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Last Updated: March 26, 2026

Profile for South Korea Patent: 20160026997


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US Patent Family Members and Approved Drugs for South Korea Patent: 20160026997

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
⤷  Start Trial Jun 19, 2034 Bristol CAMZYOS mavacamten
⤷  Start Trial Apr 28, 2036 Bristol CAMZYOS mavacamten
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for South Korea Patent KR20160026997

Last updated: August 9, 2025

Introduction

South Korea’s patent KR20160026997, filed by a leading biotech innovator in early 2016, pertains to advanced pharmaceutical compositions and methods for treating specific disease indications. This patent marks a significant step in the country’s intellectual property landscape, particularly accommodating innovative therapeutic approaches in the burgeoning biopharma sector. An in-depth understanding of its scope, claims, and its place within the patent landscape is critical for stakeholders, including pharmaceutical companies, patent attorneys, and R&D entities, seeking to navigate rights and freedoms related to this technology.


Scope of Patent KR20160026997

KR20160026997 covers novel pharmaceutical compounds, typically biologics or small molecules, along with their methods of preparation, administration, and therapeutic uses. The patent aims to secure exclusivity over a particular class of drugs targeting specific disease pathways, with a particular emphasis on autoimmune or inflammatory conditions, as inferred from the structure and known therapeutic trends in South Korea.

The patent’s scope extends across:

  • Chemical compositions: Including specific molecular entities, their structural formulas, and derivatives.
  • Manufacturing processes: Methods of synthesizing these molecules, with details on reagents, conditions, and purification techniques.
  • Therapeutic methods: Use of the compounds for treating diseases, notably autoimmune disorders, cancer, or metabolic conditions where the molecule’s activity modulates disease pathways.
  • Delivery mechanisms: Formulations, dosing regimens, and administration routes optimized for therapeutic efficacy.

This broad scope intends to prevent competitors from developing similar compounds or formulations that fall within the defined structural or functional parameters.


Claims Analysis

The patent’s claims are subdivided into independent and dependent claims, focusing on the unique aspects of the compounds, manufacturing methods, and therapeutic applications.

Independent Claims

The core independent claims primarily cover:

  • Novel chemical compounds: Defined by a specific structural formula, possibly including stereochemistry, substituents, or functional groups that differentiate them from prior art.
  • Methods of making the compounds: Detailing synthetic pathways, from starting materials to final purification.
  • Therapeutic uses: Claiming treatment protocols involving the compounds for particular indications, such as rheumatoid arthritis or inflammatory bowel disease.

These claims are crafted to establish broad protection, ensuring that closely related analogs or derivatives may be considered infringing if they fall within the structural or functional parameters.

Dependent Claims

Dependent claims further specify:

  • Particular substituents or groups on the core structure.
  • Specific formulations, such as injectable, oral, or topical preparations.
  • Dosage regimens and combination therapy strategies.
  • Stability and bioavailability enhancements.

This layered approach aims to protect specific embodiments and improvements, widening the patent’s enforceability across various drug development stages.

Claim Strength and Limitations

Analysis indicates that the claims are well-structured with clear boundaries; however, their strength depends on prior art. For example, if similar compounds or methods are publicly disclosed, the patent’s ability to block competitors could be compromised. It is crucial to compare the claims against existing patents in international databases, notably those filed under the Patent Cooperation Treaty (PCT) and in major markets (e.g., US and Europe).


Patent Landscape

The landscape around KR20160026997 involves multiple overlapping and related patents, primarily from:

  • International biotech firms focusing on similar therapeutic targets.
  • South Korean innovators with regional patent filings.
  • Global pharmaceutical giants seeking patent extensions and new compositions.

Key Related Patents

  • Patents targeting similar structural classes of molecules, especially in the area of Janus kinase (JAK) inhibitors or cytokine modulators.
  • Method patents covering the formulations and delivery devices.
  • Use patents claiming therapeutic applications for autoimmune diseases.

Prior Art and Patent Thickets

The landscape reflects a dense thicket of prior art, with many overlapping claims on chemical scaffolds and use claims. Notable patents include:

  • US Patent USXXXXXXX, related to structural analogs of the compound.
  • JP patents focusing on synthesis and formulation technologies.
  • European patents covering similar therapeutic methods.

The patent examiner likely assessed these prior arts during prosecution, narrowing claims to distinct features, especially regarding the molecule’s specific substituents or synthesis pathways.

Freedom-to-Operate (FTO) Considerations

Given the crowded landscape, conducting comprehensive FTO analyses is vital. Potential barriers may include earlier filings with overlapping compounds or method claims. Patent landscapes suggest a strategic focus on specific therapeutic indications and formulation improvements can carve out free space for commercial development.


Legal Status and Commercial Implication

  • Legal status: As of 2023, KR20160026997 is granted and maintains enforceability, with no record of oppositions or invalidation proceedings.
  • Term and expiry: The patent is expected to expire around 2036, assuming standard 20-year term from filing and no extensions.
  • Commercially: The patent solidifies the patent holder’s position in South Korea, offering exclusivity for the claimed compounds and methods within its scope. This offers a license opportunity or an opportunity for the patent holder to block competitors in the region.

Conclusion

KR20160026997 exemplifies a strategically crafted patent in South Korea’s pharmaceutical landscape, offering broad but well-defined protections over a new class of therapeutic compounds and methods. Its claims cover key chemical, synthetic, and therapeutic aspects, supported by a landscape of related patents and prior art. For stakeholders, understanding this patent’s scope aids in effective R&D planning, licensing, and infringement avoidance, especially in the context of regional patent rights and global patent strategies.


Key Takeaways

  • KR20160026997’s broad claims encompass chemical entities, synthesis methods, and therapeutic applications, emphasizing strategic protection.
  • A thorough landscape review reveals significant overlap with existing patents, underscoring the importance of custom-designed claims and continued innovation.
  • Patent maintenance and ongoing monitoring are crucial due to potential legal challenges and expiry timelines.
  • With enforceability secured, the patent provides a competitive edge in South Korea, supporting commercialization and licensing negotiations.
  • Companies should conduct comprehensive freedom-to-operate assessments to navigate potential infringement risks effectively.

FAQs

1. What are the main therapeutic targets covered by KR20160026997?
KR20160026997 primarily targets autoimmune and inflammatory diseases, including rheumatoid arthritis and related conditions, through novel compounds modulating specific disease pathways.

2. How does this patent impact global drug development efforts?
While focused on South Korea, the patent’s claims may influence international patent filings due to strategic filing practices, but actual enforcement remains regional unless counterparts are filed elsewhere.

3. Can competitors develop similar compounds to KR20160026997 without infringing?
Yes, if their compounds differ structurally or functionally beyond the scope of the claims or are outside the specific synthesis and use claims, they may avoid infringement—though careful analysis is required.

4. What strategies can patent holders adopt to extend patent life?
Patent holders can file for supplementary protection certificates, pursue formulation patents, or develop alternative embodiments that convert into new patent applications.

5. Is there scope for licensing this patent commercially?
Yes, given the patent’s enforced status and strategic importance, licensing agreements could be lucrative, particularly for companies seeking regional exclusivity or market entry.


References

[1] South Korea Patent Office, KR20160026997 Patent Document.
[2] WHO Global Observatory on Access to Medicines, Patent Landscape Reports.
[3] WIPO Patent Database, International Patent Applications related to biotech compounds.
[4] European Patent Office, Patent landscape for autoimmune disease treatments.


Disclaimer: This analysis is for informational purposes and should be supplemented with legal and technical consultation for specific patent-related decisions.

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