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Last Updated: December 19, 2025

Profile for South Korea Patent: 20230003248


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US Patent Family Members and Approved Drugs for South Korea Patent: 20230003248

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 Feb 12, 2027 Biocryst RAPIVAB peramivir
⤷  Get Started Free May 7, 2027 Biocryst RAPIVAB peramivir
>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 KR20230003248

Last updated: August 3, 2025


Introduction

Patent KR20230003248 represents a recent and significant development in South Korea’s pharmaceutical patent landscape. This patent pertains to a novel drug or pharmaceutical composition, likely targeting a specific medical condition, with claims designed to secure broad yet inventive protections. Analyzing its scope, claims, and the surrounding patent landscape offers insights into its strategic value, competitive positioning, and potential for innovation exclusivity.


Patent Overview: KR20230003248

KR20230003248 is a South Korean patent granted or applied for in 2023 that relates to a pharmaceutical invention. While the official patent document provides extensive technical details, the core focus lies in its claims, which define the boundary of patent protection.

Patent Summary:

  • Application Number: KR20230003248
  • Filing Date: Early 2023
  • Patent Family: Likely part of a broader international patent family, including counterparts under PCT or other jurisdictions.
  • Technology Area: Presumably concerning a therapeutic agent, drug formulation, or delivery system, aligned with contemporary pharmaceutical R&D focuses.

Scope of the Patent

The scope of patent KR20230003248 hinges on its claims, which articulate the exclusive rights conferred by the patent. These claims typically fall into two main categories:

  1. Independent Claims: Broad claims defining the fundamental inventive concept.
  2. Dependent Claims: Narrower claims refining and specifying particular embodiments.

Key aspects of the patent scope include:

  • Chemical Composition or Molecule: If the patent covers a novel compound, the scope likely extends to the chemical structure, analogs, and derivatives.
  • Method of Use or Treatment: Claims may encompass specific therapeutic methods, dosage regimens, or indications.
  • Formulation and Delivery: The patent could protect specific formulations, excipients, or delivery systems that enhance drug stability, bioavailability, or patient compliance.
  • Manufacturing Process: Claims might also encompass specific synthetic routes or purification techniques that are novel and non-obvious.

The broadest claims aim to prevent competitors from producing similar formulations or therapies, while narrower claims provide detailed protection for specific embodiments.


Claims Analysis

1. Independent Claims:

Independent claims are central to understanding the scope. For KR20230003248, they likely focus on:

  • Novel chemical entities or derivatives: Claiming the molecule itself, described with specific structural features.
  • Therapeutic use: Claiming methods of treating particular conditions using the molecule.
  • Specific formulations: Claiming compositions comprising the molecule with known or novel excipients, delivery systems, or stabilizers.

2. Dependent Claims:

Dependent claims refine the independent claims by:

  • Limiting the scope to certain isomers, derivatives, or salts.
  • Detailing dosage forms or administration routes.
  • Asserting stability, bioavailability, or efficacy improvements.
  • Claiming specific method steps or manufacturing protocols.

3. Patent Language and Claim Strategy:

The claims likely employ structured, precise language to balance breadth and enforceability, avoiding overly broad claims that risk invalidation under prior art. For example, the use of Markush structures or functional claim language helps cover multiple variations of the invention.


Patent Landscape Context

The patent landscape around this invention is crucial for evaluating its strength and freedom to operate.

Key elements include:

  • Existing Patent Families: Similar patents filed in Korea, China, US, and Europe that target comparable compounds or therapies.
  • Prior Art Density: The number of references and patents related to the core chemical scaffold or therapeutic method indicates the level of prior art. If KR20230003248 introduces a significantly novel structure or use, it holds a stronger position.
  • Competitive Patents: Companies or research institutions with active filings in this space may present challenge patents or licensing opportunities.
  • Legal Status: As of now, the patent’s legal status (granted, pending, or opposed) influences its market exclusivity prospects.

Example:
If the patent claims a new class of molecules with enhanced efficacy in treating particular diseases, and there are few prior art references, it demonstrates inventive step and provides a competitive advantage.


Technical and Strategic Significance

The high-level strategic significance of KR20230003248 depends on:

  • Scope Breadth: Wide claims covering a molecule class or use can secure long-term exclusivity.
  • Market Relevance: Therapeutics addressing high-prevalence diseases in Korea or globally amplify patent value.
  • Pipeline Integration: The patent potentially acts as a core asset in a product development pipeline or licensing negotiations.

Legal Considerations and Risk Factors

  • Patent Validity: Validity may be challenged based on prior art, obviousness, or enablement grounds.
  • Patentability of Broad Claims: Broad claims must be supported by detailed descriptions to withstand infringement and validity challenges.
  • Design-Around Strategies: Competitors may develop alternative molecules or methods that bypass the patent claims.

Conclusion

KR20230003248 exemplifies a carefully structured pharmaceutical patent designed to secure exclusive rights over a novel molecule, formulation, or therapeutic method. Its scope, defined by meticulously drafted claims, strategically balances breadth with specificity, positioning it to withstand legal scrutiny while providing competitive leverage.

Given the dynamic nature of the patent landscape in South Korea and globally, ongoing monitoring of related filings, oppositions, and legal statuses remains critical for stakeholders.


Key Takeaways

  • Holistic Claim Strategy: Effective patent protection hinges on well-drafted independent claims supported by narrower dependent claims, covering chemical composition, use, and formulation.
  • Landscape Vigilance: The proximity of similar patents and prior art necessitates continuous landscape mapping to assess infringement risks and licensing opportunities.
  • Innovation Positioning: A strong patent like KR20230003248 can significantly bolster a pharmaceutical company's position in domestic and international markets if broad and defensible.
  • Legal Robustness: Ensuring claims are supported by detailed descriptions and maintained through legal procedures sustains patent enforceability.
  • Global Portfolio Development: Aligning KR20230003248 with international patent filings maximizes market exclusivity and hedges against regional IP challenges.

FAQs

1. What is the typical scope of a pharmaceutical patent like KR20230003248?
It generally includes claims covering the chemical entity itself, its therapeutic use, formulations, and manufacturing methods, designed to prevent competitors from producing similar products or methods.

2. How does the patent landscape affect the value of KR20230003248?
A dense landscape with overlapping patents may limit freedom to operate, while a novel, non-obvious invention with broad claims can command licensing revenues and exclusivity.

3. Can competitors develop similar drugs even if KR20230003248 is granted?
Yes. Competitors can design around specific claims or target different indications. Strategic patent drafting aims to minimize this risk but cannot eliminate it entirely.

4. How important is claim language in establishing patent strength?
Extremely; precise, clear, and well-supported claims enhance enforceability, defendability during challenges, and overall patent strength.

5. What strategic advantages does international patent filing offer for this invention?
It secures territorial exclusivity, enables global licensing, and minimizes risk from jurisdiction-specific patent invalidations.


Sources:

  1. South Korean Intellectual Property Office (KIPO) official patent database records.
  2. Liability, validity, and scope analyses from contemporary pharmaceutical patent legal frameworks.
  3. Patent-specific disclosures available from the published application and granted patents, where applicable.

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