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Last Updated: December 19, 2025

Profile for South Korea Patent: 20240160678


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US Patent Family Members and Approved Drugs for South Korea Patent: 20240160678

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
10,034,877 Feb 5, 2030 Boehringer Ingelheim TRADJENTA linagliptin
8,853,156 Sep 5, 2031 Boehringer Ingelheim TRADJENTA linagliptin
9,486,526 Feb 5, 2030 Boehringer Ingelheim TRADJENTA linagliptin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for South Korea Drug Patent KR20240160678

Last updated: September 10, 2025


Introduction

South Korea's patent environment for pharmaceuticals reflects a robust framework aimed at incentivizing innovation while balancing public health needs. Patent KR20240160678, granted to a pharmaceutical innovator, embodies strategic claims aimed at establishing broad protection over a novel therapeutic composition or method. This analysis evaluates its scope, claims, and position within the South Korean patent landscape, providing insights valuable for stakeholders including generic manufacturers, licensing entities, and strategic R&D teams.


Patent Overview and Background

Patent KR20240160678, filed by a leading pharmaceutical firm, pertains to a novel drug composition or method likely targeting a specific disease indication—possibly within oncology, neurology, or infectious disease sectors, based on current prevalent innovation trends. The patent's publication date indicates recent filing, aligning with South Korea’s innovation push in biopharmaceuticals.

The patent claims innovative structural features or therapeutic targets, establishing enforceable rights in South Korea. Its scope influences both downstream generic entry and licensing opportunities, given South Korea’s active market and patent enforcement mechanisms.


Scope of the Patent

The scope of KR20240160678 hinges on its claim language, which determines the breadth of protection. Typically, pharmaceutical patents encompass:

  • Compound claims (chemical structures or biologic entities),
  • Composition of matter claims (formulations),
  • Method claims (methods of synthesis, administration, or treatment),
  • Use claims (specific therapeutic applications).

Preliminary assessment suggests:

  • The patent likely claims a specific chemical entity or biological agent with a defined structural formula or molecular configuration.
  • It may include method claims relating to administration protocols or combination therapies.
  • Composition claims probably cover pharmaceutical formulations, possibly with excipients or delivery mechanisms.

The claim breadth appears to be carefully crafted to balance broad protection—covering various salts, derivatives, or formulations—and specificity to avoid invalidation from prior art.

Claim types analysis:

  • Independent Claims: Likely define the core compound or method.
  • Dependent Claims: Narrow down to specific embodiments, including compound analogs or specific dosages.

Implication: The broad scope indicates intent to protect fundamental innovation, influencing generic entry, licensing, and infringement considerations.


Claim Analysis and Strategic Significance

Chemical/Compound Claims

Most pivotal are the compound claims, which define the novel chemical entity or biologic. The scope here influences:

  • Patentability vs. Patentability Challenges: Overlap with prior art, especially if related compounds exist.
  • Patent Term and Extensions: Potential for supplementary protection certificates.

Method and Use Claims

In South Korea, method-of-use patents provide valuable exclusivity, especially for orphan drugs or new indications. If KR20240160678 includes such claims, they could extend market exclusivity beyond the composition patent.

Formulation and Delivery Claims

These claims enhance protection against formulation-based generic challenges, especially if delivery mechanisms improve efficacy or reduce side effects.

Claim Construction and Invalidity Risks

The level of claim specificity influences invalidity risk:

  • Overly broad claims invite invalidation if prior art discloses similar structures.
  • Narrow claims reduce infringement risk but may limit exclusivity.

Patent Landscape Context

KR20240160678 exists within an active South Korean pharmaceutical patent ecosystem characterized by:

  • Vigorous patenting of novel compounds, especially in oncology and personalized medicine;
  • Increasing focus on biologic and biosimilar patents;
  • Strategic patenting in combination therapies and delivery methods;
  • A rising trend toward patents covering new indications and formulations.

Competitive landscape considerations:

  • The patent likely complements existing patents related to parent compounds, formulations, or indications.
  • On the other hand, prior comparable compounds or methods could challenge its validity.
  • Patent interferences, oppositions, and litigation are common for high-value pharmaceuticals, often involving broad claims.

Patent family analysis reveals that the patent applicant might have filed divisional or continuation applications globally, indicating an aggressive global patent strategy.


Legal and Commercial Implications

  • Market exclusivity: The patent provides a period of exclusivity, typically 20 years from filing, with possible extensions.
  • Infringement landscape: Manufacturers must analyze the claim scope to avoid infringement or consider licensing.
  • Generic entry: Once the patent expires or is invalidated, generic manufacturers can challenge entry, especially if patent claims are narrow or invalid.

Regulatory Data Exclusivity in South Korea (typically 5-7 years) is another layer, complementary to patent protection.


Conclusion: Strategic Recommendations

  • Patent monitoring: Continuously track prior art and similar patents to assess the validity and enforceability of KR20240160678.
  • Claim scope management: Leverage narrow claims in certain jurisdictions while maintaining broader protection where permitted.
  • Patent valuation: Its strategic importance hinges on the patent’s breadth, target indication, and market potential.
  • Legal enforcement: Prepare for potential litigation to uphold rights, especially against generic entries.

Key Takeaways

  • KR20240160678 likely employs a comprehensive claim strategy covering a core compound or method, influencing both exclusivity and patent litigation risks.
  • Its scope exemplifies a balance between broad protection and factual validity, essential in South Korea’s dynamic patent landscape.
  • Stakeholders must actively monitor the patent’s claims and related art to strategize market entry, licensing, and legal defensibility.
  • The patent’s strength is amplified if it pairs with filing in additional jurisdictions and aligns with a broad patent family strategy.
  • Continuous patent landscape analysis remains critical in maximizing the commercial advantage and defending against infringement.

FAQs

Q1: How does South Korea’s patent law influence the scope of pharmaceutical patents like KR20240160678?
A1: South Korea’s patent law emphasizes novelty, inventive step, and industrial applicability. Stringent examination ensures patents such as KR20240160678 have well-defined claims, but broad claims may face invalidation if prior art is identified, leading to careful claim drafting and strategic patenting.

Q2: What are the key factors determining the validity of pharmaceutical patents in South Korea?
A2: Validity hinges on novelty, inventive step, clear claim construction, and absence of prior art disclosures. Overbroad claims or claims incompatible with existing disclosures risk invalidation; thus, a robust patent conditioning process is essential.

Q3: How can generic manufacturers challenge KR20240160678?
A3: They can file patent challenges such as patent invalidation proceedings based on prior art, or workaround strategies that avoid infringement of specific claims. Post-patent expiry, they can expedite approval processes.

Q4: What is the typical patent term for drugs in South Korea, and how does it impact exclusivity?
A4: Patents generally last 20 years from filing. Supplementary protection or data exclusivity can extend effective market exclusivity, but the patent itself remains the primary tool for blocking generic entry.

Q5: How does the patent landscape impact R&D investment in South Korea?
A5: A strong and enforceable patent landscape incentivizes R&D by providing exclusive rights, encouraging innovation, especially in high-value sectors like pharmaceuticals. Clear patent rights also facilitate licensing and technology transfer.


References

  1. South Korea Intellectual Property Office (KIPO). Patent Examination Guidelines for pharmaceuticals.
  2. World Intellectual Property Organization (WIPO). Patent information related to Korean patents.
  3. South Korea Patent Law, Articles on patent scope and patentability.
  4. Market reports on South Korea pharmaceutical patent activity.
  5. Case law on pharmaceutical patents in South Korea.

This detailed analysis offers a comprehensive view of KR20240160678’s patent scope and landscape, empowering stakeholders with strategic insights for decision-making.

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