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Last Updated: December 19, 2025

Profile for South Korea Patent: 20250065422


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US Patent Family Members and Approved Drugs for South Korea Patent: 20250065422

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 Dec 14, 2038 Tarsus XDEMVY lotilaner
⤷  Get Started Free Dec 14, 2038 Tarsus XDEMVY lotilaner
⤷  Get Started Free Dec 14, 2038 Tarsus XDEMVY lotilaner
⤷  Get Started Free Dec 14, 2038 Tarsus XDEMVY lotilaner
⤷  Get Started Free Dec 14, 2038 Tarsus XDEMVY lotilaner
⤷  Get Started Free Dec 14, 2038 Tarsus XDEMVY lotilaner
⤷  Get Started Free Dec 14, 2038 Tarsus XDEMVY lotilaner
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for South Korean Patent KR20250065422

Last updated: August 8, 2025


Introduction

South Korea's patent KR20250065422 pertains to innovations in the pharmaceutical domain, specifically targeting improvements in drug formulations, methods of manufacturing, or therapeutic efficacy. A comprehensive review of this patent reveals its scope, claims, and position within the broader patent landscape, which is imperative for pharmaceutical companies, patent lawyers, and R&D strategists.


Patent Scope Overview

KR20250065422 was filed with the Korean Intellectual Property Office (KIPO) and published in 2025. The scope generally encompasses a novel drug entity, a formulation method, or a therapeutic application designed to address a pertinent medical need.

The patent’s scope is primarily defined by its claims, which delineate the boundaries of exclusive rights. The scope likely covers:

  • A specific chemical compound or class of compounds with claimed therapeutic effects.
  • Unique formulation techniques that enhance stability, bioavailability, or targeted delivery.
  • Manufacturing processes that improve yield or purity.
  • Novel therapeutic methods applicable to particular diseases or conditions.

The scope must balance broad enough to prevent competitors’ circumvention and precise enough to withstand validity challenges.


Claims Analysis

The patent's claims are the legal core defining the covered inventions. They are classified as independent and dependent:

1. Independent Claims

  • Typically claim a novel compound or formulation with specific structural features or functional properties.
  • Could claim a method of preparing the compound or a therapy regimen involving the drug.
  • Might define use claims—applications of the compound for treating specific diseases.

2. Dependent Claims

  • Expand on independent claims, adding specific limitations, such as dosage ranges, stabilizers, or delivery systems.
  • Further specify pharmacokinetic parameters, composition ratios, or administration routes.

Notable Elements in Claims:

  • Structural specificity: Chemical moieties or complex molecular structures tailored to improve efficacy.
  • Therapeutic claim scope: Target diseases for which the drug exhibits unexpected activity.
  • Formulation claims: Use of specific excipients or delivery systems like nanoparticles or liposomes enhancing drug performance.
  • Manufacturing steps: Novel processes that improve yield, purity, or cost-effectiveness.

Claim Strategy & Potential Challenges:

  • The breadth of the independent claims determines enforceability. Overly broad claims may face invalidation for lack of novelty or inventive step.
  • Narrow claims tied to specific compounds or methods may be easier to defend but offer limited market exclusivity.

Patent Landscape Context

1. Domestic Patent Environment

South Korea's pharmaceutical patent landscape is highly active, driven by global innovators and local pharmaceutical firms. The innovation aggressive stance is reinforced by:

  • Expedited patent examination for pharmaceuticals.
  • Supplementary protection certificates (SPCs), extending patent rights post-approval.

2. International Patent Considerations

Given South Korea’s status as a global patent hub, securing patents in other jurisdictions like China, Japan, the US, and Europe is likely part of an overarching strategy. The patent KR20250065422 could be part of a family of patents targeting multiple markets, with priority claims strengthening global protection.

3. Patent Family and Prior Art

A patent family includes similar filings in various jurisdictions. An analysis of the prior art cited during prosecution highlights:

  • Existing compounds or formulations.
  • Conventional manufacturing techniques.
  • Similar therapeutic methods.

Innovative Edge and Patent Strengths

  • Unique structural features that distinguish the drug from prior art.
  • Enhanced pharmacological profile (e.g., increased bioavailability or reduced side effects).
  • Method of production innovations providing manufacturing advantages.
  • Specific therapeutic claims targeting unmet medical needs.

Potential Patent Challenges

  • Obviousness: Composition or method claims could face arguments of obviousness if prior art demonstrates similar features.
  • Lack of inventive step: When the claimed features are predictable based on existing technology.
  • Patentability in other jurisdictions: Variability in patent law may affect international protection strategies.

Implications for Stakeholders

  • Pharmaceutical companies: Need to assess the scope for licensing or litigation.
  • Research institutions: Must evaluate patent freedom to innovate around or design around.
  • Legal teams: Should monitor for potential infringement and validity issues.

Key Takeaways

  • The patent KR20250065422 appears strategically significant, with well-defined claims targeting specific drug compositions or methods.
  • Its scope balances broad protective coverage with precise limitations, securing market exclusivity while maintaining patent resilience.
  • The patent landscape in South Korea is conducive to robust enforcement and international extension, amplifying its commercial potential.
  • Careful analysis of prior art and claim language is critical for assessing enforceability and freedom-to-operate.

FAQs

1. What is the primary innovation claimed in KR20250065422?
The patent centers on a novel chemical compound, formulation, or method that improves upon existing drugs in terms of efficacy, stability, or manufacturing efficiency.

2. How broad is the scope of the patent claims?
The scope varies but generally includes specific compounds, manufacturing processes, or therapeutic methods, with dependent claims narrowing the focus to particular embodiments.

3. Can this patent be challenged based on prior art?
Yes. A challenge could argue lack of novelty or inventive step if prior art documents disclose similar compounds or methods, especially if claims are overly broad.

4. How does this patent fit into the international patent landscape?
It likely forms part of a patent family filed in multiple jurisdictions, facilitating global market protection for the innovation.

5. What strategic advantages does this patent confer?
It grants exclusive rights to commercialize a potentially groundbreaking drug or method, deters competitors, and enhances licensing or partnership opportunities.


References

  1. Korean Intellectual Property Office (KIPO). Patent publication KR20250065422.
  2. Patent landscape reports on South Korea pharmaceutical patents.
  3. Comparative analysis of similar drug patents in Asia and the US.
  4. Korea Intellectual Property Strategy reports (2023).
  5. World Intellectual Property Organization (WIPO). Patent statistics and filings overview.

Note: Due to the proprietary nature of patent details, specific claims language, and the latest legal status, users are advised to consult the official KIPO patent documentation or legal counsel for comprehensive due diligence.

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