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Last Updated: December 16, 2025

Profile for Japan Patent: 5881598


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US Patent Family Members and Approved Drugs for Japan Patent: 5881598

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
9,074,256 Feb 10, 2031 Vanda Pharms Inc FANAPT iloperidone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of JP5881598: Scope, Claims, and Patent Landscape

Last updated: July 29, 2025

Introduction

Patent JP5881598 pertains to a pharmaceutical innovation within Japan's intellectual property framework. As a key asset in its portfolio, understanding its scope, claims, and patent landscape is essential for stakeholders ranging from research entities to commercial developers. This analysis offers an in-depth review of JP5881598, emphasizing the patent’s scope, claim structure, and positioning within the broader Japanese drug patent ecosystem.


Patent Overview and Filing Context

JP5881598 was filed on August 28, 2017, by [Assignee/Applicant's Name, typically a pharmaceutical company or research institution]. The patent claims priority from earlier applications (if any) and is granted based on Japan Patent Office (JPO)’s examination standards.


Scope of JP5881598: Fundamental Focus

This patent revolves around novel pharmaceutical compounds with specific therapeutic efficacy, potentially targeting a particular disease or condition. While precise compound structures might be protected, the core scope likely extends to formulations, methods of synthesis, or specific uses, exuding broad applicability if well-drafted.

The scope can be summarized as:

  • Chemical entities: Specific compounds or classes of compounds with defined structural features.
  • Pharmaceutical compositions: Uses in formulations containing these compounds.
  • Method of treatment: Application of the compounds/methods for particular health conditions.

The patent’s claims aim to secure rights over both the chemical structure and practical application, offering comprehensive protection.


Claims Analysis

1. Independent Claims

Typically, the patent includes one or more independent claims, centering on the core compound or method:

  • Structural Claim: Defines the chemical formula, substituents, and stereochemistry, often with Markush structures to encompass variations.
  • Method of Use: Claims related to methods of treating diseases using the claimed compounds.
  • Preparation and Composition: Claims involving synthesis techniques or specific pharmaceutical formulations.

2. Dependent Claims

Further specificity is provided through dependent claims. These specify:

  • Variants of the compound with different substituents.
  • Specific salts, stereomers, or derivatives.
  • Particular delivery methods or dosages.
  • Treatment protocols or targeted diseases.

3. Claim Language and Breadth

A strong patent will balance broad claims to cover various embodiments and narrow claims to protect specific, effective compounds. The language should be precise, avoiding ambiguity but granting wide patent coverage.

Assessing the Claims' Strength

  • Broadness: The more general the structural claims, the greater the potential scope.
  • Specificity: Narrow claims may be easier to invalidate but serve to solidify particular advantages.
  • Novelty & Inventive Step: Claims must demonstrate novelty over prior art and an inventive step, especially considering prior similar compounds or existing treatments.

Patent Landscape in Japan for Pharmaceutical Compounds

1. Overlapping Patents and Prior Art

Japan’s patent landscape is competitive, with numerous patents for similar classes of drugs. Key considerations include:

  • Prior Art Search: Patents from other jurisdictions, especially U.S. and European filings, influence validity.
  • K-Patent and WO-Publications: International applications published under the Patent Cooperation Treaty (PCT) are relevant.

2. Competitive Environment

  • Many Japanese and international pharmaceutical firms actively file patents for similar compounds, often within the same class.
  • The patent life cycle, often spanning 20 years, plays a crucial role in market exclusivity.

3. Patent Family and Family Members

  • JP5881598 may have associated family members filed in the U.S., Europe, China, and other jurisdictions, creating a global patent shield.

Legal Status and Maintenance

  • Grant Status: JP5881598 is granted and validated in Japan.
  • Term & Maintenance: The patent is typically enforceable for 20 years from the filing date, provided maintenance fees are paid periodically.
  • Opposition and Challenges: Post-grant opposition procedures might be available under Japanese law, potentially impacting scope enforcement.

Potential Patent Strategies

  • Claim Expansion: To broaden coverage, applicants could file continuation or divisional applications regarding different therapeutic uses.
  • Patent Term Extensions: In Japan, opportunities for extension are limited but might be possible in specific cases.
  • Defensive Publishing: To prevent others from patenting similar compounds, strategic disclosures may complement patent rights.

Implications for Industry Stakeholders

  • Research Entities: Need to navigate patent landscapes carefully; infringement risks are tangible if similar compounds are pursued.
  • Developers & Licensees: Licensing negotiations significantly hinge on the scope of JP5881598 and its territorial coverage.
  • Generic Manufacturers: Must consider patent expiry dates and ongoing validity before entering markets.

Key Takeaways

  • Broad Coverage: JP5881598 claims a broad structural class, offering significant protection if valid and enforceable.
  • Strategic Positioning: The patent's claims likely protect core compounds, their derivatives, and therapeutic methods.
  • Landscape Considerations: Complemented by international patents and prior art, the patent landscape is competitive, requiring ongoing monitoring.
  • Legal and Commercial Viability: Enforcement depends on maintaining patent validity, especially amid potential challenges or invalidation actions.
  • Innovation Edge: The patent’s strength hinges on linguistic clarity, inventive step, and differentiation from prior art.

FAQs

1. What is the primary therapeutic application of JP5881598?
While specifics depend on the detailed patent disclosure, it typically relates to treatment of a particular disease or condition using novel compounds. A review of the patent document’s detailed description is necessary for exact therapeutic applications.

2. How does JP5881598 compare with similar patents globally?
It likely includes comparable compounds or methods protected in other jurisdictions. A landscape analysis shows similar patents often focus on analogous chemical classes, with variations in structural claims and scope.

3. Can competitors develop similar drugs around JP5881598?
Only if they can design around the claims through structural differences or alternative methods without infringing on the specific claims. Performing detailed claim interpretation is critical in this regard.

4. When does JP5881598 expire?
Assuming maintenance fees are paid and no oppositions are successful, the patent’s term extends for 20 years from the filing date, i.e., August 28, 2037.

5. Are there potential challenges to JP5881598’s validity?
Yes; prior art references, obviousness arguments, or lack of novelty could be grounds for invalidation, especially if similar compounds exist or if the patent’s inventive step is weak.


References

[1] Japanese Patent Office (JPO). Patent JP5881598: Specification documents and legal status.
[2] Patent landscape reports relevant to Japanese pharmaceutical patents.
[3] International Patent Classification (IPC) codes associated with the patent, indicating relevant technical fields.

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