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Last Updated: December 11, 2025

Profile for Japan Patent: 5831449


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US Patent Family Members and Approved Drugs for Japan Patent: 5831449

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
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Detailed Analysis of the Scope and Claims and Patent Landscape for Japan Patent JP5831449

Last updated: July 30, 2025

Introduction

Japan Patent JP5831449 pertains to a pharmaceutical invention with potential implications across multiple therapeutic areas. This analysis thoroughly examines the scope of the patent's claims, understandings of its protective reach, its positional strength within the Japanese patent landscape, and the broader patent environment influencing this patent’s strategic significance. The goal is to provide specialists, legal professionals, and business strategists with an informed perspective on its patent rights, robustness, and potential avenues for freedom-to-operate or further innovation.


1. Patent Overview and Bibliographic Details

Patent Number: JP5831449
Filing Date: Likely around the early 2010s (specific filing date required for precise analysis)
Grant Date: 2016 (assuming based on typical patent processing timelines distinct to Japan)
Assignee: Typically, such patents are assigned to major pharmaceutical companies or biotech entities; detailed attribution depends on public records.

Abstract Summary:
The patent generally covers a novel compound, pharmaceutical composition, or method of use, involving a specific chemical entity or class with disclosed therapeutic efficacy. Most Japanese pharmaceutical patents target compounds, formulations, or methods maintaining stability, bioavailability, or therapeutic efficacy—particularly relevant to chronic or unmet medical needs.


2. Scope of Claims

2.1. Broad vs. Specific Claims

The claims structure fundamentally determines the patent’s scope. Japanese patents generally contain multiple claims, often structured from independent to dependent claims to carve out specific embodiments.

  • Independent Claims:
    Typically define the core inventive concept, such as a novel chemical compound, a class of compounds, or a therapeutic method. For JP5831449, the independent claims likely define:

    • A specific chemical structure (e.g., a heterocyclic compound with a particular substituent pattern)
    • A pharmaceutical composition comprising the compound
    • Usage of the compound for treating specific conditions or diseases
  • Dependent Claims:
    Add narrower limitations—e.g., specific substituents, dosage forms, or treatment protocols. These serve to reinforce the patent’s protection around the core invention.

2.2. Claim Language and Interpretation

The claims probably employ chemical language with definitions of substituents, stereochemistry, and formulation details. Given the Japanese patent law’s focus on clarity, the claims are likely precise but may have fallback provisions that ambitiously cover a broad scope.

The scope hinges on:

  • Chemical Structural Claims:
    If the claims cover specific compound classes, the scope remains relatively narrow, potentially easier to design around.

  • Markush-type Claims:
    If present, these could cover a large number of structural variants, broadening the scope significantly.

  • Method Claims:
    Covering methods of synthesis or specific therapeutic uses extends protection beyond just compounds, potentially encompassing treatment claims.

2.3. Potential Limitations or Narrowing Factors

  • Backbone Limitations:
    The scope may be limited to the described chemical core. Any structural deviations outside this scope would potentially not infringe.

  • Functional Language:
    Claims emphasizing specific functional features (e.g., activity, bioavailability) could be interpreted narrowly.

Overall, the scope of JP5831449 likely aims to balance breadth with enforceability—covering core compounds and methods but potentially with limitations to specific chemical embodiments.


3. Patent Landscape and Strategic Positioning

3.1. Prior Art and Patent Family

The patent’s strength correlates with existing prior art:

  • Pre-Existing Patents:
    The patent filing probably addresses known compounds or methods, with claims tailored to novel features. Extensive search indicates whether it builds on core chemical entities or presents unique modifications.

  • Patent Family:
    JP5831449 is likely part of a broader international patent family, including equivalents under the Patent Cooperation Treaty (PCT) or filings in other jurisdictions (e.g., US, EU, China), amplifying global protection.

3.2. Overlap with Existing Patents

  • Overlap Analysis:
    Patents covering similar chemical scaffolds or therapeutic areas may lead to potential patent thickets or freedom-to-operate (FTO) challenges.

  • Blocking and Infringement Risks:
    Active patent holders in similar fields could threaten licensing, litigation, or settlement strategies. Conversely, if JP5831449 is pioneering, it can serve as a foundational patent for further patent applications.

3.3. Competitor Landscape

Major pharmaceutical players often file patents in Japan aligned with global patent strategies. The presence of overlapping IP could influence market entry, licensing negotiations, or patent litigations.

  • Existing patents by competitors might block or limit the scope of future filings or require licensing agreements.
  • Conversely, in innovator’s favorable position if JP5831449 covers a key chemical innovation or therapy.

3.4. Patent Term and Maintenance

  • Patent Term:
    Typically 20 years from the filing date. Assuming filings from the early 2010s, the patent could approach expiration around the early 2030s, impacting exclusivity timelines.

  • Maintenance:
    Ongoing in force through annual fees, which if paid, extend the patent's enforceability.


4. Related Patent and Innovation Strategies

  • Complementary Patents:
    Innovations in formulations, delivery methods, or combination therapies could expand the patent landscape.

  • Design-around Strategies:
    Competitors may design around the claims by modifying chemical structures or synthesis pathways while avoiding infringement.

  • Patent Licensing and Alliances:
    Licensing strategies could leverage JP5831449’s protective rights, especially in Japan’s significant pharmaceutical market.


5. Implications for Stakeholders

5.1. For Patent Holders

  • Solidify claim scope through patent maintenance and potential continuations or divisional applications.
  • Consider international extensions to protect global markets.
  • Use the patent as leverage in licensing or partnerships.

5.2. For Competitors

  • Conduct freedom-to-operate (FTO) assessments focusing on claim scope.
  • Explore design-arounds by modifying chemical structures or using different therapeutic modalities.
  • Monitor patent enforcement for potential litigation or licensing negotiations.

5.3. For Innovators

  • Identify gaps or limitations in the claims for developing next-generation compounds.
  • Investigate adjacent patent portfolios to expand patent coverage or avoid infringement.

6. Conclusion & Key Takeaways

  • JP5831449's claim scope appears to encompass specific chemical compounds and associated therapeutic methods, typical of pharmaceutical patents aiming for targeted protection.
  • Its scope depends on the breadth of structural claims and functional language, balanced against prior art to maintain enforceability.
  • It is likely part of a strategic patent family with potential international counterparts, influencing a firm's global IP stance.
  • Competitors must critically evaluate claims to ensure freedom-to-operate, considering design-around options and patent landscapes.
  • The patent’s lifespan and maintenance influence future market exclusivity, licensing potential, and R&D direction.

7. FAQs

Q1: What is the primary therapeutic area covered by JP5831449?
A1: While specific therapeutic coverage depends on the claims, patents like JP5831449 typically relate to chemical compounds with potential uses in treatments such as oncology, neurology, or metabolic disorders. Precise details require review of the claims and description.

Q2: How does the scope of claims impact infringement risk assessment?
A2: Broader claims increase infringement risk but may be more vulnerable to invalidation; narrower claims are easier to circumvent but provide limited coverage.

Q3: Can a competitor develop similar compounds without infringing JP5831449?
A3: Yes, by designing structural modifications outside the scope of claims or pursuing different therapeutic pathways not claimed.

Q4: How does the patent landscape in Japan influence global patent strategies?
A4: Patents filed in Japan often serve as strategic bases for broader international patent portfolios, especially in Asia-Pacific markets. They can also impact global licensing negotiations.

Q5: When does JP5831449 likely expire, and how does that influence market exclusivity?
A5: Assuming a typical 20-year patent term from the filing date and an early 2010s filing, expiration could occur around the early 2030s, opening the market for generics or biosimilars.


References

  1. Japan Patent Office (JPO) Patent Database. (Accessed 2023).
  2. WIPO PatentScope. International Patent Data. (Accessed 2023).
  3. Patent Law of Japan, Japan Patent Office. (Official legal framework).
  4. Pharmaceutical Patent Strategy in Japan, IP Watchdog, 2021.
  5. Relevant scientific literature and patent filings for contextual understanding.

Note: For precise claim language and legal interpretation, consulting the official patent document JP5831449 is recommended.

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