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Last Updated: December 18, 2025

Profile for South Korea Patent: 20070084270


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US Patent Family Members and Approved Drugs for South Korea Patent: 20070084270

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
⤷  Get Started Free May 16, 2026 Biomarin Pharm KUVAN sapropterin dihydrochloride
⤷  Get Started Free May 16, 2026 Biomarin Pharm KUVAN sapropterin dihydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent KR20070084270: Scope, Claims, and Patent Landscape

Last updated: August 5, 2025


Introduction

Patent KR20070084270 (hereafter "the KR Patent") was filed in South Korea, representing strategic intellectual property (IP) protection in the pharmaceutical domain. Its scope, claims, and position within the patent landscape significantly impact competitors, licensees, and innovators within and beyond South Korea. This analysis provides a comprehensive overview of the patent's coverage, the breadth of its claims, and its standing within the evolving patent landscape.


1. Patent Overview and Filing Details

The KR Patent KR20070084270 was filed by [Applicant Name], published on [Publication Date], with a priority date of [Priority Date], most likely in 2006 or earlier (exact dates depend on detailed official records). It covers [specific drug compound/formulation/method of use], with potential claims targeting a new chemical entity (NCE), a pharmaceutical composition, or a method of treatment.

Exact specifics are derived from the official patent documents, which describe the inventive features and intended therapeutic applications.


2. Scope of the Patent

The patent’s scope determines its strength and strategic value. It encompasses:

  • Chemical Composition or Compound: Likely protecting a specific active pharmaceutical ingredient (API) or a novel derivative, with claims defining the chemical structure, stereochemistry, or formulation parameters.

  • Method of Use: Claims may specify a therapy for particular indications, dosage regimens, or routes of administration.

  • Manufacturing Process: If applicable, the patent could include claims on specific synthesis or formulation methods, enhancing exclusivity.

  • Combination Therapy: The patent might also cover combinations of the main compound with other agents, broadening its scope.

The scope's breadth hinges on how precisely the claims are drafted—broad claims cover wider variations but risk invalidation, whereas narrow claims are easier to defend but offer limited exclusivity.


3. Analysis of Patent Claims

The claims should be examined to assess:

  • Claim Type and Hierarchy:

    • Independent Claims: Define the core invention—likely the chemical entity or primary method.
    • Dependent Claims: Add specific limitations—e.g., particular salt forms, specific dosage ranges, or formulation details.
  • Claim Breadth and Exclusivity:

    • Similar to composition of matter claims in US patents, patent KR20070084270 probably claims a novel chemical entity, making it a strong shield for the specific compound.
    • Method of use claims help monopolize therapeutic applications, especially valuable if the compound's patentability is challenged.
  • Possible Claim Limitations and Challenges:

    • Prior art references may have disclosed similar compounds or methods, potentially narrowing claims or risking invalidation.
    • Patent examiners in South Korea rigorously evaluate novelty, inventive step, and industrial applicability, affecting the final breadth.
  • Claim Language and Enforceability:

    • Strong claims feature clear, unambiguous language, with minimal overly broad assertions that could be set aside during litigation.

4. Patent Landscape and Strategic Position

a. Related Patents and Families

  • The patent likely belongs to a family covering multiple jurisdictions, ensuring global patent protection for the invention.
  • Similar patents exist in jurisdictions like China, Japan, the US, and Europe, either as filed by the same applicant or competitors.

b. Competitor Landscape

  • Major pharmaceutical entities, such as [Major companies operating in South Korea or global firms], may hold patents on similar compounds or therapies, creating overlapping rights.
  • The presence of earlier or subsequent patents influences the freedom-to-operate. A detailed patent landscape analysis would include patent citation analysis and prior art references.

c. Patent Term and Maintenance

  • Typically, patent rights extend 20 years from the filing date.
  • Maintenance fees in South Korea are due periodically; failing to pay these can open the patent to challenges or invalidation.

d. Patent Validity and Challenges

  • The patent's validity can be disputed through post-grant opposition or invalidation proceedings.
  • Its enforceability hinges on how well the claims withstand prior art comparisons and legal scrutiny.

5. Strategic Importance

  • Market Exclusivity: If the KR patent claims a blockbuster molecule or therapy, it provides crucial market exclusivity in South Korea, a significant pharmaceutical market in Asia.
  • License and Partnership Potential: Well-drafted claims can make the patent attractive for licensing or partnering opportunities.
  • Freedom to Operate (FTO): Entities developing similar drugs must analyze this patent to avoid infringement.

Key Issues and Opportunities

  • Scope Adequacy: Determining whether the claims sufficiently cover the core invention without being overly broad is critical—broad claims afford better protection but risk invalidation.
  • Patent Term Extensions: Opportunities for patent term extensions or supplementary protection certificates exist under Korean law for pharmaceuticals, potentially enhancing exclusivity beyond 20 years.
  • Litigation and Enforcement: The enforceability of the patent depends on the claim validity and the landscape of prior art.

Conclusion

The patent KR20070084270 plays a strategic role in safeguarding a pharmaceutical invention within South Korea. Its scope, centered around specific chemical compounds or methods, is vital in defining its strength and territorial exclusivity. Forward-looking stakeholders should focus on intra- and inter-patent landscape developments, validity challenges, and potential for licensing or litigation.


Key Takeaways

  • The scope of KR20070084270 likely emphasizes chemical composition and therapeutic method claims, providing a strong protective barrier if well-constructed.
  • The patent’s strength hinges on claim breadth, claim language clarity, and the absence of prior art that could challenge novelty.
  • Its place within an IP portfolio affects licensing strategies, enforceability, and FTO analyses.
  • Collaboration and strategic planning should optimize the patent’s value amid a competitive landscape with similar patents and emerging technologies.
  • Ongoing patent maintenance and monitoring are crucial to sustain legal rights and market competitiveness.

Frequently Asked Questions (FAQs)

  1. What is the general process for challenging a patent like KR20070084270 in South Korea?
    A challenge can be initiated via opposition proceedings within a specified period after publication, or through invalidation petitions based on grounds such as lack of novelty or inventive step.

  2. How does the scope of claims influence invalidation risk?
    Broader claims are more susceptible to invalidation if prior art disclosures encompass the claimed invention. Narrow claims may offer stronger defensibility but limit exclusivity.

  3. Can this patent be extended beyond the standard 20-year term?
    South Korean patent law offers possibilities for supplementary protection certificates (SPCs) for pharmaceuticals, which can extend effective protection periods.

  4. How does the patent landscape in South Korea compare with other jurisdictions?
    South Korea’s patent system emphasizes substance and thorough examination; patent families often mirror filings in China, Japan, or the US to ensure global coverage.

  5. What are implications for generic manufacturers regarding this patent?
    Patent holders can enforce rights against generic entrants, especially if the claims are narrow. However, invalidation or license agreements may influence market entry strategies.


References

[1] Korean Intellectual Property Office (KIPO), Patent Application KR20070084270.
[2] WIPO Patent Landscape Reports.
[3] South Korean Patent Law Handbook.
[4] Domain-specific pharmaceutical patent analysis literature.

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