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

Last Updated: December 18, 2025

Profile for South Korea Patent: 20110041580


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for South Korea Patent: 20110041580

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
7,709,517 Aug 13, 2027 Astellas XTANDI enzalutamide
8,183,274 Aug 24, 2026 Astellas XTANDI enzalutamide
9,126,941 May 15, 2026 Astellas XTANDI enzalutamide
>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 KR20110041580

Last updated: August 7, 2025


Introduction

Patent KR20110041580, filed in South Korea, exemplifies the strategic approach to protecting pharmaceutical innovations within a highly competitive intellectual property environment. Analyzing the scope, claims, and patent landscape surrounding this patent provides critical insights into its scope of exclusivity, potential validity, and its positioning within the broader patent ecosystem. This assessment is particularly pertinent to stakeholders involved in drug development, licensing, and patent litigation.


Patent Overview

Patent Number: KR20110041580

Publication Date: March 31, 2011

Filing Date: August 31, 2009

Applicant: [Assumed, as the specific applicant's information isn't provided here; typically, pharmaceutical companies or research institutions]

Title: "Pharmaceutical Composition Containing a Specific Compound for Treatment of [Disease/Condition]" (hypothetical based on typical pharmaceutical patents)

Note: Precise details such as the chemical entity, therapeutic indication, and inventors would require access to the full patent document. Here, the analysis is based on typical patent structures within this context.


Scope of the Patent and Its Claims

1. Claims Analysis

The core of patent scope resides in its claims, particularly independent claims, which articulate the broadest legal rights conferred by the patent.

  • Independent Claims: Typically define the primary inventive concept—likely covering a novel pharmaceutical compound or composition, potentially with specific chemical structures or formulations.

  • Dependent Claims: Narrower and specify particular embodiments, such as dosage forms, methods of use, or specific sub-variants of the compound.

For KR20110041580, the claims likely encompass:

  • A chemical entity with a specific structural formula showing improved bioactivity or stability.

  • Pharmaceutical compositions comprising the compound, possibly with excipients, carriers, or delivery mechanisms.

  • Methodologies for treating a specific condition (e.g., cancer, infectious disease) using the compound.

Claim Language & Scope: The breadth of claims can range widely. Broad claims might cover any compound within a chemical class, while narrower claims target specific derivatives or usages. The scope depends on the language's specificity and the legal strategy to balance enforceability against patentability.

2. Patent Scope Considerations

  • The novelty and inventive step must be demonstrated relative to prior art, particularly prior patents and publications.

  • The claims likely include ranges for pharmacologically active amounts and administration routes, increasing enforceability breadth.

  • The inclusion of a specific chemical structure allows for protection of derivatives and analogs that do not significantly alter the core structure, potentially impacting freedom-to-operate.


Legal and Strategic Significance in South Korea

South Korea’s patent system recognizes pharmaceutical patents, with particular considerations for inventive step and patentable subject matter. Key aspects include:

  • Patent Term: Generally 20 years from filing date, providing substantial exclusivity for the innovator.

  • Data Exclusivity: Pharmaceutical products often benefit from data exclusivity for periods that complement patent rights, impacting generic manufacturing.

  • Patentability Criteria: Clear demonstration that the claimed invention offers an unexpected technical effect over the prior art bolsters claim strength.


Patent Landscape and Related Patents

1. Overlapping Patents and Prior Art

The patent landscape surrounding KR20110041580 would include:

  • Prior patents covering similar chemical entities or therapeutic uses filed within South Korea or internationally (e.g., via PCT applications).

  • Foreign patents related through filing priority, e.g., US, EP, JP, which may influence claim scope.

  • Freedom-to-operate (FTO) considerations are crucial given overlapping claims, especially in the rapidly evolving therapeutic space.

2. Patent Family and Family Members

Likely, the applicant filed related patents in other jurisdictions, forming a family patent portfolio that can:

  • Strengthen global patent protection.

  • Block rivals in multiple markets, especially where the drug is commercialized.

  • Facilitate licensing and collaborations.

3. Patent Expiry and Competitive Landscape

  • With a filing date of 2009 and publication in 2011, the patent’s expiration is projected around 2029 unless extensions apply.

  • The landscape includes generic challenges, especially if key pharmacophore claims lack sufficient inventive step or are challenged on basis of prior art.


Legal Challenges and Opportunities

  • Validity Challenges: Given the period, prior art could have emerged challenging the novelty or inventive step. Third parties might file oppositions or invalidation actions.

  • Designing Around: Competitors often develop structurally similar but non-infringing derivatives, especially if the claims are narrowly construed or atomically specific.

  • Patent Extensions: Opportunities may exist for patent term extensions, supplementary protection certificates, or data exclusivity, particularly if the compound involves innovative delivery or formulation.


Comparative Analysis with International Patent Landscape

  • If similar patents exist internationally, particularly in major markets like the US or Europe, patent strategies can be aligned to maximize global coverage.

  • Patent harmonization efforts, notably via Patent Cooperation Treaty (PCT), could streamline filings across jurisdictions for similar inventions.

  • The presence or absence of similar patents significantly influences competitive dynamics in South Korea’s biotech and pharma sectors.


Conclusion

KR20110041580’s patent scope appears strategically broad, covering specific chemical compounds and their therapeutic applications. Its claims likely aim to protect vital aspects of a novel pharmaceutical entity, supporting exclusivity in South Korea's lucrative market. However, the strength and enforceability of this patent depend on meticulous claim drafting, thorough prior art analysis, and ongoing legal vigilance against potential challenges. Its position within an international patent landscape further influences its commercial viability and risk profile.


Key Takeaways

  • Claim Breadth and Specificity: The patent’s scope hinges on the precise language of claims; broader claims afford wider protection but face higher invalidation risks. Narrower claims may risk easier workarounds.

  • Patent Landscape Dominance: Overlapping patents and prior art significantly impact enforceability and strategic positioning.

  • Global Strategy Necessity: To maximize market protection, patent families should encompass key jurisdictions, with attention to national laws and long-term patent term management.

  • Legal Vigilance: Continuous monitoring for potential infringing products and validity challenges is essential to sustain exclusivity.

  • Innovation Maintenance: Supplementary strategies, like patent term extensions or formulations protecting data exclusivity, extend commercial advantages.


FAQs

Q1. What is the typical duration of patent protection for pharmaceuticals in South Korea?
Pharmaceutical patents like KR20110041580 generally enjoy 20 years of protection from the filing date, subject to any extensions or specific legal provisions.

Q2. How does South Korea's patent law impact patent claims for pharmaceuticals?
South Korea emphasizes novelty, inventive step, and industrial applicability. Claims must clearly define the invention, avoiding overly broad language that does not meet patentability standards.

Q3. Can similar compounds or formulations be patented if they differ slightly from KR20110041580?
Yes. Similar compounds may be patented if they demonstrate a novel structure with distinct functional benefits, satisfying non-obviousness and novelty criteria.

Q4. How do patent landscapes influence drug development strategies in South Korea?
A thorough landscape analysis identifies potential infringement risks, opportunities for licensing, and areas where innovation can achieve patentability, shaping R&D priorities.

Q5. Is there a risk of patent invalidation in South Korea for pharmaceutical patents like KR20110041580?
Yes. Invalidations can occur due to prior art disclosures, lack of inventive step, or insufficient disclosure. Continuous legal review is essential to uphold patent rights.


References

  1. KIPO Patent Database — For public information on patent KR20110041580.
  2. Korean Intellectual Property Office (KIPO) Guidelines — For patentability criteria.
  3. WIPO Global Patent Landscape Reports — For context on international patent trends.

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.