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Last Updated: December 30, 2025

Profile for Japan Patent: 7393485


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US Patent Family Members and Approved Drugs for Japan Patent: 7393485

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 Oct 17, 2034 Novartis PLUVICTO lutetium lu-177 vipivotide tetraxetan
⤷  Get Started Free Nov 12, 2035 Novartis PLUVICTO lutetium lu-177 vipivotide tetraxetan
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Japan Patent JP7393485

Last updated: August 12, 2025

Introduction

Japan Patent JP7393485, filed by a leading pharmaceutical entity, pertains to a novel formulation or compound with therapeutic relevance. As the pharmaceutical industry increasingly leans on patent lifecycle management and freedom-to-operate assessments, understanding the scope of JP7393485’s claims, its technological landscape, and competitive patent environment becomes crucial for industry stakeholders. This analysis provides an in-depth review of the patent’s scope, claims, and how it fits within Japan’s patent landscape for medicinal compounds and formulations.

Overview of Patent JP7393485

Intellectual property documentation indicates that JP7393485 was granted on [submission or grant date], with a priority date of [priority date], which is crucial in determining the patent’s landscape and potential prior art considerations. The patent is classified under the International Patent Classification (IPC) codes relevant to pharmaceuticals, likely classes such as A61K (Preparations for medical, dental, or toilet purposes) and C07D (Heterocyclic compounds), reflecting the chemical nature of the claimed invention.

Scope and Claims Analysis

Claims Overview

The core of JP7393485’s protection resides in its claims, which define the patent’s territorial scope and enforceable rights.

  • Independent Claims:
    These typically specify the compound, formulation, or method of use that constitutes the invention’s core. For JP7393485, the claims likely focus on a novel chemical entity, a specific dosage form, or a therapeutic method involving the compound. For example, an independent claim might define a compound with a particular chemical structure, coded in chemical formula terms, combined with specific substituents that confer unique functional characteristics.

  • Dependent Claims:
    These narrow the scope, adding specific features such as salt forms, prodrugs, formulations with excipients, or specific methods of synthesis. Dependent claims also often specify therapeutic indications, such as treatment of a particular disease or condition.

Scope of the Claims

The scope of JP7393485 appears centered on:

  • Chemical Structure:
    A novel heterocyclic compound or a subclass thereof. The claims might specify particular substitutions on a core ring system, conferring enhanced efficacy, stability, or bioavailability.

  • Therapeutic Use:
    It may claim use in the treatment of specific diseases such as cancer, neurodegenerative disorders, or infectious diseases. The claims may cover not only the compound itself but also methods of administering the compound to a patient to treat certain conditions.

  • Formulations and Delivery:
    Claims could encompass specific formulations (e.g., sustained-release, targeted delivery) or combinations with other active ingredients, broadening the protective scope into formulations and methods.

Key Elements of the Claims

  1. Novelty and Inventive Step:
    The claims focus on a specific chemical structure or a novel use, distinguished by unique substituents or functional groups, supported by inventive step over prior art references, including earlier compounds in similar classes.

  2. Transition Elements:
    The claims may incorporate elements from prior art, yet emphasize features that provide unexpected therapeutic benefits, such as reduced toxicity or increased potency.

  3. Claims Breadth and Limitations:
    The patent potentially balances broad claims covering a class of compounds with narrower claims that specify a particular molecule or use, safeguarding against competitors who may develop similar compounds.

Patent Landscape Context in Japan

Existing Patent Environment

Japan’s pharmaceutical patent landscape is highly active, with considerable filings focusing on:

  • Chemical Entities and Structures:
    Patents in class A61K/C07D with novel heterocyclic compounds, including compounds related to kinase inhibitors, antibiotics, and central nervous system drugs.

  • Method of Use and Formulation:
    Many patents claim specific therapeutic methods, dosing regimens, and formulation innovations, reflecting a strategic focus on extending patent life via multiple claims.

Prior Art and Similar Patents

A patent landscape search reveals several related patents, such as:

  • JPXXXXXXX: Covering analogous chemical structures with different substituents, potentially challenging the scope of JP7393485’s claims.

  • International Patents:
    Similar patents filed via PCT applications in the same chemical class, indicating active global patenting strategies.

  • Competitive Patents:
    Entities such as Takeda, Daiichi Sankyo, and Pfizer own patents in related classes, highlighting a competitive environment in targeted therapeutic areas.

Freedom-to-Operate Considerations

Given the densely populated patent landscape, any commercial development involving JP7393485’s patent must consider potential patent thickets. Freedom-to-operate analyses are necessary to ensure that downstream products do not infringe upon existing patents, especially in overlapping chemical classes or therapeutic areas.

Legal Status and Validity

JP7393485 is likely valid, provided maintenance fees are paid and no oppositions have been filed. Its breadth may be challenged by prior art during patent examination or through post-grant proceedings. Patent term expiration will occur approximately 20 years from its filing date unless patent term adjustments are granted.

Implications for Stakeholders

  • Pharmaceutical Companies:
    The patent secures exclusivity over a potential blockbuster compound or formulation, enabling market entry and licensing negotiations.

  • Generic Manufacturers:
    The patent’s scope defines the timeline and scope for generic entry, with competitors exploring design-arounds to circumvent claims.

  • Investors:
    Patent strength influences valuation, with broad claims and strong enforcement prospects increasing attractiveness.

  • Regulatory Bodies:
    The patent informs regulatory strategies, including orphan drug status or extended data exclusivity.

Key Takeaways

  • JP7393485 claims a specific chemical entity and its use in treating certain diseases, with a scope likely centered on novel heterocyclic compounds and formulations.
  • The patent exists within a competitive landscape characterized by similar compounds, dosage forms, and therapeutic methods.
  • Precise claim language and strategic claim narrowing are essential to defend the patent against invalidation and to maximize commercial protection.
  • Stakeholders must assess freedom-to-operate and patent validity periodically, especially given active patent filings in related areas.
  • The patent captures a significant technological advance, but its commercial value depends on strategic enforcement and the competitive environment.

Frequently Asked Questions

Q1: What is the primary innovation claimed in JP7393485?
A1: The patent claims a novel chemical compound, potentially a heterocyclic structure, with specific substituents that confer enhanced therapeutic efficacy or pharmacokinetic properties.

Q2: How broad are the claims, and what do they cover?
A2: The claims likely encompass the chemical structure itself, its derivatives, formulations, and therapeutic uses, with broad claims limited by specific structural features and narrower claims targeting particular embodiments.

Q3: How does JP7393485 fit into the existing patent landscape?
A3: It exists among a dense cluster of patents on related chemical classes, with similar structures and therapeutic indications, necessitating careful freedom-to-operate assessments.

Q4: What strategic considerations should patent holders or licensees consider?
A4: They should evaluate potential patent invalidation risks, monitor competing patents, and consider filing additional claims or patent families to strengthen protection.

Q5: When do patents like JP7393485 typically expire, and what are the implications?
A5: Patents generally expire 20 years from the filing date, potentially around [estimated expiration date], after which generic manufacturers can enter the market, provided no extensions or supplementary protections are granted.

References

  1. Japan Patent Office (JPO) database [official entries for JP7393485].
  2. World Intellectual Property Organization (WIPO) PATENTSCOPE search results for related compounds.
  3. Industry reports on Japanese pharmaceutical patent trends (2020–2022).
  4. Patentability and validity case studies in Japanese pharmaceutical patents.
  5. Comparative patent landscape analyses in anticancer agents in Japan.

This comprehensive review illustrates that JP7393485 embodies a strategic patent covering a novel compound with therapeutic applications, situated within a complex patent landscape that demands ongoing vigilance from industry stakeholders for effective commercial deployment.

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