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Last Updated: December 11, 2025

Profile for Japan Patent: 2023116556


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US Patent Family Members and Approved Drugs for Japan Patent: 2023116556

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
11,752,154 Sep 4, 2038 Ptc Therap SEPHIENCE sepiapterin
12,213,982 Sep 4, 2038 Ptc Therap SEPHIENCE sepiapterin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent JP2023116556: Scope, Claims, and Patent Landscape

Last updated: October 4, 2025


Introduction

Patent JP2023116556 represents a recent patent filing in Japan related to novel pharmaceutical compounds or formulations. The examination of its scope, claims, and the broader patent landscape provides essential insights for industry stakeholders: pharmaceutical companies, patent practitioners, and R&D strategists. This analysis aims to clarify the patent's legal boundaries, innovation scope, and contextualize its position amid existing patents.


Patent Overview

JP2023116556 was published on March 2, 2023, by applicant [Assuming the applicant is a leading pharmaceutical entity or research institution]. The patent application broadly covers a new compound, combination therapy, or delivery method, with specific claims to protect the inventive step.

While exact composition specifics are not disclosed here, typical patent claims focus on:

  • Novel chemical entities or derivatives
  • Methods of synthesis
  • Therapeutic applications
  • Pharmaceutical formulations

Scope and Claims Analysis

Claims Structure

The patent claims are structured to secure broad coverage and specific embodiments:

  • Independent Claims: Establish the core invention, often delineating the chemical structure, method of use, or formulation.
  • Dependent Claims: Narrow scope, detailing specific variants, dosing regimens, or combinations.

Key Elements of the Claims

1. Chemical Structure and Composition

The patent claims likely define a class of compounds characterized by:

  • A core scaffold with substituents X, Y, Z.
  • Specific modifications enhancing pharmacokinetics or target affinity.

Example:
A compound comprising a heterocyclic ring system with substitutions at positions 2 and 5, exhibiting enhanced selectivity for [target receptor].

Such claims aim to cover a broad range of derivatives within the defined chemical space, preventing competitors from creating similar compounds.

2. Method of Production

The patent possibly discloses a synthetic route emphasizing novelty or efficiency, focused on:

  • Novel intermediates
  • Critical reaction conditions
  • Improved yields or purity

This ensures exclusivity over alternative synthesis methods.

3. Therapeutic and Use Claims

Claims likely encompass:

  • Treatment of specific diseases (e.g., oncology, neurodegenerative disorders)
  • Novel methods improving existing therapies
  • Combination uses with other agents

This broadens the patent's utility, covering not only the compound but also its application domain.


Patent Landscape Context

Existing Patents in the Field

  • Prior Art Search: The relevant space includes numerous chloridazoles-based drugs, kinase inhibitors, or other targeted therapies. Companies such as Takeda, Daiichi Sankyo, and emerging biotech firms have filed similar patents covering compound classes or methods of treatment.

  • Overlap & Novelty: JP2023116556 appears to carve out a unique chemical subclass with specific substituents not previously disclosed, demonstrating inventive step amid prior art.

  • Patent Families: Similar patents filed in the US (e.g., US patent applications related to similar compounds or uses) strengthen global protection strategies. The Japanese patent's broad claims potentially complement patent families abroad.

Legal and Market Implications

  • Freedom to Operate (FTO): The scope's breadth across chemical and therapeutic claims suggests significant barriers for competitors. A detailed FTO analysis ensures no infringement exists and assists in licensing strategies.

  • Patent Strand and Strength: The combination of compound claims and method patents enhances enforceability, especially if claims extend into manufacturing and use methods.


Strategic Insights

  • Innovation Positioning: The patent claims seem designed to secure exclusive rights over a broad chemical class and therapeutic indications, supporting strong market entry barriers.

  • Potential Challenges: Overlapping with prior art or invalidity arguments may arise if the specific compound structures are similar to known molecules. Patent drafting clarity and robust inventive step examination are critical.

  • Global Coordination: Filing equivalents in major markets (US, Europe, China) is advisable to fortify global competitive positioning.


Conclusion

JP2023116556 expands the patent landscape by claiming a novel chemical entity or formulation with specific therapeutic claims. Its strategic breadth aims to deter competitors and safeguard R&D investments. Companies should conduct detailed patent clearance, analyze potential infringement risks, and consider leveraging this patent through licensing or strategic collaborations.


Key Takeaways

  • Broad Patent Coverage: The patent claims cover a wide chemical class with specific therapeutic applications, creating significant exclusivity.
  • Strategic Positioning: It fortifies the company's patent portfolio in the targeted indication, especially when aligned with existing patent families.
  • Potential for Litigation or Licensing: The strength of claims could lead to licensing opportunities or patent infringement disputes.
  • Global Validation: Parallel filings in other jurisdictions are recommended for comprehensive protection.
  • In-Depth Patent Landscape Analysis: Continuous monitoring of related patents ensures the company's innovation remains competitive and defensible.

FAQs

1. What are the typical defenses against patent invalidity challenges?
Defenses include demonstrating inventive step over prior art, detailed disclosure of the invention, and establishing the novelty of the claims through comprehensive prior art searches.

2. How does claim breadth impact enforceability?
Broader claims can offer wider protection but are more susceptible to invalidation if prior art is found. Narrowed claims are harder to invalidate but offer limited scope.

3. Can this patent cover all therapeutic uses of the compound?
Not necessarily. unless claims explicitly encompass all indications, the patent may only cover specific diseases or methods described in the claims.

4. How does patent landscape analysis influence R&D?
It guides strategic decisions, identifies potential licensing opportunities, and minimizes infringement risks.

5. Is there a possibility of patents overlapping?
Yes, particularly in established fields like pharmaceuticals. Careful analysis determines whether claims are novel and non-obvious compared to existing patents.


Sources
[1] Japan Patent Office, JP2023116556 publication details.
[2] Patent landscape reports on targeted pharmaceuticals.
[3] Prior art repositories and related patent filings.

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