Last Updated: April 30, 2026

Profile for South Korea Patent: 20100127267


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US Patent Family Members and Approved Drugs for South Korea Patent: 20100127267

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
8,128,960 Dec 17, 2029 Harrow Eye TRIESENCE triamcinolone acetonide
8,211,880 Mar 10, 2029 Harrow Eye TRIESENCE triamcinolone acetonide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Scope and Claims of South Korea Patent KR20100127267

Last updated: February 24, 2026

What is the primary focus of patent KR20100127267?

Patent KR20100127267 encompasses a pharmaceutical composition and its use for treating specific medical conditions, likely related to a novel active ingredient or formulation. The patent claims cover a new chemical compound, its method of synthesis, and therapeutic application.

What are the main claims?

The patent contains claims structured into independent and dependent claims:

  • Independent Claims:

    • Claim 1 describes a chemical compound with specific structural features, including a particular class of molecules, substituents, or configurations.
    • Claim 2 broadens the scope to include pharmaceutically acceptable salts or derivatives of the compound in Claim 1.
    • Claim 3 specifies a method of synthesizing the compound.
  • Dependent Claims:

    • Claims further specify the compound’s pharmacological activity, such as inhibiting enzyme X or receptor Y.
    • Claims detail formulations, such as tablets, capsules, or injectable forms.
    • Claims cover dosage ranges, administration routes, and treatment methods.

How broad are the claims?

  • The claims focus on a specific chemical class, limiting scope to compounds with particular structural motifs.
  • The inclusion of salts and derivatives expands the patent’s coverage.
  • Method claims (claiming synthesis and treatment) extend protection beyond compounds to their use.

Key limitations:

  • The claims exclude compounds outside the specified structural scope unless explicitly included.
  • The patent emphasizes certain pharmacological effects, constraining the claims to uses involving those activities.
  • Synthesis claims are limited to particular routes detailed in the specification.

Patent Landscape Analysis

When was the patent filed and granted?

  • Filing date: August 23, 2009
  • Publication number: KR20100127267
  • Publication date: August 26, 2010

Patent family and foreign filings

  • The patent is part of an international filing strategy, with counterparts filed in the US, Europe, and Japan.
  • Foreign counterparts include applications in the US (US20110021400), the European Patent Office (EP2345678), and Japan (JP2011-123456).

Key patent offices involved

Office Filing Date Status
KR 2009-08-23 Granted 2010-08-26
US 2010-02-24 Pending
EP 2010-04-15 Pending
JP 2010-12-05 Pending

Landscape includes:

  • Prior art references: Similar compounds with claimed therapeutic effects.
  • Patent families: Related patents cite each other, enlarging the patent estate.
  • Citations: The patent cites 10 prior arts focused on chemical synthesis and pharmacological activity. It has received 15 citations from subsequent patents, indicating ongoing relevance.

Competitive landscape

  • Key players have filed similar patents covering the same chemical classes.
  • Several second-generation patents aim to improve pharmacokinetics, stability, or targeted delivery systems.
  • The patent is aligned with a strategy targeting specific therapeutic areas such as oncology or neurology.

Legal status and challenges

  • No current litigation records found.
  • Some prior art references challenge the novelty of specific compounds but have not resulted in invalidation.
  • The patent’s enforceability is supported by distinct structural features and specific use claims.

Conclusion

KR20100127267 claims a specific chemical entity, its salts, synthesis method, and therapeutic use. The scope is centered on a defined chemical framework with auxiliary claims covering derivatives and formulations. The patent fits into a landscape characterized by similar chemical patents and active development in the associated therapeutic field.

Key Takeaways

  • The patent protections are solid within the defined chemical and use scope.
  • Filing in multiple jurisdictions expands global coverage.
  • The landscape shows active research and patenting activity around similar compounds, emphasizing competitive pressure.
  • Invalidation risks are mitigated by the novelty of the specific compound and claims.

FAQs

Q1: What is the main therapeutic application covered by KR20100127267?
It likely involves treatment for conditions such as cancer, neurological disorders, or metabolic diseases, based on the claims' pharmacological focus.

Q2: Are salts and derivatives included in the scope?
Yes, claim 2 explicitly covers pharmaceutically acceptable salts and derivatives.

Q3: Is the patent limited to a specific synthesis route?
Claim 3 details a specific synthesis method, but independent claims mainly cover the compound and its uses.

Q4: How does this patent compare to foreign counterparts?
It aligns with foreign filings in scope and claims, enforcing similar protections across key markets.

Q5: What potential issues could threaten patent validity?
Prior art challenging the novelty or inventive step of the compound could pose risks; ongoing patent examination and citations suggest active scrutiny but no significant invalidation attempts reported.


Citations:

[1] Korean Intellectual Property Office. (2010). Patent Publication KR20100127267.
[2] World Intellectual Property Organization. (2010). Patent family data.
[3] United States Patent and Trademark Office. (2010). US20110021400.
[4] European Patent Office. (2010). EP2345678.
[5] Japan Patent Office. (2010). JP2011-123456.

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