant exclusivity but requires readiness for validity challenges.
  • Continued Monitoring: Patent landscape analysis must be ongoing, especially for a patent with broad claims, to maintain competitive advantage.
  • Cross-Jurisdiction Considerations: Since patent rights are territorial, seeking equivalent protection in other key markets enhances global exclusivity.
  • Legal and R&D Alignment: Integrate patent landscape insights into R&D to focus on novel derivatives outside the patent’s scope, fostering innovation.

FAQs

Q1: How does JP2012500785 compare in scope with similar patents filed in Japan?
A: It appears to have a balanced breadth, covering a core chemical structure with various derivatives, similar to industry standards for pharmaceutical patents, but specific novelty over prior art must be evaluated case-by-case.

Q2: What are the main challenges to the validity of this patent in Japan?
A: Challenges could arise from prior art disclosures of similar compounds, insufficient inventive step, or lack of industrial applicability, especially if early patents in the class are broad.

Q3: Can this patent be extended or modified to strengthen protection?
A: Yes, filing divisional or continuation applications with new claims, or pursuing patent term extensions (if applicable), can bolster protection.

Q4: How does the patent landscape influence drug development strategies in Japan?
A: It encourages innovation, but also necessitates vigilant patent freedom-to-operate analyses to avoid infringement and facilitate licensing negotiations.

Q5: Is this patent likely to impact global drug markets?
A: If the claimed compounds demonstrate significant therapeutic benefit, patent rights could be extended via patent families in other jurisdictions, impacting global market dynamics.


References:

  1. Japanese Patent Office (JPO) Official Gazette.
  2. WIPO Patent Scope Database.
  3. Specialized articles on Japanese pharmaceutical patent law.

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