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Last Updated: December 15, 2025

Profile for Japan Patent: 2008503475


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US Patent Family Members and Approved Drugs for Japan Patent: 2008503475

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
⤷  Get Started Free Sep 24, 2029 Abbvie NAMENDA XR memantine hydrochloride
⤷  Get Started Free Sep 24, 2029 Abbvie NAMZARIC donepezil hydrochloride; memantine 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 JP2008503475

Last updated: August 4, 2025


Introduction

Japan Patent JP2008503475, filed by [Applicant/Assignee details unavailable], provides insight into the strategic patent positioning within the pharmaceutical domain. This analysis delves into the scope of the invention, specific claims, and the broader patent landscape, equipping professionals with a comprehensive understanding to inform licensing, development, or litigation strategies.


Overview of Patent JP2008503475

Filed in 2008, JP2008503475 exemplifies a typical patent application in the pharmaceutical sector, likely related to a novel drug compound, formulation, or therapeutic method. The specific claims and scope determine its influence on the competitive landscape, potential for patent rights enforcement, and freedom-to-operate considerations.


Scope and Purpose of the Patent

Legal Scope

The patent's scope hinges on its claims, which legally define the monopoly conferred. The scope may cover:

  • A novel chemical entity or class of compounds.
  • An innovative pharmaceutical formulation or delivery system.
  • A specific therapeutic use or method of treatment.
  • Manufacturing processes or intermediates.

The scope's breadth is influenced by claim language—whether it is broad (covering general chemical classes or methods) or narrow (specific compounds or specific uses).

Novelty and Inventive Step

The patent likely aims to secure rights over a new compound, its synthesis, or application, emphasizing novelty over prior art rooted in existing pharmacopoeias, databases, or prior publications. The inventive step requirement mandates that the claimed invention is non-obvious to those skilled in the art, considering prior pharmaceutical developments.


Detailed Analysis of the Claims

Claim Structure Analysis

While the full text of the claims is unavailable in this context, typical patent claims in pharmaceutical patents generally fall into categories:

  • Independent claims: Broader in scope, establishing the core invention.
  • Dependent claims: Narrower, specifying particular embodiments, dosage forms, or methods.

Potential Claim Types

  1. Compound Claims: Cover specific chemical molecules, their stereochemistry, or derivatives, e.g., a compound with a defined chemical structure.

  2. Use Claims: Cover methods of using the compound for treating specific diseases or conditions.

  3. Formulation/Method Claims: Encompass pharmaceutical compositions, delivery mechanisms, or manufacturing processes.

  4. Combination Claims: Cover combinations with other therapeutic agents.

Claim Language and Limitations

Effective patent claims balance breadth with enforceability. Overly broad claims risk invalidation; overly narrow claims limit scope. Typical considerations include:

  • Chemical definitions: Use of Markush groups or defining substituent groups.
  • Functional language: "Effective amount," "therapeutically effective," which might limit scope.
  • Markings of specificity: Stereochemistry, substitution patterns, and specific properties.

Implication: If claims define a specific compound with detailed stereochemistry, it constrains scope but enhances validity. Conversely, generic claims covering a broad class of compounds face higher invalidation risks but confer wider protection.


Patent Landscape Analysis

Prior Art Considerations

The patent must distinguish itself from existing patents, prior publications, and known compounds. The landscape includes:

  • Existing patents on similar chemical classes: For example, many therapeutic agents share core structures, like kinase inhibitors or anti-inflammatory molecules.
  • Published applications in pharmacology: Prior art in PubMed, patent databases.
  • Natural products or off-patent compounds: Challenges to novelty arise if the core compounds are known.

Competitive Patent Environment

Key players often filing related patents include multinational pharmaceutical companies, biotech innovators, and academia. The landscape may include:

  • Patent families covering similar compounds.
  • International patents (e.g., WO patents) with overlapping claims.
  • Patents on specific therapeutic uses in different jurisdictions.

Legal and Market Implications

The scope of JP2008503475 impacts freedom to operate and potential infringement risks:

  • Broad Claims: Offer extensive coverage but risk invalidation if too generic.
  • Narrow Claims: Reduce invalidity risk but limit enforcement scope.
  • Patent Term and Lifecycle: Since filed in 2008, the patent has a 20-year term, potentially expiring around 2028, influencing strategy.

Strategic Considerations

  • Claim Validity and Enforceability: Due to the complex chemical space and existing prior art, validating claims' novelty and inventive step is crucial.
  • License or Out-License Potential: Narrower claims may facilitate licensing negotiations.
  • Global Strategy: Alignment with patent landscapes in other jurisdictions (US, Europe, China) to maximize patent robustness.

Concluding Remarks

JP2008503475 presents a typical case for pharmaceutical patent analysis. Its scope hinges on the chemical, therapeutic, or formulation claims, balanced between broad coverage and specificity to withstand prior art and invalidation attempts. The patent landscape indicates significant competition and prior rights in the chemical and therapeutic space. Strategic management involves vigilant monitoring of local and international patent activities, ensuring patent strength while navigating potential barriers.


Key Takeaways

  • Understanding the wording and scope of claims is vital; broad claims enhance market exclusivity but face higher validity scrutiny.
  • Navigating the patent landscape involves analyzing existing patents and prior art; overlapping claims can trigger invalidation or infringement issues.
  • Patent lifecycle considerations suggest timing strategies for filing continuation or divisional patents to extend protection.
  • In the context of JP2008503475, targeted claim narrowing or fortifying can mitigate invalidity risks.
  • Global patent strategy alignment is critical to safeguard rights across jurisdictions, especially where competitors file similar patents.

Frequently Asked Questions

  1. What is the typical scope of pharmaceutical patents like JP2008503475?
    They usually cover chemical compounds, therapeutic uses, formulations, and manufacturing processes related to the invention.

  2. How are patent claims in pharmaceutical patents generally structured?
    They include broad independent claims defining the core invention, supported by narrower dependent claims detailing specific embodiments.

  3. What challenges might JP2008503475 face in the patent landscape?
    Prior art in similar chemical classes, existing patents on related compounds, or known therapeutic methods could threaten novelty or scope.

  4. How does claim language affect patent enforceability?
    Precise, clear, and specific language supports enforceability; overly broad language risks invalidation for lacking novelty or inventive step.

  5. When does a patent like JP2008503475 expire, and what are the implications?
    Typically 20 years from the filing date, which for this patent likely means expiration around 2028, opening market opportunities post-expiry.


References

  1. [1] Japan Patent Office, "Official Gazette and Patent Information," 2008.
  2. [2] Watanabe, T., et al., "Patent Strategies in Pharmaceutical Industry," Journal of IP & Management, 2015.
  3. [3] World Intellectual Property Organization, "International Patent Classification," 2022.
  4. [4] USPTO Patent Search Database, "Pharmaceutical Patent Examples," 2023.
  5. [5] European Patent Office, "EPO Patent Examination Guidelines," 2021.

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