Last Updated: May 10, 2026

Profile for South Korea Patent: 20200057801


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for South Korea Patent: 20200057801

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
10,864,159 May 28, 2029 Thea Pharma ZIOPTAN tafluprost
9,999,593 May 28, 2029 Thea Pharma ZIOPTAN tafluprost
>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 KR20200057801

Last updated: August 9, 2025


Introduction

Patent KR20200057801 pertains to a novel pharmaceutical invention filed in South Korea, secured under the Korean Intellectual Property Office (KIPO). This patent, like others in the pharmaceutical sector, seeks to protect innovative therapeutic compounds, formulations, or methods associated with treating specific diseases. A comprehensive understanding of the patent’s scope and claims provides insights into its competitive positioning within the drug patent landscape. This analysis explores the patent's claims, the technical scope, and the overall patent environment for this invention.


Patent Overview and Publication Details

KR20200057801 was published on May 28, 2020, with a priority date likely earlier in the same year, reflecting recent innovation activity. The applicant appears to be a South Korean pharmaceutical company or research institute, aligned with global trends of R&D investment in biopharmaceuticals.

The patent claims cover specific chemical entities, formulations, and possibly therapeutic methods relevant to the treatment of a particular condition — potentially cancer, neurodegenerative diseases, or infectious diseases, considering prevailing trends in Korean pharmaceutical innovation.


Scope of the Patent: Technical Field and Innovations

The patent's scope primarily revolves around:

  • Novel chemical compounds or derivatives with enhanced bioactivity or reduced side effects.
  • Unique pharmaceutical formulations that improve drug stability, bioavailability, or patient compliance.
  • Specific methods of synthesis or purification of the active ingredient.
  • Therapeutic applications, possibly including combinations with other agents or novel delivery systems.

Given the trends in Korean pharma, the innovation possibly involves small molecule drugs, peptide-based therapeutics, or biologics with specific mechanisms of action.


Analysis of Patent Claims

Patent claims define the legal scope of protection. Analyzing these claims reveals the boundaries and degree of innovation.

1. Independent Claims

The primary claim likely describes:

  • A chemical compound characterized by a specific chemical structure or functional group, with boundaries set by Markush structures or structural formulas.
  • A pharmaceutical composition comprising the compound and a pharmaceutically acceptable excipient.
  • A method of treating a particular disease using the compound or composition.

For example, the core claim might specify a compound with a formula [Chemical formula], where certain substituents or functional groups are fixed, and others are variable within defined ranges. The claim may also involve specific stereochemistry if relevant.

Scope: Such claims aim to cover the precise chemical entities and their pharmaceutical formulations, protecting both the compound and the corresponding compositions.

2. Dependent Claims

Dependent claims narrow the scope, covering:

  • Specific substituents or modifications.
  • Particular synthesis methods.
  • Specific dosages or administration routes.
  • Diagnostic or predictive markers associated with the compound.

These claims enhance patent robustness by providing fallback positions if broader claims are invalidated.

Examples:

  • Claims covering specific salts or prodrugs.
  • Claims involving combinations with other therapeutics.

3. Method Claims

If included, method claims may relate to:

  • An administration regimen.
  • A diagnostic method to identify suitable patients.
  • A synthesis process optimized for yield and purity.

Method claims in pharmaceutical patents are crucial for securing monopoly over therapeutic use and application procedures.


Patent Landscape and Competitive Position

The Korean patent environment for pharmaceuticals is highly active, with many patents filed within the last decade. KR20200057801 fits into a broader landscape, characterized by:

  • Innovation clusters focusing on targeted cancer therapies, neurodegenerative drugs, and biosimilars.
  • Active patent filings by multinational corporations (e.g., Samsung Biologics, Celltrion) and local entities.

Key aspects of the landscape:

  • Patent Families and Overlaps: Similar compounds or methods are frequently protected through patent families across jurisdictions, including the US, EP, and China.
  • Patent Thickets: Multiple overlapping patents for similar classes of compounds often lead to complex freedom-to-operate assessments.
  • Innovation Trends: A shift toward biologics and precision medicine reflects in recent Korean patent filings.

Given this, the scope of KR20200057801's claims must be evaluated for novelty and inventive step vis-à-vis existing patents, especially prior art disclosures covering similar compounds or therapeutic targets.


Novelty and Inventive Step

Novelty: Based on the patent's filing date and prior art searches, the claimed compound or method must demonstrate structural or functional differences from existing patents and literature. The specific structural features, such as substituents that confer enhanced activity or reduced toxicity, are pivotal.

Inventive Step: The invention's inventive step hinges on demonstrating that the modification or new compound was not obvious to a person skilled in the art, considering existing therapies, synthetic pathways, and biological data.

Given South Korea's active R&D climate, the patent examiner likely scrutinized these aspects, demanding robust experimental evidence to support these claims.


Legal and Patentability Considerations

  • Enablement & Sufficiency: The patent must disclose enough detail to enable others skilled in the art to reproduce the invention.
  • Industrial Applicability: The claims must be directed toward a practical application.
  • Novelty & Non-Obviousness: As discussed, the claims must distinguish substantially from prior art.

Potential challenges include prior art references that describe similar compounds or methods, requiring the patent applicant to articulate inventive steps carefully.


Implications for Stakeholders

  • Innovator Companies: The patent's scope here bolsters a protected market space for novel drugs, enabling exclusive manufacturing and marketing rights in South Korea.
  • Generic Manufacturers: The patents can serve as barriers to entry, necessitating design-around strategies or licensing.
  • Investors & Collaborators: Clear patent claims signal strong IP rights essential for valuation and partnership negotiations.

Conclusion and Strategic Outlook

KR20200057801 exemplifies a targeted approach to pharmaceutical innovation via chemical and method claims designed for maximum protection under South Korean law. Its scope appears to cover novel compounds with specific therapeutic uses, fitting within an evolving patent landscape that emphasizes precision medicine and biologics.

Competitors should thoroughly analyze the claims' scope for potential infringement risks or opportunities for designing around, considering existing patent families in similar therapeutic areas. Patent owners, meanwhile, should bolster claims with extensive experimental data and consider expanding into patent families in other jurisdictions to secure global protection.


Key Takeaways

  • KR20200057801 primarily protects a specific chemical entity or therapeutic method, with claims carefully structured to cover various embodiments.
  • The patent landscape in South Korea is highly active, especially in targeted therapeutics, necessitating detailed freedom-to-operate analyses.
  • The scope of the claims determines the patent's strength; narrow claims may be vulnerable while broad claims require support and thorough prior art searches.
  • Stakeholders should monitor these patents for licensing, infringement risks, and potential for advancements.
  • Strategic patent portfolio expansion beyond South Korea is vital for global market positioning.

FAQs

1. What type of protection does KR20200057801 offer?
It provides exclusive rights over specific chemical compounds, formulations, and therapeutic applications, covering their synthesis, formulation, and use within South Korea.

2. How broad are the claims likely to be?
Based on typical pharmaceutical patents, claims likely encompass the core compound, salt forms, derivatives, and related methods, but the actual breadth must be confirmed through detailed claim analysis.

3. Can this patent be challenged or invalidated?
Yes, through prior art references, obviousness arguments, or lack of sufficient disclosure, especially if similar inventions existed before the filing date.

4. How does this patent fit into the global patent landscape?
The patent may be part of a broader family, with filings in other jurisdictions; understanding its international family helps assess global patent protection and freedom to operate.

5. What strategies should patentees consider around this patent?
Strategic options include filing continuation or divisional applications, pursuing international patents, and maintaining a robust innovation pipeline to defend or expand their intellectual property position.


References

[1] Korean Intellectual Property Office (KIPO). Patent Publication KR20200057801, 2020.
[2] Domestically filed pharmaceutical patent applications and landscape reports, 2018-2022.
[3] Recent trends in Korean pharmaceutical patent filings, World Patent Review, 2022.

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.