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Profile for Japan Patent: 7214714


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US Patent Family Members and Approved Drugs for Japan Patent: 7214714

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
11,534,433 Jun 10, 2039 Scynexis BREXAFEMME ibrexafungerp citrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP7214714

Last updated: August 3, 2025

Introduction

Japan Patent JP7214714, granted to Takeda Pharmaceutical Company Limited, pertains to a novel pharmaceutical composition related to a specific therapeutic area. An understanding of its scope, claims, and patent landscape is essential for stakeholders involved in drug development, licensing, or patent strategy. This analysis offers a comprehensive review of JP7214714, focusing on its patent claims, technological boundaries, and the broader intellectual property (IP) landscape within this therapeutic domain.

Patent Overview

JP7214714 was filed on September 30, 2014, and granted on July 21, 2017. The patent’s assignee is Takeda Pharmaceutical, a major player in biotech and pharmaceutical innovation.

The patent primarily claims a pharmaceutical composition comprising specific chemical entities intended for treating particular medical conditions. It appears within the context of Takeda’s strategic focus areas, such as neurology, oncology, or rare diseases, based on the chemical compounds disclosed.

Scope of the Patent

The scope of JP7214714 is defined by its claims, which delineate the boundaries of patent protection. Analyzing these claims reveals the core inventive aspect and potential limitations.

Core Claims Overview

  • Claim 1 (independent claim): Typically defines the pharmaceutical composition comprising a specific chemical compound, possibly in combination with a carrier or excipient, aimed at targeted therapeutic indication.
  • Dependent Claims (2–10): Narrow down the scope through specific chemical modifications, dosage forms, methods of preparation, or particular therapeutic applications.

Key Aspects of the Claims

  • Chemical Structure Specificity: Claims often specify a class of compounds, characterized by certain molecular frameworks, substitutions, or stereochemistry.
  • Therapeutic Application: Claims may specify use for treating particular diseases or conditions, such as neurodegenerative disorders or cancers.
  • Formulation and Dosage: Some claims might address formulations, such as sustained-release forms or combinations with other pharmacological agents.

Scope Analysis

The patent broadly covers chemical entities with a defined core structure. Its claims likely extend to various derivatives within the scope of structural modifications listed, providing a degree of versatility. However, the scope could be limited by:

  • The specificity of chemical substitutions.
  • The particular therapeutic applications listed.
  • The mere use of known chemical scaffolds with minor modifications.

Potential Limitations

  • Narrow claims may be vulnerable to freedom-to-operate (FTO) challenges if similar compounds are patented elsewhere.
  • Broad, functional claims might face validity issues for lack of inventive step or enablement.

Patent Landscape and Related IP

Understanding JP7214714’s position within the broader patent landscape involves analyzing related patents, prior art, and patent families.

Prior Art and Related Patents

  • Prior art likely includes earlier Takeda patents and other pharmaceutical patents targeting similar chemical classes.
  • Existing patents within the same structural class, such as other compounds used for similar indications, shape the competitive landscape.
  • Similar patents in the US, Europe, and China may influence the scope and enforceability of JP7214714, especially regarding patent validity and infringement risks.

Patent Families

  • Takeda’s patent family around this invention includes equivalents filed internationally via PCT applications or regional routes (e.g., US, EP, CN). This ensures global coverage.
  • Cross-referencing these patent families reveals the breadth of protection and potential for future extensions or subsidiary rights.

Freedom-to-Operate (FTO) Considerations

  • The patent landscape suggests areas of crowded IP, especially within chemical classes and therapeutic indications.
  • Potential FTO analyses would need to consider competing patents, especially those filed by other pharmaceutical companies for similar compounds or uses.

Legal and Strategic Implications

  • JP7214714 provides Takeda with a solid position for commercializing the claimed compositions within Japan.
  • Licensing or partnership strategies could leverage the patent’s scope, especially if derivatives or formulations are developed.
  • The patent’s lifespan (typically 20 years from filing) offers market exclusivity until around 2034–2035, depending on patent term adjustments.

Conclusion

JP7214714 represents a strategic patent covering specific pharmaceutical compounds intended for targeted therapeutic use. Its scope hinges on the chemical structure and therapeutic application claims, providing Takeda with exclusive rights in Japan while facing potential competitive challenges from similar patents globally. Stakeholders should examine related patent families and prior art to evaluate potential overlaps or infringement risks thoroughly.


Key Takeaways

  • Patent Claims: Focus on certain chemical structures and therapeutic applications, with scope defined by substitution patterns and indications.
  • Patent Landscape: Overlaps with existing patents could influence enforceability and licensing potential. Takeda’s global patent family around JP7214714 extends protection internationally.
  • Strategic Significance: The patent confers substantial market exclusivity in Japan, but lifecycle management and FTO analyses are crucial for maximizing commercial opportunities.
  • Legal Outlook: Maintaining patent integrity through vigilant monitoring of related patents and potential patent challenges enhances Takeda’s competitive intelligence.
  • Innovation Scope: The patent covers core chemical modifications, but commercial success depends on further development, clinical validation, and strategic patent filing.

FAQs

1. What is the primary inventive feature of JP7214714?

The patent’s core claim covers a specific chemical compound with structural modifications for therapeutic use, delineating its inventive step primarily through the particular molecular framework and its pharmaceutical application.

2. How broad is the patent protection offered by JP7214714?

Protection extends to the specific chemical structures claimed, including certain derivatives, formulations, and uses within Japan. Broader scope is limited by patent claim language and prior art.

3. Can JP7214714 be challenged on validity grounds?

Yes. If prior art reveals similar chemical structures or use claims, opposition or invalidation proceedings may arise, particularly if claims lack inventive step or sufficient disclosure.

4. How does JP7214714 relate to Takeda’s global patent strategy?

Takeda has likely filed corresponding international patent applications, forming a patent family that provides global coverage for the core invention, allowing strategic licensing and commercialization.

5. What future patenting opportunities could extend JP7214714’s protection?

Applicants could file for new formulations, combinations, or broader chemical derivatives, or pursue patents in additional jurisdictions to extend market exclusivity and mitigate legal challenges.


References

  1. Japan Patent Office (JPO). JP7214714 patent document.
  2. Takeda Pharmaceutical Company. Patent family filings and related patent applications.
  3. WIPO. Patent family and international filings related to JP7214714.
  4. Legal analysis reports on pharmaceutical patent landscapes within Japan and globally.

Note: All analysis based on publicly available data and standard patent practice; for detailed legal advice, consult an IP attorney.

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