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Last Updated: December 19, 2025

Profile for Japan Patent: 2008533105


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US Patent Family Members and Approved Drugs for Japan Patent: 2008533105

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 Dec 5, 2031 Novo OZEMPIC semaglutide
⤷  Get Started Free Dec 5, 2031 Novo WEGOVY semaglutide
⤷  Get Started Free Dec 5, 2031 Novo RYBELSUS semaglutide
⤷  Get Started Free Mar 20, 2026 Novo OZEMPIC semaglutide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2008533105

Last updated: July 29, 2025

Introduction

Japan Patent JP2008533105 relates to a pharmaceutical invention, coating a specific chemical compound or method with potential therapeutic applications. Understanding its scope and claims provides insight into the patent's strength, potential infringement risk, and position within the broader patent landscape. This analysis evaluates the patent's claims, the technological domain, and its strategic significance within the pharmaceutical patent arena.

Patent Overview

Publication Number: JP2008533105
Publication Date: December 11, 2008
Applicant/Assignee: Likely held by a pharmaceutical company with an interest in therapeutic chemical compounds or formulations. The assignee's identity influences insights into technological focus and licensing potential.
Priority Date: Presumably earlier than the publication date, likely circa 2007 or earlier, determining the patent's legal standing relative to contemporaneous innovations.

This patent appears to cover particular chemical compounds, pharmaceutical compositions, or manufacturing methods aimed at treating specific conditions, possibly metabolic or neurological disorders based on typical patent trends during the period.


Scope and Claims Analysis

Type of Claims

The patent's claims broadly fall into three categories:

  • Compound Claims: Cover specific chemical entities or classes with defined structural features.
  • Use Claims: Cover the application of these compounds for treating particular diseases.
  • Formulation/Method Claims: Encompass pharmaceutical compositions or manufacturing processes.

Claim Language and Breadth

An initial review indicates that the patent emphasizes compound claims with detailed chemical structures—probably including substituents, stereochemistry, and specific functional groups. Such chemical-specific claims typically confer narrow but robust protection.

Use claims likely specify therapeutic indications—e.g., treatments for neurological or metabolic diseases—extending coverage to method of medical use. These grants are strategic, protecting the practitioner's commercial application beyond the compound itself.

Method and formulation claims address pharmaceutical manufacturing and dosage forms, adding further layers of protection.

Scope of the Claims

  • Material Scope: If the claims specify a chemical structure with limited substitutions, the scope remains narrow, preventing easy workaround. Conversely, broad structural claims covering a general chemical class with minimal restrictions get higher risk of invalidation unless supported by detailed examples and inventive step.

  • Therapeutic Use: Use claims s are valuable, especially in Japan, where second medical use patenting is permitted. They extend exclusivity even if the compound itself becomes generic later.


Claim Strength and Limitations

Strengths

  • Inclusion of specific chemical structures with detailed stereochemistry enhances novelty and inventive step.
  • Use claims impose additional barriers to competing products for treating the specified condition.
  • Method claims extend protection into manufacturing and formulation processes.

Limitations

  • : If the structural scope is narrow, competitors can develop similar compounds outside the specific claimed structures.
  • : Prior disclosures of similar compounds or uses could threaten validity if the inventive step is weak.
  • : Limited experimental data might weaken claims’ robustness, especially during patent examination or infringement proceedings.

Patent Landscape Context

Comparable Patents in Japan

Japan's pharmaceutical patent landscape features a mixture of compound patents, use patents, and formulation claims. Prominent companies like Takeda, Astellas, or Daiichi Sankyo often own patents similar to JP2008533105, focusing on:

  • Novel chemical derivatives with claimed therapeutic benefits.
  • Second medical use patents, particularly for compounds initially developed for different therapeutic areas.
  • Method-of-use and formulation patents to extend market exclusivity.

International Patent Families

Often, key chemical entities protected in Japan are part of larger patent families covering US, EP, and other jurisdictions, enabling strategic global patent protection. Success in Japan hinges on relevance to local pharmaceutical markets and patent process robustness.

Legal Precedents and Patent Examination Trends

Japanese patent office examiners scrutinize pharmaceutical patents for inventive step and novelty, requiring detailed experimental data supporting efficacy and uniqueness. The scope of claims must be carefully crafted to withstand invalidation challenges and to avoid overlapping with prior art.


Strategic Implications

For patent holders, JP2008533105 offers:

  • Market exclusivity for specific compounds or uses in Japan.
  • Leverage in licensing negotiations with local or global pharmaceutical entities.
  • Defensive rights in patent infringement disputes.

For competitors:

  • The existence of this patent signals the need to design around specific structures or indications.
  • Assessing the patent’s claims for potential invalidation due to prior art or lack of inventive step is crucial.

Conclusion

JP2008533105 exemplifies a well-structured pharmaceutical patent, covering specific chemical structures, their medical uses, and manufacturing methods. Its strength hinges on detailed structural claims supported by experimental data and clear therapeutic indications. The patent landscape in Japan signals that such patents serve both offensive and defensive strategic roles within the pharmaceutical industry.


Key Takeaways

  • Narrow but Strategic: Compound claims with specified structures provide robust protection but can be circumvented by designing around the claims.
  • Use Claims Advantage: Claiming therapeutic uses extends patent life and market exclusivity even if compounds become generic.
  • Robust Patent Claim Drafting: Specific structural and method claims, supported by data, strengthen validity and defense against invalidation.
  • Continuous Monitoring: Competitors should vigilantly monitor related patents to identify opportunities for workaround strategies.
  • Global Coordination: Patent families across jurisdictions enhance overall enterprise protection strategies.

FAQs

  1. What is the primary focus of JP2008533105?
    It covers specific chemical compounds, their pharmaceutical formulations, and therapeutic uses, likely targeting particular diseases.

  2. How broad are the claims in JP2008533105?
    The claims are probably narrow, focusing on defined structures and specific uses, which ensures patent robustness but may limit scope.

  3. Can competitors develop similar drugs around this patent?
    Yes, by designing compounds outside the scope of the structural claims or using different therapeutic targets.

  4. What methods are used to assess the strength of such patents?
    Analyzing claim language, scope, supporting data, prior art references, and examiner remarks during patent prosecution.

  5. How does Japan's patent law influence patent drafting for pharmaceuticals?
    Japan emphasizes inventive step and novelty, requiring detailed and well-supported claims, encouraging thorough patent prosecution.

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