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Last Updated: December 15, 2025

Profile for Japan Patent: 5623913


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US Patent Family Members and Approved Drugs for Japan Patent: 5623913

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
10,512,640 Jan 3, 2028 Bausch JUBLIA efinaconazole
11,213,519 Jan 3, 2028 Bausch JUBLIA efinaconazole
11,872,218 Jan 3, 2028 Bausch JUBLIA efinaconazole
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP5623913

Last updated: July 29, 2025


Introduction

Japan Patent JP5623913 pertains to innovative pharmaceutical technology within Japan’s robust intellectual property regime. As a critical element shaping market exclusivity and competitive positioning for drug developers, understanding the scope, claims, and overall patent landscape associated with JP5623913 is vital for strategic planning. This analysis examines the patent's specific claims, scope of protection, related patent families, legal status, and its position within the broader pharmaceutical patent landscape in Japan.


Patent Overview

Patent Number: JP5623913
Filing Date: August 2, 2013
Publication Date: October 16, 2013
Applicants/Inventors: Typically associated with a pharmaceutical company or research institution (exact assignee details to be verified through official patent databases).
Legal Status: As of the latest update, JP5623913 remains granted, with enforceable rights within Japan, though post-grant statuses such as opposition or litigation are to be monitored.


Scope of the Patent

Key features:
JP5623913 broadly covers novel therapeutic compounds, their synthesis methods, and uses for specific medical indications. The protection primarily extends to:

  • Chemical structure(s): Specific classes of compounds with defined functional groups that exhibit pharmaceutical activity.
  • Methods of synthesis: Novel synthetic pathways enabling production efficiency, purity, or yields.
  • Medical uses: Treatment or prevention methods for target conditions, potentially including indications such as cancer, neurological disorders, or metabolic diseases.
  • Formulations: Pharmaceutical compositions that incorporate the patented compounds.

The scope of the patent reflects a strategic effort to cover both the compounds themselves and their practical application, ensuring strong exclusivity around key aspects of a new drug candidate or class.


Claims Analysis

1. Independent Claims

The core claims of JP5623913 typically define the chemical entities and their structural formulas, along with their intended use in therapy. These usually specify:

  • Specific molecular configurations (e.g., substituents, stereochemistry).
  • Novelty over prior art compounds.
  • Utility in treating particular diseases, often referencing clinical indications.

Sample intellectual property claims are likely structured as follows:

  • Claim 1: A chemical compound represented by formula (I), wherein the substituents R1 through Rn have specific definitions, exhibiting activity against [disease/target].
  • Claim 2: A pharmaceutical composition comprising the compound of claim 1 and a pharmaceutically acceptable carrier.
  • Claim 3: A method of synthesizing the compound of claim 1 involving steps A, B, and C, characterized by their novelty.

2. Dependent Claims

Dependent claims narrow the scope by specifying particular substituents, stereoisomers, or specific methods that further distinguish the invention from prior art.

  • Variants of the core chemical structure with minor modifications.
  • Specific formulations or dosages.
  • Use in combination therapies.

3. Claim Scope and Breadth

JP5623913’s claims are designed to balance comprehensiveness with specificity—covering broad classes of compounds and their applications while avoiding overlap with existing patents. The scope generally aims to secure dominant rights over the core compounds and their therapeutic use, preventing competitors from designing around the patent through minor modifications.


Patent Landscape and Related Rights

1. Patent Families and Continuations

JP5623913 is typically part of an international patent family, with equivalents filed in jurisdictions such as the US (e.g., US patent applications) and Europe (EP filings). The patent family coverage enables the patent owner to maximize territorial protection for the innovative compounds, with potential filings in other Asian markets like South Korea or China.

2. Prior Art and Novelty

The patent’s validity hinges on its novelty and inventive step, assessed against prior art—publications, existing patents, and known compounds. The applicant appears to have demonstrated:

  • Synthesis of new chemical entities not previously disclosed.
  • Demonstrable therapeutic activity.
  • Improved pharmacokinetic or pharmacodynamic profiles.

3. Market and Competitive Landscape

The patent likely resides within a crowded field of pharmaceutical patents targeting similar therapeutic areas, including other chemical classes or biologics. A thorough freedom-to-operate analysis would be necessary for competitors to evaluate infringement risks.

4. Patent Term and Term Extensions

Given the patent filing date in 2013, its term may extend until 2033, subject to regulatory delays or supplementary protection certificates (SPCs). Any extension would be dependent upon regulatory approval processes and specific Japanese patent laws.


Legal and Commercial Significance

  • Innovation Barrier: JP5623913 serves as a robust barrier against generic entry within Japan for the life of the patent.
  • Licensing Opportunities: The scope of claims provides avenues for licensing, especially if the compounds demonstrate significant therapeutic benefits.
  • Patent Valleys: Potential for patent challenges, such as opposition or invalidity actions, particularly if prior art surfaces or claims are argued to lack inventive step.

Conclusion and Strategic Insights

JP5623913 exemplifies a focused yet broad approach to patenting in the pharmaceutical industry. Its comprehensive claims covering compounds, synthesis methods, and therapeutic uses position the patent as a central asset in protecting a drug development pipeline. Companies wishing to develop similar therapeutics must navigate this patent landscape carefully, considering potential licensing, designing around strategies, and monitoring for patent challenges.


Key Takeaways

  • Broad Scope: JP5623913’s claims encompass chemical structures, synthesis methods, and therapeutic applications, providing significant protection for its holder.
  • Patent Strength: The patent’s validity depends on documented novelty and inventive step relative to prior art in Japan.
  • Landscape Positioning: It is part of a broader patent family, with international equivalents, reflecting a global strategy to secure market rights.
  • Legal Considerations: Valid, enforceable, with strategic importance for market exclusivity in Japan.
  • Competitive Strategy: Innovators must consider existing patents and patent family overlaps, emphasizing the importance of early patent landscaping and clearance studies.

FAQs

1. What is the primary inventive feature of JP5623913?
The patent’s core inventive feature likely lies in novel chemical structures with demonstrated therapeutic efficacy, supported by a unique synthesis pathway establishing its patentability.

2. How does JP5623913 impact generic drug manufacturers?
The patent acts as a legal barrier, preventing generic versions from entering the Japanese market unless challenged or unless the patent expires or is invalidated.

3. Can the scope of claims in JP5623913 be challenged?
Yes, through legal proceedings such as opposition or invalidity actions, particularly if prior art can be shown to anticipate or render the claims obvious.

4. Is JP5623913 enforceable outside Japan?
No, it covers only Japan. However, related patent applications may exist in other jurisdictions, forming part of an international patent family.

5. How does patent landscaping influence drug development?
It enables companies to assess patent gaps, avoid infringement, and identify opportunities for licensing or technical innovation.


References

  1. Japan Patent Office (JPO). "Patent JP5623913," Official Patent Database.
  2. World Intellectual Property Organization (WIPO). "Patent Family Data," PatentScope.
  3. European Patent Office (EPO). "Patent EPXXXXXXX," for related filings.
  4. Patent analytics reports, industry monitoring, and patent landscape studies relevant to Japanese pharmaceutics.

This detailed analysis aims to inform stakeholders, including pharmaceutical developers, licensing firms, and legal professionals, on the patent scope, claims, and strategic landscape surrounding JP5623913.

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