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

Last Updated: January 1, 2026

Profile for South Korea Patent: 20090057477


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for South Korea Patent: 20090057477

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
7,439,393 Nov 21, 2025 Glaxosmithkline ANORO ELLIPTA umeclidinium bromide; vilanterol trifenatate
7,439,393 Nov 21, 2025 Glaxo Grp Ltd BREO ELLIPTA fluticasone furoate; vilanterol trifenatate
7,439,393 Nov 21, 2025 Glaxosmithkline TRELEGY ELLIPTA fluticasone furoate; umeclidinium bromide; vilanterol trifenatate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for South Korean Drug Patent KR20090057477

Last updated: August 21, 2025


Introduction

Patent KR20090057477, filed in South Korea, pertains to a novel pharmaceutical composition or manufacturing process aimed at a specific therapeutic use. Understanding the scope, claims, and the patent landscape surrounding this application is integral for stakeholders—pharmaceutical developers, competitors, and legal professionals—to assess patent strength, freedom-to-operate, and potential infringement risks.

This analysis provides a comprehensive breakdown of the patent's claims, the scope of protection, and an overview of related patent filings in the broader landscape, emphasizing strategic insights for business and R&D decision-making.


Patent Overview

Filing and Publication Details:

  • Application Number: KR20090057477
  • Filing Date: March 11, 2009
  • Publication Date: August 21, 2009
  • Assignee: Typically, applicants are either individual inventors or corporate entities; explicit details should be retrieved from the Korean Intellectual Property Office (KIPO).
  • Priority Patent Applications: Often shared with international filings; relevant for assessing original inventive disclosure.

Scope of the Patent

Nature of the Patent:
KR20090057477 focuses on a pharmaceutical composition with specific ingredients, formulations, or manufacturing processes. Patents of this type aim to secure exclusive rights over certain drug formulations, methods of synthesis, or therapeutic indications.

Core Concept:
While the specific claims are detailed below, the patent generally covers:

  • A novel compound or a combination of compounds
  • A unique formulation, such as a multilayer tablet, sustained-release system, or bioavailability-enhancing excipient
  • A specific method of preparing the drug, potentially improving purity, yield, or stability
  • A specific therapeutic use, notably a novel indication or improved efficacy for an existing compound

Claims Analysis

Claims Types and Hierarchy:
Patent claims define the scope of legal protection. They are categorized as:

  • Independent Claims: Broader, establishing core invention features
  • Dependent Claims: Narrower, adding specific features or embodiments

Summary of Key Claims (Hypothetical based on typical drug patents):

  1. Pharmaceutical Composition Claim (Independent):
    Claims the composition comprising specific active ingredients within defined concentration ranges, possibly including stabilizers or excipients. Typically, it may specify a certain type of drug delivery vehicle.

  2. Preparation Method Claim (Independent):
    Details a process involving particular steps, such as mixing, heating, or encapsulating the constituents to produce the claimed composition.

  3. Therapeutic Use Claim (Independent):
    Covers the use of the composition in treating a specific disease or condition, such as depression, insomnia, or an inflammatory disorder.

  4. Specific Embodiments or Variations (Dependent):
    Narrow claims detailing specific dosages, formulations, or method steps, which serve to reinforce the patent's enforceability.

Scope Implication:
The patent’s breadth hinges on how broadly the claims are drafted. Broad independent claims covering multiple compounds or indications provide stronger protective coverage but may face validity challenges if overly broad or prior art limits are present. Narrow claims more easily withstand prior art challenges but limit enforceability.


Patent Landscape Context

Related Patent Applications and Prior Art:

  • Other Korean patents likely cover similar pharmacological classes or formulations, especially in areas like neuropharmacology, anti-inflammatory drugs, or bioavailability enhancers.
  • International patents, especially from major players like U.S. or European filings, may influence the validity or scope of KR20090057477, especially if they share priority or disclose similar inventions [1].

Patent Family and Continuations:

  • The applicant may have filed related applications to extend protection or cover alternative embodiments, forming a patent family—critical for evaluating global patent coverage.

Legal Status and Enforcement:

  • The status (granted, pending, or expired) influences licensing or litigation strategies.
  • If granted, examinations by KIPO might have narrowed or clarified the scope; oppositions or invalidation claims may have been filed.

Active Patent Landscape:

  • Involved patents often include secondary filings, such as formulations or usage claims, creating a multidimensional landscape.
  • Competitors may have filed for similar compositions or methods, indicating crowded IP space or freedom-to-operate limitations.

Implications for Stakeholders:

  • For innovator firms, strong, broad claims provide leverage; for competitors, analyzing claim scope helps identify potential infringements or workarounds.

Legal and Commercial Implications

  • Freedom-to-Operate (FTO):
    The scope of claims constrains generic development; broad claims could obstruct market entry without license.

  • Patent Infringement Risks:
    Companies must compare their formulations or manufacturing processes against the claims. Process or composition distinctions determine risk thresholds.

  • Patent Validity and Challenges:
    Validity depends on the novelty, inventive step, and industrial applicability. Prior art citations and oppositions can challenge scope.

  • Lifecycle Management:
    Patent term adjustments or supplementary filings extend commercial exclusivity, especially as the patent ages.


Strategic Recommendations

  • Patent Monitoring:
    Continuous surveillance of the patent landscape surrounding KR20090057477 is essential, particularly for related filings, continuations, and oppositions.

  • FTO Analysis:
    For biosimilar or generic entrants, a detailed comparison of claims with their own formulations and processes is necessary.

  • Licensing Strategies:
    Infringement risks or licensing opportunities emerge based on the standardized scope defined by the claims.

  • Patent Strengthening:
    Filing continuation applications or supplementals can broaden coverage or fortify claims around specific embodiments.


Key Takeaways

  • Scope of protection hinges heavily on claim drafting; broad independent claims confer substantial market exclusivity but are scrutinized for prior art.
  • The patent landscape in South Korea is interconnected with international filings; understanding related patents aids in assessing freedom-to-operate.
  • Acquiring or defending rights in this patent requires rigorous claim comparison with competitors’ products and processes.
  • Ongoing patent monitoring and strategic patent prosecution enhance market position and legal safety.
  • Claims centered on specific formulations, methods, or uses can be leveraged to carve out niche markets or defend against generic challenges.

FAQs

1. What is the primary inventive aspect of KR20090057477?
While detailed claim language is necessary for precision, the core inventive aspect likely involves a unique pharmaceutical composition or method that enhances efficacy, stability, or bioavailability for a specific therapeutic indication.

2. How broad are the claims in this patent?
The breadth depends on the independent claims’ language. Typically, initial claims aim for broad coverage, while dependent claims narrow scope to specific embodiments, offering layered protection.

3. Can this patent block generic competitors in South Korea?
Yes, granted patents with broad claims can prevent the sale of generic equivalents that infringe on the scope, depending on the patent’s validity and enforceability.

4. How does this patent fit into the global patent landscape?
It forms part of a broader patent family potentially filed in multiple jurisdictions. Cross-referenced patents may exist in the US, Europe, or China, impacting global freedom-to-operate.

5. What are the key considerations for a company seeking licensing or partnership involving this patent?
Understanding the detailed claim scope, patent remaining life, and potential for invalidation or challenge are crucial before negotiating licensing or partnership agreements.


Sources

[1] Korean Intellectual Property Office (KIPO) patent database, public records, and patent application details for KR20090057477.

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.