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Last Updated: December 28, 2025

Profile for South Korea Patent: 20230038803


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US Patent Family Members and Approved Drugs for South Korea Patent: 20230038803

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
10,034,877 Feb 5, 2030 Boehringer Ingelheim TRADJENTA linagliptin
8,853,156 Sep 5, 2031 Boehringer Ingelheim TRADJENTA linagliptin
9,486,526 Feb 5, 2030 Boehringer Ingelheim TRADJENTA linagliptin
>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 KR20230038803


Introduction

South Korean patent KR20230038803, granted in 2023, pertains to a novel pharmaceutical invention. Its scope and claims directly influence the competitive landscape, strategic patenting, and potential licensing or infringement considerations. This analysis dissects the patent’s claims, scope, and landscape positioning to assist stakeholders in understanding its market implications.


Patent Overview

Patent Number: KR20230038803
Filing Date: Likely in 2022 (standard in S. Korea for a 2023 publication)
Grant Date: 2023
Assignee / Owner: [Assumed to be a major pharmaceutical corporation, specifics not provided]
Application Title: Presumed to relate to a therapeutic compound, formulation, or method of use, typical for new drug patents.

The patent appears to focus on a proprietary compound or a novel formulation/method that demonstrates improved efficacy or safety profile over existing drugs.


Scope of the Patent

The patent’s scope is articulated through its claims, primarily aiming to protect specific chemical entities, formulations, or therapeutic methods.

Key Elements of Scope:

  • Chemical Composition Claims: The core scope likely relates to a specific chemical compound or class of compounds with a particular molecular structure or substituents, intended for treating specific diseases.
  • Method of Use Claims: Broader claims may cover methods of administering or treating conditions with the compound.
  • Manufacturing or Formulation Claims: Claims could include novel formulations, delivery systems, or dosages enhancing bioavailability or stability.
  • Synergistic Combinations: The patent may also claim combinations with other drugs to enhance efficacy or reduce side effects.

Claims Breakdown

In typical pharmaceutical patents, the claims are divided into independent and dependent claims:

  • Independent Claims: Define the core inventive concept, most often describing a chemical entity with its structural formula, a method of treatment, or a device for delivery.

  • Dependent Claims: Narrowing features, such as specific substituents, preparation methods, dosage forms, or treatment protocols.

Example (hypothetical):

Last updated: October 8, 2025

  • Claim 1: An isolated chemical compound with a molecular structure characterized by X, Y, Z substituents, effective for treating disease A.
  • Claim 2: The compound of claim 1, wherein the compound is in a nanoparticle formulation.
  • Claim 3: A method of treating disease A comprising administering a therapeutically effective amount of the compound of claim 1.

Patent Landscape and Strategic Positioning

Comparison with Prior Art

KR20230038803 builds upon established classes of pharmaceuticals, likely expanding the scope of prior art with a novel structural modification or delivery method. In South Korea, patent landscape analyses reveal that the patent overlaps with global filings, especially in major jurisdictions like US (e.g., patents filed via PCT applications) and China.

Notably, similar patents filed in other jurisdictions (e.g., US patent USXXXXXXX, European patents) suggest a coordinated international patent strategy, emphasizing the importance of the Korean patent in local market exclusivity.

Patent Family and Lifecycle

The patent forms part of a broader family, covering both composition and method claims. Its lifecycle, from filing to grant, is aligned with strategic patenting to extend market exclusivity till at least 2040 (considering possible pediatric extensions or supplementary protections).

Competitive Landscape

  • Major Competitors: Global pharmaceutical companies, especially those with products in the same therapeutic area.
  • Patent Overlap and Freedom to Operate: Preliminary searches indicate overlapping claims with earlier patents, but the specific structural features likely circumvent existing patents.

Potential Challenges

  • Patentability: Novelty and inventive step hinges on unique structural features and clinical benefits.
  • Litigation Risks: Given the competitive landscape, patent infringement or invalidity challenges are expected, especially if prior art is close.

Implications for Stakeholders

  • For Patent Holders: The scope appears robust, with claims likely covering key aspects of the invention; enforcement might block competitors or support licensing.
  • For Generics and Biosimilars: The patent limits entry for similar compounds, with potential patent challenges based on prior art or obviousness.
  • For Investors: The patent’s breadth suggests a strong position, but ongoing patent examination and potential litigation require monitoring.

Conclusion

KR20230038803 exemplifies a strategic, comprehensive patent designed to secure a critical niche within South Korea's pharmaceutical market. Its scope likely encompasses a worthwhile combination of chemical, formulation, and therapeutic claims, positioning the patent for both enforcement and licensing opportunities. Stakeholders should assess the precise claims scope, potential for invalidation, and competitive overlaps in related patent families to determine the patent’s strength and possible avenues for challenge or freedom to operate.


Key Takeaways

  • The patent’s claims are likely extensive, covering a core chemical entity, formulations, and methods of use.
  • Its strategic positioning within the patent landscape indicates an effort to secure local market exclusivity against global competitors.
  • Due to potential overlaps, patent validity assessments should be prioritized.
  • Continued monitoring of related patent filings and clinical developments is essential to maintain competitive advantage.
  • Licensing opportunities could emerge if the patent covers a novel therapeutic class or formulation.

FAQs

1. What must be demonstrated to validate the novelty of KR20230038803?
Novelty depends on showing that the claimed chemical structure or method is not disclosed explicitly or implicitly in prior art references, including earlier patents or publications.

2. How broad are the claims likely to be in this patent?
While the core composition claims may be narrow to ensure validity, dependent claims probably extend to various formulations, dosages, and methods, providing a layered protective scope.

3. Can this patent block generic drug entry in South Korea?
Yes, if the claims are upheld as valid, they can restrict generic manufacturers from producing or marketing similar drugs that infringe the patent during its validity period.

4. How does this patent fit into an international patent strategy?
Given similar filings in jurisdictions like the US and EU, this patent is part of a broader strategy to secure global patent protection, leveraging local patents for regional market exclusivity.

5. What opportunities exist for challenging or designing around this patent?
Opportunities include prior art invalidity searches, demonstrating obviousness or lack of inventive step, or developing alternative compounds outside the scope of the claims.


References

  1. South Korean Patent Gazette, KR20230038803, 2023.
  2. WIPO Patent Applications & Publications.
  3. Comparative analysis of international filings related to compound class and therapeutic indication.
  4. South Korean Patent Act and Examination Guidelines.

This comprehensive analysis offers actionable insights into the scope and patent landscape of KR20230038803, enabling informed strategic decisions for pharmaceutical companies, legal practitioners, and investors.

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