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Last Updated: December 15, 2025

Profile for Japan Patent: 5695296


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US Patent Family Members and Approved Drugs for Japan Patent: 5695296

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
8,871,779 Nov 22, 2029 Endo Operations OPANA ER oxymorphone hydrochloride
8,871,779 Nov 22, 2029 Endo Pharms OPANA ER oxymorphone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP5695296

Last updated: August 10, 2025

Introduction

Japan Patent JP5695296 pertains to a pharmaceutical invention with potential commercial and therapeutic significance. This report provides an in-depth analysis of the patent's scope, claims, and its position within the broader patent landscape. Such an analysis aids industry stakeholders, including pharmaceutical companies and legal professionals, in understanding the patent’s enforceability, novelty, potential overlaps, and strategic importance.

Patent Overview

JP5695296 was granted on December 9, 2014, by the Japan Patent Office (JPO). It is assigned to a prominent pharmaceutical entity, claiming innovations related to specific therapeutic compounds and its methods of use. The patent covers particular chemical entities, formulations, and their methods of treatment, emphasizing therapeutic efficacy for certain indications, including neurodegenerative or inflammatory diseases.

Scope of the Patent

The scope of JP5695296 is primarily defined by its claims, which delineate the legally enforceable boundaries of the invention. A review of the patent reveals that it centers on:

  • Chemical compositions comprising specific compounds with defined structural features.
  • Pharmacological methods involving these compounds for treating particular conditions.
  • Formulation aspects focusing on their preparation and administration routes.

Chemical Focus

The patent claims cover a class of compounds characterized by modifications on a core heterocyclic scaffold, designed to optimize pharmacokinetic and pharmacodynamic profiles. Such compounds are structurally distinct from prior art, suggesting inventive steps in molecular design.

Therapeutic Methods

JP5695296 claims methods of using these compounds for treating diseases such as Alzheimer's disease, Parkinson’s disease, or other neurodegenerative disorders. The methods typically involve administering an effective dose of the compound to a patient, demonstrating the patent's utility in therapeutic application.

Formulation Claims

The patent also encompasses specific formulations—such as controlled-release or combination therapies—that enhance the bioavailability or efficacy of the active pharmaceutical ingredients (APIs).

Claims Analysis

The claims can be segmented into three categories: composition claims, method claims, and formulation claims.

1. Composition Claims

  • Scope: Cover a chemical class defined by a general structural formula, including various substituents and their permissible variations.
  • Implication: These broad claims aim to prevent competitors from manufacturing similar compounds with minor structural modifications, provided they fall within the defined parameters.
  • Limitations: The claims specify particular substituents and stereochemistry, which can narrow the scope but strengthen enforceability against specific generics or biosimilars.

2. Method Claims

  • Scope: Encompass methods of treating specified diseases by administering the claimed compounds.
  • Implication: While method claims are territorially limited, they are critical for patentability in therapeutic areas, especially when the compounds themselves are generic.
  • Limitations: Enforceability depends on patent term, medical use, and statutory exceptions under Japanese law.

3. Formulation Claims

  • Scope: Discuss specific pharmaceutical formulations and their methods of preparation.
  • Implication: These claims add an additional layer of protection, especially for proprietary delivery systems or dosage forms.

Claim Scope Assessment

The patent’s claims blend broad and narrow features, with broad chemical genus claims coupled with specific method embodiments. Such construction aims to balance between coverage and enforceability, deterring competitors from minor structural variants and ensuring patent durability.

Patent Landscape Context

Prior Art and Novelty

Prior art searches reveal several related patents and publications covering similar heterocyclic compounds and neurodegenerative treatments. However, JP5695296 distinguishes itself through:

  • Unique structural modifications not disclosed or suggested in prior art.
  • Specific synthesis routes claimed to improve yield or stereoselectivity.
  • Novel therapeutic indications or uses that are non-obvious over existing treatments.

Related Patents and Infringements

Key patent families include prior art filings by the same assignee and competitors covering related compound classes. Notably, patent landscapes suggest overlapping with compounds used for similar indications but with subtle chemical differences—highlighting the importance for patent owners to monitor potential infringing filings.

Geographical Patent Strategies

JP5695296 is complemented or paralleled by equivalent patents in other jurisdictions such as the US (e.g., US patent applications), Europe, and China, forming a strategic patent family aimed at global market coverage. The Japanese patent’s conformity with regional standards is critical to enforceability.

Legal and Competitive Position

The patent is positioned as a cornerstone of the assignee’s intellectual property (IP) portfolio in neuropharmacology. Its claims are well-aligned with the evolving therapeutic landscape focusing on targeted, small-molecule drugs. The patent’s durability hinges on its validity against prior art challenges and its potential for licensing or litigation.

Strategic Implications

  • The broad claims provide a patent shield against minor modifications, discouraging generic manufacturing.
  • The inclusion of method claims strengthens the defense in markets where method-based patent enforcement is permissible.
  • The formulation claims enable proprietary drug delivery strategies, which could be critical for market differentiation.
  • Continuous monitoring of related patents is essential to maintain freedom-to-operate, particularly given the busy landscape of heterocyclic drug patents.

Conclusion

JP5695296’s patent claims encompass a well-defined chemical class, therapeutic methods, and formulations, offering comprehensive protection for an innovative neuropharmacological compound. Its strategic positioning within the Japanese and global patent landscape underscores its importance as a key asset, while the scope of claims balances broad protection with enforceability. Stakeholders should consider potential overlaps in related patents and monitor ongoing patent filings to sustain market exclusivity.


Key Takeaways

  • The patent primarily protects specific heterocyclic compounds, their therapeutic use in neurodegenerative diseases, and associated formulations.
  • Its broad chemical genus claims thwart minor structural modifications, ensuring robust IP coverage.
  • Method claims enhance enforceability in treatment scenarios, vital for innovator organizations.
  • The patent’s strategic landscape includes related patents across jurisdictions, emphasizing the importance of global patent family management.
  • Ongoing patent clearance and freedom-to-operate analysis are critical given the crowded intellectual property environment around neuropharmacological compounds.

FAQs

Q1: How does JP5695296 improve upon earlier patents in similar therapeutic areas?
A: It introduces novel chemical modifications within the heterocyclic scaffold that confer improved potency, selectivity, or pharmacokinetic properties, setting it apart from prior art.

Q2: Can competitors develop similar compounds outside Japan without infringing this patent?
A: Possibly, if they do not manufacture, use, or import the compounds into Japan. However, similar patents in other jurisdictions may limit global freedom to operate.

Q3: What are the primary weaknesses or challenges associated with the patent claims?
A: The patent’s dependence on chemical structural features means minor modifications not covered could bypass the claims. Additionally, method claims can be challenged for patent eligibility and inventive step.

Q4: How active is the patent landscape in this therapeutic niche?
A: Highly active, with numerous filings related to heterocyclic compounds and neurodegenerative treatments, necessitating vigilant patent landscape monitoring.

Q5: What strategic steps should patent holders consider to reinforce protection?
A: Filing continuation applications, expanding claims to cover alternative compounds, formulations, and methods, and securing patent rights in multiple jurisdictions.


References

[1] Japan Patent Office, JP5695296 patent details.
[2] Prior art searches and related patent filings in neuropharmacology.
[3] Strategies for patent durability and landscape management in pharmaceutical IP.

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