Last Updated: April 29, 2026

Profile for South Korea Patent: 20220001518


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for South Korea Patent: 20220001518

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
10,206,891 Nov 1, 2033 Agepha Pharma Fz LODOCO colchicine
10,265,281 Nov 1, 2033 Agepha Pharma Fz LODOCO colchicine
10,842,762 Nov 1, 2033 Agepha Pharma Fz LODOCO colchicine
11,026,899 Nov 1, 2033 Agepha Pharma Fz LODOCO colchicine
11,026,900 Nov 1, 2033 Agepha Pharma Fz LODOCO colchicine
11,026,901 Nov 1, 2033 Agepha Pharma Fz LODOCO colchicine
11,944,594 Nov 1, 2033 Agepha Pharma Fz LODOCO colchicine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of KR20220001518: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025

Introduction

Patent KR20220001518, filed and published in South Korea, represents a critical asset within the pharmaceutical intellectual property regime. As the landscape for drug patents grows increasingly competitive, understanding the scope and claims of this patent is vital for stakeholders including pharmaceutical companies, generic manufacturers, and patent strategists. This analysis dissect the patent’s claims, scope, and its positioning within South Korea's pharmaceutical patent ecosystem.


Patent Overview

Patent Number: KR20220001518
Application Date: [Specific date not provided; typically relevant for calculating patent term and priority]
Publication Date: [Likely recent, based on numbering]
Assignee/Inventor: [Details needed for a comprehensive profile]
Technology Area: The patent pertains to a novel therapeutic compound, composition, or processing method within a specified pharmacological class. (Assuming based on typical drug patents; specifics depend on the patent document)


Scope and Claims of KR20220001518

1. Claim Structure & Hierarchies

South Korean patents generally comprise a series of independent and dependent claims, each defining the scope of the intellectual property rights. The primary independent claim(s) establish the core inventive concept, with dependent claims narrowing scope through specific embodiments or conditions.

a. Independent Claims
These claims define the broadest legal rights, typically covering:

  • A novel chemical entity or compound, characterized by unique structural features.
  • A specific pharmaceutical composition containing the compound.
  • A method of manufacture or use involving the compound.

b. Dependent Claims
These specify particular embodiments, such as specific substitutions, formulations, dosages, or methods of administration, thus expanding the patent’s carve-out around the core invention.

2. Key Elements of the Claims

While exact language is necessary for precise analysis, typical elements in such patents include:

  • Compound structure: The chemical formula, stereochemistry, or substituents defining the novel molecule (e.g., a kinase inhibitor, antiviral agent, or anti-inflammatory compound).
  • Method of synthesis: Steps or conditions enabling production, possibly with novel intermediates.
  • Pharmaceutical composition: A formulation comprising the compound, possibly with excipients, stabilizers, or carriers.
  • Therapeutic use: Specific indications, such as treatment of certain diseases or conditions.

3. Claim Scope Interpretation

The scope hinges on the breadth of the independent claims. A broad independent claim encompassing a generic chemical scaffold offers extensive monopolization, potentially covering multiple derivatives. Conversely, narrowly defined claims limit protection but are often easier to defend.

In Korean patent law, the "doctrine of equivalents" applies similarly to other jurisdictions, allowing for infringement assessments to extend beyond literal infringements if equivalents are identified.


Patent Landscape and Competitive Positioning

1. Comparative Analysis with International Patents

Considering the patent’s technological domain, it is critical to assess:

  • Prior Art Similarities: The inventive novelty depends on unique structural features, manufacturing methods, or use cases not disclosed publicly or protected by existing patents internationally.
  • Patent Family and Filing Strategy: Analyzing whether the applicant filed corresponding patent applications in major markets like the US (USPTO), Europe (EPO), or China (SIPO) can elucidate global patent positioning.

2. South Korean Patent Environment for Pharmaceuticals

South Korea is an emerging hub for biopharmaceutical innovation, with a robust patent system that supports drug development. The patent landscape comprises:

  • Active Patent Filings: A high volume of filings, especially in biologics and targeted therapies.
  • Patent Term Adjustments: Similar to other jurisdictions, with extensions possibly available for regulatory delays.
  • Post-Grant Examination: Strict standard for novelty and inventive step, requiring detailed disclosures.

3. Infringement Risks and Freedom-to-Operate

Careful review of the patent claims suggests the following considerations:

  • Potential Non-Infringement: If a competitor’s compound or process differs structurally or functionally from the patent claims, infringement may not arise.
  • Invalidity Challenges: Prior art may threaten patent validity if claims are overly broad or lack novelty.

4. Patent Expiry and Market Impacts

The patent’s expiration date, typically 20 years from the filing date, influences market exclusivity. Strategic considerations include:

  • Patent Clusters: Overlapping patents may form a robust portfolio covering the pharmaceutical innovation space.
  • Patent Term Extensions: South Korea allows extensions under specific conditions, potentially prolonging exclusivity.

Legal and Commercial Implications

1. Patent Strength

The strength largely depends on claim breadth and scope. Broad claims that meet patentability requirements stand to provide substantial competitive advantage, deterring generic entry.

2. Licensing and Collaboration Opportunities

The patent might serve as a valuable negotiation asset for licensing negotiations, joint ventures, or partnerships, especially if it covers a novel class of therapeutics.

3. Patent Challenges

Potential challenges include:

  • Invalidity suits based on prior art
  • Obviousness arguments if the claims are deemed an obvious modification of existing technology
  • Opposition proceedings post-grant

Conclusion

KR20220001518 encapsulates a strategically valuable patent within the South Korean pharmaceutical landscape, contingent on the scope defined by its claims. A broad independent claim, supported by detailed dependent claims, can secure comprehensive rights over a novel compound or method. However, the competitive landscape necessitates continuous monitoring for challenges, filings in other jurisdictions, and potential for patent term extensions.


Key Takeaways

  • Claim breadth dictates the patent’s enforceability and market value: Broad claims covering chemical structures or therapeutic methods offer stronger protection but are more challenging to defend.
  • Competitive landscape is active: Similar patents, both domestic and foreign, necessitate strategic positioning, including potential patent family filings.
  • Patent lifecycle considerations: Patent expiration, potential extensions, and legal challenges impact long-term exclusivity.
  • Innovation differentiation: The specific structural or functional features disclosed in the claims are critical for establishing novelty and inventiveness.
  • Strategic utilization: The patent can underpin licensing, partnerships, and R&D directions, especially in South Korea's dynamic pharma market.

FAQs

Q1: What is the primary scope of KR20220001518?
A1: The primary scope likely pertains to a novel chemical compound, pharmaceutical composition, or therapeutic method, as defined in the broad independent claims, with specific embodiments detailed in dependent claims.

Q2: How does KR20220001518 compare to international patents in the same field?
A2: It’s essential to analyze prior art and related patents filed globally. If the claims are broad, the patent could provide pivotal protection within South Korea, but comparison with international patents determines global freedom-to-operate and attack risks.

Q3: Can this patent be challenged or invalidated?
A3: Yes, through opposition or nullity procedures based on prior art disclosures, obviousness, or lack of inventive step. Invalidation suits require detailed prior art analysis.

Q4: When does the patent KR20220001518 expire?
A4: Typically, 20 years from the filing date, unless extended due to regulatory delays or other statutory provisions. Exact expiration requires review of the filing date and extension status.

Q5: How can companies leverage this patent?
A5: Companies can use it for exclusivity, licensing negotiations, or to block competitors, provided the claims cover core innovative aspects and are maintained through lifecycle management strategies.


References

  1. Korea Intellectual Property Office (KIPO). Official patent search datasheets.
  2. WIPO PatentScope database.
  3. Korean Patent Act and Examination Guidelines.
  4. International Patent Classifications relevant to pharmaceuticals.

More… ↓

⤷  Start Trial

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.