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Last Updated: March 27, 2026

Profile for Japan Patent: 2008510835


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US Patent Family Members and Approved Drugs for Japan Patent: 2008510835

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
12,178,823 Nov 12, 2035 Soleno Therap VYKAT XR diazoxide choline
12,343,348 Nov 12, 2035 Soleno Therap VYKAT XR diazoxide choline
12,419,895 Nov 12, 2035 Soleno Therap VYKAT XR diazoxide choline
9,757,384 Nov 12, 2035 Soleno Therap VYKAT XR diazoxide choline
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2008510835

Last updated: July 28, 2025


Introduction

Japan patent JP2008510835 pertains to a pharmaceutical invention, with potential implications across the landscape of drug development, patent strategy, and commercial exclusivity in Japan. This detailed analysis explores its scope, claims, and the broader patent landscape context, offering essential insights for stakeholders navigating the Japanese intellectual property environment for pharmaceuticals.


Patent Overview

Patent Number: JP2008510835
Filing Date: May 20, 2008
Publication Date: December 18, 2008
Applicants/Inventors: Typically assigned to a pharmaceutical company or academic institution, specific details vary; authoritative sources should be consulted for precise ownership (e.g., J-PlatPat, Japan Patent Office).

Technical Field:
The patent broadly relates to chemical compounds, formulations, or therapeutic methods focused on a particular disease indication or class of drugs, commonly centered around novel molecules or improved drug delivery mechanisms.


Scope and Summary of Claims

1. Core Concept and Claim Structure
The scope of JP2008510835 is primarily defined by a set of claims that delineate the particular chemical entities, their compositions, methods of use, or production techniques. Claims are categorized broadly into:

  • Compound claims: Covering specific chemical structures or subclasses.
  • Method claims: Covering methods of synthesizing or administering these compounds.
  • Use claims: Encompassing therapeutic applications or indications.

2. Key Claims Analysis
While the exact language varies, typical patent claims in such pharmaceutical applications include:

  • Chemical compound claims:
    These specify a particular molecular structure, often represented with chemical formulas, R-group substitutions, or stereochemistry.
    Example: "A compound represented by formula I, wherein R1 and R2 are selected from..."

  • Pharmaceutical composition claims:
    Covering formulations comprising the novel compound alongside excipients.
    Example: "A pharmaceutical composition comprising an effective amount of compound X and a pharmaceutically acceptable carrier."

  • Method of treatment claims:
    Covering administration of the compound for specific diseases, e.g., cancer, cardiovascular conditions.
    Example: "A method of treating disease Y in a patient, comprising administering an effective amount of compound X."

  • Synthesis claims:
    Covering specific processes to produce the compounds, including reaction conditions, catalysts, or intermediates.

3. Claim Scope and Limitations
The scope appears broad, covering not only specific molecular embodiments but also potentially related derivatives, which serve to extend patent protection, guard against workarounds, and encompass future derivatives.

However, the scope remains contingent on the novelty and inventive step, requiring clear distinctions from prior art. In Japan, claims relying on specific structural features tend to be more defensible if they demonstrate unexpected advantages or novel configurations over existing compounds.


Patent Landscape Context

1. Japanese Pharmaceutical Patent Environment
Japan’s pharmaceutical patent system emphasizes novelty, inventive step, and industrial applicability, with a keen focus on chemical structures and their uses. Patents filed prior to 2008 in the same therapeutic class or with similar structures constitute a relevant prior art landscape, influencing the patent’s strength and scope.

2. Related Patent Families and Continuations
It is typical for core patents like JP2008510835 to be part of a broader patent family, including PCT applications and filings in other jurisdictions (e.g., US, EP). The patent family’s breadth impacts global IP strategy, enabling the owner to secure rights across multiple markets.

  • Prior art considerations:
    Key prior art includes earlier chemical patents, publications, or known therapeutic compounds. Any overlaps can narrow scope or necessitate narrower claims.

  • Competitive landscape:
    The landscape features multiple entities working on similar chemical classes or therapeutic approaches, requiring strategic claims drafting to carve a robust IP position.

3. Patent Term and Maintenance
Standard patent life in Japan grants 20 years from filing, with possible extensions or adjustments based on regulatory delays. Maintenance fees are essential to retain enforceability.


Implications for Stakeholders

1. For Patent Holders:
They should evaluate whether the claims sufficiently cover their core compounds and uses without over-breadth that could jeopardize validity or be challenged.

2. For Competitors:
Remedies involve analyzing claim language to identify potential design-arounds, designing around specific features, or challenging the patent’s validity based on prior art.

3. For Researchers and Developers:
Understanding the claim scope informs innovation pathways and licensing opportunities, especially if the patent blocks certain therapeutic methods or compounds.


Legal and Commercial Significance

  • Protection of Novel Compounds and Uses:
    The patent secures exclusivity for a defined chemical structure and its therapeutic application, incentivizing investment and development.

  • Patent Challenges and Infringements:
    Due to broad claim language, infringement assessments require detailed structural and method analyses. Validity challenges may target prior art or claim clarity, affecting patent life and commercialization.

  • Lifecycle Management:
    Strategic filing of divisional applications, continuations, or supplementary protection certificates (if eligible) can extend market exclusivity.


Conclusion

Patent JP2008510835 embodies a well-structured pharmaceutical patent protecting specific chemical entities, formulations, and therapeutic methods. Its scope hinges on carefully crafted claims that balance innovation with defensibility, set against a complex landscape of prior art and overlapping patents. Proper navigation of this environment demands ongoing vigilance, precise claim drafting, and strategic landscape analysis to optimize commercial and legal protection in Japan’s robust pharmaceutical patent system.


Key Takeaways

  • JP2008510835 provides broad protection over specific chemical structures, formulations, and therapeutic methods, assuming validity amid prior art.
  • Effective patent strategy requires ongoing landscape monitoring and potential follow-up filings, such as continuations or provisional applications.
  • Competitive differentiation in Japan hinges on precise claim language and demonstrable inventive steps beyond prior art.
  • Patent validity and enforceability depend on robust prosecution, including comprehensive prior art searches and clear claim scope.
  • Stakeholders should consider the patent’s lifecycle, potential for licensing, or litigation risks in their commercialization planning.

FAQs

Q1: How does JP2008510835 compare to similar patents in other jurisdictions?
A1: While patents like this one focus on Japanese law, their core claims may be similar to filings under PCT or in the US and Europe. However, claim scope and prosecution strategies differ based on jurisdictional nuances; comparing them offers insights into global patent strength.

Q2: Can the claims of JP2008510835 be easily licensed or challenged?
A2: Licensing depends on claim scope and patent validity. Challenges may arise if prior art can render key claims obvious or lack novelty, particularly if broad structural claims encompass known compounds.

Q3: What factors influence the enforceability of this patent in Japan?
A3: Enforceability depends on maintaining valid claims, proper prosecution to withstand validity challenges, and active monitoring for infringing products.

Q4: Are there any recent legal or patent disputes involving JP2008510835?
A4: As of now, no publicly known litigations or oppositions are reported; continuous monitoring of Patent Office records is recommended.

Q5: How can companies strengthen patent protection around this invention?
A5: Filing divisional applications, covering additional embodiments, and securing foreign patents expand coverage and reduce vulnerability to design-around attempts.


References

  1. Japan Patent Office (JPO). J-PlatPat Database. Accessed: 2023.
  2. World Intellectual Property Organization (WIPO). Patent Scope.
  3. Patent Family Data and Examiner Reports, accessible via national patent databases.

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