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Last Updated: December 19, 2025

Profile for South Korea Patent: 20220028125


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US Patent Family Members and Approved Drugs for South Korea Patent: 20220028125

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
10,028,995 Dec 18, 2034 La Jolla Pharma GIAPREZA angiotensin ii acetate
10,493,124 Dec 18, 2034 La Jolla Pharma GIAPREZA angiotensin ii acetate
11,096,983 Dec 18, 2034 La Jolla Pharma GIAPREZA angiotensin ii acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of South Korean Patent KR20220028125: Scope, Claims, and Patent Landscape

Last updated: August 8, 2025

Introduction

Patent KR20220028125, granted by the Korean Intellectual Property Office (KIPO), pertains to a novel pharmaceutical compound or formulation. This patent reaffirms South Korea's strategic focus on advanced drug innovation, aligning with its broader national initiatives to bolster biopharmaceutical competitiveness. This analysis explores the scope, claims, and the evolving patent landscape surrounding this patent, providing critical insights for stakeholders navigating the South Korean pharmaceutical patent environment.

Patent Overview and Context

Adopted in 2022, KR20220028125 encapsulates an inventive pharmaceutical entity, which could embody a new molecular compound, a novel therapeutic composition, or an innovative delivery method. South Korea's patent system emphasizes protection of pharmaceutical inventions, especially those that demonstrate novelty, inventive step, and industrial applicability [1].

The patent likely leverages existing molecular frameworks, enhancing efficacy, reducing side effects, or improving stability. Its strategic significance hinges on granting exclusivity in South Korea, potentially expanding into Asian markets under patent harmonization agreements.


Scope of the Patent

Legal Scope and Patentability

The scope of KR20220028125 is defined by its claims, which specify the boundaries of the patent’s protection. In pharmaceutical patents, claims typically encompass:

  • Compound Claims: Covering specific molecules or analogs.
  • Use Claims: Covering novel therapeutic uses.
  • Formulation Claims: Encompassing specific compositions or delivery systems.
  • Method Claims: Covering manufacturing or treatment methods.

The scope is primarily expressed in the independent claims, supported by dependent claims that narrow or specify embodiments.

Nature of Claims in KR20220028125

While the actual claims text requires access to the official patent document, typical pharmaceutical patents follow a structure emphasizing composition of matter claims, which provide broad protection for the active ingredient, often combined with use claims that specify particular indications.

For example:

  • Composition of Matter Claim: A pharmaceutical composition comprising a specific compound or a mixture of compounds with certain characteristics.
  • Method of Treatment Claim: Use of the compound to treat specific diseases, e.g., cancer, autoimmune disorders.

The scope's breadth determines the patent’s enforceability: broader claims offer wider protection but are more challenging to patent due to the requirement for non-obviousness.

Potential Limitations and Constraints

South Korean patent law adheres to standards similar to the European Patent Convention (EPC) and the World Trade Organization’s Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS) [2]. Claims that are overly broad, lack inventive step, or are obvious over prior art may face invalidation.


Patent Claims Analysis

Composition of Matter Claims

In pharmaceutical patents, these claims protect the chemical entity itself. If KR20220028125 encompasses a new molecular structure, the claims likely specify:

  • The molecular formula.
  • Specific substitutions or modifications.
  • Stereochemistry considerations.

A well-drafted claim would avoid overly broad language that could be invalidated for encompassing known compounds.

Use and Method Claims

Claims may extend to specific therapeutic methods:

  • Symptom relief.
  • Disease-specific indications.
  • Novel drug delivery modalities (e.g., nanoparticle encapsulation).

Use claims significantly extend patent protection, especially when composition claims are anticipated to be challenged based on prior art.

Formulation and Delivery Device Claims

If the patent introduces a novel formulation or device component, the language will delineate the specific excipients, release profiles, or delivery mechanisms.

Claim Strategy and Patent Scope Balance

An optimal patent claims strategy balances broad protection with patent validity. Excessively broad claims risk invalidation, while narrow claims might limit commercial exclusivity.


Patent Landscape and Competitive Environment

Global Patent Filings and Priority

South Korean pharmaceutical innovation is often synchronized with filings in major markets like the US, China, Europe, and Japan. Judging by similar filings, a corresponding application may exist in these jurisdictions, granting cross-jurisdictional exclusivity or priority.

Prior Art and Patentability Challenges

The landscape indicates intense patenting activity around drug compounds and formulations. Prior art includes:

  • Previously granted patents in Korea and abroad.
  • Published patent applications disclosing similar molecules or uses.
  • Scientific literature on similar compounds.

The applicant's strategic focus might entail claiming novel structural features, unexpected efficacy, or unique formulation techniques to overcome prior art.

Patent Family and Litigation Risk

A robust patent family encompassing composition, use, and manufacturing claims enhances enforcement strength. However, complex pharmaceutical patenting often invites challenges based on patent’s inventive step or obviousness, especially from generic competitors.

Patent Expiry and Lifecycle Management

Assuming the patent’s issue date is 2022, the patent lifecycle extends into the late 2030s, providing exclusivity during critical commercialization phases. Lifecycle management strategies may include:

  • Filing divisional applications.
  • Securing supplementary protection certificates (SPCs).
  • Pursuing patent term extensions via regulatory delays.

Implications for Stakeholders

For Innovators

KR20220028125 signals significant R&D investment and a commitment to securing market exclusivity. It underscores the importance of meticulous claim drafting, comprehensive patent family building, and strategic prosecution to maximize protection.

For Generic Manufacturers

The patent’s scope informs potential design-around approaches and litigation risks. A detailed understanding of claims aids in assessing the likelihood of patent infringement or invalidation.

For Investors and Licensing Firms

Patent strength influences licensing valuations and market entry decisions. The patent landscape suggests promising collaboration opportunities with entities holding complementary patents or development rights.


Key Takeaways

  • Scope Determination: The scope hinges on the specificity and breadth of claims, emphasizing composition, use, or formulation.
  • Claims Strategy: A balanced approach ensures wide protection without risking invalidation. Use claims can significantly expand patent coverage.
  • Patent Landscape: South Korea’s patent environment remains crowded, with active filings that focus on structural innovation, methods, and formulations in pharmaceuticals.
  • Enforcement and Lifecycle: Long-term protection depends on strategic patent drafting, national filings, and lifecycle management.
  • Market Impact: Robust patent protection bolsters commercialization efforts and attracts licensing opportunities, reinforcing South Korea’s position as a biopharmaceutical hub.

FAQs

Q1. How does South Korean patent law influence pharmaceutical patent scope?
South Korea emphasizes novelty, inventive step, and industrial applicability. Patent claims must demonstrate non-obviousness over prior art, influencing the breadth and enforceability of pharmaceutical patents like KR20220028125.

Q2. Can the scope of KR20220028125 be challenged post-grant?
Yes. Generic competitors or opposing parties can file invalidation actions citing prior art, obviousness, or lack of inventive step, requiring careful patent drafting and prosecution strategies.

Q3. What are common strategic filings related to this patent?
Filing in other jurisdictions (US, China, Europe), creating patent families with divisional applications, and securing regulatory exclusivities like SPCs extend protection beyond South Korea.

Q4. How does the patent landscape impact drug commercialization?
A strong patent portfolio prevents competition, enables licensing, and extends revenue streams, impacting a company's valuation and strategic market presence.

Q5. What future trends should stakeholders watch in South Korea’s pharmaceutical patent space?
Focus on AI-driven compound discovery, personalized medicine, and combination therapies. Patent filings increasingly emphasize method claims and formulations alongside structural innovations.


References

[1] Korean Intellectual Property Office (KIPO). Patent Examination Guidelines. 2022.
[2] World Trade Organization. TRIPS Agreement. 1994.

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