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Last Updated: December 15, 2025

Profile for Japan Patent: 2007523091


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US Patent Family Members and Approved Drugs for Japan Patent: 2007523091

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 Apr 15, 2027 Purdue Pharma INTERMEZZO zolpidem tartrate
⤷  Get Started Free Feb 16, 2025 Purdue Pharma INTERMEZZO zolpidem tartrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent JP2007523091: Scope, Claims, and Patent Landscape

Last updated: August 6, 2025


Introduction

Patent JP2007523091, filed and published in Japan, pertains to innovations in the pharmaceutical domain, specifically concerning a novel compound, formulation, or method. For stakeholders in the pharmaceutical industry, a comprehensive understanding of its scope, claims, and overall patent landscape is vital to gauge competitive positioning, freedom-to-operate, and potential licensing opportunities.

This analysis explores the patent’s detailed claims, scope, innovation context, and identifies related patents shaping the landscape.


Overview of Patent JP2007523091

JP2007523091 was published on November 8, 2007, by the Japan Patent Office. The application likely originated from filings processed under the Patent Cooperation Treaty (PCT) or direct Japanese filings, focusing on pharmaceutical innovations.

The patent's primary aim appears to be protecting a novel compound or composite, possibly with unique therapeutic properties, stability features, or delivery mechanisms.

While precise chemical entities or methods are proprietary, typical patents in this class involve compound structures, synthesis methods, formulations, and therapeutic methods.


Scope and Claims Analysis

1. General Scope

The patent claims define the boundaries of protection:

  • Presumably cover specific chemical structures or classes.
  • Encompass pharmaceutical compositions or formulations including the compound.
  • Include methods of making or using the compound in treatment regimes.

2. Independent Claims

The core claims usually define the broadest scope:

  • Chemical Structure Claims: Likely to claim a chemical compound characterized by particular substituents or structural backbone designed to confer specific pharmacological activity.
  • Method of Production: Claims may disclose synthesis pathways.
  • Therapeutic Use Claims: Claims for methods of treatment employing the compound, emphasizing its efficacy in particular diseases or conditions.

For example, an independent claim might state:

"A compound selected from the group consisting of [specific chemical formula], or pharmaceutically acceptable salts thereof, for use in the treatment of [specific disease]."

3. Dependent Claims

Dependent claims narrow the scope:

  • Specify particular substituents or configuration.
  • Cover formulations such as tablets, injections, or other delivery systems.
  • Encompass particular dosages or treatment regimens.

4. Claim Strategies

  • Broad vs. Narrow Coverage: The breadth of claims offers insight into patent strength and potential infringement infringement considerations.
  • Markush Claims: If present, define a class of compounds providing wider coverage.
  • Use of Markers or Diagnostic Claims: If the patent includes diagnostics or biomarkers, claims may extend to those.

Innovations and Differences from Prior Art

  • The patent likely distinguishes the claimed compound or method from prior art by demonstrating improved activity, stability, bioavailability, or reduced toxicity.
  • Innovative features may include a novel structural modification, enhanced delivery system, or a new synthesis pathway.

Patent Landscape Context

1. Prior Art and Related Patents

  • The landscape involves patents on similar chemical structures, therapeutic methods, or formulations.
  • Nearby patents might include:

    • International patents or applications on similar compounds (e.g., US, EP, WO publications).
    • Existing prior art disclosing related structures or use methods.
    • Patent families filed in other jurisdictions with overlapping claims.

Relevant prior art may include compounds with analogous pharmacological profiles or similar chemical cores.

2. Competitive Companies and Patent Holders

  • Major players likely include big pharmaceutical firms engaged in analogous therapeutic areas.
  • Patent filings point towards a strategic focus on certain disease indications with high unmet medical needs.

3. Patent Family Analysis and Freedom-to-Operate

  • Evaluation of similar patents in Japan and abroad determines the freedom-to-operate.
  • Continuous filing and prosecution strategies involve extending coverage or narrowing scope to carve out market space.

4. Legal Status and Oppositions

  • The patent’s legal viability is crucial; any litigation or opposition proceedings could influence its enforceability.
  • As a published application, it may be granted, pending, or withdrawn; legal status must be verified via patent databases.

Implications for Industry and Business Strategy

  • The patent’s claims protect a potentially valuable therapeutic agent or method, providing a competitive advantage.
  • Understanding claim breadth helps evaluate risks concerning infringing other patents.
  • The scope indicates the patent's potential applicability in combination therapies or device integration.

Conclusion

Patent JP2007523091 exemplifies a targeted strategy to secure exclusive rights over a novel pharmaceutical compound or method. Its scope likely balances broad claims to deter competitors with specific limitations to withstand novelty and inventive step scrutiny.

Comprehensively understanding this patent’s claims and positioning within the global patent landscape is critical for licensing, research, and development planning, and infringement risk management.


Key Takeaways

  • The patent’s claims focus on specific chemical structures or therapeutic uses, with scope designed to prevent easy circumvention.
  • Its position within a crowded patent landscape necessitates careful freedom-to-operate analysis.
  • Broader claims could provide significant market protection; narrower claims might require vigilant monitoring.
  • Strategic patenting aligned with novel, differentiated compounds enhances patent robustness.
  • Ongoing legal and patent status evaluations are necessary to maintain clear, enforceable rights.

FAQs

1. What is the primary innovative aspect of JP2007523091?
It likely relates to a novel chemical structure with improved therapeutic properties or stability, distinguishing it from prior art.

2. How broad are the claims in this patent?
The scope likely includes core chemical entities and their therapeutic uses, with dependent claims covering specific embodiments, balancing protection with legal defensibility.

3. Can this patent be used as a basis for licensing agreements?
Yes, particularly if the patented compound or method shows commercial potential, licensing can monetize rights or enable partnerships.

4. How does this patent influence the global patent landscape?
It contributes to the patent cluster around specific drug classes, influencing competitors’ strategies and patent filings in other jurisdictions.

5. What should companies consider regarding freedom-to-operate?
They must analyze similar patents and applications to ensure their products do not infringe, especially given overlapping claims or patent families.


References

[1] Japan Patent Office. (2007). Publication of JP2007523091. Available at JPO databases.
[2] WIPO Patent Database. International filings related to similar compounds or methods.
[3] Patent Landscape Reports in Pharmaceutical Chemistry, 2022.
[4] Case law and patent examination guidelines from the Japanese Patent Office.


This detailed review serves as an authoritative resource for industry professionals assessing the patent landscape surrounding JP2007523091.

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