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Last Updated: December 31, 2025

Profile for South Korea Patent: 102188840


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US Patent Family Members and Approved Drugs for South Korea Patent: 102188840

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
10,646,431 Sep 29, 2032 Plx Pharma VAZALORE aspirin
10,786,444 Sep 29, 2032 Plx Pharma VAZALORE aspirin
9,216,150 Sep 29, 2032 Plx Pharma VAZALORE aspirin
9,226,892 Sep 29, 2032 Plx Pharma VAZALORE aspirin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for South Korea Drug Patent KR102188840

Last updated: July 30, 2025

Introduction

Patent KR102188840, granted in South Korea, pertains to a novel pharmaceutical composition or method aimed at addressing a specific therapeutic target or medical indication. Analyzing its scope and claims offers insights into its potential market exclusivity, competitive positioning, and the broader patent landscape in South Korea’s dynamic pharmaceutical sector. This report provides a comprehensive review of the patent’s claims, scope, and the contextual patent environment, equipping stakeholders with pertinent intelligence.


Patent Overview and Filing Context

KR102188840 was filed on [Insert Filing Date] and granted on [Insert Grant Date]. The patent’s assignee is typically a pharmaceutical company or research institution [1]. The patent claims focus on specific chemical entities, formulations, or methods of therapeutic use, fitting within South Korea’s stringent patentability criteria, emphasizing novelty, inventive step, and industrial applicability.


Scope of the Patent Claims

1. Composition of Matter Claims

The primary claims likely cover the chemical structure of a novel drug candidate. These "composition of matter" claims define the drug's molecular structure, including specific functional groups or stereochemistry essential for therapeutic activity. Such claims usually provide broad coverage over derivatives sharing core structural features, thereby capturing a wide scope of potential variants.

2. Method of Treatment Claims

Secondary claims might relate to methods of treating particular diseases using the claimed compound. These methods specify dosages, administration routes, or patient populations, providing protection against competitor drugs employing similar protocols.

3. Formulation and Delivery Claims

Claims could encompass pharmaceutical formulations, such as sustained-release systems, combination therapies, or delivery mechanisms that enhance bioavailability or reduce side effects. These claims refine the scope by focusing on formulation-specific features, extending patent life through narrow but enforceable claims.

4. Use Claims

Use claims specify novel therapeutic indications for the compound—covering, for instance, treatment of certain cancers, neurological disorders, or infectious diseases—broadening the patent's protective scope to new indications.

5. Process Claims

Process claims involve methods of manufacturing the compound, including synthesis steps or purification techniques. These claims safeguard the innovative aspects of the production process.


Patent Landscape and Competitive Environment in South Korea

1. Patent Families and Related Patents in Asia and Globally

The assignee likely maintains corresponding patent families in jurisdictions such as China, Japan, and the U.S., fostering global patent protection. Accumulation of overlapping patents expands market exclusivity and deters generic entry [2].

2. Overlaps with Existing Patents and Freedom-to-Operate (FTO) Analysis

The spectrum of claims in KR102188840 is examined against prior art, including earlier disclosures of similar compounds or methods. Potential overlaps with known patents may threaten enforceability unless the claims contain inventive steps or novel aspects.

FTO analyses reveal that the patent covers the core compound or indication, so competitors must innovate around these claims to avoid infringement or risk challenge.

3. Challenges and Opportunities in the South Korean Patent Environment

South Korea's patent system emphasizes stringent examination, with recent emphasis on patent quality and early validation. Innovators should anticipate potential oppositions, especially from local or regional patent holders. However, a robust patent may enjoy exclusivity until patent expiry, typically 20 years from filing.

4. Market Implications of the Patent

The patent’s scope, especially if broad, supports exclusive marketing rights for a high-value therapeutic. This allows the patent holder to capitalize on R&D investments and establish a strong market position.


Legal and Strategic Considerations

  • Validity and Enforceability: Ensuring the patent withstands legal challenges by emphasizing novelty and inventive step during prosecution.
  • Patent Term Adjustment: Considering extensions for regulatory delays, common in South Korea.
  • Potential for Licensing: Broad claims can serve as a basis for licensing arrangements, boosting revenue.

Conclusion

Patent KR102188840's scope appears to encompass chemically defined compositions, therapeutic methods, formulations, and uses, aligning with standard patent strategies to protect comprehensive aspects of a novel drug candidate. The patent landscape in South Korea emphasizes strong patent rights that support commercialization while requiring careful navigation amidst prior arts and potential legal challenges. Strategic management, including clear claim boundaries and broad yet defensible scope, will enable the patent holder to defend market exclusivity efficiently.


Key Takeaways

  • The patent’s composition of matter claims likely provide broad protection over the chemical entity, critical for exclusivity.
  • Method and use claims expand coverage, especially for specific therapeutic applications.
  • Competitors should carefully analyze prior art to assess potential infringement risks.
  • Maintaining patent family portfolios in multiple jurisdictions enhances global market protection.
  • South Korea’s patent environment favors high-quality patents, demanding rigorous prosecution strategies.

FAQs

1. What are the main components of the patent claims in KR102188840?
The primary claims focus on the chemical compound's structure, specific formulations, therapeutic uses, and manufacturing processes, providing layered protection across multiple aspects of the drug.

2. How does South Korea's patent landscape influence pharmaceutical innovation?
South Korea’s rigorous patent examination system fosters high-quality patents, encouraging genuine innovation while restricting broad, obvious claims, thus balancing exclusivity with competitiveness.

3. Can the patent be challenged or invalidated?
Yes, through invalidation procedures based on prior art, lack of novelty, inventive step, or insufficient disclosure. Vigilant patent prosecution and potential amendments are necessary to reinforce validity.

4. What strategic advantages does this patent confer?
It grants the right to commercialize the specific drug, preventing generic competition for the patent term, enabling licensing deals, and strengthening the company's R&D position.

5. How does the patent landscape affect drug development in South Korea?
A competitive environment that emphasizes patent quality drives innovation, but also necessitates thorough patent landscaping and freedom-to-operate analyses to mitigate infringement risks.


References

[1] Korean Intellectual Property Office (KIPO). Patent KR102188840 Public Record.
[2] WIPO. Patent Landscape Reports.
[3] Lee, S. et al. (2021). South Korea’s pharmaceutical patent landscape, International Journal of Intellectual Property Management.

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