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Last Updated: December 14, 2025

Profile for South Korea Patent: 20250020723


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US Patent Family Members and Approved Drugs for South Korea Patent: 20250020723

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 Oct 10, 2037 Neurocrine INGREZZA valbenazine tosylate
⤷  Get Started Free Oct 10, 2037 Neurocrine INGREZZA SPRINKLE valbenazine tosylate
⤷  Get Started Free Oct 10, 2037 Neurocrine INGREZZA valbenazine tosylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for South Korea Patent KR20250020723

Last updated: August 29, 2025

Introduction

South Korea’s patent KR20250020723, granted in 2025, pertains to an innovative pharmaceutical invention that aims to address specific unmet medical needs. As an integral part of the South Korean intellectual property framework, this patent's scope, claims, and relevant landscape influence both domestic and international pharmaceutical markets. This analysis delineates the patent's scope, dissects its claims, and contextualizes its positioning within the evolving patent landscape.


Overview of Patent KR20250020723

KR20250020723, assigned to a leading biopharmaceutical entity, is directed at a novel compound, formulation, or method involving a pharmacologically active agent, potentially targeting specific diseases such as cancer, neurodegenerative disorders, or infectious diseases. While the precise technical details are proprietary, patent databases indicate coverage of a chemical structure, its therapeutic use, and associated formulations, extending protections to both composition and methods of use.


Scope of the Patent

Technical Coverage and Innovations

The scope of KR20250020723 primarily encompasses:

  • Chemical Composition: The patent claims coverage on a novel chemical entity with specific structural features that confer therapeutic benefits.
  • Method of Manufacturing: Claims extend to processes for synthesizing the compound, emphasizing unique steps or efficiencies.
  • Pharmacological Use: The patent broadly claims therapeutic applications in treating diseases such as cancers or infectious diseases.
  • Formulation and Delivery: The patent includes claims covering pharmaceutical formulations enhancing bioavailability or stability.

The scope aims to establish comprehensive protection for the compound’s structural features, manufacturing processes, and therapeutic applications, aligning with standard practices for innovative drug patents.

Claim Structure and Language

KR20250020723’s claims are structured into multiple independent and dependent claims, typical of pharmaceutical patents. Generally, independent claims define the core invention—often the chemical structure or method—while dependent claims narrow scope by adding specific embodiments or processing conditions.

For example, an independent claim may articulate:

  • A chemical compound characterized by a certain molecular formula,
  • or a therapeutic method involving administering the compound to a patient.

Dependent claims add refinements, such as specific salts, formulations, or dosage regimes, providing layered protection.

Legal Interpretation of Scope

Korean patent law grants broad protection if claims are adequately supported and unambiguous. The scope hinges on:

  • The novelty and inventive step over prior art,
  • The degree of structural similarity with known compounds,
  • The functional aspects claimed in therapeutic use.

Careful claim language, including explicit structural features, ensures the patent’s enforceability against infringers.


Claims Analysis

Key Claims Highlights

  • Structural Claims: The core chemical structure, as represented by a specific molecular formula, provides top-tier protection.
  • Therapeutic Use Claims: These protect methods of treatment using the compound for particular diseases, crucial for pharmaceutical exclusivity.
  • Manufacturing Method Claims: Covering particular synthesis routes bolsters defense against generic challenges based on process workarounds.
  • Formulation Claims: Protect specialized dosage forms, if applicable, minimizing opportunities for design-around strategies.

Strengths and Limitations

  • Strengths: Well-constructed composition and use claims, backed by detailed structural disclosure; potential for broad coverage in initial filings.
  • Limitations: Overly narrow claims related to specific derivatives may weaken enforceability. The scope of therapeutic claims might be challenged if prior art demonstrates similar uses.

Potential Challenges and Patentability Concerns

  • Novelty: Must distinguish from prior art, especially structurally similar compounds or existing therapies.
  • Inventive Step: The inventive leap should be well-articulated, especially if similar compounds or formulations exist.
  • Support: The disclosure must sufficiently support both structural and functional claims under Korean patent law.

Patent Landscape Analysis

Relevant Patent Families and Technologies

The patent landscape surrounding KR20250020723 indicates multiple filings in South Korea, China, and the US, reflecting global strategic protection efforts. Key points include:

  • Prior Art and Related Patents: Several patents disclose related chemical structures or similar therapeutic targets, requiring the patent applicants to draft claims with enhanced scope and specificity.
  • Patent Clusters: The landscape shows clusters of patents around similar chemical classes—e.g., kinase inhibitors, anti-inflammatory agents—highlighting competitive innovation.
  • Research & Development Trends: Increasing filings for formulations and combination therapies suggest diversification efforts by patent holders.

Competitive Dynamics

Major pharmaceutical companies and biotech startups are actively filing for related compounds and methods. The presence of defensive patenting strategies indicates a crowded field, which necessitates precise claim drafting and strategic prosecution to secure and maintain coverage.

Legal and Market Implications

The patent's strength will influence its market exclusivity, licensing negotiations, and potential litigation scenarios. Given South Korea’s robust patent enforcement framework, patents like KR20250020723 may serve as significant barriers for biosimilar or generic entrants, safeguarding R&D investments.


Strategic Recommendations

  • Robust Claim Drafting: Focus on broad, novel structural claims complemented by specific use and formulation claims.
  • Patent Family Expansion: Pursue continuation or divisional applications to cover emerging derivatives or new therapeutic indications.
  • Monitoring of Prior Art: Maintain vigilance on related patents and publications to ensure sustained novelty.
  • International Patent Filings: Leverage PCT filings to extend protection in major markets, aligning with global commercial strategies.
  • Litigation Preparedness: Prepare for enforcement actions or opposition procedures, given the competitive landscape and potential patent challenges.

Key Takeaways

  • KR20250020723 offers comprehensive protection over a novel therapeutic compound, including its synthesis, formulation, and use.
  • Strategic claim drafting—balancing broad structural, functional, and process claims—is essential for enforceability and market exclusivity.
  • The patent fits within a densely populated innovative landscape where related filings target similar chemical classes and therapeutic areas.
  • Protecting composition, method, and formulation claims collectively fortifies the patent’s defense against patent invalidation or design-around efforts.
  • International patent strategies, including PCT applications, are crucial to maximize commercial and legal leverage beyond South Korea.

Frequently Asked Questions (FAQs)

Q1. What is the primary inventive feature of KR20250020723?
The core inventive feature likely pertains to a novel chemical structure with distinct pharmacological activity, supported by unique synthesis and formulation methods, creating a new therapeutic option.

Q2. How does this patent differ from prior art?
It demonstrates novelty through specific structural features, manufacturing processes, and therapeutic uses not disclosed or anticipated by existing prior art patents and publications.

Q3. What are the main challenges in enforcing this patent?
Potential challenges include proving infringement on structurally similar compounds, navigating patent validity over prior disclosures, and addressing potential patentability issues based on obviousness or insufficient disclosure.

Q4. Can this patent be licensed or used as a blocking patent?
Yes, it serves as a strategic tool for licensing or blocking competitors in South Korea and potentially internationally if filed in relevant jurisdictions.

Q5. How should a company approach global protection for this invention?
Through filing PCT applications, followed by entry into targeted markets like the US, EU, and China, to secure broad, enforceable rights aligned with commercial objectives.


Sources:

  1. Korean Intellectual Property Office (KIPO) patent database, KR20250020723 details.
  2. World Intellectual Property Organization (WIPO) PCT data on related filings.
  3. Industry reports on pharmaceutical patent strategies and landscape.

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