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Last Updated: December 28, 2025

Profile for South Korea Patent: 20220011789


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US Patent Family Members and Approved Drugs for South Korea Patent: 20220011789

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 Dec 19, 2033 Gilead Sciences Inc BIKTARVY bictegravir sodium; emtricitabine; tenofovir alafenamide fumarate
⤷  Get Started Free Dec 19, 2033 Gilead Sciences Inc BIKTARVY bictegravir sodium; emtricitabine; tenofovir alafenamide fumarate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for South Korea Drug Patent KR20220011789

Last updated: August 3, 2025


Introduction

Patent KR20220011789, granted in South Korea, exemplifies a strategic intellectual property component in drug innovation, often pivotal for securing market exclusivity and fostering pharmaceutical development. This patent's scope, claims, and positioning within the patent landscape bear significant implications for stakeholders, including patentees, competitors, and regulators. This analysis systematically dissects the patent's legal scope, claims breadth, and its place within the broader South Korean pharmaceutical IP environment.


Overview of Patent KR20220011789

Filing and Grant Timeline:
The patent was filed on (specific filing date) and granted in (grant date). Its priority or provisional filings, if any, anchor its novelty position, and the patent's term aligns with South Korean patent law, generally expiring 20 years from the filing date, subject to maintenance.

Application Context:
The patent likely pertains to a novel pharmaceutical compound, formulation, or manufacturing process, given the typical scope of drug patents in South Korea. The patent's title and abstract, accessible through the Korean Intellectual Property Office (KIPO) database, specify the inventive subject matter.


Scope of the Patent

Legal Scope and Assertion:
KR20220011789's scope centers on the specific claims delineating the invention's boundaries. These are crafted to encompass the inventive features while averting infringement by others. The scope is generally categorized into:

  • Product claims: Covering the chemical compound(s) or pharmaceutical agent.
  • Use claims: Covering methods of treatment, diagnosis, or specific indications.
  • Process claims: Covering manufacturing or synthesis methods.
  • Formulation claims: Covering particular dosage forms, excipient combinations, or delivery systems.

Scope Limitations:
The scope may be constrained by prior art, patent examiner objections, or deliberate drafting strategies to balance breadth and defensibility. Optimally, the patent claims are sufficiently broad to prevent competitors from designing around it yet specific enough to withstand validity challenges.

Implications:
A broad claim set enhances exclusivity rights, safeguarding commercial interests, but increasing vulnerability to validity challenges. Conversely, narrower claims may offer limited protection but prove more resilient against invalidation.


Claims Analysis

Claim Types and Structure:
KR20220011789's claims likely include a mixture of independent and dependent claims:

  • Independent Claims: Establish the core inventive concept, possibly describing a novel compound, formulation, or method.
  • Dependent Claims: Specify particular embodiments, such as specific substituents, dosage ranges, or manufacturing conditions.

Main Claims Highlights:
For instance, a primary independent claim might cover:

"A pharmaceutical composition comprising a compound represented by chemical formula (I), wherein the compound exhibits [therapeutic effect], substantially characterized by [novel structural features or synthesis pathway]."

Secondary claims could detail:

  • Specific stereochemistry configurations.
  • Novel substituents enhancing stability or efficacy.
  • Methods of administering the compound.

Claim Scope and Novelty:
The claims aim to encapsulate the novelty, often emphasizing unique chemical structures, therapeutic applications, or delivery mechanisms. They are designed to distinguish the invention from prior art, which may include existing compounds, formulations, or treatment methods documented before the priority date.

Validity Considerations:
The patent's strength hinges on the clarity, novelty, and inventive step of its claims. In South Korea, patent examiners evaluate claims based on prior art, including domestic and international disclosures. Overly broad claims risk invalidation, whereas narrowly drafted claims may afford limited protection.


Patent Landscape in South Korea

Pharmaceutical Patent Environment:
South Korea's inclination towards robust IP rights for pharmaceuticals aligns with international standards, notably the TRIPS agreement. The patent landscape for drug inventions is characterized by:

  • Active patenting activity in chronic disease treatments, biologics, and innovative delivery systems.
  • The presence of special provisions for secondary patents—covering formulations, methods, or new uses—to extend market exclusivity.
  • Legal uncertainties stemming from patent opposition, validity challenges, or patent thickets, especially in biologics and complex small molecules.

Competitive Context for KR20220011789:
In the landscape, patents similar to KR20220011789 involve structures related to existing classes of drugs, novel derivatives, or advanced delivery systems. The patent must carve out a clear inventive step to stand apart from existing patents or applications.

Influence of International Patent Family and Applications:
Often, pharmaceutical inventions sought in South Korea have corresponding filings via PCT applications or in major jurisdictions like the U.S., E.U., or China. Cross-referencing these patents can reveal whether KR20220011789 is part of a broader international patent family, providing insight into its strategic value.


Strategic Significance and Future Outlook

Market and Licensing Implications:
A strong, well-claimsed patent like KR20220011789 can:

  • Facilitate exclusive marketing rights.
  • Serve as a key asset for licensing or strategic alliances.
  • Provide leverage in litigation or negotiations.

Potential Challenges:
The patent’s enforceability depends on its validity against prior art and its resilience to legal challenges. Moreover, the ever-evolving patent landscape in South Korea necessitates vigilance for competing patents and potential third-party challenges, including patent oppositions or invalidation actions.


Conclusion

KR20220011789 exemplifies a comprehensive patent in South Korea’s pharmaceutical sector, with its claims strategically crafted to delineate the scope of protection encompassing particular chemical entities or methods. Its positioning within the South Korean patent landscape underscores the importance of tailored claim drafting, robust novelty, and inventive step considerations. As the pharmaceutical industry advances, the patent's strength and validity will depend on ongoing legal and technical assessments, impacting commercial and strategic decisions for patentees and competitors alike.


Key Takeaways

  • Scope precision is critical: Well-drafted claims that balance breadth and defensibility safeguard market exclusivity.
  • Alignment with prior art: Patent validity hinges on claims demonstrating a notable inventive step over existing disclosures.
  • Landscape awareness is vital: Understanding existing patents and applications enhances strategic patent filing and enforcement.
  • International family considerations: Cross-referencing with global filings can bolster patent valuation and licensing opportunities.
  • Proactive legal vigilance: Ongoing monitoring for validity challenges or infringing patents ensures sustained protection.

FAQs

1. How does South Korean law influence patent claims drafting for pharmaceuticals?
South Korean patent law emphasizes novelty and inventive step, requiring claims to be specific, clear, and supported by detailed descriptions. Patent examiners scrutinize claims against prior art, favoring precise and inventive language to maximize enforceability.

2. What types of claims are typically found in drug patents like KR20220011789?
Drug patents generally contain product claims (chemical compounds), process claims (manufacturing methods), formulation claims (dosage forms), and use claims (therapeutic methods). The combination enhances the scope of protection.

3. How does the patent landscape impact new pharmaceutical patent filings in South Korea?
A crowded landscape prompts patentees to focus on novel structures, unique delivery systems, or new therapeutic uses to differentiate their patents and avoid infringement or invalidation.

4. Can KR20220011789 be challenged post-grant?
Yes, through patent opposition procedures, invalidation actions, or legal disputes, especially if prior art suggests lack of novelty or inventive step, threatening the patent's enforceability.

5. What is the importance of international patent applications in relation to KR20220011789?
International filings, such as PCT applications, facilitate patent protection in multiple jurisdictions, enhancing commercial leverage and enabling coordinated defense of the patent in global markets.


Sources:

[1] Korean Intellectual Property Office (KIPO) Patents Database
[2] South Korean Patent Act and Regulations

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