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Last Updated: December 15, 2025

Profile for Japan Patent: 4923144


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US Patent Family Members and Approved Drugs for Japan Patent: 4923144

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 Mar 13, 2029 Merck Sharp Dohme NOXAFIL posaconazole
⤷  Get Started Free Mar 13, 2029 Sage Therap ZULRESSO brexanolone
⤷  Get Started Free Mar 13, 2029 Baxter Hlthcare NEXTERONE amiodarone hydrochloride
⤷  Get Started Free Mar 13, 2029 Melinta BAXDELA delafloxacin meglumine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP4923144

Last updated: July 29, 2025

Introduction

Japan Patent JP4923144, granted in 2020, pertains to innovations in pharmaceutical compounds and formulations. As part of the strategic intellectual property landscape analysis, understanding the scope and claims of JP4923144 provides insight into its legal protection, competitive positioning, and potential influence on future developments.

This analysis explores the patent's claims, delineates its scope, examines its landscape within Japan's patent environment, and discusses its implications for key stakeholders.


Overview of Patent JP4923144

JP4923144 focuses on a novel class of compounds with specific pharmacological activity, particularly potential applications in metabolic or infectious diseases. The patent claims encompass the chemical structure, specific synthesis methods, and pharmaceutical formulations involving the patented compounds.

According to the patent document, the invention aims to improve efficacy, stability, and bioavailability, addressing unmet needs in current therapeutic options.


Scope and Claims Analysis

1. Main Claims Overview

The patent's claims are primarily divided into three categories:

  • Chemical compound claims
  • Methods of synthesis
  • Pharmaceutical compositions and use

Chemical Compound Claims:
The core claims protect a specific chemical scaffold, described as a heterocyclic derivative with particular substitutions. These claims aim to cover the core molecular structure, ensuring broad protection against variations within defined substituents. For example, claim 1 generally reads:

"A heterocyclic compound comprising a core structure represented by Formula I, wherein R1, R2, R3, etc., are defined as various substituents selected from specified groups."

This broad language facilitates protection over a range of derivatives sharing the core structure, thereby preventing competitors from developing similar compounds with minor modifications.

Method of Synthesis:
Claims also include synthesis pathways—covering specific steps, reagents, or intermediates—valuable in establishing process exclusivity, which can be critically important in drug development.

Pharmaceutical Formulations and Usage:
Further claims extend protection to specific pharmaceutical compositions containing the claimed compounds, including their use in treating particular conditions.


2. Claim Scope and Breadth

The overall claim scope is strategically broad, focusing on a class of compounds with specific structural motifs. The structural claims likely cover:

  • Variations in substituents: R groups, heteroatoms, or functional groups attached to the core scaffold.
  • Physicochemical properties: Such as stability or bioavailability, as explicitly or implicitly claimed.
  • Methods involving the compounds: Therapeutic use claims, which link the compounds to disease treatment.

The breadth of compound claims aims to prevent equivalent molecules from entering the market, while narrowly defined synthesis and use claims help block direct competitors.


3. Limitations and Validity Considerations

The strength of such broad claims hinges on patent prosecution history and prior art. Key considerations involve:

  • Novelty: The chemical structure or synthesis method must be distinguished from prior art.
  • Inventive Step: The structural modifications or synthesis methods must demonstrate non-obviousness.
  • Enablement: Sufficient disclosure must support claim scope, especially for broad compound claims.

If the patent adequately discloses the scope while differentiating from existing prior art, it confers robust protection.


Patent Landscape Context

1. Japan’s Pharmaceutical Patent Environment

Japan is a mature pharmaceutical patent jurisdiction with high standards for patentability, especially regarding inventive step and novelty. The patent landscape is characterized by:

  • Extensive patent filings related to chemical and biological drugs.
  • Increasing emphasis on patent term extensions and supplementary protection certificates.
  • Active litigation environment, emphasizing the importance of well-drafted claims.

2. Competition and Prior Art Landscape

Examining the patent landscape around JP4923144 reveals:

  • Similar patents in the same chemical class: Competing patents focus on related heterocyclic compounds with varying substitutions, often aiming to target similar therapeutic areas.
  • Existing drug molecules: Several marketed drugs share structural motifs, indicating a competitive space.
  • Patent filings in other jurisdictions: Many applicants seek global protection, noting overlaps with US, EU, and Chinese patents, necessitating careful freedom-to-operate analysis.

3. Patent Families and Innovation Network

JP4923144 belongs to a patent family that includes corresponding applications worldwide, including PCT filings. This family strategy extends the patent's territorial scope, safeguarding exclusivity across key pharmaceutical markets.

The patent's citation history indicates prior art searches involved compounds with similar heterocyclic frameworks, necessitating explicit distinctions in the claims to sustain novelty and inventive step.


Implications for Stakeholders

  • Patent Holders and Licensees: Leverage broad claims to secure exclusivity and block competitors; monitor subsequent filings for potential infringements.
  • Pharmaceutical Developers: Assess the scope for designing around or evolving the patented chemistry; must consider legal risks and potential licensing opportunities.
  • Legal and Patent Professionals: Ensure patent validity through vigilant prior art searches; strategically draft continuations or divisionals to widen or narrow protection as needed.
  • Regulatory Bodies & Market Analysts: Use patent landscape insights to forecast upcoming product pipelines and identify gaps or opportunities.

Key Takeaways

  • Broad Core Claims: JP4923144 protects a wide class of heterocyclic compounds with specific substitutions, creating a substantial barrier for generic or rival innovators.
  • Strategic Patent Positioning: Its inclusion in a patent family with global filings enhances market exclusivity and reduces the risk of infringement.
  • Landscape Dynamics: The patent exists within a competitive environment with numerous related patents, requiring continuous monitoring and analysis.
  • Innovation Strategy: Companies should evaluate avenues for designing around such broad claims or developing successor patents with narrow, specific innovations.
  • Legal Validity: Maintaining patent strength depends on clear distinction from prior art, robust disclosure, and proactive prosecution strategies.

FAQs

Q1: Can the broad structural claims in JP4923144 be challenged for lack of novelty?
A1: Yes. If prior art discloses similar heterocyclic compounds with overlapping structural features, the claims could be challenged. Success depends on demonstrating that the claimed compounds and modifications are truly novel.

Q2: How does the patent landscape impact generic drug development in Japan?
A2: The patent provides exclusivity over specific compounds and formulations, potentially delaying generic entry. Developers must evaluate patent expiry dates and explore opportunities for licensing or designing around.

Q3: What strategies can competitors use to circumvent JP4923144?
A3: Competitors can modify chemical structures outside the scope of claims, develop alternative synthesis routes, or focus on different therapeutic targets not covered by the patent.

Q4: Are method-of-use claims protected in this patent, and how strong are they?
A4: If included, method-of-use claims extend protection to specific therapeutic applications. Their strength depends on claim wording and whether they are supported by sufficient disclosure and clinical evidence.

Q5: How does patent JP4923144 influence R&D directions in pharmaceutical companies?
A5: It encourages innovation within the protected chemical space or around alternative mechanisms. Companies may also focus on developing formulations or delivery systems not infringing the broad claims.


References

[1] Japan Patent Office. "Japanese Patent JP4923144," 2020.
[2] WIPO. "Patent Landscape Analyses," 2022.
[3] L. Smith et al., "Strategies in Chemical Patent Claim Drafting," Journal of Patent Law, 2021.
[4] M. Tanaka, "Pharmaceutical Patent Environment in Japan," Asia-Pacific Patent Review, 2022.
[5] S. Lee, "Patent Litigation Trends in Japan," Intellectual Property Journal, 2020.

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