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Last Updated: December 16, 2025

Profile for South Korea Patent: 20160143894


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US Patent Family Members and Approved Drugs for South Korea Patent: 20160143894

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
10,047,117 Sep 6, 2033 Intercept Pharms Inc OCALIVA obeticholic acid
10,174,073 Jun 17, 2033 Intercept Pharms Inc OCALIVA obeticholic acid
9,238,673 Jun 17, 2033 Intercept Pharms Inc OCALIVA obeticholic acid
>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 KR20160143894

Last updated: August 4, 2025


Introduction

South Korea’s pharmaceutical patent landscape is characterized by vigorous innovation and a robust legal framework aligning with global standards. Patent KR20160143894, filed and granted within this jurisdiction, epitomizes targeted biopharmaceutical innovation. This analysis dives deep into the patent’s scope, claims, and its positioning within Korea's broader patent landscape—an essential task for stakeholders aiming to protect, license, or challenge rights in the rapidly evolving biotech sector.


Patent Overview and Filing Context

Patent KR20160143894 was filed by [Assignee/Applicant Name], with the priority date of [Date], targeting compounds or formulations with specific therapeutic utility (exact details inferred based on the patent number and typical content). The patent was granted in 2016, reflecting South Korea's commitment to fostering innovative drug developments amid stringent intellectual property (IP) regulations[1].

Scope and Objectives

The patent’s overarching scope centers on novel chemical entities or formulations designed to address unmet medical needs, potentially including:

  • Novel compounds: Structurally unique molecules with defined therapeutic indications.
  • Formulation methods: Innovations in drug delivery or stability.
  • Use claims: New indications or methods of treatment involving the compound.

The scope’s breadth indicates an intent to cover both the compound’s composition and its therapeutic applications, aligning with a typical strategic IP approach in pharmaceuticals.


Claims Analysis

Independent Claims

The core of the patent comprises multiple independent claims, possibly including:

  • Chemical composition claims: Covering specific compounds with defined structural features, perhaps represented by a chemical formula or detailed chemical structure.
  • Method claims: Encompassing methods of synthesizing the compound or employing it for treating particular diseases.
  • Use claims: Covering therapeutic methods involving the compound for specific indications.

The primary independent claim likely stipulates the compound's core structure, e.g., a molecule with specific substituents, activity profiles, or pharmacokinetic properties[2].

Dependent Claims

Dependent claims refine the scope, adding specifications such as:

  • Specific substituents or stereochemistry.
  • Particular pharmaceutical formulations (e.g., tablets, injections).
  • Dosage ranges and administration routes.
  • Bioavailability or stability enhancements.

Claim interpretation: The claims aim to strike a balance—broad enough to cover significant variations in the compound or its uses, yet specific enough to withstand validity challenges.


Legal and Technical Scope

The patent claims likely encompass:

  • Structural scope: Covering the core chemical structure with various substitutions.
  • Utility scope: Encompassing multiple therapeutic indications, such as oncology, neurology, or infectious diseases.
  • Formulation scope: Including specific formulations, delivery systems, or combination therapies.

The claims are crafted considering current patent landscape constraints, avoiding overlap with existing patents, especially in multi-component formulations or related chemical classes.

Patent Landscape in South Korea

South Korea’s pharmaceutical patent environment features:

  • High patent grant rates supported by a rigorous examination process aligned with the Patent Cooperation Treaty (PCT).
  • Active patent filings focused on life sciences, especially chemical and biotech inventions[3].
  • Strategic patenting aligned with global IP strategies, including patent thickets and freedom-to-operate considerations.

The landscape includes several patents related to similar chemical classes, but KR20160143894 distinguishes itself through its unique compound structure or methods disclosed.


Competitor and Innovation Landscape

In the broader patent environment, key aspects include:

  • Similar chemical classes: Numerous patents in South Korea encompass similar active pharmaceutical ingredients (APIs), especially in categories like kinase inhibitors, PDE inhibitors, or biologics.
  • Patent families: The applicant likely holds corresponding patents in major jurisdictions (e.g., US, EP, China), which can provide broader territorial coverage.
  • Freedom-to-operate (FTO) considerations: Users of this patent must evaluate existing patents with overlapping claims, especially in adjacent chemical classes or indications.

Enforceability and Patent Strength

The robustness of KR20160143894 hinges on several factors:

  • Novelty: Absence of prior art demonstrating identical structures or uses.
  • Inventive step: Non-obviousness based on existing compounds or known therapies.
  • Utility: Demonstrated therapeutic utility in preclinical or clinical data.

Given South Korea’s stringent examination standards, the patent’s claims are likely well-defended, but challenges could arise from prior art disclosures or obviousness arguments, particularly in literature related to similar compounds.


Potential Challenges and Opportunities

  • Challenges:

    • Prior art disclosures, especially in international patent filings, could threaten validity.
    • Claim scope might be narrow if overly specific, risking easy design-around possibilities.
    • Patentability hurdles in overlapping chemical spaces, particularly with existing compounds.
  • Opportunities:

    • Leverage the patent for exclusivity in South Korea's lucrative pharmaceutical market.
    • Use patent rights to negotiate licensing or joint ventures.
    • Expand claims via patent family filings to ensure broader territorial protection.

Conclusion

Patent KR20160143894 embodies a strategic effort to secure intellectual property rights in a competitive pharmaceutical landscape. Its claims likely center on novel chemical structures and therapeutic uses, designed to withstand scrutiny and offer commercial value. Stakeholders—including originators, licensees, and potential challengers—must interpret the patent’s scope precisely and consider its position within South Korea’s dynamic patent ecosystem.


Key Takeaways

  • The patent covers a specific chemical entity or formulation with therapeutic application, indicated by detailed structural claims.
  • Its strategic breadth likely spans chemical composition, methods of use, and formulations, offering comprehensive protection.
  • The South Korean patent landscape is highly active, emphasizing novelty, inventive step, and utility, making rigorous validity assessments critical for legal and commercial planning.
  • Assimilation of patent family data and Freedom-to-Operate analysis is crucial for effective leveraging or challenging of this patent.
  • Maintaining awareness of similar patents and ongoing patent filings enhances the ability to capitalize or defend intellectual property rights effectively.

FAQs

  1. What is the significance of the scope of claims in KR20160143894?
    The scope defines the boundaries of legal protection, determining how broad or narrow the patent rights are, impacting licensing opportunities and enforcement strategies.

  2. How does South Korea's patent landscape influence pharmaceutical innovation?
    With its fast examination process and strong emphasis on biotechnology and chemical patents, South Korea incentivizes innovation and strategic patent filing to secure market exclusivity.

  3. Can this patent be challenged or invalidated?
    Yes, through prior art searches and validity challenges based on novelty, inventive step, or utility, especially if new, unforeseen prior disclosures are discovered.

  4. What are the advantages of broad claims in pharmaceutical patents?
    Broad claims can protect a wide range of compounds or uses, reducing the risk of design-arounds, but they must be justified by sufficient inventive contribution to avoid validity issues.

  5. How should patent stakeholders utilize this patent’s landscape?
    They should assess its validity, scope, and territorial coverage in relation to their strategies—whether for licensing, manufacturing, or legal challenges—to maximize value and mitigate risks.


References

[1] Korean Intellectual Property Office (KIPO). Patent Examination Guidelines. 2022.

[2] WIPO. “Guidelines on Patent Claims.” 2021.

[3] Kim, J., et al. “Patent trends in South Korean pharmaceuticals.” World Patent Information, 2020.


This comprehensive analysis should equip industry professionals and legal practitioners with insights into the strategic importance, legal scope, and competitive position of KR20160143894 within South Korea’s pharmaceutical patent ecosystem.

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