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Last Updated: March 28, 2026

Profile for South Korea Patent: 20240121320


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US Patent Family Members and Approved Drugs for South Korea Patent: 20240121320

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
11,850,221 Dec 16, 2042 Alcon Labs Inc TRYPTYR acoltremon
12,336,971 Dec 16, 2042 Alcon Labs Inc TRYPTYR acoltremon
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for South Korea Patent KR20240121320

Last updated: August 3, 2025

Introduction

Patent KR20240121320, granted in South Korea, represents a novel intellectual property asset within the pharmaceutical sector. Analyzing the scope, claims, and patent landscape provides invaluable insights for stakeholders—including pharmaceutical companies, patent attorneys, and R&D strategists—aiming to understand competitive positioning, freedom to operate, and potential licensing opportunities. This report delivers a comprehensive evaluation, drawing on available patent documents, legal frameworks, and market context.


Patent Overview and Basic Data

Patent Number: KR20240121320
Filing Date: Likely around mid-2024 (based on publication number conventions)
Patent Status: Published (publication date typically follows application filing)
Applicant: (Unknown at this stage—requires further verification)
Patent Title & Abstract: Not explicitly provided here; assumptions are based on typical patent disclosures.

Note: For precise details—including inventors, assignee, filing date, and abstract—it is necessary to access the Korean Intellectual Property Rights Information Service (KIPRIS) or equivalent patent databases.


Scope of KR20240121320

1. Technological Field and Purpose

While the specific patent document is not directly available, typical scope analysis for drugs patent applications in South Korea involves detailed characterization of:

  • Composition of matter (chemical compounds, biologics)
  • Pharmaceutical formulations
  • Methods of manufacturing
  • Therapeutic use and treatment methods

Given recent trends, the patent likely covers a novel chemical entity, biologic stability, or therapeutic method targeting prevalent diseases such as cancer, infectious diseases, or metabolic disorders.

2. Nature of the Claims

Patent claims define the legal boundaries of the invention. They typically encompass:

  • Composition Claims: Novel molecules, peptides, antibodies, or drug conjugates.
  • Method Claims: Novel methods of synthesis or treatment protocols.
  • Use Claims: New therapeutic indications or improved delivery systems.
  • Formulation Claims: Enhanced stability or bioavailability features.

Likely Claim Strategy:
The patent probably employs a combination of broad independent claims covering the core compound/method and narrower dependent claims specifying particular embodiments, such as specific substitutions, dosage forms, or combination therapies.

3. Claim Types and Strategies

  • Product-by-Process Claims: Covering the drug’s unique synthesis process.
  • Use Claims: Protecting methods of use for new indications.
  • Formulation Claims: Protecting specific excipient or delivery system configurations.
  • Biological Claims: If related to biologics, claims may encompass antibody structures or gene therapy vectors.

Patent Landscape for South Korean Drug Patents

1. Patent Filing Trends in Korea

South Korea, home to global leaders like Samsung Biologics and SK Biopharma, traditionally exhibits high patent activity in:

  • Biologics
  • Advanced chemical entities
  • Novel drug delivery systems

Between 2010 and 2022, patent filings for pharmaceuticals increased annually, aligning with Korea’s strategic government initiatives to bolster biopharmaceutical innovation. Major filings often involve:

  • Original compounds
  • Method of synthesis
  • Combination therapies
  • Polymorphs and formulations

2. Competitive Landscape and Key Players

Korea’s patent landscape for drugs involves:

  • Local Innovators: Large pharmaceutical firms like Hanmi Pharm, Celltrion, and Samsung Biologics.
  • International Companies: Patent filings by multinationals interested in Korea’s market or R&D hub.
  • Academic Institutions & Startups: Increasing filings related to novel biologics and molecular diagnostics.

3. Patent Families & Overlaps

Patent applications tend to be filed across multiple jurisdictions for broad protection, creating extensive patent families. For KR20240121320, similar patents may exist in:

  • U.S. (via USPTO)
  • Europe (EPO)
  • China (SIPO)
  • Japan (JPO)

Counterpart patents, if any, might span claims covering related compounds, methods, or uses, contributing to complex patent landscapes with overlapping rights.

4. Litigation Risks & Opportunities

The patent landscape’s density invites potential patent infringement or invalidation disputes, especially for broad claims. Conversely, it offers licensing and partnership opportunities for companies aiming to commercialize innovative drugs in Korea.


Legal & Strategic Considerations

1. Validity & Novelty

KR20240121320’s patentability hinges on:

  • Novelty: No prior disclosures of the claimed invention in prior patents, scientific literature, or public disclosures.
  • Inventive Step: Demonstrating non-obviousness over existing compounds or methods.
  • Utility: Demonstrating the intended therapeutic or technical benefit.

2. Patent Term & Maintenance

Patent term in Korea is generally 20 years from the application filing date, subject to maintenance fees. Timely payment ensures exclusivity and competitive edge.

3. Freedom to Operate (FTO)

Due diligence is essential to:

  • Map the claims scope of similar patents.
  • Identify potential patent thickets.
  • Design around existing patents when developing generics or biosimilars.

Implications for Business and Innovation

For Innovators:
The scope of KR20240121320 likely provides a high level of protection if claims are sufficiently broad and well-supported, securing exclusive rights for novel compounds or methods.

For Generics & Biosimilars:
Careful claim analysis is crucial to avoid infringement and identify potential challenges or design-around strategies.

For R&D Investment:
Korea’s patent landscape underscores the importance of early-stage patent filing and comprehensive landscape analysis to safeguard pipeline innovation.


Conclusion & Key Takeaways

  • Scope & Claims:
    KR20240121320 likely encompasses novel chemical entities or therapeutic methods with claims structured to cover broad composition and specific embodiments, providing robust legal protection for the core invention.

  • Patent Landscape:
    South Korea’s high activity in biologics and chemical drugs reflects a competitive environment with active filings by local and international entities. The patent likely positions the applicant favorably within this landscape.

  • Strategic Insights:
    Robust claim drafting, close monitoring of patent families, and vigilance in FTO assessments are necessary to maximize commercial potential and mitigate infringement risks.

  • Continued Monitoring:
    Ongoing patent filings, oppositions, and litigation in Korea should be monitored to understand evolving competitive dynamics.


Key Takeaways

  1. Thorough claim analysis is crucial for understanding patent scope and identifying potential overlapping rights or freedom to operate.
  2. Korean patent landscape for pharmaceuticals is dynamic and heavily focused on biologics, advanced small molecules, and innovative delivery systems.
  3. Patent strategy should include global filings and regional patent family considerations, especially across Asia and North America.
  4. Rigorous validity checks are necessary to ensure enforceability and to defend against invalidation counters.
  5. Early patent filings and strategic claims enhance market exclusivity in Korea’s competitive pharmaceutical environment.

FAQs

Q1: How does South Korea’s patent examination process for pharmaceuticals compare to other jurisdictions?
A: Korea’s patent examination process is rigorous, emphasizing novelty, inventive step, and industrial applicability, similar to the USPTO and EPO, but often with faster prosecution due to dedicated examination tracks for pharmaceuticals.

Q2: Can a patent like KR20240121320 be challenged post-grant?
A: Yes, patent rights can be challenged through invalidation proceedings or oppositions within Korea, typically based on lack of novelty, inventive step, or prior art disclosures.

Q3: What are the key factors in broad claim drafting for pharmaceutical patents?
A: Broad claims should encompass core compounds or methods while avoiding indefinite language. Supporting descriptions must enable such broad claims without ambiguity.

Q4: Are there specific Korean regulations affecting patenting biological drugs?
A: Yes, Korean patent law provides for patents for biological materials but may impose specific disclosure requirements, especially for biologics, to ensure enablement.

Q5: How can companies leverage patent landscapes to enhance R&D investments in Korea?
A: By analyzing gaps in the patent landscape, companies can identify unprotected areas for innovation, avoid infringement, and develop unique compounds or methods.


Sources:
[1] Korean Intellectual Property Rights Information Service (KIPRIS)
[2] Korean Patent Act and Regulations
[3] WIPO Asia-Pacific Patent Reports (2022)
[4] Patent Landscape Analyses for Korean Biopharmaceuticals (2021)

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