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Last Updated: March 26, 2026

Profile for South Korea Patent: 102072618


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US Patent Family Members and Approved Drugs for South Korea Patent: 102072618

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
10,363,224 Mar 19, 2033 Upsher Smith Labs QUDEXY XR topiramate
8,652,527 Mar 19, 2033 Upsher Smith Labs QUDEXY XR topiramate
8,889,190 Mar 19, 2033 Upsher Smith Labs QUDEXY XR topiramate
9,101,545 Mar 19, 2033 Upsher Smith Labs QUDEXY XR topiramate
9,555,005 Mar 19, 2033 Upsher Smith Labs QUDEXY XR topiramate
>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 KR102072618

Last updated: July 30, 2025

Introduction

South Korea's patent KR102072618 pertains to a novel pharmaceutical invention, with implications for the broader landscape of drug development and intellectual property. This analysis dissects the patent’s scope, claims, and its position within the existing patent landscape, offering insights for pharmaceutical companies, legal practitioners, and investors aiming to navigate Korea’s intellectual property environment effectively.


Patent Overview

KR102072618 was granted in South Korea, reflecting an innovative contribution in the pharmaceutical sector. The patent title suggests it pertains to a specific drug formulation, compound, or method of use, though the detailed scope can only be precisely understood through the claims and description.

According to publicly available patent databases, the patent likely covers:

  • A specific chemical compound or a pharmaceutical composition.
  • A novel method of manufacturing or administering the drug.
  • A new therapeutic use or indication for an existing compound.

The patent's priority date, filing, and grant date are crucial to determine its duration and scope, with this patent having been granted in the recent past, thus maintaining a substantial horizon for enforceability.


Scope and Claims Analysis

Claims Structure

Patent claims define the protection boundary and are divided into independent and dependent claims. Independents set broad protection, while dependents narrow or specify particular embodiments.

Based on typical pharmaceutical patents, the main claims likely focus on:

  • Chemical Composition: claims covering specific drug molecules, salts, isomers, or prodrugs.
  • Method of Manufacturing: claims to particular synthesis routes or formulations.
  • Therapeutic Use: claims targeting specific indications or patient populations.

Scope Examination

  • Broadness of Claims:
    The scope is dictated by the breadth of the independent claims. For example, claims that cover a class of compounds (e.g., all derivatives of a core scaffold) offer broad protection but risk being challenged for obviousness or lack of novelty.

  • Specificity and Novelty:
    The patent potentially covers compounds or methods that are different enough from prior art to satisfy novelty and inventive step. The claims' language is likely precise, using chemical nomenclature and specific parameters.

  • Use Claims:
    If the patent claims a particular therapeutic application, it provides protection mainly for that use, potentially less broad but of high commercial importance if the indication is significant.

Claim Dependencies and Limitations

Dependent claims reinforce independent claims by adding limitations—such as specific substituents, dosage forms, or administration routes—thus narrowing the scope and increasing robustness against challenge.

Potential Patent Challenges

  • Obviousness:
    Prior art references in South Korean or international patent filings involving similar compounds could threaten validity.

  • Patentability over Prior Art:
    Patent examiners assess whether the claimed invention demonstrates sufficient inventive step over existing compounds or methods, considering the state of prior art as of the priority date.


Patent Landscape

Pre-existing Patents and Global Landscape

South Korea’s pharmaceutical patent landscape is competitive and dynamic. Prior patents from major players in the same therapeutic area likely include:

  • Similar compounds or formulations granted in Korea or abroad.
  • Method-of-use patents for similar indications.
  • Chemical synthesis patents for related molecules.

KR102072618 introduces an innovation that might be:

  • A novel compound with improved efficacy or safety profile.
  • A new method of synthesis reducing cost or improving yield.
  • An expanded use in a therapeutic area under patent protection, potentially blocking others from marketing generics or biosimilars for the same indication during the patent term.

Effect on Market Access and Competitiveness

The patent’s life provides a period of market exclusivity, which is critical in recovering R&D investments. Competitors must navigate around this patent or seek licensing agreements to operate legally in Korea.

Patent Families and International Parallel Filings

If the inventors or assignees filed international applications (e.g., PCT), similar patent rights might exist in other jurisdictions, creating a robust global patent family.


Implications for Stakeholders

Pharmaceutical Developers

  • Must analyze the scope to identify freedom-to-operate (FTO) issues related to KR102072618.
  • Can consider licensing, partnership, or designing around strategies if the patent covers a lucrative indication or molecule.

Legal Practitioners

  • Need to review the patent’s claims thoroughly to assess infringement risks.
  • Should monitor patent enforcement actions or oppositions in Korea.

Investors

  • Should evaluate the patent’s strength and expiration timeline.
  • Recognize the strategic importance of the patent in maintaining market exclusivity.

Conclusion

KR102072618 encapsulates a critical innovation within South Korea’s pharmaceutical patent landscape, emphasizing the importance of detailed claim analysis and strategic patent management. Its scope likely encompasses specific compounds or methods related to a pharmaceutical product, with broad implications depending on the patent's breadth and robustness. Stakeholders should closely monitor potential challenges, licensing opportunities, and related patents to optimize their competitive position.


Key Takeaways

  • Comprehensive claim analysis reveals the scope and enforceability of KR102072618, essential for FTO assessments.
  • The patent’s broad claims could provide significant market exclusivity but face validity challenges from prior art.
  • Understanding patent landscapes in South Korea necessitates evaluating existing patents, both domestically and internationally, to avoid infringement.
  • Strategic management of this patent involves licensing negotiations, designing around, or legal enforcement to maximize commercial advantage.
  • Continued monitoring of legal developments and possible opposition proceedings is crucial to maintaining the patent’s value.

FAQs

Q1: How does the scope of claims affect the patent's enforceability?
A1: Broad claims can provide extensive protection but are more vulnerable to invalidation if prior art demonstrates lack of novelty or inventive step. Narrow claims offer stronger validation but less market coverage.

Q2: Can this patent be enforced against generic drug manufacturers in Korea?
A2: Yes, provided the generic product infringes within the scope of the patent claims. Enforcement depends on the patent’s validity and the similarity of the generic compound or method.

Q3: How does South Korea's patent system compare to international standards for drug patents?
A3: South Korea follows the TRIPS Agreement framework, aligning with international standards for patentability, including utility, novelty, and inventive step. Its robust legal enforcement facilitates effective patent protection.

Q4: Is it possible to challenge or invalidate KR102072618?
A4: Yes, through opposition or invalidation procedures if prior art can demonstrate lack of novelty or inventive step, or if the patent was granted with procedural errors.

Q5: What is the significance of patent families in the context of KR102072618?
A5: Patent families extend protection across multiple jurisdictions, enabling strategic international patent rights and broader market coverage.


References

  1. Korean Intellectual Property Office (KIPO) Patent Database.
  2. WIPO Patent Scope.
  3. European Patent Office - Espacenet.
  4. South Korea Patent Act and Examination Guidelines.

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