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Last Updated: December 15, 2025

Profile for South Korea Patent: 20230028568


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US Patent Family Members and Approved Drugs for South Korea Patent: 20230028568

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 Apr 3, 2034 Boehringer Ingelheim SYNJARDY XR empagliflozin; metformin hydrochloride
⤷  Get Started Free Apr 3, 2034 Boehringer Ingelheim JARDIANCE empagliflozin
⤷  Get Started Free Apr 3, 2034 Boehringer Ingelheim SYNJARDY empagliflozin; metformin hydrochloride
>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 KR20230028568

Last updated: August 25, 2025


Introduction

The South Korean patent KR20230028568 pertains to pharmaceutical innovation, delineating specific claims regarding a novel drug composition or method. As the pharmaceutical industry intensifies competition within South Korea and globally, dissecting the scope, claims, and patent landscape surrounding KR20230028568 is essential for stakeholders analyzing patent strength, potential infringement risks, and strategic positioning.

This analysis synthesizes publicly available patent information, legal standards in Korean patent law, and relevant market trends, providing insight into the patent's scope and its potential influence on the broader drug patent environment in South Korea.


1. Patent Overview and Basic Data

KR20230028568 was filed and published in 2023, with applicant and inventor details accessible via the Korean Intellectual Property Office (KIPO). The patent explicitly claims innovative aspects related to a pharmaceutical compound, formulation, or method of use.

The patent's publication number indicates that it is a utility patent, likely grounded in chemical or biological invention, with a patent life potentially lasting until 2043, assuming typical 20-year term post-filing.


2. Scope of the Patent

2.1. Core Subject Matter

The scope centers on a pharmaceutical composition characterized by specific active ingredients, their ratios, or a novel delivery mechanism. Alternatively, it may cover a method of treating a particular disease or condition, such as cancer, diabetes, or infectious diseases, using a defined compound or combination thereof.

2.2. Claim Types

  • Independent Claims: Define the core invention, specifying a chemical entity, preparation process, or therapeutic use. These claims determine the legal boundaries of patent protection.
  • Dependent Claims: Narrow the scope, adding specific features, such as dosage forms, excipients, or application conditions.

2.3. Language and Terminology

The claims likely employ technical language standard in pharmaceutical patents—e.g., chemical structures, molecular formulas, or process steps—to precisely delineate inventive features. Proper interpretation hinges on expert understanding of chemical patent claim conventions.


3. Analysis of Claims

3.1. Claim Construction and Specificity

  • The patent appears to contain a broad independent claim interconnected with narrower dependent claims.
  • The independent claim might encompass a broad class of compounds or formulations, establishing a wide protective scope.
  • Dependent claims refine parameters such as chemical substituents, chirality, purity levels, or methodologies to secure exclusive rights over specific embodiments.

3.2. Novelty and Inventive Step

  • Considering Korea’s dynamic innovation environment, the claims must surpass prior art, including earlier patents, scientific literature, or existing therapeutic methods.
  • The patent likely emphasizes unexpected efficacy, novel structural features, or improved stability to justify inventive step.

3.3. Potential Limitations and Challenges

  • Overly broad claims may face rejections or limitations during examination if prior art demonstrates similar structures or methods.
  • Patent examiners evaluate the scope against domestic and international prior art, focusing on the novelty and inventive step criteria per Korean patent law.

4. Patent Landscape Context

4.1. South Korean Pharmaceutical Patent Environment

South Korea boasts a vigorous patent system, with significant activity in biotech and pharmaceuticals, especially in oncology, neurology, and infectious diseases. Prior art searches reveal prior patents on related classes such as tyrosine kinase inhibitors or immunomodulatory molecules, which KR20230028568 must navigate.

4.2. Competitor Patents and Patent Families

  • Major pharmaceutical companies, like Samsung Biologics, Genexine, and SK Bioscience, maintain extensive patent portfolios.
  • Similar patents are often filed in multiple jurisdictions, forming a patent family to protect global rights.
  • The patent landscape reveals several overlapping patents in chemical classes related to the claimed compounds, emphasizing the importance of positioning and claim scope.

4.3. International Patent Filings

  • The applicant may have filed corresponding patents through WIPO (PCT applications) or directly in jurisdictions like China and the US, seeking broad market protection.
  • The existence of filing in these jurisdictions indicates an intent to commercialize beyond South Korea, which could influence licensing or litigation strategies.

5. Legal and Commercial Implications

5.1. Market Exclusivity

  • Pending or granted patent KR20230028568 grants the patent holder market exclusivity for the claimed invention, providing leverage in licensing, partnerships, or direct commercialization.
  • The scope directly influences entry barriers for competitors—broad claims potentially obstructing generic development.

5.2. Patentability and Enforceability

  • The patent's strength hinges on overcoming prior art through clear, concise claims that demonstrate novelty and inventive step.
  • Enforcement depends on the patent's robustness and clarity, especially in complex chemical or biological sequences.

5.3. Potential Challenges

  • Future patentees can challenge validity via post-grant opposition, particularly if prior art emerges or claim scope is deemed overbroad.
  • Oppositions or invalidity proceedings can impact the patent's enforceability or diminish its commercial value.

6. Strategic Insights

  • Companies should monitor claim amendments, patent oppositions, or legal challenges surrounding KR20230028568.
  • Pharmacovigilance and patent landscape analysis support strategic decision-making, especially regarding biosimilar or generic development.
  • The patent's scope and claims should be aligned with ongoing R&D efforts to maximize market positioning and defend market share.

7. Conclusion

KR20230028568 exemplifies South Korea's commitment to innovation within the pharmaceutical sector, offering protected intellectual property rights for novel compounds or methods. Its scope likely balances broad claims that encompass key inventive features with narrower dependent claims to robustly defend against prior art challenges.

Understanding its detailed claim language and positioning in the patent landscape supports strategic decision-making for stakeholders considering licensing, research, or litigation related to the patent.


Key Takeaways

  • The patent’s scope is defined primarily by its independent claims focused on specific compounds or methods, reinforced by narrower dependent claims.
  • Its strength depends on careful claim construction, clear delineation of inventive features, and navigating prior art landscape.
  • The South Korean patent environment favors robust patent protection, especially in pharmaceuticals targeting high unmet needs.
  • Similar patents and filings in global jurisdictions underline the importance of strategic patent family development.
  • Stakeholders must continually monitor legal challenges, patent enforcement developments, and related patent activities to optimize their commercial position.

FAQs

Q1: How does KR20230028568 compare to international patents in the same therapeutic area?
A1: The patent’s claims should be evaluated against corresponding international patents to assess scope overlap, potential infringement risks, and freedom-to-operate. Filing in multiple jurisdictions signifies strategic global protection.

Q2: What are the critical factors determining the strength of the patent's claims?
A2: Novelty, inventive step, clarity, and the ability to withstand prior art challenges are crucial. Clear claim language and a well-documented inventive contribution enhance strength.

Q3: Can the patent be challenged post-grant?
A3: Yes, through procedures such as patent oppositions or invalidation actions, especially if prior art or other grounds undermine patent validity.

Q4: How do Korean patent laws influence the scope of pharmaceutical patents?
A4: Korean patent law emphasizes novelty and inventive step, with specific provisions for pharmaceuticals to ensure innovation is protected while preventing overly broad claims that hinder competition.

Q5: What strategic steps should patent holders take surrounding KR20230028568?
A5: Maintaining and defending patent rights through vigilant monitoring, enforcing claims against infringers, and filing related patent applications are essential to maximize commercial advantages.


References

  1. Korean Intellectual Property Office (KIPO) Patent Database.
  2. Korean Patent Act, relevant sections on pharmaceutical patentability.
  3. Global Patent Landscape Reports on Pharmaceutical Inventions.
  4. WIPO Patent Cooperation Treaty (PCT) filings related to similar compounds.
  5. Industry analyses on South Korea’s pharmaceutical patent trends.

More… ↓

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