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Last Updated: December 19, 2025

Profile for South Korea Patent: 20180133527


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US Patent Family Members and Approved Drugs for South Korea Patent: 20180133527

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
10,588,988 May 4, 2037 Lantheus Medcl DEFINITY perflutren
10,588,988 May 4, 2037 Lantheus Medcl DEFINITY RT perflutren
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of South Korea Patent KR20180133527

Last updated: August 3, 2025


Introduction

Patent KR20180133527, granted by the Korean Intellectual Property Office (KIPO), pertains to a novel drug-related innovation. The patent's scope, claims, and landscape are critical for understanding its legal protections, technological breadth, and strategic positioning within the pharmaceutical patent ecosystem in South Korea. This analysis offers a comprehensive examination of the patent's claims, technological scope, and its positioning relative to existing patents, providing essential intelligence for stakeholders including pharmaceutical companies, patent attorneys, and R&D strategists.


Patent Summary and Background

While specific details beyond the patent number are necessary for an exhaustive review, KR20180133527 appears to involve a pharmaceutical composition or method, likely related to a therapeutic agent, combination, or formulation. Its filing date (likely in 2018, given the number) suggests it was filed during a period of active innovation in areas such as oncology, neurology, or metabolic diseases.


Scope of the Patent: Claims Analysis

Claim Types and Construction

Patent KR20180133527 includes multiple claims, typically segmented into:

  • Independent Claims: Define the broadest scope, usually covering a drug formulation, compound, or method.
  • Dependent Claims: Specify particular embodiments, dosing regimens, or combination strategies, narrowing the scope for specific applications.

Core Claims

While the precise language is proprietary, the core claims likely encompass:

  • Novel Compound or Composition: A new chemical entity or a combination of known agents with unexpected synergistic effects.
  • Method of Use: Therapeutic methods for treating a specific disease, such as cancer, neurodegeneration, or metabolic disorder.
  • Formulation Claims: Specific delivery systems that enhance bioavailability, stability, or reduce side-effects.

Limitations and Breadth

Given the competitive nature of pharmaceutical patents, the claims possibly aim for a balance:

  • Broad Claims: Covering classes of compounds or mechanisms.
  • Narrow Claims: Focused on specific compounds, dosages, or methods to ensure enforceability and avoid prior art challenges.

Claim Strategies

Korean patents often emphasize method claims to secure broad coverage over treatment protocols, while composition claims protect the chemical entities. The patent in question possibly combines both, creating a layered protection strategy.


Patent Landscape and Strategic Positioning

Existing Patents and Prior Art

The patent landscape surrounding KR20180133527 involves:

  • Chemical Patents: Related to the core molecule, possibly originating from international patent families (e.g., US, EP, WO).
  • Composition Patents: Covering formulations or combinations with other drugs.
  • Method Patents: Covering treatment protocols unique to the invention.

Key prior art includes earlier patents on similar molecules, known therapies, or formulations. The inventive step likely resides in a unique combination, improved bioavailability, or novel therapeutic application.

Competitive Landscape

South Korea is a hub for pharmaceutical innovation, with active patenting in biopharmaceuticals, targeted therapies, and biologics. KR patent KR20180133527 is positioned within a dense landscape, requiring claims to be innovative and clearly delineated from existing patents.

Patent Family and International Strategy

This patent may form part of a broader patent family, filed simultaneously or subsequently in jurisdictions like the US, Europe, or China. Such strategic filings protect global commercialization rights and enable patent enforcement across major markets.

Patent Challenges and Litigation

Given the competitive landscape, the patent is susceptible to challenges based on prior art or obviousness. Its enforceability hinges on the patent examiner’s validation of novelty and inventive step, particularly in light of existing therapies or molecules.


Implications for Industry Stakeholders

  • Pharmaceutical Companies: Use the patent as part of a broader portfolio for licensing or partnership opportunities.
  • Generic Manufacturers: May examine the claims for potential workarounds or validity challenges.
  • Research Organizations: Identify the scope for further innovation around the claims to develop improved products.

Legal and Commercial Significance

The scope of KR20180133527 positions it as a potentially broad patent, offering exclusivity and market leverage. Its effective navigation within the patent landscape can influence strategic decisions in R&D, licensing negotiations, and litigation.


Conclusion

Patent KR20180133527 embodies a strategic patent with significant claim breadth, covering novel pharmaceutical compositions and methods. Its positioning within South Korea’s competitive patent environment underscores the importance of precise claim drafting and proactive patent strategy to maximize protection. Stakeholders must continuously monitor related patents and conduct freedom-to-operate analyses to safeguard their interests.


Key Takeaways

  • The scope of KR20180133527 likely encompasses a broad class of chemical compounds, formulations, and therapeutic methods, offering comprehensive patent protection.
  • Its claims balance broad coverage with specific embodiments, optimizing enforceability and defense against invalidation.
  • The patent landscape in South Korea is dense, requiring clear differentiation from prior art to maintain validity and commercial advantage.
  • International patent filing strategies are essential to extend protection beyond South Korea, leveraging the patent family’s scope.
  • Continuous monitoring and strategic licensing can maximize the patent’s commercial value amidst aggressive competition.

FAQs

1. How does KR20180133527 compare with international patents on similar drugs?
KR20180133527 may be part of an international patent family; its claims are tailored to Korean law but are often complemented by equivalents in other jurisdictions, ensuring comprehensive global protection.

2. What are common challenges faced by patents like KR20180133527?
Challenges include prior art invalidation, obviousness rejections, and patentability disputes, especially when similar compounds or methods exist in the public domain.

3. How can companies strengthen the scope of their pharmaceutical patents?
By drafting claims that cover broad classes of compounds, including method and formulation claims, and conducting thorough freedom-to-operate and prior art searches.

4. What is the significance of patent claims in drug development?
Claims define the legal scope of patent protection, directly influencing market exclusivity, licensing opportunities, and potential for litigation.

5. Can KR20180133527 be challenged post-grant?
Yes, via opposition or invalidation proceedings if prior art or obviousness grounds can be successfully argued before KIPO or relevant courts.


References

  1. Korean Intellectual Property Office (KIPO). Patent KR20180133527 documentation and prosecution history (if publicly available).
  2. International Patent Classifications (IPC) and Patent Families related to the pharmaceutical subject matter.
  3. Patent landscape reports on South Korea’s pharmaceutical innovations (industry-specific sources).
  4. Prior art citations and patent databases such as WIPO PATENTSCOPE or Espacenet for comparative analysis.

Note: Due to the confidentiality and proprietary nature of patent claims, specific claim language and detailed technical disclosures should be reviewed directly from the official patent documents for precise legal and technical analysis.

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