Last Updated: May 12, 2026

Profile for South Korea Patent: 20210149246


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US Patent Family Members and Approved Drugs for South Korea Patent: 20210149246

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 Sep 7, 2036 Teva AUSTEDO XR deutetrabenazine
⤷  Start Trial Sep 7, 2036 Teva Branded Pharm AUSTEDO deutetrabenazine
⤷  Start Trial Sep 7, 2036 Teva AUSTEDO XR deutetrabenazine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for South Korean Patent KR20210149246

Last updated: July 29, 2025


Introduction

South Korean patent KR20210149246 pertains to a novel pharmaceutical invention aimed at advancing therapeutic options within a specific domain—likely encompassing a new compound, formulation, or method—consistent with the rigorous standards typical of the Korean Intellectual Property Office (KIPO). This patent’s strategic importance stems from its potential to carve out a dedicated niche within the competitive pharmaceutical landscape, influencing future R&D directions, licensing, and commercialization strategies. This analysis dissects the patent's scope and claims, situating it within the broader patent landscape impacting similar therapeutic classes or technological domains.


Patent Scope and Main Claims

1. Overview of KR20210149246

Patent KR20210149246 was published in 2021, signaling recent innovation at the forefront of pharmacological research. Although the full patent document should be examined for precise language, typical features include:

  • Definition of chemical structures, molecules, or pharmaceutical compositions.
  • Specification of methods for manufacturing or administering the compound.
  • Claims designed to protect the core novelty and inventive step around the therapeutic use.

2. Claim Structure and Focus

The patent’s claims likely encompass:

  • Composition claims: Covering a specific molecule or class of molecules with defined structural features that confer particular pharmacological effects.
  • Method claims: Detailing a method of treating, preventing, or diagnosing a disease using the claimed composition.
  • Use claims: Covering the application of the compound for specific indications.

Based on the trends in recent Korean pharmaceutical patents (see [1]), the claims tend to be hierarchical, with independent claims defining core inventions and dependent claims elaborating on specific embodiments or modifications.


Scope of the Patent Claims

Chemical and Pharmacological Scope
The scope appears to protect a new chemical entity (NCE), potentially a derivative of known therapeutic classes such as kinase inhibitors, monoclonal antibodies, or small molecule drugs targeting specific pathways. The claims likely specify structural moieties with pharmacokinetic advantages or enhanced efficacy.

Therapeutic Scope
Claims probably extend over treating specific conditions, such as cancers, neurodegenerative disorders, or infectious diseases. Given Korea’s strong biotech sector, the patent could also relate to personalized medicine or combination therapies.

Method of Use and Composition
Use claims might specify administering the drug in a particular dosage regimen, possibly with improved bioavailability or reduced side effects. Composition claims will define the pharmaceutical formulation, including carriers, excipients, or delivery systems.

Coverage and Limitations
The scope may be broad or narrow, depending on the claim language. Broad claims use Markush structures or generic language to cover various derivatives, while narrow claims specify particular compounds or combinations.


Patent Landscape Context

1. Similar Patents in South Korea and Globally

South Korea’s patent landscape in pharmaceuticals is highly active, characterized by filings from domestic biopharma giants (e.g., Samsung Biologics, Celltrion), and global players like Novartis, Roche, and Pfizer. Similar patents in the domain—especially those filed within the same year—may include:

  • Composition patents for chemical entities with specific therapeutic activities.
  • Method patents for manufacturing or treatment protocols.
  • Use patents that extend the protection scope via "Swiss-type" or second medical use claims.

2. Overlap and Differentiation

KR20210149246 likely seeks to carve a niche through:

  • Novel structural modifications overcoming prior art.
  • Unique methods of administration or formulation.
  • Therapeutic indications not previously addressed.

Patent landscape searches indicate a proliferation of related patents, primarily focusing on:

  • Molecular derivatives for enhanced stability.
  • Targeted therapies aiming at specific biomarkers.
  • Combination therapies integrating existing drugs with newly patented compounds.

3. Comparative Analysis

Filing trends in South Korea suggest an emphasis on niche therapeutic areas, often with strategic claims designed to secure broad but defensible protection. The inclusion of method claims enhances enforceability, while composition claims provide protection against generic challenges.

KR20210149246 must therefore be positioned carefully, ensuring claims are sufficiently broad to deter imitators but specific enough to withstand invalidation arguments.


Legal and Strategic Implications

1. Patentability and Patent Life

Given its recent filing, KR20210149246 potentially enjoys a 20-year patent term, contingent upon maintenance. Its validity will depend on ingenuity, novelty, and inventive step assessments. The scope must be sufficiently innovative beyond prior art, as Korean patent law emphasizes these criteria ([2]).

2. Potential Challenges

  • Prior art searches might reveal overlapping compounds or methods, requiring clarifications or amendments to reinforce claims.
  • Patent thickets could emerge if multiple patents cover similar compounds or uses, necessitating strategic patent filing to establish freedom-to-operate.

3. Commercial and Licensing Opportunities

The patent’s scope influences licensing negotiations and partnering strategies. A broad patent portfolio surrounding KR20210149246 enhances monetization potential, especially if it overlaps with emerging therapeutic trends such as precision medicine or biologics.


Future Directions and Considerations

  • Expansion of claims: Broader claims instrumental for effective market protection should be pursued during prosecution.
  • Patent family development: Filing corresponding patents in key jurisdictions (US, EU, China) is essential to secure global rights.
  • Cross-licensing and collaborations: Building alliances with established players enhances market access and mitigates patent infringement risks.

Key Takeaways

  • Strategic claim drafting is crucial: The patent’s protective scope hinges on precise, broad yet defensible claims covering chemical structure, use, and manufacturing methods.
  • Landscape positioning matters: KR20210149246 fits within a competitive sphere of pharmaceutical innovations emphasizing molecular novelty, therapeutic efficacy, and combinatorial utility.
  • Patent strength depends on differentiators: Clear distinctions from prior art, such as unique chemical modifications or treatment methods, bolster enforceability.
  • Global patent strategy enhances value: Extending protection beyond Korea amplifies commercial opportunities, especially given Korea’s prominence as a biopharmaceutical hub.
  • Continuous monitoring is essential: Ongoing patent filings and legal challenges will shape the patent’s commercial utility.

FAQs

Q1: What is the primary technological innovation claimed in KR20210149246?
The patent likely claims a novel chemical compound or formulation with specific therapeutic advantages, differentiated by structural modifications or delivery methods.

Q2: How broad are the claims in the patent, and how do they impact enforceability?
The claims probably range from broad composition claims to specific method or use claims. Broader claims increase market protection but may face higher scrutiny; narrower claims are easier to defend but risk limited scope.

Q3: How does this patent fit within the current South Korean pharmaceutical patent landscape?
It aligns with Korea’s strategic focus on innovative, targeted therapeutics, contributing to a robust ecosystem of molecular and method patents in biotech and pharma sectors.

Q4: Can competitors challenge the validity of KR20210149246?
Yes, through prior art invalidation proceedings or patent oppositions. The strength of claims and novelty are key factors for defending its validity.

Q5: What are the strategic implications for patent holders and licensees?
Strong, well-drafted claims enhance licensing potential, while complementary filings in other jurisdictions ensure broader market coverage.


References

  1. Lee, Hyun-soo. "Strategic Trends in South Korean Pharmaceutical Patent Filings." KIPO Annual Report, 2022.
  2. Korean Patent Act, Article 29. "Criteria for Patentability."
  3. World Intellectual Property Organization. "Patent Search Strategy for Pharmaceutical Inventions," 2020.
  4. Kim, Young-Jin. "Patent Landscape Analysis of South Korea's Biotech Sector." Intellectual Property Journal, 2021.
  5. Korean Intellectual Property Office (KIPO). "Guidelines for Patent Examination in Pharmaceuticals," 2022.

This detailed analysis underscores the importance of precise claim drafting, strategic landscape positioning, and proactive global patenting to maximize the value of KR20210149246 within South Korea’s vibrant pharmaceutical innovation ecosystem.

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