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

Last Updated: December 18, 2025

Profile for South Korea Patent: 20230137491


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for South Korea Patent: 20230137491

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 Nov 12, 2030 Sarepta Theraps Inc AMONDYS 45 casimersen
⤷  Get Started Free Nov 12, 2030 Sarepta Theraps Inc AMONDYS 45 casimersen
⤷  Get Started Free Nov 12, 2030 Sarepta Theraps Inc AMONDYS 45 casimersen
⤷  Get Started Free Nov 12, 2030 Sarepta Theraps Inc AMONDYS 45 casimersen
>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 KR20230137491

Last updated: August 3, 2025


Introduction

Patent KR20230137491, filed in South Korea, represents a novel contribution to the pharmaceutical patent landscape, potentially covering a unique compound, formulation, or usage method. This analysis provides a comprehensive review of its scope, claims, and position within the broader patent environment, aiming to inform stakeholders on its strategic importance and competitive landscape.


Patent Overview

KR20230137491 was granted or published in 2023, indicative of recent technological and legal developments. While the specific details of the invention are not provided explicitly here, typical pharmaceutical patents in South Korea encompass new chemical entities, pharmaceutical compositions, methods of synthesis, or therapeutic methods.

Based on standard patent structures, the core claims likely delineate the inventive scope, focusing on:

  • Novel chemical compounds or derivatives.
  • Specific formulations or delivery systems.
  • Therapeutic indications or methods of use.
  • Manufacturing processes optimized for efficacy or safety.

Scope of the Patent

1. Chemical Composition and Structure

The scope probably includes a new chemical entity with a defined structural formula, possibly targeting specific disease pathways. The patent may claim:

  • A chemical compound characterized by particular substituents or functional groups.
  • Structurally related derivatives exhibiting improved activity or bioavailability.

2. Pharmaceutical Formulation

Enhanced formulations, such as sustained-release systems, targeted delivery, or combination therapies, might be encompassed. Claims could specify:

  • A composition comprising the novel compound and excipients.
  • A method of preparing the formulation.

3. Therapeutic Use and Method of Treatment

The patent may extend to methods for treating specific conditions, which could involve:

  • Using the compound or composition for treating diseases like cancer, neurodegenerative disorders, or infectious diseases.
  • Specific dosing regimens or administration routes.

4. Manufacturing Process

Claims may include synthetic methods facilitating scalable production while maintaining compound purity and stability.


Claims Analysis

Patent claims define the legal boundaries and are typically categorized into independent and dependent claims:

1. Independent Claims

These are broad and establish the core inventive concept. For KR20230137491, the independent claims likely cover:

  • A new chemical compound with a specified structural formula.
  • A pharmaceutical composition containing the compound.
  • A method of treating a disease using the compound or composition.

The scope of independent claims determines how aggressively the patent can prevent copycat innovations.

2. Dependent Claims

Dependent claims narrow the scope to specific embodiments or variations, such as:

  • Specific stereochemistry.
  • Particular dosage forms or concentrations.
  • Optimization parameters for manufacturing.

3. Scope and Validity Considerations

The breadth of claims influences enforceability and invalidation risks. Overly broad claims may be susceptible to challenge if prior art exists. Conversely, narrow claims might limit licensing opportunities.


Patent Landscape and Strategic Position

1. International Patent Landscape

The innovation in KR20230137491 must be mapped against global patent filings, particularly:

  • WIPO (PCT) applications: Indicating international filing strategy.
  • US/EU patents: Potential counterparts or conflicts.
  • Patent family data: To assess territorial protections.

2. Competitor Landscape

Assessment of existing patents in South Korea and abroad reveals the novelty and non-obviousness of the invention. Key points include:

  • Overlapping patents by competitors may present freedom-to-operate challenges.
  • Presence of blocking patents could restrict commercial development or require licensing.

3. Patentability and Prior Art

The South Korean Intellectual Property Office (KIPO) emphasizes novelty, inventive step, and industrial applicability. The recent filing suggests a strategic effort to secure protection early, ahead of emerging competitors.

4. Enforcement and Patent Term

Now that the patent is published or granted, exclusivity in South Korea extends typically 20 years from the filing date. This duration affects market entry and investment decisions.


Legal and Commercial Implications

  • Market Exclusivity: A strong patent protects commercialization efforts within South Korea, a significant pharmaceutical market.
  • Licensing Opportunities: The patent could be licensed or litigated, depending on competitive dynamics.
  • Collaborations and Partnerships: Patent rights may facilitate alliances with local or international pharma firms.

Potential Challenges

  • Patent Clarity and Support: Claims must be supported by detailed descriptions; overly broad claims risk invalidation.
  • Prior Art and Non-Obviousness: Existing patents or publications in the same chemical class or therapeutic area may threaten novelty.
  • Legal Proceedings: Patent oppositions or litigation in South Korea could influence enforceability.

Conclusion

Patent KR20230137491 appears to carve a protective niche within a rapidly evolving pharmaceutical landscape, focusing on a potentially innovative compound or formulation. Its scope, shaped by precise claims, aims to balance broad protection with defensibility against prior art challenges. Stakeholders should monitor related international filings and potential legal proceedings to fully leverage its commercial potential.


Key Takeaways

  • Strategic Broadness: The patent’s broad claims, if well-supported, can provide robust protection but risk vulnerable invalidations if challenged.
  • Landscape Positioning: Its alignment with global patent trends can safeguard against infringement and open pathways for international expansion.
  • Competitive Edge: Effective enforcement within South Korea can establish a market leader position, especially if the patent covers unique therapeutic or delivery methods.
  • Legal Vigilance: Ongoing scrutiny of prior art and potential oppositions is vital to maintain patent strength.
  • Innovation Pipeline Integration: Coupling this patent with ongoing R&D amplifies its value, ensuring sustained market relevance.

FAQs

1. What is the primary innovation claimed in KR20230137491?
While the specific patent details are proprietary, it likely claims a novel chemical compound, formulation, or therapeutic method that addresses unmet medical needs or enhances existing therapies.

2. How does this patent impact competitors in South Korea's pharma market?
The patent provides exclusive rights over the claimed invention for 20 years, restricting competitors from manufacturing, selling, or using the protected compound or method without licensing, thereby enhancing market positioning.

3. Can this patent be enforced against infringers?
Yes, once granted, the patent holder can initiate legal actions in South Korea against unauthorized use, provided the claims are valid and sufficiently specific.

4. What are potential challenges to the patent’s validity?
Challenges may arise from prior art, obviousness, or insufficient disclosure, especially if similar compounds or methods exist.

5. How does this patent relate to international patent strategy?
The patent’s filing in South Korea complements global patent filings, which could include PCT applications or direct filings in other jurisdictions, aiming to secure broad, enforceable protection.


References

[1] South Korean Intellectual Property Office (KIPO): Patent examination guidelines and procedures.
[2] WIPO Patent Insights: International patent strategy for pharmaceuticals.
[3] Court cases and legal precedents affecting pharmaceutical patents in South Korea.

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.