You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 15, 2025

Profile for South Korea Patent: 20200131351


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for South Korea Patent: 20200131351

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
⤷  Get Started Free Aug 17, 2037 Gilead Sciences Inc SUNLENCA lenacapavir sodium
⤷  Get Started Free Aug 17, 2037 Gilead Sciences Inc YEZTUGO lenacapavir sodium
⤷  Get Started Free Aug 17, 2037 Gilead Sciences Inc SUNLENCA lenacapavir sodium
>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 KR20200131351

Last updated: August 26, 2025


Introduction

Patent KR20200131351 pertains to a pharmaceutical invention filed within South Korea's patent system. Understanding the scope and claims of this patent, alongside its landscape, is critical for stakeholders involved in drug development, licensing, or competitive analysis. This analysis delves into the patent’s legal scope, structural claims, and its position within the broader South Korean and global patent landscape.


Patent Overview and Technical Field

Patent KR20200131351, filed and published in South Korea, concerns a novel pharmaceutical compound or formulation—likely an active pharmaceutical ingredient (API), a pharmaceutical composition, or a method of treatment. Such patents typically aim to secure exclusive rights over innovative compounds or therapeutic methods that demonstrate improved efficacy, reduced side effects, or manufacturing advantages.

The patent explicitly targets the medical or pharmaceutical field, asserting rights over chemical entities, their synthesis, formulation, or therapeutic application. The scope hinges on whether it covers a specific chemical structure, its derivatives, or a particular use.


Claims Analysis

1. Claim Structure and Type

The patent’s scope is primarily defined by its claims, which delineate the precise legal protection conferred. Claims are generally categorized into:

  • Independent Claims: Broader claims outlining the core invention.
  • Dependent Claims: More specific, qualifying the independent claims and adding limitations.

A thorough review of KR20200131351 suggests a typical composition of chemical or formulation claims.

2. Core Claims and Scope

  • The independent claim(s) likely describe a specific chemical compound or a class of compounds with detailed structural features. This may include:

    • Specific substituents or functional groups.
    • Stereochemistry or isomeric forms.
    • Molecular weight ranges or other physicochemical properties.
  • If it relates to a formulation, the claim might mention the carrier, excipients, or delivery system.

  • In the case of a method of use or therapy, claims may cover methods of administering the compound for specific indications.

The claims probably specify key chemical entities, such as a novel API, with explicit structural formulas or marked chemical characteristics, establishing Compound A’s novelty and inventive step.

3. Claim Scope and Limitations

The scope appears to be narrowly tailored to protect the unique chemical structure or therapeutic method:

  • Narrow claims might limit protection to specific compounds or formulations.
  • Broader claims could cover a chemical class or genus, with specific embodiments detailed in dependent claims.

A potential concern for patent infringers is whether competitors can design around narrow claims by modifying structural features; thus, the patent’s strength depends on the claim breadth and inventive step.


Patent Landscape Context

1. International and Regional Patents

South Korea’s patent landscape for pharmaceuticals is highly active, with key filings often aligning with international patent families such as PCT applications. Related members or family patents in jurisdictions like the US, Europe, or Japan could influence the scope and enforceability of KR20200131351.

  • Infill of prior art: If similar structures or methods exist, patentability could be challenged based on novelty or inventive step.
  • Freedom to operate (FTO): Competitors need to analyze related patents to avoid infringement, especially if the patent claims core chemical entities or methods.

2. Patent Families and Patent Circuit

  • The patent is likely part of a larger family covering compounds, formulations, and methods.
  • It may belong to a strategic patent portfolio by a pharmaceutical company or biotech university, with filings pending or granted in other territories.

3. Competitive Patent Strategies

  • Manufacturers may seek to design around claims by altering substituents or synthesis pathways.
  • Opponents or generic challengers could file post-grant oppositions or invalidation claims if prior art surfaces.

4. Legal and Market Implications

  • The patent, valid until approximately 20 years from filing (assuming a 10-year patent term from the application date), can serve as a formidable barrier to generic entry.
  • The scope often guides licensing negotiations and partnership developments.

Conclusion

KR20200131351 appears to be a carefully drafted patent aimed at protecting a novel chemical entity or therapeutic method. Its scope, determined by specific structural claims, provides a robust barrier to competitors, depending on its breadth and the comprehensiveness of its claims. The patent landscape indicates a strategic filing, with potential overlaps or related patents in international jurisdictions, emphasizing the importance of a comprehensive patent clearance and freedom-to-operate analysis.


Key Takeaways

  • The patent's scope centers on specific chemical structures or therapeutic methods, with narrower claims potentially limiting broad protection.
  • Its position within the patent landscape underscores the importance of analyzing related patents in multiple jurisdictions.
  • Maintaining a global patent portfolio enhances market exclusivity and strategic value.
  • Competitors should scrutinize claim language for potential design-around opportunities.
  • Regular monitoring for patent extensions, oppositions, or invalidations is vital to sustaining patent rights.

Frequently Asked Questions

1. What is the primary inventive element of KR20200131351?
It likely covers a novel chemical compound or specific formulation with therapeutic use, characterized by unique structural features or a new method of medical application.

2. How broad are the claims in KR20200131351?
The claims are probably structurally specific, potentially limiting protection to particular derivatives or forms, which influences the scope's breadth and enforceability.

3. How does KR20200131351 fit within the global patent strategy?
It may be part of a broader patent family filed in multiple jurisdictions, forming a core element of a multinational patent strategy for exclusive commercialization.

4. Can competitors modify the claimed compound to avoid infringement?
Yes, if the claims are narrow, competitors can alter substituents or synthesis methods; broader claims mitigate this risk but are more challenging to obtain.

5. What are the implications for generic drug entrants?
The patent effectively blocks generic entry into the South Korean market until its expiry unless challenged or invalidated.


References

  1. South Korea Intellectual Property Office (KIPO) patent database.
  2. Patent KR20200131351 published information and claims analysis.
  3. International patent classification and patent landscape reports related to pharmaceutical compounds.

Note: The specific structural details, claims, and claims dependencies depend on the official patent document, which should be reviewed for an in-depth legal and technical examination.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.