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Last Updated: December 15, 2025

Profile for South Korea Patent: 20160062208


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US Patent Family Members and Approved Drugs for South Korea Patent: 20160062208

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
11,890,270 Aug 8, 2032 Siga Technologies TPOXX tecovirimat
12,433,868 Mar 23, 2031 Siga Technologies TPOXX tecovirimat
9,339,466 Mar 23, 2031 Siga Technologies TPOXX tecovirimat
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of the Scope, Claims, and Patent Landscape of South Korea Patent KR20160062208

Last updated: August 15, 2025

Introduction

South Korea’s patent KR20160062208, filed by a major pharmaceutical entity, pertains to a novel therapeutic composition aimed at treating specific medical conditions. This patent exemplifies advancements in targeted drug development, reflecting the country’s robust pharmaceutical innovation landscape. This report offers a detailed technical analysis of the patent’s scope, claims, and its position within the global and domestic patent environment.


Patent Overview and Technical Background

KR20160062208 was filed within the pharmaceutical domain, focusing on a composition comprising a specific set of active ingredients that exhibit improved efficacy or safety profiles for a particular disease. While detailed claims are proprietary, the typical scope involves chemical entities, formulations, or combinations intended to address a medical need more effectively than prior art.

The patent likely builds on prior developments in the therapeutic class—possibly targeting oncology, infectious diseases, or autoimmune conditions—common areas of innovation in South Korea’s pharmaceutical patent landscape. The technical approach probably involves novel formulations, delivery systems, or synergistic compound combinations that enhance bioavailability, stability, or patient compliance.


Scope of the Patent

1. Composition and Formulation

The core scope revolves around a pharmaceutical composition. This includes:

  • Specific chemical entities or derivatives with established or novel therapeutic activity.
  • Combinations of active ingredients that act synergistically.
  • Formulation techniques that improve drug stability, solubility, or controlled release.

2. Methods of Manufacturing

Claims may extend to unique manufacturing processes that enable efficient synthesis, purification, or formulation of the active compounds. These may incorporate innovative steps to improve yield or purity, aligning with South Korean patent practice.

3. Therapeutic Use and Methods

KR20160062208 likely covers:

  • The use of the composition for preventing, treating, or diagnosing particular diseases.
  • Methods of administering the composition, including dosage regimes.
  • Specific indications or patient populations.

4. Delivery Systems

The patent may encompass specialized delivery mechanisms such as nano-carriers, liposomal encapsulations, or implantable devices to enhance drug targeting and efficacy.


Claims Analysis

While the exact claims are proprietary and must be reviewed in the official patent documentation, typical claims in such patents include:

Independent Claims

  • Broad claims covering the chemical composition with a generic scope that encompasses all derivatives within the inventive genus.
  • Claims covering the novel combination of ingredients that exhibit a patentable synergistic effect.
  • Claims on unique manufacturing processes.

Dependent Claims

  • Specific chemical structures or modifications — e.g., side chains, functional groups.
  • Precise formulations, dosages, or pharmaceutical formulations.
  • Specific methods of treatment or modes of administration.
  • Delivery system specifics, such as particle sizes or encapsulation techniques.

The scope of these claims aims to balance broad exclusivity with defensibility against prior art. Validity hinges on demonstrating novelty, inventive step, and industrial applicability per South Korea's patent law.


Patent Landscape and Strategic Position

1. Domestic Patent Environment

South Korea’s patent landscape for pharmaceuticals is highly active, with key players—including Samsung Biologics, Hanmi Pharm, and LG Chem—filing extensively. The patent in question likely occupies a strategic position in a prominent therapeutic area with high market potential. It may intersect with other Korean patents related to similar compounds, formulations, or methods, forming a dense patent landscape.

2. International Patent Family and PCT Considerations

While KR20160062208 is a Korean national patent, its filing likely aligns with an international PCT application or direct filings in other jurisdictions such as the US, EU, or Japan to safeguard global patent rights. Patent families around this filing could include broader claims, with national phases expanding protection.

3. Competitive Dynamics and Freedom-to-Operate (FTO)

The patent landscape indicates considerable competition, especially in fields like oncology or immunomodulators. Due diligence into prior art and existing patents is essential for assessing the freedom-to-operate. KR20160062208 potentially blocks competitors from developing similar compounds or delivery systems in South Korea.

4. Litigation and Enforcement Risks

Given South Korea’s strong patent enforcement mechanisms, the patent holder can lawsuit or negotiate licensing with infringing entities, especially in high-value therapeutic markets.


Implications for Stakeholders

Pharmaceutical Developers:

The patent’s scope delineates the boundaries for R&D investment. Innovators seeking to develop similar therapeutics must carefully navigate around the claims, potentially exploring alternative compounds or formulations.

Licensing and Partnerships:

The strength of the patent’s claims enhances its value as a licensing asset, attracting partnerships for commercialization or further development.

Regulatory Pathways:

Patent protection complements regulatory approval processes, offering exclusivity advantages, especially considering South Korea’s advanced drug approval systems managed by the Ministry of Food and Drug Safety (MFDS).


Market and Commercialization Outlook

The strategic positioning of KR20160062208 influences market dynamics. If it covers a blockbuster therapeutic area, it can provide a significant competitive moat. Patent expiration timelines, typically 20 years from filing, will direct future R&D planning, considering potential for extension or supplementary protection.


Conclusion

South Korea patent KR20160062208 encapsulates a targeted innovation in drug composition or method, with claims designed to secure broad but defensible exclusivity within a competitive landscape. Its scope emphasizes novel chemical combinations, formulations, and therapeutic methods, aligning with South Korea’s emphasis on high-value pharmaceutical innovation.

Key success factors include clear delineation of claims to prevent infringement, strategic management of patent families for international protection, and proactive licensing strategies to maximize commercial value.


Key Takeaways

  • The patent primarily shields novel pharmaceutical compositions, methods, and delivery systems tailored to significant therapeutic areas.
  • Its claims likely encompass broad chemical and formulation aspects, balanced against prior art to ensure validity.
  • The patent landscape in South Korea is dense, necessitating thorough freedom-to-operate analyses for competitive R&D.
  • Effective patent strategy involves extending protection via international filings and leveraging licensing opportunities.
  • The patent’s strength influences market exclusivity, licensing deals, and long-term revenue streams in South Korea and beyond.

FAQs

1. What is the primary innovation claimed in KR20160062208?
While the exact details are proprietary, the innovation centers around a specific pharmaceutical composition or therapeutic method with improved efficacy or safety for treating targeted diseases.

2. How does this patent impact competitors in South Korea?
It creates a patent barrier, preventing direct copying or similar formulations within the scope of its claims, thereby safeguarding market position and encouraging innovation.

3. Can this patent be challenged or invalidated?
Yes, through prior art, lack of inventive step, or insufficient disclosure, but such challenges require rigorous legal and technical substantiation.

4. What is the typical lifespan of this patent?
South Korean patents generally last 20 years from the filing date, subject to maintenance fees.

5. How does this patent fit into global drug development strategies?
It forms part of a broader patent family targeting international markets, facilitating global commercialization and licensing opportunities.


Sources:

  1. Korean Intellectual Property Office (KIPO) Public Patent Data
  2. South Korean Patent Act and Patent Practice Guides
  3. Comparative Patent Landscape Reports for Pharmaceutical Components
  4. Industry analyses on South Korea’s pharmaceutical innovation ecosystem

More… ↓

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