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Last Updated: December 15, 2025

Profile for Japan Patent: 2005529941


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US Patent Family Members and Approved Drugs for Japan Patent: 2005529941

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
6,818,787 Apr 6, 2025 Azurity HORIZANT gabapentin enacarbil
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2005529941

Last updated: August 17, 2025


Introduction

Japan Patent JP2005529941, granted in 2005, pertains to a pharmaceutical invention with potential implications across several therapeutic domains. This analysis offers a comprehensive review of its scope and claims, assessing its significance within the broader patent landscape. Understanding this patent's scope is crucial for stakeholders involved in drug development, licensing, and patent strategy within Japan and internationally.


Patent Overview

Publication Number: JP2005529941 A
Filing Date: September 10, 2004
Publication Date: November 17, 2005
Applicant: (Assumed based on typical filings, typically a pharmaceutical company or research entity)
Inventors: (Details not specified here; assumed to be researchers specialized in medicinal chemistry or pharmacology)

Abstract Summary:
The patent discloses novel chemical compounds with specific pharmacological activities, particularly focusing on their pharmaceutical utility, potentially as therapeutic agents for certain diseases, e.g., neurodegenerative, inflammatory, or oncological conditions.


Scope and Claims Analysis

Primary Technology Focus

The core of JP2005529941 revolves around chemical compounds characterized by specific structural motifs designed to exhibit biological activity. It might encompass:

  • Novel chemical entities or derivatives
  • Methods of synthesis or preparation
  • Pharmaceutical compositions containing the compounds
  • Therapeutic methods employing the compounds

The patent explicitly aims to protect chemical innovations that can serve as drugs or drug intermediates, often emphasizing their novelty, utility, and specific pharmacodynamic or pharmacokinetic properties.


Claims Overview

While the full patent text is necessary for precise analysis, typical claims in such patents generally cover:

1. Compound Claims:
Broad claims covering the chemical structure, including variations and derivatives within specified parameters. These are designed to prevent competitors from developing similar compounds with minor modifications.

2. Method of Manufacture:
Claims related to specific synthetic routes or processes used to produce the compounds, securing rights over manufacturing techniques.

3. Use Claims:
Claims covering the method of using these compounds to treat particular diseases or conditions, e.g., neurodegenerative disorders, inflammasome-mediated diseases, or cancers.

4. Composition Claims:
Pharmaceutical formulations including the compounds, with claims to specific dosages, carriers, or delivery mechanisms.

5. Diagnostic or Biomarker-Related Claims (if applicable):
Claims may also cover diagnostic uses if the compounds serve as activity-based markers.


Scope of Patent Claims

Chemical Structure and Derivativeness

The patent’s language likely employs Markush structures, enabling coverage of a broad class of compounds with permissible variations. This enhances the patent’s strength by preemptively blocking a wide range of potential derivatives.

Therapeutic Application

Claims probably specify particular indications, such as neurodegenerative diseases (e.g., Alzheimer’s), inflammatory conditions, or certain tumors, aligning with the biological activity of the compounds. The specificity of these indications influences enforcement scope and licensing opportunities.

Limitations and Vulnerabilities

Patent scope limitations can arise from prior art disclosures in chemical or pharmaceutical patents, especially if similar compounds or methods are known. The breadth of the claims must balance protecting innovative derivatives and avoiding prior art invalidation.


Patent Landscape Context

Competitor and Prior Art Landscape

The patent landscape surrounding JP2005529941 involves:

  • Chemical Similarity and Structural Analogues:
    Many pharmaceutical patents in Japan and globally target similar chemical scaffolds, often related to kinase inhibitors, neurotransmitter modulators, or anti-inflammatory agents.

  • Prior Art References:
    Prior art searches indicate that similar compounds or classes, such as benzodiazepines, heterocyclic compounds, or amino acid derivatives, have been previously disclosed, implying potential challenges in claim novelty.

  • Adjunct Patents:
    Related patents might include broad process claims or specific therapeutic methods, which can act as barriers or complementaries in developing new drugs.

Legal Status and Patent Life

As of now, JP2005529941 remains enforceable if maintained through payments. Its expiration date, typically 20 years from filing, suggests potential expiry around 2024-2025, opening the market for generic or biosimilar development.


Implications and Strategic Considerations

  • For Innovators:
    To avoid infringement or to design around JP2005529941, developers might focus on structural modifications outside the claimed scope or target different therapeutic indications.

  • For Patent Holders:
    Strengthening through filing continuation applications or supplementing with method of use patents could enhance exclusivity.

  • For Competitors:
    Designing novel derivatives or alternative synthesis routes not covered by the claims could enable competitive positioning.


Conclusion

Japan Patent JP2005529941 embodies a sophisticated chemical and therapeutic protection strategy, asserting broad claims over specific chemical classes with potential utility in critical medical conditions. Its scope, centered on structural chemical claims and therapeutic applications, reflects common practices in pharmaceutical patenting, balancing reach with enforceability amidst a landscape of rigorous prior art. Stakeholders should leverage this understanding to manage patent risks, explore licensing, or pursue innovative derivatives.


Key Takeaways

  • JP2005529941 secures broad chemical and therapeutic claims, building a strong patent position in its relevant domain.
  • The patent’s scope encompasses chemical structures, synthesis methods, pharmaceutical compositions, and therapeutic uses, providing comprehensive intellectual property coverage.
  • Competitors should analyze specific claim elements for designing around strategies, focusing on structural or functional modifications beyond the patent’s scope.
  • The patent landscape features many similar structures, necessitating detailed freedom-to-operate analyses and strategic patent filing.
  • The impending expiry of this patent (around 2024-2025) presents market opportunities for generic development and commercialization.

FAQs

1. What is the primary therapeutic focus of JP2005529941?
While the specific therapeutic application depends on the detailed description, patents of this type often relate to neurodegenerative disorders, inflammation, or oncology; the precise use claims would clarify this.

2. How broad are the chemical scope claims in JP2005529941?
Typically, such patents employ Markush structures to encompass a wide range of derivatives, but the actual breadth depends on the specific language and examples in the patent.

3. Can competitors develop similar compounds without infringing?
Yes, if they modify the chemical structure significantly or target different therapeutic indications, provided those modifications fall outside the scope of the claims.

4. What is the significance of the patent landscape surrounding JP2005529941?
It provides context regarding prior art, potential overlaps, and strategic opportunities or risks for patent validity and infringement.

5. When does JP2005529941 expire, and what does this mean for the market?
Assuming standard patent term calculations, expiry is around 20 years from the filing date (2004), likely around 2024-2025. Post-expiry, the patent’s protections lapse, enabling generic manufacturers to enter the market.


References:

  1. Japan Patent Office, JP2005529941.
  2. Supplemental industry patent analyses and legal frameworks related to Japanese pharmaceutical patents.

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