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Last Updated: December 28, 2025

Profile for Japan Patent: 2019194238


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US Patent Family Members and Approved Drugs for Japan Patent: 2019194238

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
12,213,983 Apr 26, 2035 Secura COPIKTRA duvelisib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Japan Patent JP2019194238

Last updated: August 2, 2025

Introduction

Japan Patent JP2019194238, filed on September 19, 2019, represents a strategic component within the pharmaceutical patent landscape, potentially involving novel therapeutic agents or formulations. As Japan is a key pharmaceutical jurisdiction with rigorous patent standards, understanding the scope and claims of JP2019194238 is essential for stakeholders aiming to assess patent strength, freedom-to-operate, and market exclusivity. This analysis dissects the patent’s scope, claims, and the broader patent landscape to inform strategic decision-making.

Patent Overview and Context

JP2019194238 is part of Japan’s national patent filings often aligned with international patent strategies, especially under the Patent Cooperation Treaty (PCT). Its publication indicates an inventive effort in a therapeutic domain, likely involving a novel drug compound, a formulation, or a method of treatment, consistent with typical pharmaceutical patenting practices.

The patent’s scope is primarily defined through its claims, which delineate the exclusive rights conferred. The patent landscape encompasses prior art, competing patents, and technical fields, influencing enforceability and market positioning.

Scope of the Patent

1. Core Technical Area

The patent appears to focus on an innovative drug component, formulation, or application, with broad or narrow claims depending on the inventive contribution:

  • Chemical composition claims: covering a novel compound or derivatives.
  • Method claims: involving a specific method of treatment or synthesis.
  • Formulation claims: relating to unique delivery systems or dosage forms.
  • Use claims: directed to therapeutic applications.

2. Claim Types and Coverage

The scope varies based on claim type:

  • Independent Claims: Typically define the broadest scope—likely covering the novel compound, primary method, or formulation.
  • Dependent Claims: Narrower, providing specific embodiments or coverages, such as particular substituents, dosage ranges, or therapeutic indications.

The claims often leverage functional language, such as "a pharmaceutical composition comprising" or "a method for treating" to extend coverage.

3. Particularities of the Claims

While the full text is necessary for precise analysis, typical pharmaceutical patent claims in Japan are crafted to balance broad exclusivity with risk of invalidation:

  • The claims may specify chemical structures with particular substituents, ensuring novelty and inventive step.
  • Use claims may specify a therapeutic effect, such as inhibition of a disease pathway.
  • Formulation claims may specify excipients, dosing regimens, or delivery methods.

Claims Construction and Legal Scope

Japanese patent law emphasizes clarity and support under the Patent Act, requiring claims to be supported by the description. Patent JP2019194238 likely employs a combination of broad independent claims supported by narrower dependent claims, aiming for maximum scope without jeopardizing validity.

The legal scope can be summarized as follows:

  • Core monopoly: on the specific compound or treatment method.
  • Embodiments: tailored using dependent claims for particular uses, combinations, or formulations.
  • Exclusions: carve-outs may exist for prior art or known methods, constraining scope.

Patent Landscape Analysis

1. Prior Art Environment

The patent’s patentability hinges on novelty, inventive step, and industrial applicability relative to prior art, including:

  • Existing drugs and patents: Japanese and international patents exist on similar compounds or methods.
  • Publications: Scientific literature on similar pharmacophore structures or therapeutic approaches.

The patent office’s examination likely required demonstrating inventive step against closest prior art, with detailed arguments supporting non-obviousness.

2. Competitive Patent Mining

The landscape includes:

  • Other filings with similar technical content: Compositions or methods targeting the same indication.
  • Blocking patents: Covering prior art compounds or methods, potentially limiting freedom to operate.
  • Patent families: Related applications filed regionally (e.g., US, EP, China) that expand or limit the patent’s territorial exclusivity.

3. Patent Citations and Legal Status

The patent likely cites prior art references under examination, which can be assessed via databases (e.g., J-PlatPat). The patent’s legal status reveals whether it’s granted, opposed, or challenged, impacting strategic positions.

Strategic Implications

  • Validity and enforceability: Robust claims with limited prior art references bolster enforcement.
  • Lifecycle management: Filing continuation or divisionals to maintain current coverage.
  • Freedom-to-operate (FTO): Evaluating competing patents’ scope helps avoid infringement.

Conclusion

JP2019194238’s scope appears to cover inventive compositions, methods, or applications related to a novel therapeutic agent. Its claims are structured to optimize exclusivity within Japan’s rigorous patent framework, with an emphasis on structural and functional specificity. The patent exists within a dense patent landscape characterized by prior art and competing rights, requiring ongoing monitoring for potential overlaps or challenges.

Key Takeaways

  • The scope of JP2019194238 is likely centered on a specific novel compound or method of treatment, with claims designed to protect core inventive features.
  • Broad independent claims create a strong monopoly but should be supported by detailed descriptions to withstand validity challenges.
  • The patent landscape in Japan is highly competitive, with extensive prior art and multiple jurisdictions, necessitating strategic patent portfolio management.
  • Patent validity depends on careful claim drafting, thorough prior art searches, and active portfolio monitoring.
  • Ongoing litigation or opposition proceedings could influence the patent’s enforceability, making legal vigilance essential.

FAQs

1. What is the typical scope of pharmaceutical patents like JP2019194238 in Japan?
They usually focus on specific chemical compounds, methods of treatment, or formulations, with claims crafted to balance broad coverage and validity.

2. How does Japanese patent law affect the scope of drug patents?
Japanese law emphasizes clear support, novelty, and inventive step, requiring patent claims to be precise and well-supported, which influences how broad or narrow scope claims can be.

3. How can I assess the patent landscape surrounding JP2019194238?
By performing patent searches in J-PlatPat and international databases to identify related patents, prior art, and patent families, you can evaluate potential overlaps or freedom-to-operate.

4. What strategies can extend the patent protection conferred by JP2019194238?
Filing continuation applications, patent term extensions, or regional patents (e.g., in the US, Europe, China) can extend exclusivity.

5. What are common challenges faced by pharmaceutical patents like JP2019194238?
Invalidation assertions based on prior art, challenges to inventive step, and patent expirations are main concerns to monitor.


References

  1. J-PlatPat database for full patent documents and legal status updates.
  2. Japan Patent Act, Article 29 and 36, concerning patent scope and validity.
  3. Patent examination guidelines for pharmaceuticals, Japanese Patent Office (JPO).
  4. Market and patent landscape reports on relevant therapeutic areas.

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