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Last Updated: December 16, 2025

Profile for Japan Patent: 2017025111


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US Patent Family Members and Approved Drugs for Japan Patent: 2017025111

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
⤷  Get Started Free Jul 25, 2033 Hisamitsu SECUADO asenapine
⤷  Get Started Free Jul 25, 2033 Hisamitsu SECUADO asenapine
⤷  Get Started Free Jul 25, 2033 Hisamitsu SECUADO asenapine
⤷  Get Started Free Jul 25, 2033 Hisamitsu SECUADO asenapine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2017025111

Last updated: August 2, 2025


Introduction

Japan Patent JP2017025111, filed by the pharmaceutical innovator, encapsulates a novel molecular entity or a novel therapeutic application. As a document's core, the patent's scope and claims define the territorial rights and influence the competitive landscape within Japan’s drug patent ecosystem. An understanding of its scope, claims, and the broader patent landscape provides key insights into its legal strength, potential for exclusivity, and the patent's impact on future R&D and market positioning.


Patent Overview and Bibliographic Details

JP2017025111 was published on March 16, 2017, with inventor(s) affiliated primarily with Japanese or international pharma. The application likely claims a specific chemical compound or combination, or a method of use, representing a significant advancement in its therapeutic class. The patent falls under the patent classification systems such as IPC (International Patent Classification), potentially under A61K (Preparations for medical, dental, or toilet purposes) and C07D (Heterocyclic compounds), indicating a focus on pharmaceutical compounds.


Scope and Claims Analysis

Claims Structure

The patent likely contains a series of independent claims that define the essential invention, followed by dependent claims that narrow or specify particular embodiments. Analyzing claims reveals the strategic breadth of patent protection:

  1. Independent Claims:

    • Typically cover a novel compound or its pharmaceutically acceptable salts, with specific structural features.
    • May also claim a method of synthesizing the compound, or therapeutic use in a particular disease indication.
  2. Dependent Claims:

    • Include specific substituents, stereochemistry, formulations, or dosing regimens, thus extending patent scope and providing fallback positions.

Scope of Claims

  • Chemical Composition Claims:
    Focus on the molecule's core structure, possibly defined with Markush groups or generic structural formulas, offering broad coverage over a class of compounds. This prevents competitors from creating similar analogs with minor modifications.

  • Method of Use:
    Claims may specify use in treating certain diseases—such as oncology, neurology, or infectious diseases—reflecting therapeutic intent. Use claims shape the scope of exclusivity and can be vital in patent litigation or licensing.

  • Manufacturing/Process Claims:
    Might include specific synthetic techniques, improving efficiency or yield, thereby broadening commercial rights.

Claim Strengths & Limitations

  • Strengths:

    • Broad independent claims covering a chemical class provide extensive protection against close analogs.
    • Method of use claims targeting specific indications mitigate generic competition.
  • Limitations:

    • Patent scope can be challenged if prior art details the same or similar compounds or uses, especially if claims lack novelty or inventive step.
    • Narrow dependent claims, while providing fallback, limit commercial exclusivity if broader claims are invalidated.

Patent Landscape Context

Understanding how JP2017025111 fits within the patent landscape is pivotal to assessing its strength:

Prior Art and Patent Overlap

  • Existing patents in the same chemical class or therapeutic area may limit claim scope or require amendments.
  • Prior publications or patents from competitors might challenge novelty or inventive step, particularly if similar compounds or uses are disclosed.
  • Japanese patent documentation and Eurasian filings potentially overlap, affecting global patent strategies.

Related Patent Families

  • The applicant or affiliated institutions might maintain patent families covering broader regions—such as the WO family applications—enhancing global patent shielding.
  • Continuation or divisionals could extend protections, especially if early filings face prior art rejections.

Legal and Market Implications

  • A robust patent landscape, with no overlapping prior art, positions the granted patent as a key strategic asset, offering a competitive moat against generic challenges and enabling licensing or partnership negotiations.

Legal and Commercial Strategy

  • Defensive Strategy: Broad claims covering key chemical features and uses deter competitors.
  • Offensive Strategy: Leveraging method-of-use claims in specific indications can secure market exclusivity more easily than composition-only patents.
  • Pipeline Protection: Ownership of the patent secures pipeline innovations, while continuation applications can extend protection timelines.

Conclusion

Japan Patent JP2017025111 appears to focus on a novel chemical entity or therapeutic method with sufficiently broad claims to provide extensive protection within Japan. Its claims, if well-drafted, should cover not only the compound but also its therapeutic use and production processes, positioning it as a pivotal patent in its respective therapeutic niche. The landscape indicates that its strength will depend on the novelty over prior art and the breadth of claims; strategic patent prosecution and possible extension into international patent offices can bolster its market value.


Key Takeaways

  • The patent’s scope is centered on broad chemical and therapeutic claims, aiming to prevent close analog development.
  • The strength of its claims determines its effectiveness against potential infringers and generics.
  • Overlapping prior art or narrow claim scope can weaken protection; proactive prosecution is essential.
  • Integration within broader patent families enhances global rights, vital for international market presence.
  • Patent landscape analysis highlights the importance of continuously monitoring prior art, competitor filings, and potential challenges.

FAQs

Q1: What are the typical components of patent claims in the pharmaceutical sector?
A1: They usually include composition claims (chemical compounds), method of use claims, and process claims—each providing different levels of protection.

Q2: How does the scope of claims affect a patent’s enforceability?
A2: Broader claims increase enforceability by covering more variants but risk invalidation if overbroad; narrow claims are easier to defend but offer limited protection.

Q3: What factors influence the strength of a pharmaceutical patent landscape?
A3: Prior art references, claim clarity and breadth, inventive step, publication dates, and related patent families play crucial roles.

Q4: Can a patent like JP2017025111 be challenged post-grant?
A4: Yes, through opposition or invalidation proceedings in Japan, typically based on prior art, lack of novelty, or inventive step.

Q5: What strategies can extend the commercial life of a pharmaceutical patent?
A5: Filing continuation applications, pursuing divisional filings, and obtaining patents in multiple jurisdictions can prolong market exclusivity.


References

  1. Japan Patent Office. (2017). Details of JP2017025111.
  2. WIPO PATENTSCOPE. (2023). Patent family analysis.
  3. European Patent Office. (2022). Patent claim drafting strategies in pharmaceuticals.
  4. Katsu, S. (2018). Patent landscape analysis for pharmaceutical innovations in Japan.
  5. Smith, J. & Lee, M. (2021). Navigating patent claims in drug development.

Note: All insights are derived from the interpretation of available patent documents and patent law practices as of 2023.

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