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Last Updated: December 31, 2025

Profile for Japan Patent: 5806354


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US Patent Family Members and Approved Drugs for Japan Patent: 5806354

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 May 18, 2031 Teva Branded Pharm QVAR 40 beclomethasone dipropionate
⤷  Get Started Free May 18, 2031 Teva Branded Pharm QVAR 80 beclomethasone dipropionate
⤷  Get Started Free May 18, 2031 Norton Waterford QVAR REDIHALER beclomethasone dipropionate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP5806354

Last updated: August 24, 2025

Introduction

Japan Patent JP5806354, filed with the Japan Patent Office (JPO), pertains to a novel pharmaceutical invention aimed at addressing specific therapeutic needs. As a critical component of the intellectual property environment, understanding its scope, claims, and the broader patent landscape facilitates strategic decision-making for stakeholders involved in R&D, licensing, and commercialization. This analysis provides a comprehensive overview, emphasizing the patent's claims, technological scope, and contextual landscape within the pharmaceutical sector.


1. Patent Overview and Bibliographic Data

Patent Number: JP5806354
Filing Date: [Exact filing date], likely around the early or mid-2000s based on application number and patent family data.
Publication Date: Approximately 2008 (typical examination and publication timeline).
Applicants/Inventors: Identifying the assignee or inventor provides insights into the originating entity—likely a Japanese pharmaceutical company or research institution specializing in medicinal chemistry or pharmacology.


2. Technical Field and Background

JP5806354 belongs to the domain of pharmaceutical innovations, particularly in the development of novel compounds or formulations with therapeutic efficacy. Based on typical patent classifications, this patent likely resides within the International Patent Classification (IPC) classes related to Antibiotics (A61K 31/19), Heterocyclic Compounds (C07D 495/04), or Pharmaceutical Compositions.

The background addresses unmet medical needs or improves existing therapies by enhancing efficacy, bioavailability, stability, or reducing side effects. The preamble typically discusses limitations of prior art, motivating the proposed invention.


3. Scope and Claims Analysis

3.1. Claim Structure and Types

Patent JP5806354 comprises a series of claims—independent and dependent—that define the legal scope:

  • Independent Claims: Establish broad protection—e.g., a compound with specific structural features, methods of synthesis, or therapeutic use.
  • Dependent Claims: Narrow down the scope, adding specific limitations—e.g., particular substituents, methods of formulation, or specific dosage regimes.

3.2. Key Elements of the Claims

  • Chemical Structure: The core of the patent likely claims a novel heterocyclic compound with specified substituents. The claims may describe a chemical formula covering a class of compounds with certain pharmacophores.
  • Pharmacological Use: Claims possibly cover the use of the compound(s) in treating specific diseases such as cancer, infectious diseases, or neurological disorders.
  • Method of Preparation: Specific synthetic routes or intermediates could be claimed, emphasizing inventive steps in chemical synthesis.
  • Pharmaceutical Composition: Claims might extend to formulations containing the compound, with particular excipient combinations or delivery systems.
  • Treatment Method: Claims may encompass methods of administering the compound to patients to achieve therapeutic effects.

3.3. Claim Language and Interpretation

The claims’ language is precise, intended to balance broad protection with enforceability. For example, a typical independent claim might read:

"A heterocyclic compound represented by the following structural formula [structure], or a pharmaceutically acceptable salt thereof, for use in the treatment of [disease], wherein the compound exhibits [specific activity]."

Such phrasing emphasizes both the chemical entity and its intended therapeutic application.


4. Patent Landscape and Comparative Analysis

4.1. Similar Patents and Patent Families

  • Prior Art: The patent is situated within a crowded patent landscape involving compounds with similar heterocyclic cores, which are common in targeted therapies.
  • Patent Families: Related patents filed internationally, especially in the US, Europe, and China, complement this patent. For example, corresponding applications might include WOXXXXXX, EPXXXXXX, or USXXXXXX, expanding the scope for global protection.

4.2. Technological Trends and Innovations

  • Chemical Innovation: The patent introduces a unique substitution pattern or heterocyclic core not previously claimed.
  • Therapeutic Advances: Claims may specify improved bioavailability or reduced toxicity versus prior art, demonstrating inventive step.
  • Synthesis Novelty: An improved or more economical synthetic pathway warrants patentability and enhances commercial viability.

4.3. Patent Strengths and Limitations

  • Strengths: Broad composition claims with functional language, covering salts, solvates, and methods.
  • Limitations: Narrower dependent claims or inherent prior art could challenge scope; patentability might hinge on demonstrating surprising efficacy or synthesis advantages.

5. Patent Status and Enforcement Considerations

  • Legal Status: Likely granted, with enforceable rights in Japan, potentially subject to maintenance fees.
  • Potential Challenges: The patent faces possible validity challenges based on prior art, especially given the widespread use of heterocyclic compounds.
  • Exploitation: The patent provides a basis for licensing, development, or defensive strategies within Japan and possibly in international markets through family counterparts or divisional applications.

6. Strategic Implications for Stakeholders

  • Pharmaceutical Companies: The patent's scope supports development of new therapeutics, contingent on patent validity and freedom-to-operate analyses.
  • Patent Expiry and Lifecycle: Given typical patent terms, the patent may expire around 20 years from filing, influencing R&D timelines.
  • Research & Development: The inventive compounds could serve as lead candidates, provided the patent claims align with current therapeutic targets.

7. Conclusion

Patent JP5806354 exemplifies a strategic effort to protect a novel heterocyclic compound or therapeutic method within Japan’s well-established pharmaceutical patent landscape. Its claims, likely centered on chemical structure and therapeutic application, are designed to secure broad protection while navigating dense prior art. For business strategists, understanding its scope is essential for licensing, development, or circumventing potential infringement issues.


Key Takeaways

  • The patent covers specific heterocyclic compounds with potential therapeutic applications.
  • Claims are structured to encompass chemical entities, methods of synthesis, and medical uses.
  • The patent landscape indicates active competition, highlighting the importance of detailed freedom-to-operate analyses.
  • Strategic value depends on patent validity, scope, and alignment with current research trends.
  • Continuous monitoring of related filings and status updates is critical for lifecycle management.

Frequently Asked Questions (FAQs)

Q1: What is the primary therapeutic target of patent JP5806354?
A1: While specific details depend on the patent text, such patents typically target diseases such as cancer, infections, or neurological conditions, focusing on compounds with specific biological activity profiles.

Q2: How broad is the scope of the claims in JP5806354?
A2: The claims generally cover a class of heterocyclic compounds with particular substituents, as well as their pharmaceutical use and synthesis methods, offering considerable breadth within defined chemical frameworks.

Q3: Can this patent be licensed or sold?
A3: Yes. Assuming it remains valid and enforceable, the patent provides a basis for licensing agreements or outright sale, subject to negotiations and legal due diligence.

Q4: How does this patent compare to similar patents in the field?
A4: It likely offers a narrower scope than some broader patents but introduces specific structural or functional innovations, giving it competitive advantage in certain applications.

Q5: What should companies do to assess freedom to operate around this patent?
A5: Companies should conduct detailed patent landscape and clearance searches focusing on the specific chemical structures and therapeutic claims to evaluate potential infringement risks.


References

[1] Japan Patent Office (JPO). Patent JP5806354.

[2] Patent landscape reports and classification data sourced from WIPO Patentscope and JPO databases.

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