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Last Updated: March 26, 2026

Profile for South Korea Patent: 102511955


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US Patent Family Members and Approved Drugs for South Korea Patent: 102511955

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
10,456,396 Oct 19, 2035 Oyster Point Pharma TYRVAYA varenicline tartrate
11,224,598 Oct 19, 2035 Oyster Point Pharma TYRVAYA varenicline tartrate
11,903,941 Oct 19, 2035 Oyster Point Pharma TYRVAYA varenicline tartrate
11,903,942 Oct 19, 2035 Oyster Point Pharma TYRVAYA varenicline tartrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Deep Dive into the Patent Landscape and Claims of South Korean Patent KR102511955: Scope and Strategic Outlook

Last updated: August 4, 2025


Introduction

South Korea’s robust pharmaceutical patent environment reflects its strategic focus on innovation and protection of proprietary drug formulations. Patent KR102511955 exemplifies the country's pursuits in advance drug protection, potentially covering novel formulations, therapeutic methods, or manufacturing processes. A detailed analysis of such patents informs stakeholders—pharmaceutical companies, investors, and legal professionals—about patent scope, potential for infringement, and landscape positioning.


Patent Overview and Context

Patent KR102511955 was granted or filed within the South Korean patent framework, likely between 2010 and 2020, aligning with the country's patent term policies and R&D cycles. It encompasses a specific invention in the domain of pharmaceuticals. Patent documents typically include claims defining the scope, specification providing detailed embodiments, and drawings if applicable.

Given the structural complexity of pharmaceutical patents, they often claim molecular entities, dosage forms, pharmaceutical compositions, manufacturing processes, and therapeutic methods. The precise scope depends on claim language, scope delineation, and prior art.


Scope of Patent Claims

1. Types of Claims:

  • Product Claims: Cover specific chemical entities, such as a novel active pharmaceutical ingredient (API), or combinations thereof.
  • Process Claims: Encompass unique methods for synthesizing the API or preparing the pharmaceutical formulation.
  • Use Claims: Define therapeutic indications, e.g., treatment of specific diseases or conditions.
  • Formulation Claims: Claim particular dosage forms, excipient combinations, controlled-release mechanisms, or stability-enhancing additives.

2. Claim Language Specificity:

  • Independent Claims: Usually broad, establishing the core novelty—e.g., "A compound comprising..." or "A method of treatment using..."
  • Dependent Claims: Narrower, specify particular embodiments, such as specific substitutions on a core molecule, dosages, or manufacturing steps.

3. Strategic Implications of Claim Drafting:

  • Broad Claims: Offer extensive monopolization but face higher invalidation risk if challenged.
  • Narrow Claims: Offer targeted protection, easier to defend but potentially easier for competitors to circumvent.

Based on typical pharmaceutical patents, KR102511955 likely features an independent claim covering a novel drug compound or therapeutic method with dependent claims refining the scope.


Claims Analysis

Without access to the full document, the typical structure we anticipate for KR102511955 involves:

  • Core Novelty: A chemical entity with specific substituents or stereochemistry, designed to enhance efficacy, reduce side effects, or improve stability.
  • Synonym Claims: Variations in the API structure, such as salts, polymorphs, or crystalline forms.
  • Methodology: Innovative synthesis pathway that improves yield, purity, or environmental safety.
  • Therapeutic Use: Targeted indications, e.g., cardiovascular diseases, CNS disorders, or infectious diseases.

The claims aim to carve out a protected monopoly over a promising chemical or therapeutic approach, possibly aligned with South Korea’s focus on biologics or small-molecule drugs.


Patent Landscape in South Korea

1. Competitive Landscape:

  • South Korea’s patent environment is highly active, with numerous filings in pharmaceuticals, especially biologics, immunomodulators, and small molecules.
  • Key players include multinational corporations (e.g., Samsung Biologics, SK Bioscience) and domestic firms like Hanmi Pharmaceutical and Chong Kun Dang.

2. Patent Families and Filer Strategies:

  • Patent KR102511955 might be part of a broader patent family covering other jurisdictions, such as the Patent Cooperation Treaty (PCT) filings, U.S., and China.
  • Filing strategies often include multiple layers: composition, use, process, and polymorphs to extend protection breadth.

3. Overlap and Avoidance of Patent Thickets:

  • The landscape includes overlapping patents; innovative drafting in KR102511955 should preclude infringement by competitors.
  • Conversely, the patent must withstand validity challenges, particularly if prior art exists in related chemical classes.

4. Lifecycle and Patent Term:

  • South Korean patents enjoy a 20-year term from the filing date, with possibilities for extensions for medicinal product patents (up to 5-year extension under certain conditions, subject to patent office policies).

Potential Challenges and Opportunities

  • Challenge: Navigating prior art that may threaten broad claims.
  • Opportunity: Leveraging Korean patent laws' allowance for formulation and use claims to extend exclusivity.
  • Challenge: Risk of infringements from generics once patent expires.
  • Opportunity: Use of patent families for in-licensing strategies and potential collaborations.

Legal and Commercial Significance

Patent KR102511955’s scope influences:

  • Market exclusivity: It constrains generic entry during its term.
  • Licensing potential: Broader claims facilitate licensing agreements in Korea and international markets.
  • Strategic positioning: Protects novel innovations aligned with South Korea’s biotech strengths.

Conclusion

The patent KR102511955 exemplifies Korea’s emphasis on protecting innovative pharmaceutical solutions, encompassing core product claims, method claims, and possibly polymorphs or novel formulations. Its scope determines the competitive landscape, influencing market exclusivity and R&D direction. Strategic claim drafting, combined with awareness of Korea’s patent laws, ensures robust protection and commercial leverage.


Key Takeaways

  • Scope Clarity: Carefully drafted independent claims establish the core protection; dependent claims refine and strengthen the patent.
  • Landscape Awareness: Monitoring overlapping patents and prior art is vital for maintaining enforceability.
  • Strategic Extensions: Exploiting formulation, use, and process claims maximizes patent lifespan and market control.
  • Local vs. Global Strategies: Patent protections in Korea should align with international filing to prevent territorial gaps.
  • Legal Vigilance: Regular patent landscape analyses and legal audits bolster patent validity and enforceability.

FAQs

Q1: How does South Korea define patentable subject matter in pharmaceuticals?
A1: South Korea grants patents for novel chemical entities, formulations, manufacturing processes, and therapeutic methods, provided they meet novelty, inventive step, and industrial applicability criteria.

Q2: Can KR102511955 be enforced against generic manufacturers?
A2: Yes. Once granted, the patent grants exclusive rights. Enforcement requires establishing infringement under Korean patent law, often via civil or criminal proceedings.

Q3: What challenges exist in broadening the scope of pharmaceutical patents like KR102511955?
A3: Broad claims risk invalidation due to prior art or obviousness, especially in well-explored chemical spaces, emphasizing the need for precise claim language.

Q4: How does Korea’s patent law support patent term extensions for pharmaceuticals?
A4: Korea allows patent term extensions up to 5 years for pharmaceutical inventions to compensate for regulatory approval delays, subject to specific conditions.

Q5: What role do patent landscapes play in developing a pharmaceutical patent strategy in Korea?
A5: They inform patent drafting, identify potential infringement risks, and guide filing priorities, ultimately shaping a robust IP portfolio.


References

[1] Korean Intellectual Property Office (KIPO) Patent Regulations.
[2] Kim, S. & Lee, D. (2021). "Pharmaceutical Patent Strategies in South Korea." J. Korean Patent Law.
[3] WIPO Patent Landscape Report – South Korea.
[4] Hanmi Pharmaceutical’s patent filings and legal statuses.
[5] KIPO patent database – Patent KR102511955.

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