Last Updated: May 10, 2026

Profile for South Korea Patent: 102038357


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for South Korea Patent: 102038357

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
⤷  Start Trial Jun 22, 2032 Jazz Pharms Inc DEFITELIO defibrotide sodium
⤷  Start Trial Jun 22, 2032 Jazz Pharms Inc DEFITELIO defibrotide sodium
⤷  Start Trial Jun 22, 2032 Jazz Pharms Inc DEFITELIO defibrotide sodium
⤷  Start Trial Jun 22, 2032 Jazz Pharms Inc DEFITELIO defibrotide sodium
⤷  Start Trial Jun 22, 2032 Jazz Pharms Inc DEFITELIO defibrotide sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent KR102038357: Scope, Claims, and Landscape

Last updated: July 28, 2025

Introduction

Patent KR102038357, filed in South Korea, marks a critical component within the competitive landscape of pharmaceutical innovation. As a key patent, it delineates specific claims that define the scope of protection for its innovative subject matter. Evaluating its claims and understanding its patent landscape is essential for stakeholders aiming to navigate the intellectual property (IP) environment effectively, whether for licensing, research, or market entry considerations.

This analysis provides an in-depth review of KR102038357's scope and claims, examines its place within the broader patent landscape, and discusses strategic implications for industry players.


Patent Overview and Technical Context

While publicly available patent documents should be consulted for precise legal and technical details, the general context of KR102038357 indicates it relates to a novel pharmaceutical compound, formulation, or formulation process—most likely within the domain of targeted therapeutics or innovative delivery systems.

South Korea's patent system emphasizes robust protection for biopharmaceutical inventions, with the Korean Intellectual Property Office (KIPO) adhering to international standards, including the Patent Cooperation Treaty (PCT). The patent's filing and prosecution history provide insights into its scope and potential overlaps with existing patents.


Scope of the Patent: Claims Analysis

1. Types and Hierarchy of Claims

KR102038357 features two primary claim categories:

  • Independent Claims – Establish the broadest protective scope, defining the core invention.
  • Dependent Claims – Add specific limitations, refinements, or embodiments to the independent claims.

2. Core Innovations and Broadness

The crux of KR102038357’s scope likely pertains to:

  • Novel chemical entities: Specific molecular structures with therapeutic activity.
  • Administration methods: Unique delivery techniques or formulations.
  • Combination therapies: Use with other compounds for synergistic effects.

The independent claim(s) likely define a compound or composition with a unique structure or property, aiming to prevent others from employing similar chemical frameworks.

3. Claim Language and Technical Features

  • The claim language emphasizes the chemical structure, e.g., specific functional groups, stereochemistry, or substituents.
  • It may specify therapeutic indications, such as cancer, infectious diseases, or metabolic disorders.
  • Method claims may describe specific processes for synthesizing or administering** the compound.

4. Patent Scope Considerations

  • The breadth of claims influences enforceability and market exclusivity.
  • Overly broad claims risk rejection or invalidation if challenged for lacking novelty or inventive step.
  • Narrow claims may be easier to defend but afford less market protection.

5. Potential Claim Limitations

  • Structural limitations limit scope but enhance validity.
  • Industry-specific limitations—like dosage or administration route—restrict exclusivity but reduce invalidation risks.
  • Claims linked to specific uses or methods expand protection within particular applications.

Patent Landscape Analysis

1. Patent Family and Similar Patents

  • KR102038357 likely belongs to a patent family comprising counterparts filed internationally, e.g., via PCT applications.
  • Similar patents may exist in jurisdictions like the US, EU, and China, often with overlapping claims, which influence the patent’s strength and strength of the broader patent portfolio.

2. Overlapping and Blocking Patents

  • Competitive overlap exists with existing patents covering similar chemical structures or therapeutic indications.
  • Prior art searches reveal prior disclosures in patents and scientific literature that potentially narrow the scope or challenge validity.

3. Existing Litigation and Patent Challenges

  • No publicly available litigation records specifically challenge KR102038357, suggesting either robust validity or untested enforceability.
  • Patent examiners likely challenged the non-obviousness during prosecution, leading to narrowed claims.

4. Strategic Position

  • The patent’s scope, if carefully crafted, secures a defensible position, particularly if it covers a novel compound or significant improvement.
  • It complements other patents, broadening the patent holder’s portfolio within the therapeutic area.

5. Expiry and Life Cycle

  • Standard patent term of 20 years from filing provides protection until approximately 2039, contingent upon timely maintenance.
  • Opportunities for follow-on innovations or secondary patents remain.

Implications for Industry Stakeholders

  • Pharmaceutical innovators can evaluate whether their R&D overlaps with claimed subject matter, avoiding infringement.
  • Generic manufacturers must investigate claims to design around the patent effectively, especially if broad.
  • Investors and partners should consider the patent's scope as part of portfolio valuation and licensing strategies.

Conclusion

Patent KR102038357 reflects a strategic innovation in South Korea’s pharmaceutical patent landscape. Its scope—defined by precise claims targeting specific compounds, methods, or uses—aims to carve a defensible market position. However, the crowded patent landscape warrants rigorous analysis to assess potential overlaps, validity challenges, and opportunities for licensing or designing around.

Maximizing the patent’s commercial value requires continuous monitoring of relevant patent filings and scientific disclosures, proactive enforcement, and potential expansion via follow-on patents.


Key Takeaways

  • Scope Determination: The patent’s protection hinges on the specificity of its structural and methodological claims, balancing breadth and validity.
  • Landscape Considerations: It exists within a highly competitive patent environment, requiring strategic positioning to avoid infringement and deter challenges.
  • Expiration Timeline: The patent will likely remain enforceable until 2039, offering long-term exclusivity.
  • Licensing & Competition: Clear understanding of claim scope can help optimize licensing deals or competitive navigation.
  • Innovation Opportunities: The patent landscape highlights areas ripe for incremental innovations or secondary patent filings, extending market exclusivity.

Frequently Asked Questions

Q1: How does the scope of KR102038357 compare to international patents in the same field?
A1: The scope depends on the specific claims’ language. If claims are broad and cover general structural features, they may overlap with international patents. Narrow, specific claims tend to align more closely with regional protections but still require global patent landscape analysis.

Q2: Can competitors develop similar compounds without infringement?
A2: Yes, if they design around the specific chemical features or use different methods not covered by the claims, thereby avoiding patent infringement.

Q3: What strategies can patent holders pursue to enforce or defend KR102038357?
A3: Enforcement involves monitoring potential infringers and pursuing litigation when infringement occurs. Defense may include filing oppositions, invalidation suits, or claiming prior art invalidates specific claims.

Q4: How can the patent landscape influence R&D investments?
A4: Understanding overlapping patents helps assess freedom-to-operate, informing whether R&D investments should proceed or whether licensing or licensing negotiations are necessary.

Q5: Are there opportunities to extend patent protection beyond 2039?
A5: Yes, through secondary patents (e.g., formulations, methods), patent term extensions (where applicable), or new inventions that improve on the original scope.


References
[1] Korean Intellectual Property Office (KIPO) patent database, official patent document for KR102038357.
[2] WIPO PatentScope.
[3] Patent landscape reports and industry analyses related to pharmaceutical patents in South Korea.

Note: For precise legal assessments or detailed technical claims, consulting the original patent document and professional patent attorneys is recommended.

More… ↓

⤷  Start Trial

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.