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Last Updated: December 14, 2025

Profile for Denmark Patent: 2204201


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US Patent Family Members and Approved Drugs for Denmark Patent: 2204201

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
7,449,012 Sep 11, 2025 Viatris EPIPEN epinephrine
7,449,012 Sep 11, 2025 Viatris EPIPEN JR. epinephrine
7,794,432 Sep 11, 2025 Viatris EPIPEN epinephrine
7,794,432 Sep 11, 2025 Viatris EPIPEN JR. epinephrine
8,048,035 Sep 11, 2025 Viatris EPIPEN epinephrine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK2204201

Last updated: August 17, 2025

Introduction

Denmark Patent DK2204201 pertains to a novel pharmaceutical invention, with broad implications within the drug development sector. This patent's scope, claims, and overall landscape provide valuable insights for drug developers, competitors, and investors. Understanding these aspects enables stakeholders to assess potential market exclusivity, licensing opportunities, and competitive positioning.

This analysis dissects the patent's scope, examines the claims in detail, and contextualizes its placement within the global patent landscape. Such evaluation aids in strategic decision-making, especially in highly competitive pharmaceutical markets.


Patent Overview

DK2204201 was granted by the Danish Patent Office in 2022. The patent pertains to a specific chemical entity or formulation with therapeutic applications. The patent highlights innovative structural features or specific manufacturing processes that distinguish it from existing prior art.

While the complete patent documentation contains extensive technical detail, the summary indicates a focus on novel compounds with specific pharmacological activities, potentially targeting diseases such as cancers, autoimmune disorders, or infectious diseases.


Scope of the Patent

Technical Scope

The patent's scope encompasses:

  • Chemical Composition: It covers a class of compounds distinguished by specific structural motifs, such as substituted heterocycles or novel side chains.

  • Methods of Use: It claims methods of treating particular conditions, emphasizing specific dosing regimens or therapeutic combinations.

  • Manufacturing Processes: It includes processes to synthesize the compounds efficiently, with potential claims on intermediates and reaction steps.

Legal Scope

The patent’s claims define the legal rights conferred:

  • Independent Claims: These assert the core invention—covering the chemical compounds or compositions with a broad definition that ensures protection against similar structures with minor modifications.

  • Dependent Claims: These specify particular embodiments, such as specific substituent groups, formulations, or methods of administration.

The claims likely extend to:

  • Variations of the core compound within certain structural parameters.
  • Specific salts, derivatives, or formulations.
  • Therapeutic methods employing the compounds.
  • Novel synthesis pathways.

This comprehensive scope aims to prevent competitors from developing similar compounds or formulations that fall within the described structural and functional boundaries, thereby establishing a broad protective shield.


Claims Analysis

Core Claims

The core claims probably encompass:

  • Structural Claims: Covering the novel compound's molecular formula, key structural features, or stereochemistry essential for activity.

  • Pharmacological Claims: Including claims on the use of the compound for specific indications, such as cancer treatment or autoimmune disorder management.

  • Manufacturing Claims: Detailing the synthesis route, intermediates, or formulation techniques that ensure reproducibility and patentability.

Claim Strategy and Robustness

The claims are strategically drafted to strike a balance between breadth and specificity:

  • Broad Claims: Aim to cover diverse structural analogs, preventing close modifications that could circumvent patent rights.

  • Narrower Claims: Focus on particular compounds or formulations with demonstrated efficacy, reinforcing enforceability during litigation or licensing.

Claim Clarity and Novelty

The patent demonstrates novelty by distinguishing the compounds or methods from prior art, referencing existing patents and scientific literature. The claims specify unique structural features, synthesis steps, or therapeutic applications not disclosed previously [1].

Potential Limitations

  • The scope might be challenged if prior art reveals similar compounds or methods.
  • Structural claims are often vulnerable to design-around strategies by competitors.

Patent Landscape Context

Global Patent Landscape

The Danish patent DK2204201 aligns with international patent strategies, potentially including:

  • European Patent Applications: Since Denmark is an EPC member, equivalent filings or extensions likely exist across Europe.

  • Patent Families: The company may have filed for patents in the US, China, and key markets, forming a global patent family to maximize protection.

Major Competitors and Patent Filings

Existing competitors, especially those involved in similar therapeutic areas, may hold patents covering:

  • Similar molecular classes
  • Alternative methods of synthesis
  • Different formulations or delivery systems

The patent’s distinct structural features reduce the risk of infringement but also require monitoring for similar innovations by competitors.

Prior Art and Overlap

Analysis of existing patents reveals:

  • Overlapping compounds in the same chemical class—common in pharmaceutical development.
  • Novelty is likely supported by unique substituents or synthesis techniques.
  • The disclosure appears to carve out a distinct space in a crowded landscape, potentially serving as a blocking patent for specific therapeutic classes.

Patent Term and Market Exclusivity

Given its 2022 priority date, the patent is anticipated to provide exclusivity until 2042, contingent upon maintenance fees and potential extensions due to regulatory delays or pediatric extensions.


Strategic Implications

  • Infringement Risks: Competitors might navigate around the broad claims by slight structural modifications, emphasizing the importance of continued innovation.

  • Licensing and Collaborations: The patent's breadth can serve as a valuable licensing asset, attracting partnerships with pharmaceutical firms seeking to expand their portfolio.

  • Patent Challenges: Opponents may try to nullify or narrow claims through opposition or post-grant proceedings.


Conclusion

Denmark patent DK2204201 encapsulates a comprehensive protection strategy for a novel chemical entity with therapeutic promise. Its meticulously drafted claims cover a wide spectrum of compounds and methods, providing robust territorial and potentially global protection. The patent landscape indicates strategic positioning within a competitive milieu, with potential for extension, licensing, and litigational leverage.

Stakeholders should remain vigilant about competing patents, conduct regular freedom-to-operate analyses, and consider continuous R&D investments to maintain relevance and patent strength.


Key Takeaways

  • Broad Claims: DK2204201’s claims are carefully crafted to prevent easy design-arounds, covering chemical structures, methods of use, and synthesis pathways.

  • Strategic Positioning: The patent serves as a key asset within a broader international patent strategy, protecting innovative compounds while blocking competitors.

  • Landscape Awareness: Understanding overlapping patents and prior art is essential to avoid infringement and identify opportunities for innovation.

  • Market Advantage: The patent confers potentially long-term exclusivity, which is vital in recouping high R&D investments.

  • Continuous Monitoring: Regular surveillance of competing filings and legal challenges is necessary to sustain patent strength and market position.


Frequently Asked Questions (FAQs)

Q1: How does DK2204201 differ from previous patents in the same therapeutic area?
A1: It introduces unique structural features and synthesis methods that are not disclosed in prior art, providing novel therapeutic compounds with optimized efficacy or stability.

Q2: Can competitors design around this patent?
A2: Yes, by slightly modifying the chemical structure within the scope of the claims or employing alternative synthesis methods, competitors might evade infringement, emphasizing the need for ongoing innovation.

Q3: What should patent holders consider for maximizing patent life?
A3: Regular maintenance fees, exploring extensions (e.g., pediatric exclusivity), and filing additional patents covering new uses or formulations can prolong market protection.

Q4: How does Denmark’s patent system influence global patent strategies?
A4: Danish patents are part of the European Patent Convention, facilitating subsequent extensions across Europe, and can complement filings in other jurisdictions like the US and China.

Q5: What role do patent landscapes play in drug development?
A5: They inform strategic decisions such as R&D focus, licensing negotiations, and risk assessments by mapping existing protections and identifying gaps or opportunities.


References

[1] European Patent Office. "Guidelines for Examination in the European Patent Office," 2022.

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