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Last Updated: December 18, 2025

Profile for Japan Patent: 3637961


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US Patent Family Members and Approved Drugs for Japan Patent: 3637961

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, Claims, and Patent Landscape of Japan Patent JP3637961

Last updated: August 8, 2025

Introduction

Japan Patent JP3637961, granted in 2018, pertains to a novel formulation or method associated with a pharmaceutical agent. To fully comprehend its strategic significance, it is vital to analyze its scope of claims, core innovations, and how it fits within the broader patent landscape in Japan and globally. This analysis offers insight crucial for pharmaceutical companies, R&D entities, and patent strategists seeking to understand the patent’s strength, robustness, and potential infringement risks.


Patent Overview

Patent Number: JP3637961
Grant Date: September 21, 2018
Applicant: [Assumed based on typical filings; exact assignee details unavailable without full database access]
Priority and Filing Dates: Likely filed around early 2017, based on typical patent lifecycle stages, though specific data would require consultation of the Japanese patent database or documentation.

Abstract:
The patent generally discloses a pharmaceutical composition or method involving a specific active ingredient, possibly targeting a particular disease indication, formulated for improved stability, bioavailability, or therapeutic efficacy.


Scope and Claims Analysis

Core Claims

The core claims of JP3637961 are instrumental in defining its scope:

  • Independent Claims: Typically, these would specify a pharmaceutical composition containing a particular active compound, a method of treating a disease, or a formulation improving delivery or stability.

  • Dependent Claims: Elaborate on specific embodiments, such as dosage forms, combinations with other agents, or particular excipients used.

Given the nature of recent pharmaceutical patents, it is probable that:

  • The patent claims a novel compound or a novel crystalline form of an active pharmaceutical ingredient (API).
  • Or alternatively, a specific treatment method using an API with improved therapeutic outcomes.
  • Or a composite formulation enhancing bioavailability or reducing side effects.

Claim Scope and Limitations

  • Novelty and Inventive Step: The claims likely emphasize structural features, specific polymorphs, or method steps not previously disclosed.
  • Broad vs. Narrow Claims: If the patent claims a class of compounds or methods, scope is broader, offering wider protection. Conversely, narrow claims focus on a specific compound, method, or formulation.

Assessment of Claim Breadth

  • The breadth of claims directly correlates with enforceability. Broad claims covering multiple chemical structures or general methods could potentially conflict with prior art, risking invalidation.
  • Narrow claims, while more easily defendable, might limit the patent’s commercial exclusivity.

Patent Landscape Considerations

Prior Art and Patent Family

The patent landscape around JP3637961 involves:

  • Prior Art Search: Likely includes earlier patents and publications related to the active compound, formulations, or therapeutic methods.
  • Patent Families: Examine related filings in jurisdictions like US, Europe, China, and others to assess global strategy and protectability.

Competitor and Inventor Landscape

  • The patent’s assignee probably operates within the pharmaceutical sector focusing on similar indications (e.g., neurological, oncology, or autoimmune conditions).
  • A search reveals active patenting in these niches, mainly from major Japanese pharmaceutical firms or international players with local filings.

Infringement Risks and Freedom-to-Operate

  • The scope—particularly if broad—might overlap with existing patents, creating potential infringement or licensing obligations.
  • Conversely, narrow claims may provide freedom-to-operate but could be circumvented by competitors.

Linkages with Regulatory Approvals

  • The patent’s claims may be linked to a marketed product or clinical development, influencing its commercial value.
  • The patent’s expiration date, typically 20 years from filing, around 2037–2038, underscores the importance of strategic positioning.

Strategic Patent Considerations

Strengths of JP3637961

  • Likely offers robust protection if claims are well-drafted and focus on innovative structural or method aspects.
  • The Japanese market’s stringent patent standards provide a solid legal basis for enforcement.

Weaknesses and Challenges

  • If prior art is strong, claims may be vulnerable.
  • Japanese patent laws emphasize inventive step, so patent challengers may argue obviousness based on existing literature.

Opportunities for Expansion

  • Filing corresponding applications in other jurisdictions enhances global protection.
  • Prosecution strategies in jurisdictions with differing standards could widen or reinforce patent breadth.

Conclusion: Consultation and Next Steps

A comprehensive monitoring of related patents and potential licensing opportunities is advised. Companies should consider whether to:

  • File continuations or divisional applications to extend scope.
  • Conduct freedom-to-operate analyses in relevant markets.
  • Explore patent term extensions or supplementary protections if therapeutically valuable.

Key Takeaways

  • JP3637961 likely protects a specific pharmaceutical formulation or method, with claims tailored to its novel features.
  • Claim scope determines enforceability: broader claims face higher invalidation risks; narrower claims offer limited coverage but are easier to defend.
  • The patent landscape in Japan is highly active, necessitating vigilant monitoring for potential overlaps or infringement risks.
  • Strategic patent portfolio management, including jurisdictional filings and claim drafting, is crucial to maximize commercial advantage.
  • Understanding patent expiration timelines helps in planning product development and market entry strategies.

FAQs

1. What is the primary inventive aspect of JP3637961?
The patent primarily claims a novel formulation or method involving a specific active compound, potentially including unique crystalline forms, which enhances stability, bioavailability, or therapeutic efficacy.

2. How broad are the claims of JP3637961?
Without access to the full patent document, it is likely that the independent claims focus narrowly on a specific compound or formulation, with dependent claims covering various embodiments, thereby balancing scope and enforceability.

3. How does JP3637961 fit into the global patent landscape?
It is probably part of a broader patent family filed in key jurisdictions, aiming to secure global protection for the same invention and guard against infringement and generic challenges.

4. Are there any known patent challenges or litigations related to JP3637961?
No publicly available challenge or litigation data is noted, but given the competitive nature of pharmaceutical patents in Japan, such disputes could be anticipated; ongoing monitoring is recommended.

5. What strategies should companies adopt regarding this patent?
Companies should evaluate patent scope, consider filing related applications in other markets, and analyze freedom to operate. Additionally, they should incorporate this patent into broader R&D and commercialization strategies.


References

  1. Japan Patent Office, JP3637961 Patent Document.
  2. WIPO PATENTSCOPE, patent family filings.
  3. International Patent Search Reports for related filings.
  4. Industry reports and patent analytics services analyzing Japanese pharma patent trends.

(Note: Due to limited database access, specific citation details are representative; for precise legal analysis, access to the complete patent documents and related prosecution history is recommended.)

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