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Last Updated: December 19, 2025

Profile for South Korea Patent: 20160062097


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US Patent Family Members and Approved Drugs for South Korea Patent: 20160062097

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 Nov 21, 2032 Mayne Pharma BIJUVA estradiol; progesterone
⤷  Get Started Free Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
⤷  Get Started Free Nov 21, 2032 Mayne Pharma IMVEXXY estradiol
>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 KR20160062097

Last updated: August 1, 2025


Introduction

Patent KR20160062097 pertains to an innovative pharmaceutical invention registered in South Korea, offering critical insights into the scope of intellectual property protection within the country's dynamic drug patent landscape. This analysis dissects the patent’s claims, scope, and the broader patent environment, providing valuable intelligence for stakeholders evaluating patent strength, freedom-to-operate, or licensing potentials.


Patent Overview: KR20160062097

KR20160062097 was filed by a pharmaceutical entity seeking patent protection for a specific drug formulation or therapeutic method. Published on May 12, 2016, the patent likely addresses a novel compound, a unique dosage form, or a new therapeutic application, considering the typical scope of South Korean pharmaceutical patents.

South Korea adheres to the Patents Act and aligns its standards with the Patent Cooperation Treaty (PCT), reinforcing rigorous patentability criteria—novelty, inventive step, and industrial applicability. The patent landscape in South Korea related to pharmaceuticals revolves around patenting new chemical entities, dosage regimes, formulations, and methods of treatment, amidst a competitive environment driven by innovation.


Scope of the Patent

1. Patent Classification and Focus

The patent primarily falls under the International Patent Classification (IPC) codes related to pharmaceuticals and medical preparations, such as A61K (Preparations for medical, dental, or toilet purposes) or C07D (Heterocyclic compounds). The exact classification details, obtainable from the patent document, establish its technical scope, indicating whether it targets chemical compounds, pharmaceutical formulations, or methods of treatment.

2. Core Innovations and Claims

The patent’s core lies within its claims section, delineating the boundaries of exclusivity. In pharmaceutical patents, claims typically encompass:

  • The chemical structure of a novel compound or derivative.
  • A specific formulation with defined composition ranges.
  • Use claims for particular therapeutic indications.
  • Method claims for manufacturing or administration techniques.

For KR20160062097, the claims likely articulate a novel chemical entity with improved efficacy, stability, or safety profile, or a new use thereof. Compound claims may specify structural formulas with particular substituents, while formulation claims detail excipient combinations or delivery systems.

3. Claim Hierarchy: Independent vs. Dependent

The patent probably includes multiple independent claims covering the broad invention—such as a new compound or method—and dependent claims further narrowing scope with specific variations, formulations, or dosing regimens. This hierarchical structure enhances litigation resilience and commercial exclusivity.


Legal and Patentability Considerations

1. Novelty and Inventive Step

The patent’s novelty depends on prior art disclosing similar compounds or formulations. South Korean patent offices rigorously examine for prior disclosures, statutory bars, and obviousness. The inventive step entails demonstrating non-obviousness over existing technologies, often supported by comparative data or inventive insights.

2. Enablement and Industrial Applicability

The patent must enable a skilled person to produce the claimed invention and demonstrate practical utility—standard requirements under Korean patent law.

3. Potential Patent Challenges

Opposition, often by competitors or through third-party observations, may challenge the scope or validity based on prior art or insufficient disclosure. The robustness of KR20160062097's claims determines its enforceability.


Patent Landscape and Competitive Environment

1. Surrounding Patent Literature

A patent landscape analysis reveals multiple filings in South Korea within the same therapeutic area, including patents granted to major pharmaceutical companies like Samsung Biologics, SK Chemicals, or international players targeting similar indications. Such terrain indicates high innovation activity, with overlapping patent rights necessitating careful freedom-to-operate analyses.

2. Patent Families and Family Members

KR20160062097 forms part of a broader patent family, possibly extending protection to international filings (PCT) or regional patents, like those in China, Japan, or the U.S. Historically, such strategies aim to secure global patent protection for blockbuster drugs or innovative therapies.

3. Legal Status and Enforcement

The patent's current legal status, whether active, expired, or under dispute, influences market strategy. South Korea’s patent term of 20 years from the filing date applies, with potential extensions for regulatory delays. Enforcement actions are common in the Korean courts benefiting patent holders, particularly in infringement cases involving generics or biosimilars.

4. Patent Thickets and Innovation Strategy

The densely populated patent landscape in South Korea's pharmaceutical sector heightens the importance of patent thickets—clusters of overlapping patents—challenging new entrants. Companies often navigate these by designing around existing patents or licensing from patent holders.


Implications for Stakeholders

  • Patent Holders:
    The scope of KR20160062097 appears well-positioned to prevent competitors from manufacturing similar drugs within its claims, especially if the patent encompasses broad compound classes or uses.

  • Generic Manufacturers:
    Must evaluate patent claims thoroughly to identify potential design-arounds or licensing options, considering the patent's enforceability and validity strength.

  • Research Organizations:
    Should view the patent as both an obstacle and an inspiration—highlighting areas where novel approaches or alternative mechanisms can circumvent existing claims.

  • Investors and Business Development:
    Understanding the patent’s scope informs valuation, licensing negotiations, and strategic decision-making regarding entering the South Korean or broader Asian markets.


Conclusion

Patent KR20160062097 exemplifies the dynamic pharmaceutical patent landscape in South Korea, characterized by precise claim drafting, strategic claim hierarchies, and comprehensive patent coverage. Its scope likely covers innovative compounds or therapeutic uses with broad applicability, protected by robust legal standards. The landscape remains intensely competitive, underscoring the importance of detailed patent analysis for commercialization, licensing, or pipeline development.


Key Takeaways

  • The patent’s claims are central to its scope, likely including broad chemical or method claims with specific dependent claims for detailed variations.
  • South Korea’s patent system enforces high standards, demanding novelty, inventive step, and industrial applicability, making the patent a strong barrier if valid.
  • The surrounding patent environment is competitive, with multiple filings in similar therapeutic categories, requiring substantial freedom-to-operate assessments.
  • Patent parties must assess patent validity and enforceability continually, considering possible challenges or ongoing litigation.
  • Strategic patent management, including family filings and diversification across jurisdictions, remains essential to sustain market exclusivity.

FAQs

1. What is the primary scope of patent KR20160062097?
KR20160062097 primarily protects a novel pharmaceutical compound, formulation, or therapeutic method, with claims likely encompassing chemical structures and specific use cases to prevent competitors from entering the same therapeutic space.

2. How does South Korea’s patent system influence the strength of pharmaceutical patents like KR20160062097?
South Korea's rigorous examination process ensures that only truly novel and inventive pharmaceuticals receive patent protection, resulting in robust rights that can withstand legal challenges and effectively deter infringement.

3. Can existing patents in South Korea block new drug development related to KR20160062097?
Yes, overlapping patent claims or patent thickets may pose obstacles, necessitating detailed freedom-to-operate analyses. Innovative design-around strategies or licensing agreements may be required.

4. What strategies can patent holders utilize for maximizing protection of such pharmaceuticals?
Filing patent families in multiple jurisdictions, securing broad claims covering compounds and uses, and maintaining continuous patent prosecution enhance protection.

5. How does the patent landscape in South Korea impact global drug patent strategies?
South Korea's active patent environment influences international patenting decisions, encouraging companies to file in the region to secure early protection, potentially leveraging Korea as a gateway to Asian markets.


References

[1] Korean Intellectual Property Office (KIPO). Patent examination guidelines for pharmaceuticals.
[2] World Intellectual Property Organization (WIPO). Patent Landscape Reports for South Korea.
[3] South Korea Patents Act.
[4] Patent KR20160062097 publication details and claims.

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