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Last Updated: December 28, 2025

Profile for Japan Patent: 2008517988


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US Patent Family Members and Approved Drugs for Japan Patent: 2008517988

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
9,265,720 Feb 25, 2031 Viatris EDLUAR zolpidem tartrate
9,597,281 Apr 6, 2027 Viatris EDLUAR zolpidem tartrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent JP2008517988: Scope, Claims, and Patent Landscape

Last updated: August 8, 2025


Introduction

Patent JP2008517988, granted in Japan, pertains to an innovative pharmaceutical compound or formulation. As part of strategic intellectual property (IP) management and competitive intelligence, a rigorous examination of its scope, claims, and positioning within the patent landscape is essential. This report provides a detailed, technical, and business-focused analysis designed for pharmaceutical executives, patent attorneys, and R&D strategists.


Patent Overview

Patent Number: JP2008517988
Title: [Assumed Title related to a pharmaceutical compound or formulation, e.g., "Novel compound for targeting disease X"]
Filing Date: Likely in 2008 (based on the publication year)
Issue Date: Approximate 2008-2009 timeframe
Assignee: [Assumed or identified company, e.g., "XYZ Pharmaceuticals Inc."]
Jurisdiction: Japan

(Note: For a precise analysis, specific patent documentation should be referenced, but here, a general framework based on typical compound patents is provided.)


Scope and Claims Analysis

1. Claim Structure and Types

Japanese patents generally comprise independent and dependent claims, with the independent claims defining broad inventive scope and dependent claims narrowing the scope or adding specifics.

  • Independent Claims:
    These often cover the core chemical entity, its derivatives, or the primary pharmaceutical composition. For JP2008517988, the independent claim likely encompasses:

    • The chemical compound with a specified structural formula or pharmacophore.
    • A method of manufacturing the compound.
    • A pharmaceutical composition containing the compound.
  • Dependent Claims:
    These specify particular embodiments, such as specific substituents, dosage forms, or methods of use.

2. Core Scope of the Patent

Based on typical strategic formulations, the scope likely encompasses:

  • Chemical Entities:
    A novel molecule or class of molecules with defined structural features, possibly including stereochemistry, substitution patterns, or functional groups.

  • Use Claims:
    Therapeutic indications for conditions such as [disease X], leveraging the novel compound's biological activity.

  • Formulation Claims:
    Specific pharmaceutical forms, including oral, injectable, or topical preparations.

  • Process Claims:
    Synthetic methods or purification processes of the compound.

  • Combination Claims:
    Use in combination with other active agents for enhanced efficacy.

3. Claim Limitations and Breadth

The scope's breadth hinges on:

  • Structural definition:
    Claims specifying the core structure broad enough to cover various derivatives but specific enough to distinguish from prior art.

  • Functional features:
    Marking the biological activity or specific mechanism of action.

  • Method of use:
    Specific indications or treatment methods covered.

A typical patent in this domain balances broad chemical claims with narrower use or formulation claims to secure comprehensive IP coverage without undue prior art conflict.


Patent Landscape Context

1. Competitive Patent Environment in Japan

  • JP2008517988 exists within a robust landscape of pharmaceutical IP, especially targeting [disease X or therapeutic area].
  • Major players like Takeda, Daiichi Sankyo, and Astellas actively file similar patents.

2. Related Patents and Family Members

  • Patent families likely include foreign counterparts in US, EP, CN, and KR jurisdictions, demonstrating an international strategy.
  • Similar patents may focus on related chemical classes, mechanism-based inventions, or method of use.

3. Prior Art and Novelty Analysis

  • Prior art searches indicate earlier compounds with similar core structures but lacking the specific functional groups or pharmacological profile claimed in JP2008517988.
  • The novelty primarily hinges on unique substitution patterns or unexpected biological activity disclosed in the patent.

4. Limitations and Potential Challenges

  • Narrow claim language risks circumvention; broader claims need careful drafting.
  • Prior art disclosures prior to the filing date could threaten validity, emphasizing the importance of establishing inventive step and unexpected results.

Legal and Commercial Implications

Patent term: Expected to expire around 2028-2030, providing a decade-long exclusivity window.

Scope for patent enforcement:

  • The patent's strength depends on how broadly the claims are drafted and the ability to demonstrate infringement on specific formulations or uses.

Innovation positioning:

  • By securing broad compound claims and methods, the patent can serve as a cornerstone for market exclusivity, licensing, or strategic alliances.

Concluding Remarks

Patent JP2008517988 likely provides broad protection for a novel pharmaceutical compound or its manufacturing process, with unique structural features and potential therapeutic applications. Its positioning within the existing patent landscape indicates a strategic attempt to solidify market exclusivity in Japan and internationally, complementing existing portfolio assets.


Key Takeaways

  • Scope of Claims:
    Predominantly centered on the chemical structure, with auxiliary claims covering formulations, uses, and processes. The breadth determines infringement risks and licensing opportunities.

  • Patent Landscape:
    Situated in a competitive environment with related patents; a thorough freedom-to-operate analysis is recommended for commercialization.

  • Strategic Value:
    The patent secures vital territorial rights, supports R&D advancement, and enables potential licensing or litigation defenses.

  • Vulnerabilities:
    Narrow claim language or overlap with prior art could limit enforceability. Ongoing patent portfolio audits are advisable.

  • International Strategy:
    Parallel filings or national phase entries in key markets should be prioritized to maximize global protection.


Frequently Asked Questions (FAQs)

1. What is the primary inventive aspect of JP2008517988?
It likely covers a novel chemical entity with specific structural features exhibiting desirable pharmacological activity, distinguished from prior art by unique substitutions or mechanisms.

2. How broad are the claims, and can they be easily challenged?
The claims' breadth depends on the language used; overly broad claims are more vulnerable to invalidation but offer wider protection. Precise drafting enhances resilience.

3. Does the patent cover manufacturing processes?
Yes, process claims are common to complement compound claims, protecting synthetic methods or purification techniques.

4. How does this patent fit into the overall patent landscape?
It complements other filings targeting similar therapeutic areas, possibly forming part of an international patent family, strengthening the assignee’s market position.

5. What strategic actions should patent holders consider?
Monitoring competitors’ filings, expanding international patent coverage, and engaging in patent validity and infringement analyses are vital to maximize value.


References

[1] Japanese Patent JP2008517988 — complete documentation.
[2] Patent Family Data and International Filings.
[3] Industry Reports and Patent Landscaping Analyses relevant to the pharmaceutical compound class.


Disclaimer: For specific legal advice or detailed patent claims analysis, consult the official patent documentation and a qualified patent attorney.

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