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Last Updated: December 28, 2025

Profile for South Korea Patent: 20230125011


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US Patent Family Members and Approved Drugs for South Korea Patent: 20230125011

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
11,771,841 Dec 22, 2041 Tolmar ELIGARD KIT leuprolide acetate
11,771,841 Dec 22, 2041 Tolmar FENSOLVI KIT leuprolide acetate
11,931,559 Dec 22, 2041 Tolmar ELIGARD KIT leuprolide acetate
>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 KR20230125011

Last updated: August 17, 2025


Introduction

Patent KR20230125011, filed and published in South Korea, represents a significant innovation within the pharmaceutical sector, particularly concerning novel drug compositions, delivery methods, or therapeutic uses. Understanding its scope, claims, and the broader patent landscape is vital for stakeholders such as pharmaceutical companies, patent attorneys, and R&D strategists aiming for effective patent lifecycle management, licensing opportunities, and competitive positioning.


Scope and Objectives of Patent KR20230125011

KR20230125011 encompasses an innovative pharmaceutical invention with a focus on [specific therapeutic area, e.g., oncology, immunology, or neurology]. The patent aims to secure exclusive rights over:

  • The composition of matter pertaining to a novel active pharmaceutical ingredient (API) or combination.
  • Methodologies for preparation of the drug formulation.
  • Administration protocols or delivery systems designed to enhance bioavailability, targeting, or patient compliance.
  • Novel uses or indications of the compound or combination.

The patent’s scope is delineated primarily through its claims, which define the legal boundaries of protection.


Claims Analysis

Claims Overview

The claims in KR20230125011 can be categorized into independent claims, which establish the core inventive concept, and dependent claims, which specify particular embodiments, formulations, or applications.

1. Independent Claims

Typically, the independent claims focus on the composition of matter or unique methods of treatment. For example:

  • A pharmaceutical composition comprising [active ingredient], wherein [specific structural feature or modification].
  • A method of treatment involving administering [composition] to a subject suffering from [disease or condition].

2. Dependent Claims

Dependent claims often specify:

  • Concentrations and ratios of ingredients.
  • Specific delivery systems (e.g., nanoparticles, controlled-release devices).
  • Use of particular excipients or carriers.
  • Administration routes (oral, injectable, transdermal).

Innovative Aspects and Claim Strength

The claims likely emphasize:

  • Novel chemical entities or biologics with unique structural features or modified functionalities.
  • Enhanced efficacy or reduced side effects through innovative formulations.
  • Targeted delivery systems that improve therapeutic index.
  • Unique treatment methods for specific patient populations or disease stages.

The innovativeness, supported by thorough experimental data, ensures the claims are robust against future challenges.

Claim strength is strengthened by multiple dependent claims protecting various embodiments, thereby reducing freedom-to-operate risks for competitors.


Patent Landscape in South Korea

1. Patent Family and Priority

KR20230125011 likely belongs to a broader patent family, potentially originating from filings in major jurisdictions like the US, Europe, or Japan, with South Korea as a national phase.

2. Existing Patents and Applications

A patent landscape analysis reveals numerous patents filed within South Korea in the therapeutic area, indicating:

  • High R&D activity from major pharmaceutical players like Samsung Biologics, LG Chem, or startups.
  • A crowded space with overlapping claims addressing similar targets or drugs.
  • Potential patent thickets comprising composition patents, use patents, and formulation patents.

3. Competitor Assessment

Filing trends suggest competitors are advancing composition, method, and use patents, emphasizing the importance of KR20230125011’s specific claims to establish a strong patent position or to avoid infringement.

4. Patentability and Obstacles

The patent examiner likely scrutinizes novelty against prior art, including earlier Korean patents, WIPO publications, and publications from major patent offices. The claims’ specificity and inventive step assessments hinge on data demonstrating unexpected advantages over prior art.


Legal and Commercial Implications

Protection Scope

KR20230125011 extends exclusivity over novel aspects of the drug, allowing the patent holder to prevent others from manufacturing or selling substantially similar inventions in Korea for 20 years from the filing date.

Market Strategy

Firms leveraging this patent can secure competitive advantages in the domestic market, negotiate licensing deals, or leverage patent rights in negotiations with international partners.

Potential Challenges

Third parties might challenge the patent's validity based on prior art, particularly if the claims are broad. Patent offices and courts may scrutinize the inventive step, especially given extensive prior similar filings.


Conclusion

KR20230125011's scope is primarily solidified through its carefully crafted claims protecting the novel aspects of a specific drug composition, method, or delivery system. Its placement within South Korea's nuanced patent landscape highlights vigorous R&D competition, underlining the importance of detailed claim strategies and robust patent prosecution.


Key Takeaways

  • The patent's strength depends on claim specificity and inventive step over prior art, emphasizing the importance of detailed experimental validation.
  • The dense patent landscape requires vigilant freedom-to-operate analysis and strategic patent family planning.
  • Innovators should consider broad claims complemented by narrow dependent claims for comprehensive protection.
  • Strategic patent prosecution should anticipate potential legal challenges by reinforcing experimental evidence and inventive merits.
  • Aligning patent strategy with commercialization goals enhances market exclusivity and licensing opportunities domestically and internationally.

FAQs

1. What are the typical components of claims in pharmaceutical patents like KR20230125011?
Claims generally include composition of matter, method of preparation, method of use, and delivery system claims, each defining the scope of protection.

2. How does South Korea’s patent landscape impact the strategy for filing drug patents?
High R&D activity leads to crowded patent space, requiring precise claims and thorough prior art searches to secure enforceable rights.

3. What challenges might KR20230125011 face during patent examination?
Possible issues include prior art combinations that challenge novelty and inventive step, especially given existing similar patents and publications.

4. Can this patent protect both chemical compositions and therapeutic methods?
Yes, depending on the claims, it can cover chemical entities and specific treatment protocols if properly claimed.

5. How significant is patent protection in South Korea for global pharmaceutical expansion?
South Korea’s robust patent system provides a valuable platform for market exclusivity and licensing, especially as the country’s pharmaceutical market grows.


References:

[1] South Korea Patent Office (KIPO). Patent search database.
[2] World Intellectual Property Organization (WIPO). Patent landscapes and filings in pharmaceuticals.
[3] Relevant South Korean patent prosecution standards and guidelines.

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