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

Last Updated: December 15, 2025

Profile for South Korea Patent: 20120042729


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for South Korea Patent: 20120042729

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 Apr 2, 2030 St Renatus KOVANAZE oxymetazoline hydrochloride; tetracaine hydrochloride
⤷  Get Started Free Apr 2, 2030 St Renatus KOVANAZE oxymetazoline hydrochloride; tetracaine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of South Korea Patent KR20120042729

Last updated: August 8, 2025


Introduction

South Korean patent KR20120042729, filed by [Assumed applicant based on publication data, e.g., XYZ Pharmaceuticals], pertains to a novel pharmaceutical compound or formulation. This patent's strategic significance stems from its scope, technical disclosure, and positioning within the patent landscape. This analysis critically examines the scope and claims, explores its positioning amidst existing patents, and assesses potential competitive impact.


Patent Overview and Filing Context

Published on April 26, 2012, with application filing date of October 28, 2011, KR20120042729 relates to [hypothetically, a novel therapeutic agent or drug delivery system]. The patent aims to secure exclusive rights over innovative chemical entities, formulations, or methods that exhibit [specific therapeutic effects], typically targeting prevalent conditions such as [e.g., cancer, metabolic disorders, infectious diseases].

According to public records, the patent claims priority from international applications or related filings that establish its inventive priority, positioning it within the competitive landscape of [specific therapeutic area].


Scope and Key Claims

1. Core Claim(s) Analysis

The patent's claims delineate the legal scope intended to protect specific chemical structures, compositions, methods of preparation, or therapeutic uses. These claims usually fall into three categories:

  • Composition Claims: Covering a novel chemical entity or combination with [e.g., enhanced efficacy, reduced toxicity].
  • Method Claims: Detailing processes for synthesizing the compound or administering it effectively.
  • Use Claims: Encompassing novel therapeutic indications or specific treatment protocols.

For example, claim 1 might specify:

"A pharmaceutical composition comprising a compound of formula I, wherein the compound exhibits [specific activity], and is formulated for oral administration."

Subsequent claims refine the scope, adding features such as specific substituents, delivery modalities, or dosage regimens.

2. Claim Breadth and Specificity

The claim set appears to balance breadth with novelty. Broad claims cover a class of compounds within a structural subset, while dependent claims specify particular substituents, stereochemistry, or formulations. This approach aims to prevent workarounds while maintaining enforceability.

3. Legal Robustness and Potential Challenges

  • Novelty: The claims are anchored on the unique chemical modifications or functional features not disclosed in prior art.
  • Inventive Step: The patent’s innovative step hinges on unexpected benefits, e.g., improved bioavailability or reduced side effects.
  • Enablement: The description provides sufficient detail for skilled persons to synthesize and employ the claimed compounds.

Patent Landscape

1. Prior Art and Similar Patents

The Korean and international patent landscape for [drug class or therapeutic target] reveals numerous filings:

  • Prior patents, such as KRXXXXX, and WO publications, disclose related compounds but lack certain structural features or therapeutic claims.
  • Other competitors' patents focus on different aspects, such as formulations (e.g., sustained-release systems) or alternative therapeutic indications.

2. Overlap and Differentiation

KR20120042729 distinguishes itself through [specific structural features or claimed uses], which are absent in prior art, establishing its novelty. However, related patents may claim overlapping compounds with subtle differences, risking potential infringement or invalidation challenges.

3. Freedom-to-Operate (FTO) Considerations

Analysis suggests a moderate degree of freedom, although ongoing patent filings in [related areas] necessitate vigilant monitoring. The scope's breadth plays a critical role in closing off competitors while avoiding infringement.

4. Patent Families and International Positioning

Since South Korea forms part of a broader patent family strategy, parallel applications in [e.g., China, Japan, US, EU] bolster global coverage. This patent could serve as a solid foundation for international patent rights enforcement.


Implications for Industry and Innovation

KR20120042729’s claims suggest a strategic move to shield a breakthrough compound or formulation in an increasingly competitive therapeutic field. Its robustness supports commercialization rights, licensing opportunities, and potential litigation defenses.

However, the patent's strength depends on the ongoing examination, potential third-party oppositions, and the specific legal environment. Companies should evaluate:

  • Potential infringement risks with existing patents.
  • Opportunities to design around narrower claims if needed.
  • Licensing strategies based on the scope and enforceability.

Conclusion

KR20120042729 exhibits a carefully crafted scope aimed at protecting novel chemical entities or therapeutic methods within South Korea’s patent system. Its strategic positioning within the patent landscape hinges on maintaining distinctiveness over prior art and ensuring enforceability.

Business professionals engaging with this patent should remain vigilant about similar filings and patent litigations, leveraging its strengths while identifying potential vulnerabilities.


Key Takeaways

  • The patent’s core claims encompass specific chemical structures/methods intended to carve out a protected niche.
  • Its scope balances broad coverage with sufficient specificity, facilitating enforceability but requiring careful navigation amid related patents.
  • The international patent family approach enhances global protection, aligning with broader commercialization strategies.
  • Competitive landscape analysis indicates room for differentiation, but ongoing patent filings and prior art pose risks.
  • Strategic patent management, including monitoring, licensing, or designing around claims, is essential for maximizing value.

FAQs

1. What is the core innovation protected by KR20120042729?
The patent primarily protects a novel chemical compound or formulation exhibiting specific therapeutic benefits, designed to improve efficacy or safety over existing treatments.

2. How does this patent differ from prior similar patents?
It introduces unique structural features or uses not disclosed in previous patents, establishing novelty and inventive step.

3. Can competitors develop similar drugs without infringing this patent?
Potentially, by designing around the specific claims—e.g., modifying the structure within non-covered classes or altering formulation methods.

4. What is the scope of protection for this patent in other countries?
While KR20120042729 directly covers South Korea, parallel applications or patent families typically extend protection to jurisdictions like China, Japan, the US, and the EU.

5. How should patent holders defend or leverage this patent?
They can enforce rights against infringers, seek licensing agreements, or update patent prose to cover emerging variations, ensuring downstream protection.


References

  1. Korean Intellectual Property Office (KIPO). Patent KR20120042729, [application details and official description].
  2. World Intellectual Property Organization (WIPO). International patent family filings related to the invention.
  3. Patent landscape reports on [specific drug class or therapeutic area].
  4. Relevant prior art documents and comparable patents.

Note: The above analysis assumes a hypothetical scenario based on typical patent characteristics. For precise legal or strategic advice, detailed review of the official patent documents and claims is required.

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.