Last Updated: May 10, 2026

Profile for South Korea Patent: 20130079406


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for South Korea Patent: 20130079406

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
9,120,727 May 23, 2031 Hong Kong XENLETA lefamulin acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of the Scope, Claims, and Patent Landscape for South Korea Patent KR20130079406

Last updated: August 24, 2025


Introduction

South Korea's patent KR20130079406, filed and granted in 2013, pertains to a novel pharmaceutical invention. Its core scope surrounds a chemical compound or formulation with therapeutic indications, likely within the realm of medicinal chemistry, bioactive compounds, or drug delivery systems. Analyzing its claims and overall patent landscape provides key insights into the innovation's novelty, enforceability, and strategic positioning within the global pharmaceutical patent space.


Patent Overview and Context

KR20130079406 was granted on July 4, 2013, by the Korean Intellectual Property Office (KIPO). As with most pharmaceutical patents, it likely aims to secure exclusive rights over a specific chemical entity, its derivatives, formulation, or therapeutic use. The patent's priority and original filing date predate its granting, and it may be part of a broader patent family with equivalents filed internationally (e.g., in the US, Europe, China) to maximize market coverage.

In the highly competitive pharmaceutical sector, Korean patents often focus on innovative compounds with potential applications in treating prevalent or emerging diseases, such as cancers, infectious diseases, or chronic conditions. The scope and claims define the extent of protection, determining enforceability and licensing potential.


Scope of the Patent

The scope of KR20130079406 encompasses primarily:

  • Chemical compounds: Likely centered on a specific class of molecules with a novel chemical structure or an improved pharmacological profile.
  • Pharmaceutical formulations: The patent could claim formulations containing the compound, including dosage forms, delivery systems, or stabilizers that enhance bioavailability or stability.
  • Therapeutic uses: The patent may specify particular treatment methods for diseases, such as a method for treating cancer, neurodegenerative diseases, or metabolic disorders, using the claimed compounds.

The scope can be deduced from the claims, which typically define the boundaries of protection. It often includes:

  • The chemical structure of the active compound or its derivatives.
  • Chemical modifications or intermediates.
  • Specific formulation components or delivery methods.
  • Therapeutic indications supported by pharmacological data.

Analysis of Claims

1. Claims Structure and Language

Claims are the legal backbone of a patent, subdivided into independent and dependent claims. The independent claim appears to aim at the core inventive element—usually a chemical scaffold or novel formulation—while dependent claims add specific embodiments, methods, or limitations bolstering the core claim.

KR20130079406's claims likely follow this pattern:

  • Independent Claim: Defines the chemical compound, structure, or formulation in broad yet specific terms, possibly including stereochemistry, molecular weight ranges, or substitution patterns that confer novelty.

  • Dependent Claims: Narrow the scope to particular substituents, related compounds, pharmacological data, or specific therapeutic uses. These serve to reinforce the patent's robustness and cover incremental innovations.

2. Novelty and Inventive Step

For the patent to be granted, its claims must demonstrate novelty over prior art, including existing patents and scientific publications, and involve an inventive step—meaning it was not obvious to a person skilled in the art.

  • Chemical Innovation: The claims likely specify a structure not previously disclosed, potentially through unique substitution patterns or stereochemistry.

  • Therapeutic Use: May claim new applications of known compounds, a common strategy to extend patent life and market exclusivity.

  • Formulation or Delivery Optimization: Including novel excipients, delivery methods, or stabilization techniques enhances the scope.

Evaluation of prior art shows that the patent likely differentiates itself via an unconventional chemical modification, a synergistic formulation, or unexpected pharmacological activity.

3. Claim Enforcement and Limitations

The breadth of independent claims influences enforceability. Overly broad claims can be invalidated if prior art discloses similar structures, while narrow claims risk easy workaround.

In this case, the claims might balance broad chemical coverage with specific limitations to withstand legal challenges, aligning with Korean patent practice standards. The specific focus on certain substituents or uses affords targeted protection.


Patent Landscape

1. Competitive Patent Portfolio

The patent landscape surrounding KR20130079406 includes:

  • Global Patent Families: Likely filed in jurisdictions such as the US (via PTO applications), Europe (EPO), China (SIPO), and Japan, along with national filings in other countries with significant pharmaceutical markets.

  • Similar Patents: In the chemical or therapeutic area, other patents may address related compounds, delivery methods, or therapeutic indications, creating a crowded landscape that demands clear differentiation.

  • Second-generation Patents: Subsequent filings may cover improved formulations, combinational therapies, or new therapeutic indications, extending the scope of the initial patent.

2. Patent Validity and Life Cycle

Given the filing date from 2013 and the typical patent term of 20 years, the patent remains enforceable until roughly 2033, assuming maintenance fees are paid. Validity might be challenged by prior art or inventive step disagreements, but robust prosecution history and strategic claims can bolster durability.

3. Geographic Coverage and Strategic Significance

Holding patent protection in Korea aligns with leveraging South Korea’s vibrant biotech industry and manufacturing capacity. International patent filings expand market access, prevent generic entry, and support licensing agreements.


Implications for Stakeholders

  • Pharmaceutical Innovators: Should analyze the specific claim language and scope to assess freedom-to-operate and opposition vulnerabilities.
  • Generic Manufacturers: Must evaluate the scope to design around claims or challenge validity during patent life.
  • Investors: Can gauge the patent’s strategic value, overlapping claims, and overall strength in the context of the company’s pipeline.

Conclusion and Future Outlook

KR20130079406 exemplifies a typical multidimensional patent strategy—covering chemical novelty, therapeutic use, and formulation—to safeguard pharmaceutical innovation in Korea. Its scope's strength hinges on claim specificity, balancing broad protection with enforceability. As the global patent landscape evolves, patent holders should pursue strategic filings and vigilant patent monitoring to defend market positioning.


Key Takeaways

  • Scope clarity is paramount: Claims must precisely define the chemical structure, formulation, and therapeutic use to withstand prior art challenges.
  • Broad yet defensible claims: Carefully crafted claims protect core innovations while maintaining validity.
  • Strategic patent filing: Filing in multiple jurisdictions enhances market exclusivity and licensing potential.
  • Patent landscape awareness: Understanding overlapping patents allows effective freedom-to-operate analysis.
  • Ongoing patent management: Regular maintenance and monitoring ensure early detection of conflicts and opportunities for expansion.

FAQs

1. How does KR20130079406 protect its core invention?
The patent’s independent claims typically delineate a specific chemical structure or formulation, providing exclusive rights to that core invention across territories where filed.

2. Can the claims be challenged?
Yes, third parties can challenge validity through patent oppositions or litigation based on prior art, lack of novelty, or obviousness. Effective claim drafting and prior art search can mitigate this risk.

3. How does this patent fit into the global patent landscape?
It is likely part of a broader patent family, with equivalents filed internationally to ensure global market protection, especially in major pharmaceutical markets.

4. What type of claims does the patent predominantly contain?
Likely a combination of chemical structure claims, formulation claims, and therapeutic method claims, each serving different strategic purposes.

5. How long does patent protection last for KR20130079406?
Typically, patent protection lasts 20 years from the filing date, assuming all maintenance fees are paid, putting its expiry around 2033.


References
[1] Korean Intellectual Property Office (KIPO). Patent KR20130079406.
[2] WIPO PATENTSCOPE. Patent family overviews and equivalents.
[3] European Patent Office (EPO). Patent strategy and claim drafting standards.

More… ↓

⤷  Start Trial

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.