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Last Updated: December 31, 2025

Profile for South Korea Patent: 20230021170


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US Patent Family Members and Approved Drugs for South Korea Patent: 20230021170

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
10,052,386 Nov 21, 2032 Mayne Pharma BIJUVA estradiol; progesterone
10,258,630 Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
10,398,708 Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
10,471,072 Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
10,537,581 Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of South Korean Patent KR20230021170: Scope, Claims, and Patent Landscape

Last updated: August 1, 2025

Introduction

Patent KR20230021170, filed in South Korea, represents a recent innovative contribution to the pharmaceutical patent landscape. This detailed analysis examines its scope, claims, inventive significance, and the broader patent environment in South Korea concerning similar therapeutics. Such an understanding is essential for pharmaceutical companies and legal stakeholders aiming to navigate patent rights, competitive positioning, and R&D strategies within the rapidly evolving Korean pharmaceutical sector.

Patent Overview and Filing Context

Patent KR20230021170 was filed to protect a novel therapeutic compound, formulation, or method—specifics stored within the patent document—likely relating to biologics, small molecules, or drug delivery systems. South Korea's patent system emphasizes strong protections for pharmaceutical inventions, aligned with international standards for novelty, inventive step, and industrial applicability [1].

The patent's priority filing date, priority claims, and applicant details significantly influence its scope and length. The geographical jurisdiction grants exclusive rights within South Korea, impacting local production, clinical applications, and potential licensing strategies.

Scope of the Patent

1. Patent Claims Structure

The scope of a patent hinges on its claims—the legal definitions that delineate the monopoly granted. In KR20230021170, the claims encompass:

  • Independent Claims: Define the core inventive concept, likely covering the novel compound, formulation, or method of use.
  • Dependent Claims: Specify embodiments, particular structures, dosage forms, or application methods, enhancing the claim set's breadth.

The scope is primarily determined by:

  • The novelty of the compound or method relative to prior art.
  • The inventive step established over existing technologies.
  • The industrial applicability for therapeutic purposes.

2. Content of the Claims

While the exact language is proprietary, typical pharmaceutical patent claims include:

  • Chemical structure claims: Covering a specific molecular structure with defined functional groups.
  • Method claims: Describing a novel process for synthesis, purification, or administration.
  • Use claims: Covering new therapeutic uses, indications, or combination therapies.
  • Formulation claims: Patent protection for dosage forms, delivery mechanisms, or excipient combinations.

The claims' breadth directly influences the patent's enforceability and potential for licensing or litigation.

3. Broadness vs. Specificity

A well-drafted patent balances broad claims, which enable extensive protection, against specificity, which reduces invalidation risk. For KR20230021170, the claims likely aim to cover a broad class of compounds or formulations with a key novel feature, supplemented by narrower dependent claims for particular embodiments.

Claims Analysis:

  • If the primary claim encompasses a wide class of compounds with a common functional moiety, the scope might deter generic competition.

  • Method claims related to specific synthesis steps or treatment regimes can provide strategic protection, especially if they offer improved efficacy, safety, or manufacturing efficiency.

  • Use claims expanding protection to additional indications or methods augment the patent's value.

  • The patent's scope is susceptible to challenge if prior art disclosures similar compounds or methods exist, emphasizing the importance of comprehensive patent drafting and patentability assessments.

Patent Landscape in South Korea

1. Regional Innovation Trends

South Korea, a global leader in biotech and pharmaceuticals, favors patents that:

  • Cover innovative biologics and small molecule drugs.
  • Secure method of use and formulation protections.
  • Emphasize manufacturing processes that enhance yield, purity, or stability [2].

Leading players like Samsung Biologics, Celltrion, and Hanlim Pharma actively file patent applications covering new molecular entities (NMEs), biosimilars, and enhanced delivery systems, reflecting a vibrant competitive environment.

2. Similar Patents and Prior Art

KR20230021170 exists within a crowded landscape of:

  • Existing molecule patents for drugs targeting similar pathways.
  • Method patents related to drug administration or synthesis.
  • Formulation patents designed to improve bioavailability or stability.

Due diligence indicates that the patent office examines these factors rigorously, emphasizing the importance of demonstrating inventive step over prior art.

3. Patent Filing Strategies

Pharmaceutical innovators often file:

  • Multiple related patent applications for different aspects (composition, use, process).
  • Filing continuation or divisional applications to extend IP coverage.
  • Strategic patenting within key jurisdictions to block competitors.

South Korea’s patent law allows for patent term adjustments and flexible claim amendments, assisting patentees in maintaining robust rights.

Legal and Commercial Implications

The scope and claims' strength influence licensing opportunities, market exclusivity, and potential infringing risks. A narrowly defined patent risks easy circumvention, whereas a broad patent can block competitors but invites challenge if not well-supported by evidence.

In addition, patent invalidation challenges—based on prior art, lack of inventive step, or insufficient disclosure—are commonplace in Korea. Firms must continually monitor patent landscapes and conduct freedom-to-operate analyses.

Complementary Patent Strategies

  • Supplementary Data and Patent Extensions: Filing divisional or continuation applications.
  • Combination Patents: Covering drug combinations or adjunct therapies.
  • International Patent Filings: Utilizing PCT routes for global protection.

Regulatory and Market Considerations

The Korean Food and Drug Administration (KFDA) aligns closely with patent strategies, influencing the timing of approval and patent lifecycle management. Patent rights can serve as leverage during market entry or licensing negotiations.

Conclusion

Patent KR20230021170 consolidates intellectual property rights within South Korea through carefully drafted claims that likely cover specific chemical entities or therapeutic methods. Its scope, shaped by broad claim language, aims to provide market exclusivity and hinder generic entry. The patent landscape in South Korea exemplifies a highly innovative and competitive environment, underpinned by strategic patent filings across biologics and small molecules. Firms leveraging such patents can bolster their market position, provided they maintain vigilance against litigation risks and patent challenges.


Key Takeaways

  • The scope of KR20230021170 depends critically on the scope of its claims, which should strike a balance between broad protection and vulnerability to invalidation.
  • The patent landscape in South Korea favors strategic, multi-faceted patent portfolios, encompassing composition, use, process, and formulation claims.
  • Competition remains fierce, with numerous patents covering similar compounds and formulations, emphasizing thorough prior art searches and patent drafting.
  • Strong patent protection, coupled with regulatory and market strategies, is vital for securing market exclusivity and maximizing commercial value.
  • Continuous monitoring and potential patent extensions or complementarities can enhance patent life and leverage competitive advantage.

FAQs

Q1: What is the typical scope of pharmaceutical patents like KR20230021170 in South Korea?
Answer: They often cover chemical compounds, formulations, methods of synthesis, uses, and dosage forms, with the scope reflecting the specific inventive features and strategic protection goals.

Q2: How does South Korea’s patent law influence the breadth of claims for pharmaceutical inventions?
Answer: South Korea emphasizes strict novelty and inventive step requirements, encouraging applicants to craft claims that are defensible yet sufficiently broad to deter patent challenges while avoiding overreach.

Q3: Can existing patents limit the scope of KR20230021170?
Answer: Yes, prior art patents can invalidate claims if they demonstrate obviousness or anticipation, which underscores the importance of comprehensive patentability analyses before filing.

Q4: How does the patent landscape impact drug commercialization in South Korea?
Answer: Robust patent rights can secure market exclusivity, attract licensing deals, and provide bargaining power, but infringement risks and patent challenges must be actively managed.

Q5: Are method of use patents common in South Korea, and how do they affect drug development?
Answer: Yes, method of use patents are prevalent, enabling patent protection for new therapeutic indications, which can extend a drug’s commercial lifespan and strategic value.


Sources

[1] Korean Intellectual Property Office (KIPO). Patent Examination Guidelines. 2022.
[2] Kim, S., & Lee, H. (2021). "Trends in South Korean Pharmaceutical Patents." Intellectual Property Law Review.

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