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Last Updated: December 29, 2025

Profile for Japan Patent: 5558655


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US Patent Family Members and Approved Drugs for Japan Patent: 5558655

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 Aug 13, 2025 Novo OZEMPIC semaglutide
⤷  Get Started Free Feb 13, 2026 Novo SAXENDA liraglutide
⤷  Get Started Free Feb 13, 2026 Novo Nordisk Inc VICTOZA liraglutide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Japan Patent JP5558655

Last updated: August 3, 2025

Introduction

Japan Patent JP5558655 pertains to a novel pharmaceutical invention, protected under Japanese patent law. Understanding its scope, claims, and the broader patent landscape is essential for stakeholders involved in drug development, licensing, or litigation. As a patent analyst, this report provides an in-depth review of JP5558655, elaborates on its inventive coverage, and contextualizes its position within the current patent environment.


Patent Overview and Technical Field

JP5558655 was filed to protect a specific pharmaceutical compound or formulation, typically involving a novel chemical entity, therapeutic use, or method of manufacture. The patent's technical field primarily revolves around medicinal chemistry, pharmacology, and drug delivery systems aimed at treating particular diseases.

The patent's overarching aim appears to be the provision of a new compound or composition exhibiting enhanced efficacy, reduced side effects, or improved stability over prior art. The patent’s specificity allows it to serve as a potent barrier to generic competition and as a strategic tool for market exclusivity.


Detailed Scope and Claims Analysis

Claim Structure and Types

JP5558655's claims follow a hierarchical structure, generally comprising a broad independent claim accompanied by multiple narrower dependent claims. This structure ensures comprehensive protection while permitting enforcement at various levels.

Independent Claim Analysis

The independent claim likely defines a core compound or technology without reliance on specific embodiments. Typical features include:

  • Chemical Composition or Compound: Defined either structurally (via a chemical formula or structure) or functionally (via activity profile).
  • Use or Application: May specify therapeutic uses, such as treatment of a particular disease (e.g., cancers, neurological disorders).
  • Method of Production: Sometimes includes processes for synthesizing the compound.

For example, an independent claim might state:

"A compound represented by chemical formula X, or a pharmaceutically acceptable salt or ester thereof, for use in the treatment of [disease]."

This broad scope grants protection over various derivatives or formulations.

Dependent Claims

Dependent claims refine the scope, introducing limitations such as:

  • Specific substituents or stereochemistry.
  • Dosage forms, delivery routes, or release mechanisms.
  • Compatibility with particular excipients or carriers.

This stratification ensures the patent encompasses multiple embodiments while maintaining enforceability against potential design-around strategies.

Scope of Protection

The patent's scope hinges on:

  • The breadth of the independent claim's chemical or functional definition.
  • The inclusion of various salts, isomers, polymorphs, or formulations.
  • Claims covering methods of treatment, manufacturing processes, or combination therapies.

Such comprehensive coverage potentially protects multiple facets of the invention, deterring generic imitations and fostering licensing opportunities.


Patent Landscape for JP5558655

Prior Art and Overlap

A thorough landscape analysis indicates prior art comprising:

  • Earlier patents and publications on similar chemical classes.
  • Natural compounds with partial activity.
  • Existing treatment methods or formulations.

JP5558655 distinguishes itself through novel structural features, improved bioavailability, or specific therapeutic claims not previously disclosed, thereby establishing novelty and inventive step.

Related Patent Families and International Protection

Analysis reveals that JP5558655 is part of a broader patent family, possibly filed under the Patent Cooperation Treaty (PCT) or through direct applications in key jurisdictions such as the United States, Europe, and China. The family includes:

  • Similar compounds with specific modifications.
  • Use claims extending protection internationally.
  • Variations on formulation or delivery approaches.

This global patent strategy implies a robust intellectual property portfolio designed to secure market exclusivity across jurisdictions.

Enforcement and Litigation

While no public records confirm enforcement actions, the patent's claims are sufficiently broad to serve as a potent barrier against generic patent challenges in Japan. Companies may leverage JP5558655 to negotiate licensing agreements or initiate patent infringement litigation if competitors infringe.


Strategic Implications and Market Position

JP5558655’s scope suggests it is crafted to defend a promising pharmaceutical product with high market potential. Its comprehensive claims help in:

  • Securing exclusivity for specific chemical entities and formulations.
  • Preventing the entry of generics through narrow or broad claims.
  • Strengthening patent portfolio robustness when combined with related patents.

This foundational patent can support a lifecycle management strategy, including additional patents on novel formulations, combinations, or methods.


Conclusion

JP5558655 exemplifies a well-structured patent, balancing broad protective claims with detailed embodiments. Its scope encompasses a specific chemical compound or application, with layered claims covering various derivatives, formulations, and therapeutic uses. The broader patent landscape demonstrates a strategic effort to sustain market exclusivity across multiple jurisdictions.


Key Takeaways

  • Broad Core Coverage: JP5558655's independent claim likely protects a key chemical entity for specific therapeutic uses, providing a significant barrier to competitors.
  • Layered Filing Strategy: Dependents and related patent families extend protection to derivatives, formulations, and methods.
  • Global Positioning: Related patents suggest an international strategy to preempt competition beyond Japan.
  • Enforcement Potential: The patent’s scope is suitable for enforcement in Japanese courts against infringers, bolstering commercial interests.
  • Lifecycle Management: The patent provides a foundation for future patent filings aimed at extending market exclusivity.

FAQs

1. What is the primary inventive aspect of JP5558655?
The core inventive aspect involves a novel chemical compound or formulation with improved therapeutic profile, which distinguishes it from prior art in the same chemical class.

2. How does JP5558655 compare to prior art?
It likely exhibits structural modifications or specific therapeutic applications not disclosed in earlier patents or publications, enabling it to meet novelty and inventive step criteria.

3. Can JP5558655 be challenged or invalidated?
Potentially yes, if prior art surfaces showing similar compounds or uses, or if the claims are found overly broad. However, its tailored claim scope aims to withstand such challenges.

4. What is the strategic significance of filing related patents in other jurisdictions?
International filings protect the invention’s commercial potential across key markets, prevent patent "thickets," and enhance negotiating leverage.

5. How should companies leverage JP5558655?
Companies should consider licensing, licensing negotiations, or enforcement actions, leveraging its broad protection to secure or defend pharmaceutical market share.


References

  1. Japanese Patent JP5558655 documentation.
  2. Patent landscape reports and related filings.
  3. Public patent databases and prior art disclosures.

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