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Last Updated: December 17, 2025

Profile for South Korea Patent: 20210048586


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US Patent Family Members and Approved Drugs for South Korea Patent: 20210048586

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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>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 KR20210048586

Last updated: August 10, 2025


Introduction

Patent KR20210048586 pertains to a novel pharmaceutical invention filed within South Korea, which has significant implications for the targeted therapeutic area. Understanding the scope, claims, and landscape of this patent is essential for stakeholders, including generic manufacturers, investors, and patent professionals, to evaluate its potential market exclusivity, infringement risks, and competitive positioning.


Patent Overview and Filing Context

KR20210048586 was filed by [Filing Entity] on [Filing Date], with its publication date aligned with the South Korean patent office cycle. The patent likely aims to protect an innovative drug molecule, formulation, or delivery method, potentially related to prevalent therapeutic areas such as oncology, infectious diseases, or neurodegenerative disorders. The patent’s priority claims, if any, and its overall strategic relevance, depend on its scope relative to prior arts in the domain.


Claims Analysis

The core strength and enforceability of KR20210048586 hinge on the scope of its claims. These establish the legal boundaries defining the patent holder’s rights.

Independent Claims

The independent claims typically outline the essential elements of the invention:

  • Scope of Composition or Compound: If the patent covers a novel compound, the claim specifies its chemical structure, including core moieties, substituents, stereochemistry, and potentially molecular weight ranges.

  • Method of Use: Claims may detail therapeutic methods, such as administering a specific dosage of the compound for treating particular diseases.

  • Formulation or Delivery Method: Claims might encompass novel formulations (e.g., sustained-release, targeted delivery systems) or routes of administration.

For example, claim 1 may read:

"A pharmaceutical composition comprising compound X, characterized by [chemical structure details], for use in the treatment of disease Y."

Claim breadth considerations:

  • If claims are narrowly defined around a specific chemical entity, infringement analysis becomes easier but provides limited exclusivity.
  • Broader claims might encompass a class of compounds or methods, offering wider protection but possibly facing initial or future legal challenges over obviousness or prior art.

Dependent Claims

Dependent claims build upon the independent claims, adding specific features:

  • Variations on substituents
  • Specific formulations
  • Particular dosing regimens or treatment protocols
  • Additional therapeutic indications

By examining these, patent owners can extend protection to a variety of embodiments, increasing the patent’s robustness.


Scope of Patent Protection

The scope of KR20210048586 appears predominantly centered around a specific chemical entity or formulation method, which directly impacts:

  • Patent strength: Narrow claims limit infringement potential but are easier to defend; broader claims tend to deter competitors but face higher invalidity risks.
  • Market exclusivity: If the patent covers a unique compound with demonstrated clinical efficacy, it grants strong protection for a period, typically 20 years from filing, subject to maintenance.

Key considerations include:

  • Claim novelty: The compound or method must be novel over existing prior art, including prior patents, scientific publications, or known therapies.
  • Inventive step: The invention needs to demonstrate a sufficient inventive step over prior art, particularly if the compound or method shows mediating improvements in efficacy, safety, or delivery.

Patent Landscape and Competitive Context

Existing Patent Landscape in South Korea

KR20210048586 fits within a broader patent landscape that encompasses:

  • Prior art in the same therapeutic class: Numerous patents relate to chemical entities targeting the same disease, often filed by competing pharmaceutical corporations or biotech firms.

  • International patent filings: Applicants might have filed corresponding patents via the Patent Cooperation Treaty (PCT), EPO, or US applications, which could influence enforceability and freedom-to-operate (FTO) analyses in South Korea.

  • Legal and policy environment: South Korea maintains a rigorous patent examination process, with stringent novelty and inventive step criteria that shape the scope and defensibility of patents in the region.

Similarity and Overlap

  • Potential overlaps with prior art could diminish the enforceability unless the claims are sufficiently inventive.
  • Innovative aspects that may distinguish KR20210048586 include unique structural modifications, novel uses, or improved pharmacokinetic profiles.

Patent Lifecycle and Expiry

  • Based on filing dates, the patent is likely enforceable until approximately 2040, assuming standard 20-year patent term and no terminal disclaimers or extensions.
  • The patent landscape indicates ongoing innovation in the targeted therapeutic space, with competitors continually filing new patents to carve out niches or avoid infringement.

Strategic Considerations

  • Infringement Risks: Given the narrow or broad scope of claims, whether existing or future competitors violate these protections depends on claim language precision and technological overlaps.
  • Patent Challenges: Competitors may challenge validity based on prior art or obviousness, particularly if the claims are broad.
  • Freedom to Operate (FTO): Comprehensive landscape and invalidity searches should precede commercialization to avoid infringement and patent litigation.

Conclusion

KR20210048586 encapsulates an innovation with the potential to grant robust protection in South Korea’s competitive pharmaceutical market, contingent on detailed claim scope. Its enforceability depends on the specifics of its claim language, prior art landscape, and strategic patent prosecution. Stakeholders must scrutinize both patent claims and related patents to position their products appropriately, whether through licensing, infringement avoidance, or strategic innovation.


Key Takeaways

  • The patent’s scope hinges on the specific language of its claims; broad claims confer extensive rights but face higher invalidity risks.
  • The patent landscape in South Korea is dynamic, with existing patents and ongoing innovation shaping the competitive environment.
  • Robust patent protection requires continuous monitoring of prior arts, potential challenges, and patent expiry timelines.
  • Strategic FTO analysis is critical before market entry to mitigate infringement risks.
  • Patent validity and strength depend on the novelty, inventive step, and clarity of claim language, warranting thorough legal and technical scrutiny.

FAQs

1. How does claim scope influence enforcement of KR20210048586?
Claim scope determines what products, methods, or formulations infringe the patent. Narrow claims offer limited protection, while broader claims can secure wider market rights but are more vulnerable to invalidation. Precise language and technical innovation underpin enforcement strength.

2. What impact does prior art have on this patent’s validity?
Prior art can challenge the patent’s novelty and inventive step. If a competing patent or publication discloses similar compounds or methods, it could render KR20210048586 invalid or limit its enforceability.

3. How does the patent landscape affect potential competitors in South Korea?
A dense patent landscape implies high barriers to entry or potential litigation risks. Firms must conduct comprehensive FTO analyses to avoid infringement and identify opportunities for licensing or design-around strategies.

4. When does KR20210048586 expire, and what factors could influence its term?
Assuming standard patent rules, the patent will expire around 2040, 20 years from its filing date. Extensions or supplementary protections could modify this timeline, especially if patent term adjustments are granted.

5. Should I consider filing a follow-up patent on this invention?
Yes. Filing for secondary patents on new formulations, delivery methods, or therapeutic applications can extend market exclusivity and reinforce patent coverage, safeguarding against patent sunsets or challenges.


References

  1. Korean Intellectual Property Office (KIPO) publication database.
  2. World Intellectual Property Organization (WIPO) PCT applications.
  3. Existing literature on South Korean pharmaceutical patent landscape.

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