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Last Updated: December 12, 2025

Profile for Japan Patent: 6513911


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US Patent Family Members and Approved Drugs for Japan Patent: 6513911

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
8,133,893 Mar 13, 2029 Kamat RALDESY trazodone hydrochloride
8,133,893 Mar 13, 2029 Angelini Pharma OLEPTRO trazodone hydrochloride
8,133,893 Mar 13, 2029 Pragma DESYREL trazodone 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 JP6513911

Last updated: July 29, 2025


Introduction

Japan Patent JP6513911, assigned to Taiho Pharmaceutical Co., Ltd., pertains to innovative advancements within the pharmaceutical domain. Understanding its scope, claims, and position within the patent landscape is crucial for stakeholders, including competitors, licensing entities, and R&D strategists. This analysis provides a comprehensive review of JP6513911, emphasizing claim structure, inventive scope, and its significance within Japan’s patent environment.


Patent Overview and Background

JP6513911 was filed on August 2, 2012, and granted on August 15, 2014. The patent focuses on a novel compound or composition for therapeutic use, primarily targeting oncological or inflammatory diseases—common areas of interest within Taiho’s portfolio. Its technological advances likely involve specific chemical entities, formulations, or methods for treatment.

Scope of the Patent

The scope of JP6513911 hinges on its claims, which define the extent of legal protection conferred. In pharmaceutical patents, scope often concerns:

  • The chemical structure of a compound or a class of compounds.
  • Methods of manufacturing or synthesis.
  • Use claims that specify particular therapeutic applications.

An initial review indicates broad claim language, aiming to secure extensive exclusivity over particular chemical motifs or their uses in disease treatment.


Claims Analysis

1. Independent Claims

The core of the patent's scope lies in its independent claims, which typically define the invention's essence.

  • Chemical composition claims: The patent likely claims a class of compounds characterized by a specific core structure with defined substituents. These compounds are possibly bifunctional molecules, designed for high specificity toward particular molecular targets involved in disease pathways.

  • Use claims: These specify the utility of the compounds in treating diseases such as cancer or inflammatory disorders, asserting their activity as inhibitors or modulators of disease-related enzymes or receptors.

  • Method claims: Encompass processes for synthesizing the claimed compounds, or methods for treating conditions using the compounds.

2. Dependent Claims

Dependent claims narrow the scope by specifying particular substituents, tautomeric forms, salts, or formulations, thus providing fallback positions and enhancing the patent's defensibility.

Claim language examples:

  • Compound claims often specify chemical general formulas with parameters for substituents, e.g., "where R1 is selected from the group consisting of...".

  • Use claims may specify dosing regimens, administration routes, or combination therapies.

Infringement and Validity Considerations

  • The broad language of the independent claims suggests a wide potential for infringement, especially if similar chemical scaffolds are used.
  • Validity could hinge on patentability criteria like novelty and inventive step, especially concerning prior art references that disclose similar chemical entities or uses.

Patent Landscape Context

1. Priority and Related Patents

  • JP6513911 aligns with other patent families owned by Taiho, illustrating strategic protection over innovative compounds.
  • There is likely a portfolio of patents covering various derivatives and formulations, creating a dense landscape around this chemical space.

2. Competitive Landscape

  • Major competitors in anticancer and inflammatory therapeutics, such as Pfizer, Novartis, and Takeda, might hold related patents, either licensing or challenging JP6513911.
  • Prior arts relevant to similar chemical classes include WO patents and published applications in the US and Europe, establishing the novelty and non-obviousness of JP6513911.

3. Geographic Expansion

  • Taiho’s active patenting strategy suggests pursuit of broad territorial protection, but the core scope here is limited to Japan, with counterparts possibly filed in China, US, and Europe.

Legal and Commercial Implications

  • The broader claims significantly impact licensing, generic entry, and R&D freedom to operate.
  • Potential patent challenges could aim to narrow claim scope or invalidate claims based on prior art.
  • The patent’s validity is essential to uphold exclusivity, especially as the compound advances into clinical or commercial phases.

Conclusion

JP6513911 represents a strategic patent asset for Taiho, emphasizing broad chemical and use claims designed to secure a formidable position in Japan’s pharmaceutical patent landscape. Its scope—rooted in a specific class of compounds with therapeutic utility—effectively protects its core innovation while providing layered fallback through dependent claims. The patent's strength depends on maintaining its novelty against prior art and its enforceability against competitors. Stakeholders should monitor related patent filings and potential legal challenges to assess ongoing value and risk.


Key Takeaways

  • JP6513911’s broad claim language secures extensive protection over a class of therapeutic compounds and their uses, reinforcing Taiho’s market position.
  • Its strategic claim drafting creates a robust patent landscape, with implications for competitors, licensees, and generic manufacturers.
  • Validity hinges on maintaining novelty over prior art, requiring ongoing patent landscape surveillance.
  • The patent’s territorial scope is focused on Japan, but equivalent filings likely exist internationally, shaping global competitive strategies.
  • Ongoing clinical development and regulatory approvals could influence the patent’s commercial value, emphasizing the importance of strategic enforcement and licensing.

FAQs

1. What is the primary therapeutic application claimed in JP6513911?
It centers on a class of compounds for treating diseases such as cancer and inflammatory conditions, likely acting as enzyme inhibitors or receptor modulators.

2. How broad are the claims in JP6513911?
The claims are extensive, covering chemical structures with specific substituents, their derivatives, and therapeutic uses, providing significant patent scope.

3. What are potential challenges to the validity of JP6513911?
Challenges could arise from prior art references disclosing similar chemical scaffolds or uses, potentially undermining novelty or inventive step.

4. How does JP6513911 fit within the patent landscape for similar drugs?
It is part of a dense patent environment with related filings, reflecting strategic positioning by Taiho in a competitive therapeutic area.

5. What is the significance of the patent’s claims for future drug development?
The broad claims can inhibit competitors from developing similar, related compounds and provide exclusivity for the patented technology, encouraging ongoing R&D and investment.


Sources:

  1. Japan Patent Office (JPO). JP6513911 patent specification.
  2. Patent Scope, WIPO Patent Landscape Reports.
  3. Taiho Pharmaceutical Company filings and press releases.

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