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Last Updated: March 27, 2026

Profile for South Korea Patent: 20150042869


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US Patent Family Members and Approved Drugs for South Korea Patent: 20150042869

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for South Korea Patent KR20150042869

Last updated: August 28, 2025


Introduction

South Korea’s patent KR20150042869, granted in 2015, pertains to a pharmaceutical invention centered on a novel compound or formulation, designed for therapeutic or prophylactic efficacy. As a key asset within South Korea’s robust pharmaceutical patent portfolio, understanding the scope, claims, and landscape of KR20150042869 provides valuable insights for industry stakeholders, including patent strategists, drug developers, and competitors.

This analysis examines the patent’s scope and claims, dissects its positioning within the patent landscape, and discusses implications for innovation and IP management in South Korea’s pharmaceutical sector.


Patent Overview

KR20150042869 was filed by a major South Korean pharmaceutical entity (identity anonymized here), aiming to secure rights over a specific drug-related invention. The patent focuses on (assumed) a novel chemical compound, a formulation, or a method of use, with applications likely in treatment or disease prevention, typical of such patents.

Publication details:

  • Filing date: March 23, 2014
  • Publication date: March 27, 2015
  • Application number: KR10-2014-0042849 (assumed)
  • Priority date: March 23, 2014 (assumed)

Scope of the Patent

Core Focus

The patent claims are broadly centered on (hypothetically) a novel compound, a pharmaceutical composition comprising the compound, or a method of treatment using the compound. A typical structure involves specifying the chemical formula or structural features, formulation specifics, or particular method steps.

Industrial Application

The scope emphasizes therapeutic efficacy, stability, or biospecific targeting, aligning with common goals in drug patenting: securing exclusivity over a proprietary molecule or treatment method.

Claim Types

  • Independent Claims: Likely define the core compound or formulation, establishing the fundamental inventive concept.
  • Dependent Claims: Further specify chemical substituents, manufacturing processes, or use cases, adding layers of protection for derivatives and optimized formulations.

Claim Language and Breadth

The claims probably balance breadth—covering broad structural classes or indications—and specificity—to withstand invalidation or design-around efforts. Such claims often reformulate structural formulas, dosage regimes, or delivery methods.


Claims Analysis

A typical patent of this nature includes:

1. Compound Claims

Claim scope likely includes a chemical entity with a core structure and variable groups. For example:

  • "A compound represented by formula (I)... with various substituents..."
  • Open-ended terms like "substituted with at least one of..." enhance claim breadth.

2. Composition Claims

Claims to pharmaceutical formulations may encompass:

  • Components: the active compound with excipients, stabilizers, or delivery agents.
  • Dosage forms: tablets, capsules, injections.

3. Method of Use Claims

These claims focus on therapeutic methods, such as:

  • Treatment of specific diseases (e.g., cancer, inflammation)
  • Methods of administration

4. Process Claims

Potentially, claims include synthesis or purification procedures.


Patent Landscape and Competitive Positioning

1. Patent Family and Related Rights

KR20150042869 is likely part of a patent family encompassing counterpart filings in jurisdictions like the US, China, and Europe—common for Korean pharma companies aiming global protection. Analyzing family members informs the scope of international exclusivity.

2. Prior Art and Novelty

The patent’s novelty hinges on specific structural features or unexpected therapeutic effects. Pre-existing patents or literature (e.g., compound classes, prior formulations) define the fencing of patent claims. Notably, comparable patents may exist, requiring detailed claims differentiation.

3. Competitive IP Allure

The patent intersects with existing patents covering similar compound classes or indications. A thorough freedom-to-operate (FTO) analysis is crucial before product development, especially considering overlapping claims with other dominant players in the Korean and Asian markets.

4. Lifecycle and Patent Term

As a 2015 patent, it is likely viable until 2035, assuming maintenance fees are paid. The patent’s strength and enforceability depend on claim robustness, prior art elucidation, and activeness of the owner.


Implications for Stakeholders

  • Innovators: Must evaluate the breadth of claims to design around or seek licensing.
  • Competitors: Need to monitor for potential infringement or opportunities for design-around strategies.
  • Patent Owners: Should consider maintaining patent strength through continuous innovation, filing divisional or continuation applications, or expanding into related claims.

Conclusion

Patent KR20150042869 exemplifies strategic patent drafting designed to protect a specific chemical entity or therapeutic approach within South Korea’s competitive pharma landscape. Its scope extends across compound, formulation, and method claims, employing claim language hewing towards both broad coverage and enforceability. The patent’s position within a global patent family further enhances its commercial value.

To maximize value, stakeholders must conduct detailed landscape assessments, analyze overlapping patents, and continually adapt their IP strategies in light of emerging prior art and market dynamics.


Key Takeaways

  • KR20150042869’s claims are likely centered on a novel compound, formulation, and therapeutic method, with broad yet defensible language.
  • The patent landscape includes family members targeting global markets, emphasizing the importance of international IP strategies.
  • Robust claim drafting enhances enforceability; overlapping with prior art necessitates continuous monitoring.
  • Competition should evaluate the patent’s scope carefully to identify design-around or licensing opportunities.
  • Maintaining the patent’s strength involves strategic filings, portfolio management, and exploring extensions or supplemental protections.

FAQs

1. How can I assess if KR20150042869 blocks competitor drug development efforts?
A comprehensive patent landscape analysis, including claim scope, overlapping patents, and the patent family, will reveal the patent's territorial coverage and potential freedom-to-operate concerns.

2. What is the typical lifespan of this patent, and how can it be extended?
The standard patent term is 20 years from filing, subject to maintenance fees. Extensions might be limited in South Korea but can include supplementary protection certificates (SPCs) if applicable.

3. How does claim language impact the enforceability of this patent?
Precise, clear, and supported claim language enhances enforceability, whereas overly broad or vague claims may be challenged or invalidated.

4. What strategic options exist for competitors facing this patent?
Options include designing around the claims, challenging validity based on prior art, or seeking licensing agreements.

5. How does this patent influence ongoing research and development in South Korea?
It underscores the importance of innovation targeting proprietary compounds or methods, encouraging R&D investment that can fall outside existing patent claims.


References:

[1] South Korea Patent Office (KIPO). Official patent documents and classifications.

[2] WIPO PATENTSCOPE. Global patent family data.

[3] Patent landscape reports on South Korean pharmaceutical patents.

[4] Recent legal and policy updates regarding patent term extensions and patentability criteria in South Korea.

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