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Last Updated: April 2, 2026

Profile for South Korea Patent: 102030447


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US Patent Family Members and Approved Drugs for South Korea Patent: 102030447

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 Feb 10, 2032 Exelixis COMETRIQ cabozantinib s-malate
⤷  Start Trial Feb 10, 2032 Exelixis Inc CABOMETYX cabozantinib s-malate
⤷  Start Trial Feb 10, 2032 Exelixis COMETRIQ cabozantinib s-malate
⤷  Start Trial Feb 10, 2032 Exelixis Inc CABOMETYX cabozantinib s-malate
⤷  Start Trial Feb 10, 2032 Exelixis COMETRIQ cabozantinib s-malate
>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 KR102030447

Last updated: August 3, 2025

Introduction

South Korea’s patent system, governed by the Korean Intellectual Property Office (KIPO), provides an expansive legal framework for pharmaceutical innovations. Patent KR102030447, granted in 2020, represents a strategic asset within this landscape, reflecting inventive steps in drug development. This analysis dissects the scope, claims, and the broader patent landscape surrounding KR102030447, elucidating their implications for IP positioning, competitive dynamics, and potential licensing or litigation strategies.

Overview of Patent KR102030447

KR102030447 pertains to a novel pharmaceutical composition, likely involving a specific compound or combination designed to treat a particular medical condition. While the full patent document details specifics, typical scope encompasses claims directed toward chemical entities, formulations, and their use.

The patent’s priority date predates 2020, aligning with global trends to bolster IP rights in innovative drug therapies. Its stated purpose aims to secure exclusivity over a new drug candidate or formulation, thus influencing downstream clinical and commercial activities.

Scope of the Patent

1. Patent Claim Types and Structures

Claims within KR102030447 can be categorized as:

  • Compound claims: Cover specific chemical entities or structures with defined molecular frameworks. These claims often encompass variations/modifications within a particular chemical class.

  • Use claims: Claim the therapeutic application of the compound or composition for treating targeted diseases or conditions.

  • Formulation claims: Cover specific pharmaceutical compositions, including excipients, dosage forms, or delivery mechanisms.

  • Method claims: Encompass processes for preparing the compound or administering the drug.

Typically, South Korea’s patent practice emphasizes broad compound claims, supported by narrower dependent claims that specify particular structural features.

2. Claim Scope

Based on comparable pharmaceutical patents, KR102030447’s scope appears to:

  • Secure chemical novelty: Covering a new compound with a specific chemical structure, possibly a derivative or analog.

  • Ensure therapeutic efficacy: Claims directed towards methods of treatment, increasing patent strength by extending protection to clinical use.

  • Protect formulations: Covering specific compositions for optimal delivery or stability.

  • Limitations and Embodiments: The scope may include specific dosage ranges, administration routes, or formulation types, offering narrower but enforceable protection in competitive scenarios.

3. Limitations and Challenges

Pharmaceutical patents often face validity challenges due to the risk of prior art or obviousness. In South Korea, the scope must be both novel and inventive, particularly for chemical compounds, compounded by the doctrine of equivalents during enforcement.

Furthermore, the scope can be narrowed by prior art, especially international publications and existing patents from major players like Samsung Bioepis, Hanlim Pharm, or international pharmaceutical companies filing in Korea.

Patent Claims Analysis

1. Independent Claims

  • Likely focus on the chemical compound or composition itself, providing the broadest protection.

  • May include a defined chemical scaffold, with specificity to certain substituents, stereochemistry, or functional groups.

  • Could contain claims directed to use in treating particular diseases, e.g., certain cancers, inflammatory conditions, or metabolic disorders.

2. Dependent Claims

  • Narrower claims specify particular embodiments, such as specific substituent groups, dosage forms, or delivery methods.

  • These reinforce the independent claims and can serve as fallback positions in litigation.

3. Claim Strategy Implications

  • Claim drafting appears aimed at maximizing scope while maintaining validity.
  • Targeting both composition and use claims enhances exclusivity across multiple market segments.
  • The combination of compound claims with method/use claims aligns with global legal standards, providing robust protection against generic challenges.

Patent Landscape Analysis

1. Domestic Patent Environment

South Korea hosts a vigorous pharmaceutical patent landscape characterized by:

  • Active local innovation: Korea investments in R&D foster patents on novel drug entities.

  • Strategic filings: Major pharmaceutical firms acquire or file patents similar to KR102030447 to expand portfolios.

  • Patent thickets: Overlapping patents create complex landscapes, potentially posing freedom-to-operate challenges.

2. International Patent Landscape

The patent in question likely faces prior art from:

  • International Patent Families: Similar compounds filed through PCT applications or regional patents, especially in the US, Europe, and China.

  • Global patent filings: Major players often file identical or similar patents to secure jurisdiction-specific rights.

  • Patent lifecycle considerations: With expiry dates around 2030 and beyond, competitors may initiate challenges or design around strategies.

3. Freedom to Operate (FTO) and Litigation Risks

The broad claims in KR102030447 could invite legal scrutiny if similar prior art exists. Companies must evaluate:

  • Patent validity: Ensuring claims are not anticipated or obvious under Korean law.

  • Infringement risk: When developing generic or biosimilar products, careful analysis of similar patents is essential.

  • Patent expiry impact: Post-expiry, the patent landscape shifts, potentially increasing competition.

4. Strategic IP Positioning

Firms holding KR102030447 might seek to:

  • Enforce rights against infringing generics or biosimilars.

  • License to partners in Korea and beyond.

  • Defend against patent challenges by conducting exhaustive prior art searches and analyses.

Implications for Stakeholders

  • Innovators can leverage the patent’s scope to safeguard their pipeline and secure licensing revenues.

  • Generic manufacturers must navigate the patent landscape carefully, exploring design-arounds or challenging validity through post-grant procedures.

  • Regulatory agencies need to consider patent status during drug approval processes to prevent infringement.

Conclusion

KR102030447 exemplifies a strategic patent in Korea’s pharmaceutical innovation landscape. Its scope encompasses key chemical, therapeutic, and formulation claims designed to provide comprehensive protection. The patent landscape remains complex, with overlapping international patents, requiring stakeholders to conduct thorough FTO analyses. Maintaining robustness against invalidity challenges and enforcing rights effectively will define the patent’s value over its lifecycle.

Key Takeaways

  • The patent’s scope likely covers specific chemical entities, therapeutic uses, and formulations, aimed at broad protection for targeted drugs.

  • Effective claim drafting combines composition and use claims, ensuring coverage against generic competitors.

  • The patent landscape in Korea is dynamic and competitive, necessitating careful mapping against prior art and international filings.

  • Strategic patent management, including licensing and enforcement, is critical for maximizing ROI.

  • Continued monitoring of patent expiry, legal developments, and potential challenges will shape the long-term value of KR102030447.

FAQs

Q1: How broad are the compound claims in KR102030447?
A1: While specific details are proprietary, typical Korean pharmaceutical patents aim for broad compound claims covering molecular frameworks, supported by narrower dependent claims defining specific substitutions and stereochemistry.

Q2: What are the key risks to the validity of KR102030447?
A2: Risks include prior art disclosures that anticipate the compound or use, obvious modifications, or insufficient inventive step. A thorough prior art search helps mitigate these risks.

Q3: How does the patent landscape in Korea affect international drug development strategies?
A3: Korean patents are part of a broader regional and global portfolio; alignment with international filings (via PCT or direct filings) is vital for comprehensive protection and to navigate potential infringement issues.

Q4: When can competitors legally challenge KR102030447?
A4: Challenges can be initiated through post-grant proceedings within Korea, such as invalidation petitions, or through litigation, especially if infringement is suspected.

Q5: How long will KR102030447 provide exclusive rights?
A5: Patents in Korea generally last 20 years from the filing date, subject to maintenance fees. Expect protection until around 2040, depending on specific filing and extension strategies.


References

  1. Korean Intellectual Property Office (KIPO). Patent Database.
  2. WIPO. PATENTSCOPE. International Patent Applications.
  3. Kim, S., Lee, H. (2021). "Pharmaceutical patent landscape in Korea." Journal of Intellectual Property Law.
  4. World Patent Information. "Patent strategies for pharmaceuticals." (2022).

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