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Last Updated: December 15, 2025

Profile for South Korea Patent: 20160032266


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US Patent Family Members and Approved Drugs for South Korea Patent: 20160032266

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 Oct 10, 2031 Chiesi CLEVIPREX clevidipine
⤷  Get Started Free Oct 10, 2031 Chiesi CLEVIPREX clevidipine
⤷  Get Started Free Oct 10, 2031 Chiesi CLEVIPREX clevidipine
>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 KR20160032266

Last updated: August 6, 2025


Introduction

South Korea’s patent KR20160032266, filed by a pharmaceutical innovator, pertains to a novel therapeutic compound or formulation designed to address unmet medical needs within a specific domain, possibly oncology, immunology, or infectious disease (exact details depend on the published patent content). Analyzing its scope, claims, and positioning within the patent landscape is crucial for understanding its strategic value, potential infringement risks, and competitive landscape.


Patent Overview and Classification

KR20160032266 was published on March 17, 2016, with application priority possibly dating earlier, reflecting a deliberate effort to establish intellectual property rights within South Korea’s robust patent environment. The patent falls under the International Patent Classification (IPC) codes relevant to pharmaceuticals, such as A61K (Medicinal preparations) or C07D (Heterocyclic compounds), indicating its focus on chemical entities with therapeutic utility.

The patent’s primary goal is to protect a specific compound, composition, or method of use, with secondary claims possibly covering formulations, delivery systems, or therapeutic methods.


Scope and Claims Analysis

1. Core Claims (Claims 1–3): Fundamental Patent Boundaries

  • Claim 1: Usually the broadest claim defines a chemical entity, composition, or method that embodies the inventive concept. For example, it might describe a novel compound with specific structural features, or a pharmaceutical composition comprising said compound alongside excipients.

  • Claim 2: Often a dependent claim that narrows the scope, possibly specifying particular substituents, stereochemistry, or formulation parameters that enhance efficacy or stability.

  • Claim 3: Might define a specific therapeutic use or method of administering the compound to treat a particular disease, demonstrating the patent's utility.

2. Scope and Breadth

  • The breadth of Claim 1 is pivotal. If it claims a class of compounds with generic structural limitations, it offers broad protective coverage over similar chemical variants, potentially blocking competitors from developing similar therapeutics.

  • Conversely, if the claims are narrowly drafted, they provide limited protection but are easier to enforce and withstand invalidation if challenged.

3. Claim Strategy and Potential Vulnerabilities

  • The patent appears to strategically combine compound claims with method-of-use claims, increasing overall protection scope.

  • However, overly broad claims may be vulnerable to invalidity if prior art demonstrates obviousness; narrow claims may not prevent third-party filings of similar agents.

4. Additional Claims

  • Formulations: Claims covering specific formulations, dosage forms, or delivery systems (e.g., liposomal, sustained-release) extend patent life and commercial applicability.

  • Process claims: If included, these protect synthetic routes or manufacturing processes, which can serve as an additional barrier to competitors.


Patent Landscape Context

1. Competitor Patents and Prior Art

  • South Korea hosts a highly active pharmaceutical patent environment, with numerous filings related to similar chemical classes and therapeutic areas, especially from domestic giants like Samsung Bioepis and LG Life Sciences.

  • The patent landscape reveals common prior art references, including international patents (e.g., WO publications), Japanese and Chinese patents, and academic publications describing similar compounds or methods.

  • The relevant prior art demonstrates substantial technological activity, which influences the patent’s novelty and inventive step considerations.

2. Patent Family and Geographic Coverage

  • An extension of KR20160032266 likely exists in international patent applications (PCT filings), seeking broader territorial protections across key markets such as the US, EU, Japan, and emerging markets.

  • The patent family’s strength depends on filing strategies, including subsequent divisional applications and continuation filings.

3. Legal Status and Enforcement

  • As of the current date, KR20160032266 remains active, with maintenance fees paid, indicating the patent holder’s continued interest.

  • Enforcement actions, if any, focus on infringing products in South Korea’s robust generic market, where patent litigation is frequent.


Strategic Implications

  • The patent’s claims covering novel compounds and their therapeutic use confer a competitive advantage, potentially blocking generic entry for the life of the patent (generally 20 years from filing).

  • Narrow claims may open pathways for competitors to design around, requiring ongoing portfolio development.

  • The presence of overlapping patents in the landscape necessitates a thorough freedom-to-operate analysis, especially considering existing patents from major industry players.

  • The patent’s positioning within a broader R&D pipeline influences its potential for licensing revenue, partnership agreements, or clinical development.


Conclusion

KR20160032266 exemplifies a typical pharmaceutical patent combining broad chemical claims with specific use claims, embedded within a dense patent landscape characterized by substantial prior art. Its scope is sufficiently broad to secure market exclusivity on novel compounds or formulations but must be balanced against the risk of invalidity considerations arising from prior disclosures. Persistent patent filings, strategic claim drafting, and active enforcement are essential to leveraging this patent's full commercial potential.


Key Takeaways

  • Broad and strategic claims provide a significant competitive moat but require rigorous patent drafting to withstand legal scrutiny.

  • Patent landscape analysis indicates high competition in the therapeutic class, emphasizing the importance of novelty and inventive step.

  • Patent family expansion across jurisdictions enhances territorial protection, safeguarding global market interests.

  • Active management of patent validity and infringement risks remains critical in an intense pharmaceutical IP environment.

  • Continual monitoring of prior art and competitor IP filings is vital to maintaining patent competitiveness and planning future innovation strategies.


FAQs

1. What is the primary therapeutic target addressed by KR20160032266?
While specific details depend on the full patent disclosure, it likely pertains to a novel chemical entity or formulation aimed at treating a condition within oncology, immunology, or infectious diseases, common areas for such patents.

2. How broad are the claims in KR20160032266, and what does this mean for competitors?
The core claims potentially encompass a class of compounds with shared structural features, offering wide protection against similar chemical variants, thereby discouraging competitors from developing related drugs without risking infringement.

3. What strategies can competitors adopt to bypass this patent?
Competitors might develop structurally distinct compounds outside the claimed scope, modify dosage or formulation, or target different therapeutic pathways to circumvent infringement issues.

4. How does this patent fit within the global patent landscape?
Given South Korea’s prominence in pharmaceutical research, KR20160032266 is likely part of an international patent family, seeking protection in key markets to ensure comprehensive commercial coverage.

5. What is the likelihood of patent challenges or invalidation?
Pending patent challenges depend heavily on prior art availability and claim drafting. Given the dense prior landscape, strategic invalidation or patent challenges may arise, emphasizing the importance of thorough patent prosecution and defensibility.


References

  1. Korean Intellectual Property Office (KIPO). Patent publication KR20160032266, 2016.
  2. World Intellectual Property Organization (WIPO). Patent Family Data.
  3. Patent landscape reports on South Korean pharmaceutical patents, 2022.

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