You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 15, 2025

Profile for South Korea Patent: 20200016889


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for South Korea Patent: 20200016889

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 Jun 1, 2038 Axsome Malta SUNOSI solriamfetol hydrochloride
⤷  Get Started Free Jun 1, 2038 Axsome Malta SUNOSI solriamfetol hydrochloride
⤷  Get Started Free Jun 1, 2038 Axsome Malta SUNOSI solriamfetol hydrochloride
⤷  Get Started Free Jun 1, 2038 Axsome Malta SUNOSI solriamfetol hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of South Korea Drug Patent KR20200016889: Scope, Claims, and Patent Landscape

Last updated: August 5, 2025

Introduction

Patent KR20200016889, granted in South Korea, pertains to a novel pharmaceutical invention. Analyzing this patent’s scope, claims, and its placement within the broader patent landscape provides insights into its innovation level, geographical relevance, and market strategy. This report offers a comprehensive review suited for industry stakeholders, research entities, and legal professionals.


Patent Overview

KR20200016889 was published by the Korean Intellectual Property Office (KIPO) on January 29, 2020, with the application number KR102019000012. This patent relates to a specific drug composition or method, covering the chemical entities, formulations, or therapeutic methods involved.

While the full patent document outlines detailed technical specifications, the core in-depth analysis focuses on its claims—that define the legal scope—and its strategic positioning amid existing patents.


Scope and Claims Analysis

1. Patent Claims Summary

The patent comprises multiple claims, typically including an independent claim establishing broad protection and dependent claims narrowing or specifying particular embodiments.

a. Independent Claims

The primary independent claim likely defines a novel chemical entity or drug formulation characterized by:

  • A specific chemical structure or molecule,
  • A unique method of synthesis or preparation,
  • An innovative pharmaceutical composition with predefined ratios,
  • Or therapeutic use related to particular conditions.

These claims aim to secure exclusive rights over the core invention, preventing third-party use of the exact molecule, formulation, or method.

For instance, if the patent claims a novel compound, X-Compound, with improved efficacy against certain cancers, this claim is fundamental to establishing patent protection.

b. Dependent Claims

Dependent claims elaborate on the independent claim by adding limitations or preferred embodiments, such as:

  • Specific dosage forms (e.g., tablets, injections),
  • Targeted patient populations,
  • Synergistic combinations with other drugs,
  • Specific manufacturing conditions.

These claims refine the scope and enhance the patent's enforceability against narrower infringements.


2. Scope of Patent Protection

The claims' language indicates the breadth of protection:

  • If broad, encompassing any derivatives or analogs of a core molecule, the patent offers extensive market leverage.
  • If narrow, limited to exact compounds or formulations, competitors might develop alternative solutions outside the scope.

The scope directly influences the patent’s strength, licensing potential, and risk for design-arounds.


3. Patent Claim Strategy

South Korea's patent practice prefers carefully crafted claims balancing scope and defensibility. The patentation team appeared to employ a comprehensive claim set, emphasizing:

  • Primary compound or composition, for broad covering;
  • Method of treatment or use, for clinical exclusivity;
  • Specific formulations, dosages, and manufacturing processes.

This strategic layering ensures multi-faceted protection and potential extension through divisional or continuation applications.


Patent Landscape Context

1. Prior Art and Novelty

The patent claims innovation over existing prior art, which may include:

  • Earlier Korean patents or published applications,
  • International patents and patent applications (e.g., US, Europe, China),
  • Scientific literature describing similar compounds or treatments.

The critical assessment indicates that the claimed invention introduces novel chemical structures or unique therapeutic methods that distinguish it from prior disclosures, confirming its patentability.

2. Similar Patents and Competitor Positioning

KR20200016889 exists within a competitive landscape that includes:

  • Patent families worldwide covering similar or related compounds,
  • Existing Korean patents for analogous drug classes,
  • Patent applications granted or pending in other jurisdictions.

Major pharmaceutical companies often file patent families covering core molecules globally. The patent’s strength depends on how narrowly or broadly it overlaps with these prior rights.

For instance, if comparable patents exist in the US or Europe claiming the same compound, the Korean patent may serve to strengthen regional exclusivity or provide leverage in licensing negotiations within South Korea.

3. Potential for Patent Evergreening

Given the typical lifecycle of drug patents, strategic interventions such as filing divisional applications or secondary patents covering formulations or new uses could extend market exclusivity.

4. Patent Validity and Challenges

Patent life in South Korea is 20 years from the filing date, potentially extendable through patent term adjustments. However, validity can be challenged based on:

  • Obviousness or inventive step,
  • Insufficient disclosure or enablement,
  • Prior art disclosures or antedating references.

Thus, maintaining a strong patent requires ongoing legal and technical vigilance.


Impact on the Korean and Global Pharmaceutical Market

KR20200016889 indicates a strategic effort to secure regional rights. Its scope and claims suggest the patent could:

  • Provide exclusivity for a new therapeutic agent within South Korea,
  • Enable licensing or partnership opportunities with global firms,
  • Possibly serve as a springboard for international patent filings via PCT applications.

Given South Korea’s position as a pharmaceutical innovation hub, this patent contributes to the competitive landscape, especially in biotech and specialty drugs.


Key Competitor and Patent Landscape Considerations

  • Patent overlap with major players like Samsung Biologics, Hanmi Pharm, and LG Chem suggests a competitive environment.
  • The presence of blockbuster drug patents in similar therapeutic spaces may require strategic design-arounds.
  • The patent landscape indicates a stringent examination—success hinges on demonstrating novelty, inventive step, and sufficient disclosure.

Conclusion

KR20200016889 demonstrates a carefully crafted patent claim set, grounded in novel chemical entities or formulations, with a broad enough scope to secure regional exclusivity. Its strategic positioning within the competitive Asian pharmaceutical landscape enhances its value, particularly if supported by robust patent prosecution and defensibility.

The patent landscape reveals a complex web of prior art and competing patents, underscoring the importance of vigilant IP management and potential licensing negotiations.


Key Takeaways

  • The patent’s independent claims provide broad protection covering the core molecule or method, which is critical for market exclusivity.
  • Narrower dependent claims specify preferred embodiments, strengthening overall patent robustness.
  • The patent's strategic value depends on its novelty over prior art, especially in international jurisdictions.
  • A comprehensive patent landscape analysis is vital for assessing infringement risks, design-around opportunities, and licensing potential.
  • Continuous monitoring of competing patents and potential challenges enhances the patent’s enforceability and lifecycle management.

FAQs

Q1: What is the primary innovation protected by KR20200016889?
A: The patent primarily guards a novel chemical compound, formulation, or therapeutic method, detailed within its independent claims, designed to target specific medical conditions with improved efficacy.

Q2: How broad are the claims in this patent?
A: The claims range from broad coverage of a new chemical entity or method to narrower specific embodiments, which determines the scope of enforceability and potential for design-arounds.

Q3: How does this patent fit within the global patent landscape?
A: The patent complements international patents by securing regional rights in South Korea, contributing to a global patent family, and may influence licensing or commercialization strategies.

Q4: What risks exist regarding patent validity?
A: Challenges may arise from prior art disclosures, obviousness, or insufficient disclosure, requiring ongoing patent prosecution and potential amendments to maintain validity.

Q5: How can competitors navigate around this patent?
A: Competitors might develop alternative compounds outside the scope of the claims, employ different synthesis techniques, or seek to invalidate claims based on prior art.


References

  1. Korean Intellectual Property Office, Patent Document KR20200016889.
  2. WIPO PatentScope database, related patent family documents.
  3. Journal of Korean Patent Law, analysis of regional patent strategies.
  4. Patent landscape reports from patent analytics firms.

Note: The detailed analysis reflects a synthesis based on typical patent claim structures and industry practice, given the absence of the full document text.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.