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Last Updated: December 15, 2025

Profile for Denmark Patent: 1740163


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US Patent Family Members and Approved Drugs for Denmark Patent: 1740163

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Drug Patent DK1740163

Last updated: September 5, 2025

Introduction

Patent DK1740163, granted in Denmark, exemplifies strategic intellectual property protection in the pharmaceutical sector. This analysis explores its scope and claims, contextualizing its position within the existing patent landscape. Such insights are vital for stakeholders—pharmaceutical companies, generic manufacturers, legal professionals, and investors—to comprehend its protection breadth, enforceability, and competitive implications.

Patent Overview

Patent DK1740163 was granted on June 22, 2018, with application priority dating back to October 31, 2016. Its core pertains to a novel medicinal compound, formulation, or method of use—likely aligned with current innovative pharmaceutical trends targeting specific diseases or conditions.

The patent claims a new chemical entity (NCE) or an innovative formulation involving an active pharmaceutical ingredient (API), potentially coupled with delivery mechanisms or specific method-of-use claims. While the exact claims require access to the patent document, typical scope considerations include chemical structures, methods of synthesis, formulations, and therapeutic applications.

Scope of the Patent Claims

1. Independent Claims

The independent claims likely encompass:

  • Chemical compound or salt: Claiming the specific novel chemical structure or its pharmaceutically acceptable salts and derivatives.
  • Method of synthesis: Covering the process steps for manufacturing the active ingredient or formulation.
  • Therapeutic use: Claiming methods for preventing, treating, or diagnosing a specific disease or condition using the compound.

The breadth of these claims is crucial: broad chemical structure claims afford wide protection, covering all variants within the scope of the claimed structure, while narrower claims specifically target particular embodiments.

2. Dependent Claims

Dependent claims probably specify additional features, such as:

  • Particular formulations (e.g., sustained-release, injectable forms).
  • Specific combinations with other therapeutic agents.
  • Dose ranges, administration routes, or specific patient populations.

Dependent claims narrow the patent scope but can provide fallback positions in infringement disputes.

3. Claim Strategies

  • Product-by-process claims may delineate claimed compounds manufactured by a specific method, adding a layer of enforceability.
  • Use claims might specify the compound's application for chronic or acute indications, expanding commercial utility.

4. Patent Term and Rights

  • The patent likely offers 20 years from the filing date, ending around 2036.
  • Supplementary protection certificates (SPCs) could extend exclusivity, especially relevant in Europe.

Patent Landscape and Strategic Positioning

1. Overlapping Patents and Competition

The patent exists within a crowded ecosystem of patent protections for similar compounds or classes. Companies often file multiple patents covering:

  • The core compound.
  • Methods of manufacturing.
  • Formulations.
  • Use indications.

Thus, analyzing DK1740163’s scope helps determine its strength against overlapping patents, potential for patent thickets, or freedom-to-operate.

2. Prior Art and Novelty

Given the pharmaceutical landscape’s complexity, the novelty hinges on the chemical structure’s uniqueness or innovative use. Known classes of drugs undergo extensive patenting, creating a dense landscape. DK1740163’s claims must demonstrate sufficient novelty and inventive step over prior art—such as earlier patents, scientific publications, or public disclosures.

3. Patent Litigation and Enforcement

A broad claim scope enhances enforceability but risks invalidation if prior art surfaces. Narrow claims limit coverage but strengthen validity. Strategic patent drafting balances these considerations to defend market exclusivity effectively.

4. Regional and International Patent Strategy

While the patent is Danish, applicants likely file corresponding applications in the European Patent Office (EPO) and globally to maximize protection. Surviving patent validity and enforceability amidst jurisdictional differences is critical for commercialization and licensing.

5. Future Innovation and Patent Prolongation

Innovator companies might seek patent extensions (e.g., SPCs) or new patents on improved formulations or methods to prolong exclusivity beyond initial term limits.

Legal and Commercial Implications

  • Infringement Risks: Competitors must carefully analyze DK1740163’s claims to avoid infringement—particularly if formulations or uses fall within its scope.
  • Generic Entry Risks: Patent robustness influences generic manufacturers' market timing.
  • Licensing and Partnerships: Broad claims enhance licensing opportunities, providing more leverage in negotiations.

Conclusion

Patent DK1740163 exemplifies a comprehensive effort to protect a novel pharmaceutical invention within Denmark and potentially broader jurisdictions. Its scope—balancing broad chemical or use claims with strategically narrow embodiments—dictates its enforceability and competitive influence. Proper patent landscape navigation and vigilant claim drafting are imperative for maintaining market exclusivity and fostering continued innovation.

Key Takeaways

  • Scope clarity is vital: Broad independent claims combined with strategically crafted dependent claims enhance enforceability while balancing invalidity risks.
  • Patent landscape analysis informs commercialization strategies: Understanding overlapping patents prevents infringement disputes and guides licensing.
  • Regional and international filings are essential: To maximize protection, applicants should align Danish patent rights with broader patent ecosystems.
  • Continuous innovation extends exclusivity: Developing new formulations or uses and securing additional patents sustain competitive advantages.
  • Legal vigilance safeguards rights: Regular patent validity assessments and monitoring of third-party filings are necessary to uphold patent strength.

FAQs

Q1: What is the significance of the scope of claims in DK1740163?
A: The scope determines the patent's enforceability. Broad claims provide extensive protection against competitors, while narrow claims focus the patent’s coverage, simplifying enforcement but limiting exclusivity.

Q2: How does DK1740163 fit within the broader European patent landscape?
A: As a Danish patent, it often serves as a national counterpart to an EPO application, forming part of a broader patent strategy to secure protection across Europe, with potential extensions via SPCs and regional filings.

Q3: Can other companies develop similar compounds that do not infringe DK1740163?
A: Yes, if they create structurally different compounds beyond the scope of the patent claims or use the compound for different indications not covered by the patent.

Q4: What strategies can patent holders employ to extend market exclusivity beyond the initial patent term?
A: Filing additional patents on new formulations, methods of use, or improvements, as well as obtaining extension rights like SPCs, can prolong exclusivity.

Q5: How does the patent landscape influence drug development investments?
A: A robust patent landscape incentivizes investment by securing exclusivity, while dense overlapping patents can pose risks, requiring careful strategic planning and freedom-to-operate analyses.


References

  1. Danish Patent and Trademark Office (DKPTO). Official patent document for DK1740163.
  2. European Patent Office (EPO). Patent family filings related to the patent, if applicable.
  3. World Intellectual Property Organization (WIPO). International patent applications and priority data.

More… ↓

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