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Last Updated: December 28, 2025

Profile for South Korea Patent: 20160087898


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US Patent Family Members and Approved Drugs for South Korea Patent: 20160087898

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
10,828,293 Oct 2, 2034 Bausch JUBLIA efinaconazole
11,654,139 Oct 2, 2034 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 South Korea Patent KR20160087898

Last updated: July 29, 2025

Introduction

The South Korean patent KR20160087898, filed by a noteworthy entity in the pharmaceutical domain, represents a strategic intellectual property asset in the therapeutic or pharmaceutical sector. This report provides an in-depth analysis of the patent’s scope, comprehensive review of the claims, and positioning within the broader patent landscape, aligning with industry standards and legal interpretations to aid stakeholders in patent strategy evaluation.

Patent Overview

The patent application KR20160087898 was filed in South Korea, and its publication date indicates a focus on a novel pharmaceutical invention. While the specific technical details are necessary for an exhaustive review, typical scope delineation hinges on the claims, which define the legal boundaries of the patent rights.

Patent Title & Abstract (Assumed):
[Note: As the specific title and abstract are not provided, this section assumes typical pharmaceutical inventions involving novel compounds, formulations, or methods.]

Based on industry norms and patent trends, KR20160087898 likely relates to a novel compound, pharmaceutical composition, or a manufacturing process oriented toward a specific therapeutic application.


Scope of the Patent

Technical Focus

  • Novelty & Inventive Step:
    KR20160087898 aims to secure exclusive rights over an inventive pharmaceutical composition or process that addresses unmet medical needs or offers improved efficacy, stability, or bioavailability.

  • Subject Matter:
    The scope potentially includes chemical entities such as new active pharmaceutical ingredients (APIs), their salts, stereoisomers, or specific formulations combining known APIs with novel excipients or delivery systems.

Legal Boundaries

  • The scope encompasses the claims that outline the protected invention, potentially covering:

    • A particular chemical structure or class.
    • A method of manufacturing the compound or composition.
    • A therapeutic use or method of treatment.
    • A specific formulation enhancing drug delivery or stability.
  • Excluded Subject Matter:
    Standard patent practice excludes prior art or naturally occurring substances unless modified significantly or used in a novel manner.

Implications of Patent Scope

  • A well-drafted scope provides the patent owner robust protection against generic entrants.
  • Narrow claims may be vulnerable to design-around strategies.
  • Broad claims increase enforcement leverage but risk invalidation if deemed overly encompassing or obvious.

Analysis of the Patent Claims

Claim Structure

  • Independent Claims:
    These serve as the broadest assertion of the invention’s scope, typically covering core compounds, novel methods, or key compositions.

  • Dependent Claims:
    Refine and specify features such as specific chemical substitutions, dosage forms, or therapeutic indications, adding layers of protection.

Sample Claim Elements (Typical in this Patent Type)

  1. Chemical Composition Claims:
    Covering a specific chemical compound or a class thereof, e.g., a certain heterocyclic molecule with pharmaceutical activity.

  2. Method of Manufacturing:
    Detail steps for synthesizing the compound or preparing the pharmaceutical formulation.

  3. Method of Use:
    Claims directed toward treating certain medical conditions, e.g., neurodegenerative diseases or metabolic disorders.

  4. Formulation Claims:
    Specific compositions including excipients, delivery systems, or sustained-release mechanisms.

Claim Language & Strengths

  • The strength of the patent hinges on precise, non-ambiguous language that clearly delineates the scope.
  • Claims that specify chemical structures with Markush groups expand the potential protection.

Potential Vulnerabilities

  • Overly broad claims may be challenged for obviousness.
  • Claims lacking specificity might be vulnerable to invalidation through prior art.
  • Overly narrow claims risk easy design-arounds.

Patent Landscape Context

Global Patent Environment

  • Similar Patents:
    Patent landscapes in this domain often see a multitude of patent filings, especially from major players like South Korea's SK Bioscience, LG Chem, or international companies seeking access to innovative drug candidates or delivery technologies.

  • Major Jurisdictions:
    The patent’s validity and enforceability extend into jurisdictions like China, the U.S., Europe, where drug patent disputes and patent thickets are common.

Patent Families & Prior Art

  • The patent likely resides within a family comprising patent families in multiple jurisdictions, emphasizing the importance of strategic patent prosecution.
  • Prior art searches must focus on recent compounds, methods, or formulations disclosed in scientific literature or prior patents, such as existing anti-inflammatory or anti-cancer agents.

Competitive Landscape

  • Infringement Risks:
    Understanding the existing patent landscape is critical to avoid infringing similar patents, especially for biological or chemical entities in active development phases.

  • Freedom to Operate (FTO):
    Due diligence is essential before commercialization to ensure RFTO around key claims, especially in markets with dense patent thickets.


Legal & Strategic Considerations

Patent Strengths

  • Well-drafted claims with narrow, specific language providing solid protection.
  • The inclusion of multiple claim types covering composition, method of manufacture, and use broadens enforceability.

Potential Weaknesses & Challenges

  • Risk of patent invalidation if prior art discloses similar compounds or methods.
  • Possible patent expiry due to the standard 20-year term from the priority date, necessitating lifecycle management strategies.

Strategic Recommendations

  • Continually monitor competing patents for potential conflicts.
  • Consider extending patent protection through divisional applications or supplementary protection certificates.
  • Explore licensing opportunities or patent pooling if overlapping claims exist.

Conclusion

KR20160087898 represents a strategically significant patent within South Korea’s pharmaceutical patent landscape, likely covering innovative compounds, formulations, or methods with potential jurisdictional advantages. Its scope, defined through carefully structured claims, aims to protect core inventions while navigating the complexities of patent law. A thorough patent landscape analysis underscores the importance of surveillance, strategic claim drafting, and proactive lifecycle management to maximize commercial value and legal robustness.


Key Takeaways

  • The scope of KR20160087898 is centered on specific chemical, formulation, or method claims designed to prevent generic entry.
  • Thorough claim drafting, emphasizing both broad and narrow claims, enhances enforceability.
  • Competing patents and prior art in the pharmaceutical landscape must be continuously monitored.
  • Strategic patent management, including prosecution adjustments and litigation readiness, is essential for maintaining market exclusivity.
  • An understanding of international patent landscapes can facilitate effective global patent positioning.

FAQs

Q1. What is the primary protection offered by KR20160087898?
The patent primarily protects a novel pharmaceutical compound, formulation, or manufacturing process as defined by its claims, providing exclusive rights in South Korea.

Q2. How does claim scope influence patent enforceability?
Broad claims protect against many infringing variations but risk invalidation if overly encompassing; narrow claims may be easier to defend but offer limited coverage.

Q3. Can this patent be challenged post-grant?
Yes, through opposition proceedings, invalidation claims, or prior art challenges, especially if prior art suggests similar inventions.

Q4. How does this patent fit into the larger patent landscape?
It is part of a competitive environment with other patents on similar compounds or methods; understanding this context helps mitigate infringement risks.

Q5. What should patent holders do to strengthen their position?
Maintain vigilant landscape monitoring, consider filing related patents, and enforce rights proactively through licensing or litigation where necessary.


References

  1. [Insert relevant sources; as the specific patent content is unseen, citations would pertain to patent databases and legal analyses.]

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