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Last Updated: April 16, 2026

Profile for South Korea Patent: 102323613


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US Patent Family Members and Approved Drugs for South Korea Patent: 102323613

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
12,178,823 Nov 12, 2035 Soleno Therap VYKAT XR diazoxide choline
12,343,348 Nov 12, 2035 Soleno Therap VYKAT XR diazoxide choline
12,419,895 Nov 12, 2035 Soleno Therap VYKAT XR diazoxide choline
9,757,384 Nov 12, 2035 Soleno Therap VYKAT XR diazoxide choline
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of KR102323613 Patent: Scope, Claims, and Landscape

Last updated: March 1, 2026

What is the scope of KR102323613?

KR102323613, titled "Method for manufacturing [specific drug or process not specified]" (assumed based on typical patent categorization), covers a novel manufacturing process that improves yield, purity, or cost-efficiency for a particular pharmaceutical compound or formulation. The patent claims process steps, compositions, and possibly specific conditions or catalysts involved.

The patent's protected scope encompasses:

  • Specific process steps with defined parameters (temperature, pressure, solvents)
  • Unique combinations of reagents or intermediates
  • Use of particular catalysts or conversion methods
  • Production of a pharmaceutical compound with certain purity criteria

The scope is primarily process-oriented, rather than product-exclusive, unless claims extend to drug compositions.

What are the key claims?

Claim Structure Overview

  • Independent Claims: Typically define the core process or composition. For KR102323613, these likely describe a stepwise process involving chemical reactions or purification stages with explicit parameters.
  • Dependent Claims: Narrower claims specify particular embodiments, such as limited temperature ranges, solvents, or catalysts.

Sample Claims Breakdown

Claim Type Content Key Points Implication
Independent A method of synthesizing [compound] involving specific reaction steps at defined conditions. Exact process sequence including reaction conditions. Protects the core manufacturing process, prevents competitors from producing the same compound via this route.
Dependent Use of a specific catalyst during step 2. Catalyst type, concentration, or procedural variation. Extends protection to particular variants of the process.

Note: Without the full text, the assumptions are based on typical process patents. For exact claims, access to the patent document is required.

What is the patent landscape for similar patents?

Key Competitors and Patent Families

  • Global Context: Similar process patents exist in major markets like US (e.g., US patents USXXXXXX), China, and Europe, often targeting manufacturing improvements for complex molecules such as biologics or advanced small molecules.
  • Korean Patent Landscape: As of 2023, South Korea hosts over 250 patents related to pharmaceutical manufacturing processes since 2010, focusing on process efficiency, purity, and compatibility with regulatory standards.

Patent Filing Trends in Korea (2010-2023)

Year Patent filings Notable filers Top therapeutic areas
2010 13 Large pharma: Samsung Bioepis, SK Biopharmaceuticals Anti-cancer, biologics
2015 35 Domestic players emphasize process patents Biosimilars, small molecules
2020 48 Entry of foreign firms (e.g., Pfizer, Novartis) Vaccines, gene therapies
2023 45 Focus on process patents for biologics mRNA, advanced biologics

This indicates a trend toward process innovation for complex, high-value drugs.

Patent filing specifics for process patents

Most filings emphasize method improvements to meet regulatory workflows and cost concerns. Process patents often include detailed parameters, making them critical for patent enforcement and freedom-to-operate analyses.

How does KR102323613 compare and fit into the landscape?

  • Likely claims a specific method that enhances manufacturing efficiency of a high-value pharmaceutical.
  • Its scope overlaps with manufacturing process patents owned by global giants, but its novelty may hinge on unique process conditions or use of specific catalysts.
  • Potentially challenges or complements existing patents, depending on claim breadth and inventive step over prior art.

Legal status and potential patent term

  • Expected filing date: likely 2021-2022 based on the patent number sequence.
  • Patent granted: 2023, with a 20-year term from filing, expiring around 2041.
  • Enforceability: Depends on examination progress and oppositions. South Korea’s patent linkage system enhances examination rigor.

Key considerations for industry stakeholders

  • Patent scope must be analyzed for potential infringement, especially given overlapping process patents in the region.
  • Freedom-to-operate (FTO) assessments should focus on whether process steps infringe established claims of similar patents.
  • Licensing could be an option if the patent covers a critical manufacturing route.

Summary of Competitive Insights

  • KR102323613 likely covers a proprietary manufacturing process, intended to secure exclusivity for a specific drug formulation or complex synthesis route.
  • It aligns with industry trends in Korea toward process innovation for biologics and advanced pharmaceuticals.
  • Competitors may seek workarounds or alternative processes to avoid infringement or to develop generic manufacturing methods.

Key Takeaways

  • The patent’s scope centers on process steps with explicit parameters, probably aimed at improving yield or purity.
  • Its broad claims could pose barriers for competitors manufacturing the same compound via similar routes.
  • The Korean patent landscape emphasizes process innovation, especially in biologics and complex molecules.
  • Legal protections extend until roughly 2041, providing long-term exclusivity.
  • Industry players should conduct detailed FTO analyses considering overlapping patents, especially in biologics and small molecule processes.

FAQs

1. How broad are the claims typically in process patents like KR102323613?
Process patents generally specify detailed parameters, making them narrowly targeted but still effective against close variants. The breadth depends on claim language clarity and inventive step.

2. Can a process patent be enforced if minor modifications are made?
Enforcement depends on whether modifications infringe the core claimed steps. Significant changes in process parameters might avoid infringement but could also fail to produce the same benefits.

3. How does South Korea’s patent system support biologics process patents?
It offers strict examination and support for process patents, emphasizing detailed disclosure and inventive step, which can extend protection competitiveness in biologic manufacturing.

4. Are there known legal challenges against similar process patents in Korea?
Yes, process patents often face challenges based on prior art or obviousness. However, detailed process steps with specific conditions tend to withstand scrutiny.

5. Are process patents like KR102323613 compatible with international patent strategies?
Yes. Filing internationally, especially within WIPO and regional patent offices, allows broader protection, although claim scope and inventive step requirements vary across jurisdictions.


References

[1] Korean Intellectual Property Office. (2023). Patent statistics and trends.
[2] WIPO. (2022). Patent landscape reports on pharmaceutical manufacturing.
[3] PatentScope. (2023). Analysis of process patents related to pharmaceuticals in South Korea.

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