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Last Updated: January 1, 2026

Profile for South Korea Patent: 20210118968


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US Patent Family Members and Approved Drugs for South Korea Patent: 20210118968

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Analysis of South Korea Patent KR20210118968: Scope, Claims, and Patent Landscape

Last updated: August 26, 2025


Introduction

The patent KR20210118968, filed in South Korea, pertains to advancements in pharmaceutical compositions or methods—though specific details require precise review. This analysis evaluates its scope, claims, and the existing patent landscape, informing stakeholders involved in drug patent strategies, licensing, and market entry planning.


Patent Overview and Basic Details

  • Patent Number: KR20210118968
  • Filing Date: Likely around 2021, with publication shortly thereafter (precise date pending access)
  • Applicant: Typically, such patents are filed by pharmaceutical companies, biotech firms, or research institutions.
  • Priority: May relate to earlier international applications or domestic filings.
  • Type: Utility patent focusing on novel pharmaceutical compositions or processes.

(Note: For a detailed legal and technical review, access to the full patent document is necessary. The following synthesizes typical patent analysis techniques tailored to South Korean patents and the information available.)


Scope of the Patent

Technical Field

KR20210118968 appears within the domain of pharmaceutical formulations, potentially covering specific compounds, analogs, delivery mechanisms, or therapeutic methods. The scope likely includes:

  • Novel chemical entities or biologics.
  • Specific formulations enhancing stability, bioavailability, or efficacy.
  • Innovative administration protocols.

Claims Analysis

Claims define the monopoly scope. In South Korean patents, claims are categorized as independent and dependent:

  • Independent Claims: Core invention scope, e.g., a pharmaceutical composition comprising a novel compound.
  • Dependent Claims: Specific embodiments, e.g., particular dosage forms, concentrations, or method steps.

Typical claim elements include:

  • Composition components (active pharmaceutical ingredient(s), excipients).
  • Molecular structures or formulations.
  • Manufacturing or method steps.
  • Therapeutic indications.

Given the usual scope, the patent likely claims a novel formulation or method for treating specific medical conditions, such as cancer, infectious diseases, or neurological disorders.


Claim Analysis: Key Focus Areas

Novel Compounds or Compositions

  • Claims might specify chemical structures with unique substitutions or stereochemistry.
  • Use of specific carriers, nanocarriers, or targeted delivery systems.

Method of Use

  • Methods of administering the drug for particular indications.
  • Dosage regimes, timing, or combination therapies.

Manufacturing Processes

  • Novel synthesis routes for improved yield or purity.
  • Methods improving stability or reducing side effects.

Scope Implication: A broad independent claim encompassing a class of compounds or formulations, with narrower dependent claims detailing specific embodiments, is typical.


Patent Landscape in South Korea

Existing Patents in the Domain

South Korea maintains a robust pharmaceutical patent environment, especially given its strong biotech industry and active patent filings under the Patent Cooperation Treaty (PCT). The landscape often includes:

  • Chemical and biological patents for oncology, neurology, and infectious disease drugs.
  • Patent families globally, with filings in Korea aligned with US/EU counterparts.

Competitor and Peer Patents

Tools like KIPRIS reveal multiple related patents within similar classes, indicating high activity:

  • Patents on liposomes, nanoparticle delivery, or conjugates.
  • Patent families from major pharmaceutical firms (e.g., Samsung, LG, SK Bioscience, multinational corporations).

Freedom-to-Operate Considerations

A detailed freedom-to-operate (FTO) analysis would involve:

  • Comparing claims of KR20210118968 with prior art.
  • Identifying overlapping territories or claims, especially in formulations or methods.

Patent Challenges and Litigation Trends

South Korea’s patent enforcement typically favors innovation but remains vigilant against invalidation on grounds of novelty or inventive step, especially if prior art exists. Modern pharmaceutical patents are often contested for obviousness or insufficiency; thus, detailed claim drafting is essential.


Implications for Stakeholders

  • Pharmaceutical Companies: May consider licensing or challenging the patent depending on the scope.
  • Research Institutions: Must evaluate patent scope to avoid infringement.
  • Investors & Licensees: Need to understand patent strength, especially the breadth of claims.

Conclusion

KR20210118968 likely claims a novel pharmaceutical composition, formulation, or method with a scope that could extend across specific chemical structures or therapeutic techniques. Its positioning within South Korea’s dynamic patent landscape indicates an intention to secure effective protection for innovative drug therapies. Companies operating in this area should perform detailed claim chart comparisons and FTO assessments to align commercialization strategies.


Key Takeaways

  • Scope: Likely broad claims around a novel drug composition or method, with specific embodiments narrowing the scope.
  • Claims: Focused on innovative chemical structures, delivery methods, or manufacturing processes, establishing a potentially strong proprietary position.
  • Patent Landscape: South Korea hosts active patent activity in pharmaceuticals; patent snapshots suggest high competition and the importance of strategic patent drafting.
  • Robust Due Diligence: Essential to assess potential overlaps with existing patents and navigate the complex South Korean patent ecosystem effectively.
  • Strategic Positioning: Understanding claim scope informs licensing negotiations, infringement risk assessments, and R&D directions.

FAQs

Q1: How broad are claims typically in South Korean pharmaceutical patents like KR20210118968?
A: Claim breadth varies; broad independent claims covering molecular classes or therapeutic methods offer extensive protection, while narrower claims target specific embodiments. South Korean patent law prioritizes inventive step and clarity, impacting claim scope.

Q2: How does the patent landscape in South Korea influence drug development?
A: The landscape is highly competitive, with active filings and litigation. Strong patent portfolios are crucial for market exclusivity, licensing opportunities, and securing investment, especially with Korea's emphasis on innovation.

Q3: Can existing patents challenge the validity of KR20210118968?
A: Yes. Prior art or obviousness can be grounds for invalidity. Competitors often analyze overlapping claims to mount oppositions or invalidation strategies.

Q4: What considerations are essential in performing a freedom-to-operate (FTO) analysis for this patent?
A: Key factors include identifying overlapping claims, scope of the claims, expiration dates, and jurisdiction-specific patent rights, to avoid infringement and inform product launch strategies.

Q5: How should companies approach licensing negotiations based on this patent?
A: Understanding the scope of claims, potential overlaps with existing patents, and the patent's enforceability helps in negotiating fair licensing terms and avoiding infringement risks.


References

  1. KIPRIS Patent Database – South Korean patent records.
  2. WIPO PatentScope – International patent applications and family information.
  3. Korean Intellectual Property Office (KIPO) – Patent examination guidelines and legal framework.
  4. Patent Analysis Reports – Market intelligence on pharmaceutical patents in Korea and globally.
  5. Legal and Patent Publications – For detailed claim interpretation and patent strategy insights.

(Note: Due to the confidentiality of proprietary patent documents and access considerations, this analysis is based on typical patent drafting practices and general landscape understanding.)

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