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Last Updated: December 15, 2025

Profile for South Korea Patent: 102318070


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US Patent Family Members and Approved Drugs for South Korea Patent: 102318070

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
9,439,906 Jan 26, 2031 Janssen Pharms INVEGA SUSTENNA paliperidone palmitate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent KR102318070: Scope, Claims, and Landscape

Last updated: August 18, 2025

Introduction

Patent KR102318070 pertains to a pharmaceutical invention filed in South Korea, which aligns with the nation’s evolving landscape for innovative therapeutics. As drug patents influence market exclusivity, licensing, and competitive positioning, a comprehensive understanding of the scope and claims of KR102318070 is essential for stakeholders. This analysis evaluates the patent’s claims, technological scope, and landscape, providing crucial insights for pharmaceutical companies, legal professionals, and R&D entities.


Patent Overview

KR102318070 was granted in South Korea with a focus on a novel pharmaceutical composition. Although detailed claim specifics are not provided here, typical patent documents in this domain cover innovations in molecular entities, formulations, methods of manufacture, or therapeutic use.

The patent appears to originate from an entity involved in developing a specific therapeutic agent or improved drug delivery system, considering common patent trends in South Korea. Its filing date and legal status are not disclosed here, but the patent’s family likely extends to other jurisdictions, reflecting strategic global coverage.


Scope of the Patent

Core Innovation

The patent’s core innovation likely revolves around a specific chemical compound, a pharmaceutical formulation, or a novel method of treatment. For example, it may pertain to:

  • A novel chemical entity with therapeutic activity.
  • An improved formulation enhancing bioavailability or stability.
  • A specific method of administration or combination therapy.

The scope is, therefore, delineated by its claims, which define the boundaries of exclusivity. The scope’s breadth depends on how narrowly or broadly the claims are drafted—broad claims can cover various modifications, while narrow claims specify particular compounds or methods.

Legal Scope

In South Korea, patent claims are interpreted based on the language of the claims themselves, considering the specification and drawings. The scope may encompass:

  • Composition claims: Covering the drug substance and its formulation.
  • Use claims: Protecting the therapeutic application.
  • Process claims: Covering methods of manufacture or administration.

Given the competitive pharmaceutical landscape, protection likely extends to both composition and method claims to maximize enforceability and market exclusivity.


Analysis of Claims

While the exact wording of the claims is unavailable without the patent document, typical claims in this context can be categorized as follows:

1. Composition Claims

These likely specify:

  • A chemical compound or derivative with defined structural features.
  • A combination of active ingredients.
  • Specific excipients or carriers providing stability or controlled release.

Example: "A pharmaceutical composition comprising compound X, characterized by its inhibitory activity against Y enzyme."

2. Method of Use Claims

  • Providing protected methods for treating particular diseases or conditions.
  • Covering individualized treatment protocols.

Example: "A method of treating disease Z comprising administering compound X to a subject in need thereof."

3. Manufacturing Claims

  • Protocols for synthesizing the active ingredient or formulation.
  • Improving yield, purity, or stability.

Example: "A process for preparing compound X involving steps A, B, and C."

Scope and Limitations

  • If claims specify particular molecular structures, the scope might be narrow but robust against design-arounds.
  • If claims are broad, covering classes of compounds, they risk invalidation but also provide extensive coverage.

Potential for Paragraphal and Functional Claims

  • Patent claim drafting often employs functional language, e.g., "a compound capable of..." which could widen scope but be more vulnerable to validity challenges under certain patent laws.

Patent Landscape in South Korea

Regional Patent Strategy

South Korea’s patent system emphasizes strong examination standards, encouraging precise claim drafting and robust disclosures. The patent landscape for pharmaceuticals is highly competitive, with many filings focusing on:

  • Innovative molecules: R&D by domestic firms like Hanmi, SK Biopharmaceuticals, and international players.
  • Patent thickets: Multiple overlapping patents to protect drug families.
  • Evergreening strategies: Adding process or formulation claims to extend exclusivity.

Related Patent Families

KR102318070 is likely part of a broader patent family, possibly filed also under the Patent Cooperation Treaty (PCT), to secure international rights. It may share priority with earlier applications, such as national or foreign filings, aiding in establishing a robust patent portfolio.

Legal and Market Implications

  • South Korea’s strict patentability criteria favor genuinely inventive claims.
  • Patent litigation and opposition proceedings are common, often initiated by generic manufacturers or competitors.
  • The patent’s strength depends on novelty, inventive step, and sufficiency of disclosure, aligning with Korea’s legal standards.

Challenges and Opportunities

  • Challenges: Navigating prior art, especially in mature therapeutic areas, to maintain claim validity.
  • Opportunities: Leveraging KR102318070 to block generic entry or negotiate licensing deals within Korea and beyond.

Competitive Landscape and Patent Validity

The field likely includes competitors holding overlapping patents for similar compounds or uses, creating a complex landscape. Validity considerations include:

  • Novelty: Confirmed if the compound or method differs significantly from known art.
  • Inventive step: Satisfied if the invention involves an unexpected technical effect.
  • Enablement: Demonstrated through sufficient disclosure in the specification.

Jurisdiction-specific factors include the South Korean Patent Act, which emphasizes inventive activity and detailed descriptions for pharmaceutical patents.


Conclusion

KR102318070 presents a strategic patent within South Korea’s pharmaceutical innovation landscape, likely encompassing chemical, formulation, and use claims. Its scope hinges on claim drafting, with broad claims offering market protection but facing validity scrutiny, whereas narrow claims afford specific coverage. Stakeholders must continuously monitor related patents and legal developments to navigate the competitive environment effectively.


Key Takeaways

  • Assess the claims carefully: The scope, whether broad composition claims or narrow process claims, dictates market exclusivity.
  • Consider global patent strategy: South Korea patent rights often complement international filings, forming a critical part of a global portfolio.
  • Monitor legal challenges: Validity and infringement issues are common, especially in crowded therapeutic classes.
  • Leverage patent claims for competitive advantage: Use robust patents like KR102318070 to block competitors or negotiate licensing.
  • Stay updated on patent landscape shifts: Evolving R&D focus areas and legal standards influence patent strength and enforcement potential.

FAQs

1. What is the typical lifespan of the patent KR102318070 in South Korea?
The standard patent term in South Korea is 20 years from the filing date, subject to maintenance fees. The specific filing and grant dates for KR102318070 determine its expiration.

2. How does South Korea’s patent law influence pharmaceutical patent claims?
South Korea emphasizes novelty, inventive step, and sufficiency of disclosure, compelling patent applicants to craft precise and well-supported claims, especially in complex pharmaceutical inventions.

3. Can the claims in KR102318070 be challenged or invalidated?
Yes. Patents can be challenged through legal procedures, such as oppositions or invalidity trials, based on prior art, lack of inventive step, or insufficient disclosure.

4. How does the scope of claims impact licensing opportunities?
Broader claims facilitate licensing across multiple applications but risk invalidation, while narrow claims offer targeted protection but limit scope. Strategic drafting balances both.

5. Are there specific trends in South Korea for patenting pharmaceuticals like those covered by KR102318070?
Yes. There’s increased focus on biologics, targeted therapies, and formulations, with companies employing patent strategies to extend exclusivity through composition, use, and process claims.


References

  1. Korean Intellectual Property Office (KIPO). Patent Information.
  2. World Intellectual Property Organization (WIPO). Patent Landscape Reports.
  3. South Korea Patent Act.
  4. Industry reports on South Korean pharmaceutical patent strategies.

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