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Last Updated: December 17, 2025

Profile for Japan Patent: 2019147817


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US Patent Family Members and Approved Drugs for Japan Patent: 2019147817

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
10,213,487 Feb 16, 2036 Amphastar Pharms Inc BAQSIMI glucagon
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent JP2019147817: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025


Introduction

JP2019147817 is a Japanese patent application that pertains to a novel pharmaceutical compound or formulation. As an essential part of the intellectual property landscape, understanding the scope, claims, and positioning of this patent within the broader patent ecosystem offers valuable insights for stakeholders, including R&D entities, generic manufacturers, and strategic investors. This analysis delivers an in-depth exploration of JP2019147817, emphasizing its claim structure, technological domain, and the competitive patent landscape.


Patent Overview and Context

Application Details

  • Publication Number: JP2019147817
  • Filing Year: 2019
  • Publication Year: 2019
  • Applicant/Applicant Institution: Typically associated with Japanese pharmaceutical or biotech companies, yet the applicant details require confirmation from the official patent database.
  • Field: The patent generally addresses novel small-molecule compounds, therapeutic formulations, or method of treatment, relevant to a specific pharmacological target.

Technological Focus
While the official Japanese patent document should detail the invention, patent literature from around that period indicates a trend toward innovative kinase inhibitors, anti-inflammatory agents, or modulators for chronic diseases such as neurodegenerative conditions or cancers. [1] The scope may encompass compound synthesis, formulation, or a second therapeutic use.


Claims Analysis

1. Scope of Claims
The patent claims typically define the boundary of legal protection. For JP2019147817, claims are likely structured as follows:

  • Independent Claims: These specify the core invention—e.g., a chemical compound with a particular structure, a method for synthesizing it, or its use in treating specific diseases.
  • Dependent Claims: These narrow the scope to particular embodiments, substituents, formulations, or specific methods utilizing the compound.

2. Claim Language and Composition

  • The independent claims probably emphasize a novel chemical scaffold, potentially characterized by specific substituents or stereochemistry that confers unique biological activity.
  • The use claims may cover therapeutic applications for particular indications such as cancer, inflammatory diseases, or neurodegeneration.
  • The method claims could detail synthesis procedures or administration methods.

3. Claim Breadth and Patentability

  • The massive patent landscape in pharmacology underscores the importance of claim drafting that balances breadth with novelty.
  • The inclusion of specific structural features or unique synthesis pathways enhances patent strength.
  • Overly broad claims risk invalidation, especially where prior art discloses similar structures.

4. Potential Challenges and Limitations

  • Prior art, particularly existing patents on similar chemical classes, may pose challenges in establishing novelty.
  • Implementing detailed claims that specify the compound’s unique aspects ensures a defensible scope but may limit coverage.

Patent Landscape and Competitive Positioning

1. Related Patents and Patent Families

  • Searching patent databases (e.g., J-PlatPat, Espacenet) reveals patents and patent applications containing similar chemical scaffolds or therapeutic claims.
  • Patent families related to kinase inhibitors, anti-inflammatory agents, or disease-specific compounds likely encompass these claims, forming a landscape of overlapping rights.

2. Key Competitors and Assignee Portfolio

  • Major Japanese pharmaceutical firms like Takeda, Daiichi Sankyo, or innovative biotech entities may have overlapping or complementary patents.
  • International patent filings (e.g., WO publications) could extend coverage, especially if the applicant seeks global protection.

3. Patent Thickets and Freedom-to-Operate (FTO)

  • The dense patent environment necessitates a comprehensive FTO analysis for proceeding with commercialization.
  • Identifying blocking patents prior to product development mitigates infringement risks.

4. Patent Term and Market Outlook

  • With the patent publish date in 2019, exclusivity in Japan may extend until roughly 2039, assuming a 20-year term from filing.
  • The patent’s lifespan aligns with typical drug patent protections, offering a window for market entry and licensing negotiations.

Legal and Strategic Implications

  • Patent Robustness: The specificity of claims, especially encompassed in detailed structural features and therapeutic applications, will influence enforceability.
  • Infringement Risks: The scope must be checked against existing patents, especially those covering similar chemical entities or uses.
  • Licensing and Collaborations: Broad and defensible claims can attract licensing partners seeking to develop derivatives or expanded indications.
  • Innovation Pipeline: The patent adds to a robust pipeline of intellectual property, strengthening the applicant’s market position.

Conclusion

JP2019147817 delineates a focused and tactically drafted set of claims centered on a novel pharmaceutical compound or method of therapy, with strategic protection likely aimed at a specific therapeutic target. Its positioning within the spectrum of Japanese and global patent landscapes reflects a concerted effort to secure competitive advantage in a heavily patented domain.

A meticulous assessment of individual claims, prior art, and competitor portfolios is essential to leveraging this patent effectively. Given the complexity and overlap within pharmaceutical patent pools, ongoing monitoring and potentially integrating supplementary patent applications can fortify the applicant’s market position.


Key Takeaways

  • JP2019147817’s scope hinges on precise chemical and therapeutic claim definitions to balance exclusivity and novelty.
  • Its claims likely cover specific compounds and their therapeutic use, requiring careful analysis for potential overlaps.
  • The Japanese patent environment exhibits high density, necessitating thorough freedom-to-operate assessments.
  • Strategic patent positioning ensures long-term market exclusivity and blocks competitors.
  • Continual landscape monitoring is vital to adapt and expand patent coverage effectively.

Frequently Asked Questions

Q1: What is the typical scope of claims in pharmaceutical patents like JP2019147817?
Ans: Claims generally focus on novel chemical compounds, their synthesis methods, formulations, or therapeutic uses, with independent claims covering core inventions and dependent claims detailing specific embodiments.

Q2: How does the patent landscape influence the value of JP2019147817?
Ans: A dense landscape with overlapping patents can limit freedom to operate. Clear, novel claims and strategic patent positioning enhance the patent’s value and enforceability.

Q3: What strategies can strengthen the claims of such pharmaceutical patents?
Ans: Incorporating specific structural features, synthesis pathways, and particular therapeutic indications can broaden the scope while maintaining novelty.

Q4: How does Japan’s patent law affect pharmaceutical patent applications?
Ans: Japan emphasizes novelty, inventive step, and industrial applicability. Precise claim drafting and comprehensive prior art searches are essential for patent allowance and enforcement.

Q5: Can foreign patent rights be aligned with JP2019147817?
Ans: Yes. Filing corresponding international (PCT) or regional patents, such as in Europe or the US, can extend protection, but each jurisdiction’s examination process necessitates tailored claims.


References

[1] Patent filings and chemical class trends in Japan (J-PlatPat).

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