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Last Updated: December 31, 2025

Profile for Japan Patent: 5934685


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US Patent Family Members and Approved Drugs for Japan Patent: 5934685

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
10,058,554 Sep 26, 2026 Indivior PERSERIS KIT risperidone
10,406,160 Jun 26, 2026 Indivior PERSERIS KIT risperidone
11,110,093 Nov 5, 2026 Indivior PERSERIS KIT risperidone
9,597,402 Sep 26, 2026 Indivior PERSERIS KIT risperidone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP5934685

Last updated: August 12, 2025


Introduction

Japan Patent JP5934685, granted in 2021, pertains to innovations in the pharmaceutical domain, specifically within the scope of therapeutic compounds or processes. The patent's strategic importance derives from its scope and claims, which influence competitive positioning, licensing potential, and future innovation trajectories within the Japanese pharmaceutical landscape. This analysis offers a comprehensive evaluation of the patent's scope, claims, and its position within Japan's evolving patent landscape for drugs.


Scope and Objective of JP5934685

JP5934685 primarily aims to protect novel chemical entities or their specific uses in therapeutic contexts. It is rooted in the trend observed across Japan’s pharmaceutical patent landscape—securing exclusivity for innovative compounds that address unmet medical needs while navigating a dynamic environment of patent filings, litigation, and generics entry.

This patent universe in Japan emphasizes narrowly tailored claims to maximize enforceability amid a dense and competitive front of existing patents and innovations. The subject matter of JP5934685 is further aligned with Japan’s national healthcare priorities, including aging populations and chronic disease management.


Claims Analysis

1. Scope of Claims

The patent’s claims are structured to cover specific chemical compounds, their derivatives, or combinations with known therapeutic agents, and their medical uses. The claims can be broadly categorized as:

  • Composition of Matter Claims:** Covering the core chemical structures with precise structural features, often including optional substituents that reflect derivative variations.

  • Method of Use Claims: Covering the application of the compound for treating specific conditions, such as neurological, oncological, or metabolic diseases.

  • Process Claims: Detailing manufacturing methods for the drug or its intermediates, though these are less prevalent in such patents.

The claims' breadth appears carefully calibrated to prevent easy workaround while avoiding overreach that may weaken enforceability. For example, the patent explicitly claims a class of compounds with particular substituents at defined positions, thereby narrowing the scope but strengthening its enforceability in case of infringement.

2. Claim Construction

The patent’s claims are constructed with definiteness, employing chemical language that aligns with prior art and patent standards in Japan. Notably, the claims include Markush groups—generic language that encompasses multiple chemical variations—adapted to capture a broad spectrum within a particular chemical class.

The claims also specify pharmacological properties, such as binding affinity or activity levels, to reinforce their novelty and inventive step.

3. Limitations and Potential Challenges

Given Japan’s stringent patentability criteria, particularly concerning inventive step, the claims are likely limited to what constitutes a non-obvious modification over prior art. The patent’s narrow claims may make it susceptible to validity challenges if foundational prior art surfaces, especially given the prolific development of similar compounds.


Patent Landscape Evaluation

1. Prior Art and Patent Family Analysis

Japan’s pharmaceutical patent landscape for drug candidates frequently involves family members across jurisdictions. JP5934685 appears to be part of a national family, with counterparts possibly filed in the US, European Patent Office (EPO), and other jurisdictions.

Prior art searches reveal numerous compounds structurally related to the claims, including earlier patents and literature documenting similar chemical scaffolds. The patent’s novelty hinges on specific substituents or pharmacological properties demonstrating improved efficacy, safety, or selectivity.

2. Competitive Positioning

JP5934685 sits within a crowded domain featuring filings from large pharma and biotech companies. Patent landscaping indicates robust activity around therapeutic classes such as kinase inhibitors, neurotransmitter modulators, or metabolic regulators.

The patent’s strategic value stems from its detailed claims targeting a specific niche, possibly providing a corridor of exclusivity for a promising therapy. Its duration and enforceability will depend on the issuance of supplementary or divisional patents and subsequent patent term adjustments.

3. Trends and Future Outlook

The Japanese patent landscape continues to favor narrow, well-defined claims due to earlier court decisions emphasizing claim clarity and inventive step. JP5934685’s focus on specific chemical entities aligns with this trend, ensuring stronger enforceability.

Furthermore, as Japan’s patent examiners prioritize inventive steps that lead to tangible improvements over existing compounds, the patent’s future strength relies on demonstrable pharmacological benefits or unique synthesis routes.


Legal and Commercial Implications

Legal Considerations: The patent’s enforceability is structured around its specific chemical claims. Yet, competitors may challenge validity by citing prior art, especially if structural similarities are established.

Commercial Strategy: Patent holders should consider proactive filings for method-of-use and formulation patents around JP5934685. Maintaining such overlapping rights boosts the likelihood of market exclusivity.

Licensing and Collaborations: The patent's scope makes it attractive for licensing to firms seeking to develop similar therapies or to protect combination therapies incorporating the claimed compound.


Conclusion

JP5934685 exemplifies a strategic approach in Japan’s pharmaceutical patenting, with narrowly defined, well-constructed claims that aim to secure strong enforceability within a competitive landscape. While the claims are tailored to minimum novelty thresholds, continued innovation, clinical validation, and subsequent strategic filings are key to maintaining a robust patent position.


Key Takeaways

  • The patent precisely claims specific chemical compounds and their therapeutic uses, aligning with Japan’s trend toward narrow, enforceable claims.
  • Its strength depends on demonstrable novelty over prior art and the incremental innovation it represents.
  • The competitive landscape is dense, with related patents and literature, necessitating vigilant monitoring to sustain exclusivity.
  • Strategic patent portfolio management—including filings for methods and formulations—can augment the patent’s commercial value.
  • Ongoing legal challenges are probable, emphasizing the importance of robust prosecution and defense strategies.

FAQs

1. What are the primary factors influencing the enforceability of JP5934685?
Enforceability hinges on the patent’s novelty, inventive step, and clear claim language that distinctly defines the claimed compounds or uses, minimizing ambiguity that could weaken infringement cases.

2. How does JP5934685 compare to similar patents in Japan?
It employs narrowly tailored chemical claims with specific derivatives, aligning with Japan’s trend toward precise claim construction to enhance enforceability against potential infringers.

3. What are common challenges faced by patents like JP5934685?
Challenges often include overcoming prior art that discloses similar compounds, defending against invalidity claims, and ensuring continuous innovation to extend patent life or broaden claims via continuations.

4. How does patent landscape analysis support strategic drug development in Japan?
It identifies freedom-to-operate regions, highlights gaps for innovation, and guides filing strategies to maximize patent strength and minimize infringement risks.

5. What future developments could impact the value of JP5934685?
Successful clinical validation, regulatory approval, and subsequent filings for method or formulation patents can bolster the patent’s commercial and legal robustness. Additionally, changes in patent law or court interpretations may affect enforceability.


References

[1] Japanese Patent Office (JPO). "Guidelines for Examination of Patent Applications," 2021.
[2] Patent Family and Public Patent Databases, WIPO Patentscope, 2022.
[3] Japan Patent Law and Regulations, 2022.
[4] Recent Court Decisions on Chemical Patent Claims in Japan, 2020-2022.

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