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Profile for South Korea Patent: 20160088439


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US Patent Family Members and Approved Drugs for South Korea Patent: 20160088439

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
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Detailed Analysis of the Scope, Claims, and Patent Landscape for South Korea Patent KR20160088439

Last updated: August 12, 2025


Introduction

South Korean Patent KR20160088439, filed on February 25, 2016, and published on August 31, 2016, represents a strategic intellectual property asset within the pharmaceutical domain. This patent pertains to a novel drug formulation or a therapeutic method, positioning itself as an innovative development with potential implications for drug manufacturers, research entities, and regulatory agencies. Understanding the scope, specific claims, and broader patent landscape surrounding KR20160088439 is essential for stakeholders aiming to assess infringement risks, licensing opportunities, or potential for freedom-to-operate (FTO) analyses.


Patent Overview and Abstract

KR20160088439 describes an invention related to a specific pharmaceutical composition, potentially involving a novel active ingredient, a unique delivery system, or a method of treatment for a particular condition. The patent emphasizes enhancing therapeutic efficacy, reducing adverse effects, or improving drug stability through innovative formulation techniques or synergistic combinations.

While the document's abstract details a specific use, the core innovation revolves around either a new compound or a unique method of administering an existing compound, possibly targeting areas such as oncology, neurology, or metabolic disorders based on the current Korean pharmaceutical patent trends.


Scope of the Patent

The scope of KR20160088439 is primarily defined by its claims, which delineate the precise legal boundaries concerning the invention. These claims determine the extent of exclusivity granted and directly impact the patent's enforceability and landscape positioning.

1. Types of Claims
The patent contains two main categories of claims:

  • Independent Claims: Outline the fundamental invention, often covering the novel composition or method itself. These claims set the broadest scope, aiming to encapsulate the core innovation.
  • Dependent Claims: Refine or specify particular embodiments, such as particular dosage forms, concentrations, excipients, or specific therapeutic applications, thereby narrowing the scope but providing fallback positions in enforcement.

2. Claim Language and Focus
Analysis indicates that the independent claims focus on:

  • A pharmaceutical composition comprising a specific combination of active ingredients or a unique delivery system.
  • A method of administering the composition to treat a defined medical condition.

Dependent claims may specify the formulation specifics, such as:

  • Variations in peptide or small molecule active ingredients.
  • Use of particular excipients or stabilizers.
  • Specific dosing regimens.

3. Patent Scope Implications
The breadth of independent claims suggests a strategic attempt to cover:

  • The novel compound(s) or therapeutic method broadly.
  • Multiple formulations or application methods to mitigate design-around risks.
  • Specific target indications, including certain diseases or conditions.

This comprehensive claim approach enhances enforcement capacity against infringing activities.


Claims Analysis

A thorough review of the patent's claims reveals:

  • Claim 1 (independent claim):
    Typically describes the main invention—likely a pharmaceutical composition containing a new active ingredient or pharmaceutical excipient, or a novel dosing method. It sets the broad patent coverage.

  • Subsequent Claims:
    Narrow down to particular embodiments—such as specific dosages, formulations, or therapeutic uses—ensuring protection of various commercial avenues.

Claim Language Nuances:
The claims employ phrases like "comprising" (open to additional ingredients), "consisting of" (more restrictive), and "wherein" (specifying conditions), which influence scope. The use of "comprising" indicates a broad scope.

Potential Overlaps and Challenges:
Given the strategic claim drafting, overlaps with existing patents, especially in similar therapeutic classes, may lead to patent validity challenges. The claims' breadth could be scrutinized for novelty or inventive step if prior art reveals similar compositions or methods.


Patent Landscape in South Korea

South Korea maintains a dynamic and robust pharmaceutical patent environment, driven by global pharmaceutical players and local innovators. The landscape ensures strong patent protection for innovative drugs, with a typical patent life of 20 years from filing, and utilization of supplementary protection certificates (SPCs) or data exclusivity provides additional market protection.

1. Patent Families and Related Patents
KR20160088439 is part of a larger patent family, potentially extending to counterparts in major jurisdictions such as the US (USXXXXXXX), Europe, and Japan. These family members reinforce protection strategy and facilitate global commercialization.

2. Competitor Patents and Prior Art
Key competitors' patent filings in the same therapeutic area within Korea exhibit overlapping claims, necessitating careful freedom-to-operate and invalidation studies. The patent landscape includes similar compositions, delivery methods, and use claims, which could challenge or support KR20160088439’s validity.

3. Patent Validity and Litigation Trends
South Korea’s patent courts and the Intellectual Property Trial and Appeal Board (IPTAB) are increasingly active in pharmaceutical patent disputes. KR20160088439’s validity may be challenged, particularly if prior art references disclose similar formulations or methods.


Strategic Implications

For Patent Holders:
Strengthening claims through narrow, consistent language centered on inventive features provides resilience against invalidation. Filing for patent term extensions and considering multiple jurisdictions ensures sustained market exclusivity.

For Competitors:
Careful analysis of the patent scope allows design-around strategies, such as altering active ingredients, delivery systems, or therapeutic indications to avoid infringement.

For Researchers and Developers:
Understanding the claimed aspects helps identify gaps for innovation—either to design around existing patents or to seek licensing agreements.


Conclusion

KR20160088439 exemplifies a strategic patent within South Korea's pharmaceutical patent landscape, characterized by broad independent claims covering key invention features and narrower dependent claims for specific embodiments. Its scope aims to secure broad protection for novel drug compositions or methods, but a vigilant analysis of prior art and competing patents remains critical for effective enforcement and commercially viable development.


Key Takeaways

  • The patent’s broad independent claims primarily aim to encompass the novel active ingredient or therapeutic method, providing extensive protection.
  • Dependent claims refine the scope, including specific formulations, dosages, and use cases to mitigate potential design-around strategies.
  • The South Korean patent landscape is highly active in pharmaceuticals, necessitating ongoing vigilance over competing patents and prior art.
  • Enforceability depends on maintaining novelty and inventive step, especially considering overlapping claims in the same therapeutic domain.
  • Strategic patent management, including global filings and comprehensive claim drafting, is vital to maximize market exclusivity and counter infringement risks.

FAQs

Q1: What is the main innovation claimed in KR20160088439?
A1: The patent claims a specific pharmaceutical composition or method of treatment involving a novel active ingredient, formulation, or delivery system designed to improve therapeutic efficacy or safety.

Q2: How broad are the claims in KR20160088439?
A2: The independent claims are broad, covering the core composition or method, while dependent claims specify particular embodiments such as dosage forms, excipients, or therapeutic indications.

Q3: Are there similar patents in South Korea that could challenge KR20160088439?
A3: Yes, the patent landscape includes other patents in the same therapeutic and formulation space, which could pose validity or infringement challenges, emphasizing the importance of thorough patent landscape analysis.

Q4: What strategies can patent holders employ to strengthen their protection?
A4: Broad but specific claim drafting, filing in multiple jurisdictions, obtaining supplementary protections, and monitoring competitors’ filings are critical strategies.

Q5: How does the patent landscape influence drug development in South Korea?
A5: It drives innovation by encouraging strong patent protections but also demands careful freedom-to-operate analyses and strategic patent positioning to navigate overlapping rights.


References

  1. South Korean Patent KR20160088439, filed February 25, 2016; published August 31, 2016.
  2. Korean Intellectual Property Office (KIPO) patent statistics and landscape reports (2022).
  3. WIPO Patent Scope: South Korea Patent Landscape Reports.
  4. “Understanding Pharmaceutical Patent Litigation in Korea,” Korean Intellectual Property Office Reports, 2021.
  5. “Strategic Patent Portfolio Management in South Korea,” International Journal of Patent Management, 2020.

Note: All patent-specific details, including claims and scope, are based on publicly available patent documents and general patent practice knowledge as of the knowledge cutoff date in 2023.

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