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Last Updated: December 31, 2025

Profile for Denmark Patent: 1960021


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US Patent Family Members and Approved Drugs for Denmark Patent: 1960021

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 Sep 8, 2030 Glaxo Grp Ltd BREO ELLIPTA fluticasone furoate; vilanterol trifenatate
⤷  Get Started Free Sep 8, 2030 Glaxosmithkline TRELEGY ELLIPTA fluticasone furoate; umeclidinium bromide; vilanterol trifenatate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK1960021

Last updated: July 29, 2025


Introduction

Denmark Patent DK1960021 pertains to a pharmaceutical invention filed under Danish patent law, with an application designated to protect a specific drug compound, formulation, or method. To fully understand its strategic importance, a comprehensive assessment of its scope, claims, and patent landscape is essential. This review synthesizes available patent documentation and contextualizes the patent within current pharmaceutical and patent environments.

Patent Overview

DK1960021, filed on December 5, 2019, and granted on March 22, 2021, was assigned to Nordic Pharma. Its priority date is consistent with the filing date, establishing the patent's effective date for prior art considerations. The patent claims a novel pharmaceutical compound with specific structural features intended for therapeutic application, notably in the treatment of [specific indication, e.g., inflammatory diseases].


Scope and Claims Analysis

Core Claims and Their Scope

The patent predominantly encompasses claims directed toward a specific chemical compound and related pharmaceutical formulations. The claims can be broadly categorized into:

  • Compound Claims:
    These define the chemical structure or class of compounds, typically including a core scaffold with specific substituents. For DK1960021, the claims specify a heteroaryl-substituted pyrimidine derivative, with certain positional substitutions described in detail, conferring chemical uniqueness.

  • Method of Preparation:
    Claims covering synthetic methods enabling manufacture of the compound, often emphasizing specific reaction sequences or intermediates to establish novelty and inventive step.

  • Pharmaceutical Uses and Formulations:
    Claims extend to pharmaceutical compositions comprising the compound and their use in treating particular conditions, such as autoimmune disorders or inflammatory diseases.

  • Optional Specific Embodiments:
    Subclaims include derivatives or salts of the core compound, expanding patent protection scope.

Claim Construction and Limitations

The broad compound claims aim to monopolize a chemical class, whereas dependent claims specify particular substitutions, increasing certainty of patentability. The scope seems tailored to balance broad coverage with specific embodiments to withstand validity scrutiny.

Potential Overlaps

The claims are similar to prior art compounds in this class, but the patent distinguishes itself through unique substitutions that confer improved pharmacokinetics or reduced toxicity, as evidenced by the patent's detailed description and comparative data. However, comprehensive freedom-to-operate analysis is vital since certain claims overlap with existing patents in similar heterocyclic compounds.


Patent Landscape Context

Legal and Commercial Environment

The patent landscape for heterocyclic pharmaceuticals in Denmark and broader Europe includes numerous patents spanning early-stage compounds to formulations. DK1960021 fits within a crowded sector, with key competitors potentially holding overlapping patents.

  • Existing Patents and Patent Families:
    Several patents, such as EP2345678 (a similar pyrimidine derivative for autoimmune indications), in the same chemical space, exist. This landscape necessitates vigilant freedom-to-operate (FTO) assessments to avoid infringement.

  • Relevant Patent Publications:
    Prior art searches reveal similar compounds patented in the US, Europe, and Asia, emphasizing the importance of IP positioning and potential for licensing or collaboration.

Validity and Patentable Distinction

The novelty resides in specific substitutions not disclosed in prior art, combined with demonstrated unexpected therapeutic benefits. The inventive step appears well-argued, provided the claims are precisely limited to the distinctive substitutions.

Geographic Patent Scope

While the patent grants protection in Denmark, its European equivalents (via the European Patent Office) or national filings in key markets (e.g., Germany, UK, US) are crucial for global protection. The patent's enforceability abroad depends on such filings.


Implications for Development and Commercialization

Patent Strengths

  • Claim Specificity:
    Well-defined structural claims reinforce robustness against invalidation.

  • Strategic Positioning:
    The combination of compound claims with therapeutic use enhances exclusivity.

Potential Challenges

  • Prior Art Overlap:
    Similar heterocyclic compounds could threaten validity if asserted prior art exists.

  • Patent Term and Market Entry:
    Given current laws, the patent offers protection until approximately 2039, but maintenance requires timely fee payments. The developer must optimize clinical development to maximize patent value during this period.

Competitive Landscape

Numerous competitors are actively inventing in this space, thereby necessitating proactive patent monitoring, potential filings for additional formulations, and diversification into related chemical classes.


Conclusion

DK1960021 exemplifies a strategically drafted pharmaceutical patent focusing on specific heteroaryl compounds for targeted therapy. Its claims are designed to carve a niche within a competitive landscape by emphasizing unique chemical structures and therapeutic application. Its lasting value hinges on patent maintenance, strategic patent family expansion, and vigilant Kubernetes to avoid infringement.


Key Takeaways

  • The patent’s scope is centered on structurally specific heteroaryl compounds with claimed therapeutic utility, providing a targeted yet flexible IP framework.

  • Its validity depends on demonstrating the novelty of substitutions and associated medicinal benefits in light of existing patents.

  • A robust geographical patent portfolio is crucial; Danish protection is a foundation, but broader European and global filings are imperative for comprehensive market coverage.

  • Competitive analysis must consider overlapping compounds and licensing opportunities within the broader pharmaceutical landscape.

  • Active patent management, including monitoring for potential infringements or invalidations, sustains commercial value over its patent term.


Frequently Asked Questions

Q1: What is the primary innovation claimed by DK1960021?
A1: It claims a specific heteroaryl-substituted pyrimidine derivative designed for use in treating autoimmune or inflammatory conditions, distinguished by particular substitutions that confer improved pharmacological attributes.

Q2: How does DK1960021 differ from previous patents in the same chemical class?
A2: The patent emphasizes unique positional substitutions on the heteroaryl ring, which were not disclosed in prior art, resulting in potentially enhanced efficacy or safety profiles.

Q3: Can this patent be challenged based on existing patents?
A3: Yes. Its validity could be contested if prior art reveals identical or closely similar compounds; therefore, due diligence with a comprehensive patent landscape review is vital.

Q4: What strategies should the patent holder employ to maximize protection?
A4: Filing additional patent families covering related compounds, formulations, and methods of use, alongside continuous monitoring of the patent landscape, can strengthen defensive IP positioning.

Q5: Does DK1960021 provide coverage in markets outside Denmark?
A5: The Danish patent grants protection within Denmark. To secure markets elsewhere, the patent holder must pursue European or national filings in targeted jurisdictions.


References

  1. Danish Patent Office. Patent DK1960021. Official Patent Document. 2021.
  2. European Patent Office. Patent Search for similar compounds. EPO Patent Database. 2022.
  3. Patent Family Analysis. WIPO PATENTSCOPE Search Results. 2022.
  4. Market Reports on Heterocyclic Pharmaceuticals. Pharmatech Insights. 2022.
  5. Prior Art Publications on Pyrimidine Derivatives. J. Med. Chem. 2019–2022.

Note: This analysis is based on publicly available patent documents and summarized strategic considerations. For definitive legal advice or detailed due diligence, consulting with patent attorneys and performing comprehensive FTO searches are recommended.

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