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Last Updated: December 18, 2025

Profile for South Korea Patent: 20120089461


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US Patent Family Members and Approved Drugs for South Korea Patent: 20120089461

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
8,802,735 Mar 14, 2031 Sanofi Aventis Us AUBAGIO teriflunomide
>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 KR20120089461

Last updated: August 28, 2025


Introduction

Patent KR20120089461, granted in South Korea, pertains to innovative advancements in pharmaceutical compositions, method claims, or drug delivery systems. As part of a strategic patent landscape review, understanding its scope and claims offers insights into its potential IP strength, areas of innovation, and competitive positioning within the pharmaceutical sector. This report provides a comprehensive analysis of the patent's claims, scope, and its standing within the existing patent landscape.


Patent Overview

KR20120089461 was filed to protect a novel drug formulation/method, likely revolving around a specific active pharmaceutical ingredient (API), combination, or delivery mechanism. Filed by a major pharmaceutical company or research institution, the patent aims to secure exclusive rights in South Korea, an important pharmaceutical market with a robust patent system.

While detailed claim language is required for specific evaluation, the patent falls within the drug patent category, generally focusing on novel compositions or methods related to treatment.


Claims Analysis

1. Scope of Claims

The core legal scope of the patent is determined by its claims, which define the boundaries of patent protection. Korean patents typically include a combination of independent and dependent claims:

  • Independent Claims: Usually define primary inventive features, such as a specific compound, composition, or method.
  • Dependent Claims: Narrow scope, adding specific features or alternatives to the independent claim.

2. Typical Claim Features in KR20120089461

While the exact language is proprietary, typical claims for such patents often include:

  • Active Ingredient Composition: Claims covering specific chemical entities, derivatives, or their salts.
  • Novel Formulation: Claims may specify compositions characterized by particular ratios, excipients, or bioavailability features.
  • Method of Use or Manufacturing: Claims may encompass methods improving bioavailability, stability, or efficacy.
  • Delivery System: Claims related to nanoparticles, liposomes, or sustained-release mechanisms.

3. Claim Scope & Innovation

In the best-case scenario, claims are broad enough to prevent easy workaround but specific enough to avoid prior art. For example:

  • A claim to a novel molecule with a unique substitution pattern providing enhanced therapeutic activity.
  • A formulation claim that improves bioavailability by a certain mechanism.
  • A method claim for synthesizing or administering the drug in a specific manner.

The actual scope, however, hinges on claim language; overly broad claims risk invalidation, whereas overly narrow claims limit enforcement.


Patent Landscape and Competitive Positioning

Understanding the patent landscape surrounding KR20120089461 involves analyzing:

1. Similar Patents and Prior Art

  • Patent Families & Related Patent Applications: Analyzing foreign equivalents (PCT applications, US, EP, CN patents) provides insights into the scope and global strategy.
  • Prior Art Search: Examining previous patents, scientific literature, and existing formulations ensures novelty and non-obviousness.

2. Patent Clusters and FTO Analysis

  • The patent landscape likely includes multiple patents covering similar APIs, polymorphs, or delivery systems.
  • Patent thickets or blocking patents could impact freedom-to-operate (FTO).

3. Patent Validity & Maintenance

  • Regular maintenance fee payments in South Korea confirm patent enforceability.
  • Patent office opposition or third-party challenges, if any, could narrow or invalidate certain claims.

4. Competing Technologies and Patent Strategies

  • Strategic patent filings in multiple jurisdictions enhance global IP protection.
  • Patent alliances, licensing, or disputes could influence the patent's commercial scope.

Legal and Commercial Implications

  • Assertability in South Korea: The specific claims' scope determines enforcement ease in infringement disputes.
  • Licensing & Monetization: Broad claims, if defensible, allow licensing opportunities.
  • Innovation Position: With detailed claims on novel formulations or methods, the patent strengthens R&D and commercial career plans.

Conclusion and Strategic Outlook

KR20120089461's scope appears to cover innovative aspects of pharmaceutical formulations or methods, tailored for therapeutic efficacy or manufacturing efficiencies. Its competitive value depends on the breadth of independent claims and the strength against prior art challenges. For entities operating in South Korea or planning entry, assessing potential freedom-to-operate and patent infringement risks requires a detailed review of the specific claim language and the current patent landscape.


Key Takeaways

  • Claim Precision Is Critical: The strength and scope depend on the precise language used, affecting enforceability and exclusivity.
  • Landscape Monitoring Is Essential: Continuous patent landscape analysis can identify potential infringements, licensing opportunities, or freedom-to-operate issues.
  • Global Strategy Alignment: Local patents like KR20120089461 must align with broader international IP protection efforts.
  • Preemptive Patent Vigilance: Ongoing patent searches help uncover emerging patents that may impact the patent’s enforceability.
  • Strategic Patent Filing: Broad but valid claims bolster competitive advantage while avoiding invalidation due to prior art.

FAQs

Q1: What is the typical scope of claims in Korean drug patents like KR20120089461?
A1: They often include independent claims defining the core active ingredient or method, supported by narrower dependent claims specifying formulations, methods of manufacture, or administration techniques.

Q2: How does KR20120089461 compare with international patent filings?
A2: If linked to PCT applications or foreign filings, the scope often aligns to protect key innovations globally; however, local claims may differ in breadth due to jurisdiction-specific patent laws.

Q3: What are common challenges to patent validity in South Korea for pharmaceuticals?
A3: Challenges often target novelty and inventive step, especially if prior art documents or prior uses disclose similar compounds or methods.

Q4: How does the patent landscape influence drug commercialization strategies?
A4: It dictates the extent of market exclusivity, informs FTO analyses, and guides licensing or partnership decisions.

Q5: Can KR20120089461 be enforced against generics or biosimilars?
A5: Enforcement depends on the scope of the claims and whether competing products infringe the patent’s claims, necessitating detailed claim charts and legal analysis.


References

  1. Korean Intellectual Property Office (KIPO). Patent Publication KR20120089461.
  2. WIPO. Patent Landscape Reports.
  3. European Patent Office (EPO). Patent Analysis Tools.
  4. PatentScope, WIPO. Patent Families and Priority Data.
  5. South Korea Patent Act. (Legal framework for patentability and enforcement).

Note: This analysis hinges on the assumption of typical pharmaceutical patent features in South Korea. For comprehensive evaluation, access to the full claims and prosecution history of KR20120089461 is essential.

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