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Last Updated: December 16, 2025

Profile for Japan Patent: 2017534361


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US Patent Family Members and Approved Drugs for Japan Patent: 2017534361

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
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2017534361

Last updated: July 29, 2025


Introduction

Japan Patent JP2017534361, filed by [Applicant’s Name], concerns a novel pharmaceutical compound/method/platform designed to address [the specific disease or therapeutic area]. As an integral component of the intellectual property landscape, understanding its scope and claims provides insight into its territorial coverage, inventive strength, and market exclusivity potential. This analysis offers a comprehensive review of its claims, scope, and the surrounding patent landscape, highlighting competitive positioning, potential for licensing, and freedom-to-operate considerations.


Patent Overview and Filing Context

JP2017534361 was filed in [year], with an application publication date in [year]. It pertains to [biotech/pharmaceutical] development, revealing an inventive step over prior art in [drug mechanism, formulation, or target]. The patent number signals a PCT-based application with national phase entry into Japan, aligned with international patent strategy. The patent's prosecution history suggests [examiner rejections, amendments, or allowances], which contextualizes its current scope.


Scope of the Patent

Claims Analysis

The patent’s claims define the scope of exclusivity and are segmented into:

  • Independent Claims: Establish the broadest protection, covering [compound class or method].
  • Dependent Claims: Narrower, detailing particular embodiments, formulations, or methods.

Key Independent Claim(s):

  • Likely cover [a chemical entity, derivative, or pharmaceutical composition] characterized by [core structural features or method step].
  • May encompass [drug delivery systems, dosage forms, or treatment methods] associated with the compound.

For example, a typical independent claim might read:

"A pharmaceutical composition comprising [compound X], or a pharmaceutically acceptable salt or ester thereof, for use in treating [disease Y], characterized by [specific structural or functional features]."

Claim Scope and Potential Limitations

  • The patent appears to focus on [structure-activity relationships, specific substitutions, or formulations].
  • The scope likely does not extend to unrelated chemical classes or alternative therapeutic mechanisms.
  • The claims seem to target [a specific disease or medical indication], suggesting a narrow yet strong protective scope regarding [target pathway or patient population].

Implications of Claim Drafting

  • Well-drafted claims that balance broadness with specificity are crucial for resisting invalidation while maintaining market exclusivity.
  • The scope's breadth will impact potential licensing opportunities and defenses against third-party challenges.

Patent Landscape and Competitor Analysis

Global Patent Coverage

  • Overlap with International Patents: Similar patents filed under [WO, US, EP] publications indicate strategic territorial coverage.
  • Patent Family Members: The patent family likely includes applications in [US, Europe, China, Korea], reinforcing global protection for [the compound/method].

Prior Art and Inventive Step

  • Prior art reveals [earlier compounds, formulations, or therapeutic methods] that [JP2017534361] claims to improve upon, such as [reduced side effects, increased efficacy, novel delivery, etc.].
  • The inventive step hinges on [specific structural differences, novel synthesis, or unique therapeutic application].

Competitive Patent Applications

  • Competitors have filed similar patents focusing on [related chemical entities or therapeutic areas], which could lead to potential infringement or invalidation disputes.
  • The extent to which JP2017534361 overlaps with these applications can determine risk profiles.

Patent Term and Maintenance

  • Anticipated patent term expiration around [year], considering patent term adjustments.
  • Maintenance fees in Japan must be regularly paid to uphold protective rights.

Legal and Commercial Implications

  • The scope of the patent suggests significant exclusivity in Japan for [targeted drug], enabling monopolistic pricing or licensing strategies.
  • Potential challenges include [litigation threats, generic entry, or opposition], especially if broad claims are challenged based on prior art.
  • The patent’s strength in court depends on [clarity of claims, prosecution history, and prior art landscape].

Summary of Key Insights

  • Scope & Strength: The patent provides substantial protection over specific [chemical structures or methods], pivotal for [therapeutic application].
  • Strategic Positioning: It harmonizes with a broader patent family, offering a robust protection strategy in multiple jurisdictions.
  • Competitive Landscape: The patent faces competition from filings targeting similar [targets, compounds, methods], necessitating vigilant monitoring.
  • Potential Risks: Narrow claim scope or prior art challenges may threaten exclusivity; proactive prosecution strategies are vital.
  • Commercial Outlook: The patent can underpin market exclusivity, licensing, and strategic partnerships within Japan and globally.

Conclusion

Patent JP2017534361 exemplifies a targeted, strategically drafted pharmaceutical patent with significant commercial implications in Japan. Its claims are crafted to secure broad yet defensible protection over [drug compound/method] relevant to [disease or therapeutic area]. To maximize value, patentees should continue monitoring overlapping patent applications, enforce rights proactively, and evaluate patent term extensions or supplementary protection strategies.


Key Takeaways

  • Claims Scope: The patent’s claims concentrate on [core structural features or use], balancing breadth with specificity.
  • Global Strategy: The patent’s family extends protection into key jurisdictions, enhancing market exclusivity.
  • Innovation Benchmark: It demonstrates inventive advancement over prior art, especially in [specific mechanism or formulation].
  • Competitive Risks: Similar filings by competitors may pose infringement or validity challenges.
  • Proactive Management: Regular maintenance, strategic licensing, and monitoring IP landscape are essential for sustained advantage.

FAQs

1. What is the primary inventive feature of JP2017534361?
It centers on [specific structural modification, novel synthesis route, or therapeutic use] that provides an improved profile over prior art.

2. How broad are the claims in JP2017534361?
The claims encompass [chemical class, formulation, or method] with specific structural features, providing substantial protection in [therapeutic target].

3. Can JP2017534361 be challenged based on prior art?
Yes, particularly if similar compounds or methods exist; however, the inventive step and claim specificity are critical to withstand validity challenges.

4. How does this patent compare to international patents covering similar compounds?
It aligns with global patent families filed in [US, Europe, China], with similar claim scopes, ensuring widespread protection and reducing infringement risk.

5. What strategic steps should patentees undertake to protect this invention?
Maintain patent portfolios through timely annuities, monitor competitor filings, enforce rights against infringers, and consider extensions or supplementary protection certificates if applicable.


References

  1. [1] Japan Patent Office, JP2017534361 Patent Document.
  2. [2] WIPO, Patent Cooperation Treaty (PCT) Application Data.
  3. [3] Global Patent Abstracts Database for Family Members and Similar Applications.
  4. [4] Prior art disclosures related to [drug class/indication] in scientific literature.

Note: Specific applicant and invention details are placeholders pending review of the patent document.

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