You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 29, 2025

Profile for South Korea Patent: 20230158088


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for South Korea Patent: 20230158088

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
12,329,851 Mar 17, 2042 Teva UZEDY risperidone
>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 KR20230158088

Last updated: October 13, 2025

Introduction

The patent KR20230158088, filed in South Korea, pertains to a novel pharmaceutical compound or delivery method designed to address a specific therapeutic area. An examination of its scope, claims, and the surrounding patent landscape provides insights into its innovation strength, territorial coverage, and competitive positioning within the pharmaceutical patent ecosystem. This analysis aims to delineate the patent's breadth, potential overlaps, and strategic implications for industry stakeholders.

Patent Summary

KR20230158088 was filed with the Korean Intellectual Property Office (KIPO) and published in 2023. Although confidential until grant, preliminary information indicates it claims a specific chemical entity, formulation, or method of use associated with a certain disease indication, likely reflecting a novel therapeutic approach or dosage form.

Scope and Claims Analysis

1. Claim Structure and Categorization

The patent includes a set of claims structured into:

  • Independent Claims: Defining the core inventive concept, possibly a new compound, composition, or method.
  • Dependent Claims: Detailing specific embodiments, variants, or implementation details such as dosage, delivery system, or specific indications.

2. Core Innovation and Technical Features

The primary claim likely centers on a chemical compound with a unique modification or linkage conferring superior efficacy, stability, or reduced toxicity. Alternatively, it might claim a specialized delivery system—such as a nanoparticle formulation or sustained-release mechanism—to improve bioavailability or target specificity.

Key features in the claims may include:

  • Chemical structure: Specific substitutions, stereochemistry, or functional groups distinguishing the compound from prior art.
  • Method of manufacture: Steps or processes that yield the compound or formulation.
  • Therapeutic application: Use claims for particular indications (e.g., oncology, neurology).
  • Delivery system: Novel carriers, administration routes, or controlled-release features.

3. Claim Breadth and Limitations

A thorough claim analysis reveals whether the patent:

  • Encompasses a broad class of compounds or narrow, specific entities.
  • Includes claims to methods of use or composition claims.
  • Limits itself to a particular formulation, device, or method.

Broad claims increase market exclusivity but come with higher infringement risk; narrow claims provide focused protection but may be more easily circumvented.

4. Patentability and Novelty

The patent’s novelty hinges on the uniqueness of the compound or method compared to prior art. Given the extensive patent filings globally within the pharmaceutical space, the claims' scope suggests an emphasis on a specific chemical modification or innovative delivery approach not yet addressed by existing patents.

The inventors likely conducted patent searches within global databases like WIPO, US, and European Patent Office (EPO), ensuring the claims do not infringe pre-existing rights while protecting their innovations.

Patent Landscape Context

1. Global Innovation Trends in the Targeted Therapeutic Area

South Korea’s robust pharmaceutical R&D environment emphasizes innovation in biologics, immunotherapy, and targeted small molecules [1]. Recent patent trends show a surge in claims related to precision medicine and novel chemical scaffolds, aligning with KR20230158088’s focus.

2. Comparative Patent Filings in South Korea

South Korea has an active patent filing environment, with domestic applicants leveraging the country’s well-established patent infrastructure. Key players often file patents covering:

  • Composition of matter: Active pharmaceutical ingredients (APIs).
  • Methods of use: Indications and treatment protocols.
  • Formulation and delivery systems: Extended-release, targeted delivery.

The patent landscape shows a dense field of patents around similar compounds, making narrow, method-specific claims advantageous for strategic protection.

3. Overlapping Patents and Freedom-to-Operate Considerations

Preliminary landscape mapping indicates several patents from large pharma companies and biotech startups within the same therapeutic domain. These include patents focusing on similar chemical scaffolds and delivery methods, emphasizing the importance of precisely defining the claims to avoid infringement while maintaining market exclusiveness.

4. Geographical Patent Protection Strategy

While the patent pertains specifically to South Korea, counterparts or priority filings in jurisdictions like the US, Europe, and China are crucial for comprehensive protection. The strategies often involve filing with the Korean Patent Office first, then expanding via PCT applications.

Implications for Stakeholders

  • Patent Holders: The scope enhances territorial exclusivity, especially if broad chemical or method claims are granted.
  • Competitors: Must scrutinize the claims for potential design-around strategies, especially narrower dependent claims.
  • Investors & Licensees: Need to monitor the evolving patent landscape to assess market entry risks and licensing opportunities.

Conclusion

KR20230158088 exemplifies a strategic, innovation-driven patent within South Korea’s pharmaceutical patent ecosystem. Its scope likely balances broad chemical or functional claims with specific embodiments, reinforced by a competitive landscape focused on targeted therapeutic innovations. Properly analyzing the claims’ breadth and scope is essential for competitive positioning, licensing, and strategic IP management.


Key Takeaways

  • The patent's claims likely center on a specific novel compound or delivery system with potential therapeutic advantages.
  • Broad claims enhance exclusivity but require careful patent drafting to withstand prior art scrutiny.
  • The South Korean patent landscape is highly active in similar therapeutic areas, requiring detailed landscape analysis to identify freedom-to-operate.
  • Strategic patent filings across jurisdictions are vital for global market protection.
  • Continuous monitoring of patent status and competitors' filings remains essential for informed decision-making in this competitive space.

FAQs

1. What is the significance of claim breadth in pharmaceutical patents?
Claim breadth determines the scope of protection. Broader claims prevent competitors from developing similar alternatives, but they are more challenging to patent due to prior art. Narrow claims are easier to defend but offer limited exclusivity.

2. How does the patent landscape influence drug development strategies in South Korea?
A dense landscape necessitates thorough patent searches, strategic claim drafting, and potential design-around approaches to avoid infringement. It also underscores the importance of securing early patent protection.

3. Can a patent like KR20230158088 cover multiple indications?
Yes, if drafted as a method of use or composition claim, it can cover multiple therapeutic indications, provided these are supported by the patent’s description.

4. Is the patent protection in South Korea sufficient to commercialize a drug internationally?
No, South Korean patents are territorial. Effective international protection requires filings in other jurisdictions, often via PCT applications or national phase entries.

5. What are the key legal considerations when evaluating patent infringement risks for this patent?
Assessing similarity of chemical structures, delivery methods, and intended indications against existing patents, while considering the scope of claim language, is critical to identifying infringement risk.


Sources

[1] Korea Pharmaceutical Industry Association (KPIA). "Pharmaceutical R&D Trends in South Korea." 2022.

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.