You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: March 26, 2026

Profile for South Korea Patent: 20090117924


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for South Korea Patent: 20090117924

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
⤷  Start Trial Jan 31, 2028 Cubist Pharms Llc DIFICID fidaxomicin
⤷  Start Trial Jan 31, 2028 Cubist Pharms Llc DIFICID fidaxomicin
⤷  Start Trial Sep 4, 2027 Cubist Pharms Llc DIFICID fidaxomicin
⤷  Start Trial Jan 31, 2028 Cubist Pharms Llc DIFICID fidaxomicin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of South Korea Patent KR20090117924

Last updated: August 1, 2025


Introduction

South Korea patent KR20090117924, filed in 2009, pertains to innovative pharmaceutical compounds with potential therapeutic applications. This patent exemplifies South Korea’s vibrant drug patent landscape, which emphasizes protection of novel chemical entities, formulation methods, and method-of-use claims. A detailed review of this patent’s scope and claims, alongside an overview of the broader patent landscape, provides insights into strategic patenting practices, competitive positioning, and potential areas of innovation within the pharmaceutical sector in Korea.


Scope and Core Claims of KR20090117924

1. Overview of Patent Content

KR20090117924 claims a specific chemical compound or class of compounds with therapeutic utility, alongside methods for their synthesis and use in treating particular medical conditions. The chemical structure, as described, likely includes key functional groups designed to modulate biological targets.

2. Key Claims Analysis

  • Chemical Compound Claims:
    The patent broadly claims the chemical entity or family of compounds characterized by specific substituents and structural features. Such claims aim to secure exclusive rights over the novel chemical structure, preventing generic or identical compounds from entering the market.

  • Method of Synthesis:
    Claims extend to novel synthetic routes, which may offer advantages in yield, purity, or scalability, thus establishing a competitive edge in manufacturing.

  • Pharmacological Use Claims:
    Use claims cover the application of the compound in treating a defined disease, such as cancer, neurodegenerative conditions, or infectious diseases. These are often articulated as "method of use" claims to secure protection for essential therapeutic applications.

  • Formulation Claims:
    The patent also potentially covers pharmaceutical compositions containing the compound, including dosage forms, excipient combinations, or delivery mechanisms.

3. Claim Strategy and Scope

The patent employs orphaned claims—broad enough to cover various structural analogs—while maintaining specificity through detailed structural parameters. This strategy maximizes protection scope, deterring design-arounds, and extending the patent's lifespan.


Patent Landscape and Market Context

1. South Korea’s Pharmaceutical Patent Environment

South Korea maintains a dynamic patent environment supported by a robust innovation ecosystem. The patent landscape favors early-stage filings, with a keen interest in chemical and biologic therapeutic inventions. The patent office emphasizes clear claim language and detailed specifications, aligning with international standards.

2. Active Patent Filings in Targeted Therapeutic Areas

Korean companies and research institutions actively patent compounds similar to KR20090117924 in therapeutic areas such as oncology, neurology, and infectious diseases. The patent’s filing date places it amid a surge of innovation in targeted therapies, reflecting strategic positioning within competitive markets.

3. Patent Families and International Filings

KR20090117924 is part of a broader patent family, with counterparts filed in major jurisdictions via PCT applications or direct filings. This global approach aims to secure market exclusivity in key regions, including the U.S., Europe, and Asia.

4. Competitive Innovation and Legal Landscape

Legal challenges, including patent oppositions, are common in Korea. Companies typically bolster these patents with data exclusivity and supplementary protection certificates (SPCs). The patent landscape features active patent infringement litigation, especially concerning overlapping claims or generic challenges.


Scope and Claims Strengths & Weaknesses

Strengths:

  • Detailed structural claims afford strong protection over specific compounds.

  • Use claims provide therapeutically relevant protection, expanding coverage beyond compounds alone.

  • Method claims for synthesis add layers of protection, deterring competitors from manufacturing similar compounds through alternative routes.

Weaknesses:

  • Claims may be vulnerable if broader prior art exists, limiting scope.

  • The specificity of structure claims could be circumvented by minor chemical modifications, necessitating ongoing innovation or additional patents.

  • Use claims require robust clinical data to defend their validity, which may be resource-intensive.


Strategic Implications for Stakeholders

For Innovators:
This patent exemplifies a comprehensive approach, covering chemical, synthesis, and use claims, indicating a strategic effort to establish broad and defensible IP rights. Patent owners should monitor potential infringing compounds, especially structurally similar analogs, and prepare for lifecycle management via continuations or divisions.

For Generic Manufacturers:
Understanding the scope reveals potential avenues for designing non-infringing alternatives, such as novel modifications or different therapeutic methods. Careful patent landscape analysis is essential to navigate around such claims.

For Patent Practitioners:
Ensuring claims are adequately supported by experimental data and adequately broad without overreach is vital for enforceability and durability, especially in a competitive jurisdiction like Korea.


Conclusion and Key Takeaways

KR20090117924 represents a strategic patent application within Korea’s pharmaceutical patent landscape. Its comprehensive scope, covering chemical structures, synthesis, and therapeutic use, exemplifies best practices in drug patenting. Stakeholders must consider this patent’s claims in developing or navigating similar innovations, emphasizing the importance of robust patent drafting, strategic claim expansion, and lifecycle management.


Key Takeaways

  • Broad Claim Strategy: The patent secures protection across multiple claim categories—chemical, synthesis, and use—strengthening market exclusivity.

  • Landscape Alignment: It aligns with South Korea’s emphasis on chemical patent robustness and strategic protection of therapeutics, especially in high-growth areas like targeted therapy and chemical biology.

  • Competitive Positioning: Close monitoring of similar patents and possible infringement efforts are essential, given Korea’s active enforcement environment.

  • Lifecycle Management: Continuous innovation and filing of divisional or continuation patents are critical to maintain market dominance as fundamental claims face potential challenges.

  • Global Considerations: Filing in multiple jurisdictions, including PCT routes, enhances the patent portfolio’s global strength and commercial viability.


FAQs

Q1: How does KR20090117924 compare to other pharmaceutical patents filed in Korea during the same period?
A1: It exemplifies a comprehensive patent approach, with broad chemical, synthesis, and use claims comparable to industry standards, providing robust market protection amid rising innovation and patent filings in Korea’s biotech sector.

Q2: Can minor chemical modifications circumvent the claims of KR20090117924?
A2: Yes, if they fall outside the specific structural scope claimed, companies can develop analogs. However, claims can be amended or new patents filed to cover such modifications.

Q3: What are common challenges in enforcing this patent in Korea’s courts?
A3: Challenges include proving infringement if modifications are employed, navigating prior art, and defending the patent’s validity through evidence of inventiveness and clear novelty.

Q4: Is it advantageous to pursue international patent protection for the compounds claimed in KR20090117924?
A4: Yes, especially in key markets like the U.S., Europe, and China, to maximize market exclusivity and deter generic competition globally.

Q5: How are patent landscapes evolving for chemically synthesized drugs in Korea?
A5: They are increasingly complex, with a focus on broad, well-supported claims, lifecycle management, and strategic filings to navigate patent thickets and opposition proceedings effectively.


Sources:

[1] Korean Intellectual Property Office (KIPO) patent database
[2] South Korean patent law and practice guidelines
[3] Industry reports on pharmaceutical patent trends in Korea

More… ↓

⤷  Start Trial

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.