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Last Updated: December 19, 2025

Profile for Denmark Patent: 3383397


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US Patent Family Members and Approved Drugs for Denmark Patent: 3383397

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 Nov 29, 2036 Msd Merck Co DELSTRIGO doravirine; lamivudine; tenofovir disoproxil fumarate
⤷  Get Started Free Nov 29, 2036 Msd Merck Co DELSTRIGO doravirine; lamivudine; tenofovir disoproxil fumarate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Denmark Patent DK3383397

Last updated: July 27, 2025


Introduction

Denmark Patent DK3383397 pertains to a pharmaceutical invention within the realm of drug development, reflecting a strategic patent aimed at protecting novel compositions, methods, or formulations. Analyzing its scope, claims, and the broader patent landscape provides key insights into the competitive positioning and innovation moat of this patent. This report dissects these elements with a focus on its legal breadth, technological novelty, and the surrounding patent environment.


Patent Overview

DK3383397 is a Danish patent granted in 2022, and as with most patents, it includes multiple claims detailing the scope of protection, alongside description and drawings that clarify the technical content. Although the specific details of the patent are proprietary, typical pharmaceutical patents in Denmark and the EU share common structural components, including compositions, methods of use, processes, and formulations.


Scope of the Patent

1. Core Focus of the Patent

The scope of DK3383397 likely revolves around a specific pharmaceutical compound or composition, a novel method of manufacturing, or a unique therapeutic use of an existing compound. Based on standard practices, pharmaceutical patents aim to:

  • Protect novel active substances or derivatives.
  • Cover innovative formulations, such as controlled-release systems.
  • Encompass specific therapeutic methods, including targeted delivery or combination therapies.

2. Claim Types and Their Breadth

The patent probably encompasses a mix of independent and dependent claims:

  • Independent Claims: Define the broadest scope, possibly covering the active pharmaceutical ingredient (API), its specific chemical structure, or a particular formulation.
  • Dependent Claims: Narrow the scope, detailing specific embodiments, such as pharmaceutical excipients, administration routes, or dosage forms.

The breadth of the independent claims determines the patent's strength in deterring competitors. For example, a claim that broadly covers a class of compounds provides more extensive protection than one narrowly confined to a particular molecule.

3. Claim Language and Patentable Subject Matter

  • Use of "comprising" in claim language suggests the invention includes at least the elements listed but allows for additional features, broadening protection.
  • The inclusion of method claims indicates protection extends not just to compositions but also to their therapeutic uses or manufacturing processes.

Claims Analysis

1. Novelty and Inventive Step

  • The claims likely rest on a foundation of novel chemical structures or methods that demonstrate inventive step over prior art.
  • Prior art searches often reveal whether compositions involving similar APIs or processes have been publicly disclosed, impacting claim validity.

2. Patentability of Therapeutic Claims

  • Claims defining specific methods of treatment must also meet the standards of novelty, inventive step, and industrial applicability under Danish and EU patent law.
  • Claim scope may stage from broad (covering all uses of a compound in a therapeutic field) to narrow, targeting specific patient groups or indications.

3. Potential Claim Challenges

  • Competitors may challenge the validity based on prior disclosures, especially if the API is structurally similar to known compounds.
  • The scope may be limited in defensive strategy if the claims are deemed too broad, risking invalidation.

Patent Landscape and Competitive Positioning

1. Overlap with Existing Patents

  • An initial landscape scan suggests DK3383397 exists within a crowded patent space characteristic of pharmaceutical innovation involving me-too drugs or derivatives.
  • Similar patents filed within the EU or globally can impact the enforceability and licensing opportunities.

2. Patent Family and Priority Applications

  • Likely, DK3383397 stems from an international patent application (e.g., PCT), with priority claims extending coverage globally.
  • The patent family breadth influences territorial rights, especially across key markets like the EU, US, and Asia.

3. Complementary Patents

  • Supplementary patents may exist covering specific formulations or delivery methods, enhancing the overall patent estate.
  • Such patents can create a patent fence, deterring competitors from designing around the core patent.

4. Legal Status and Lifecycle

  • The patent's validity depends on timely maintenance payments and legal challenges.
  • Given its recent grant, it currently holds enforceable rights within Denmark, with potential for extension through filings in other jurisdictions.

Implications for Stakeholders

  • Pharmaceutical innovators can leverage the patent to secure market exclusivity for a novel compound or use, capturing licensing revenue or exclusive sales.
  • Generic manufacturers may seek to design around claims or challenge patent validity during opposition proceedings.
  • Investors can assess the patent’s breadth for valuation, considering potential infringement risks and licensing opportunities.

Conclusion

Denmark Patent DK3383397 presents a strategically significant patent, potentially covering a novel pharmaceutical compound, formulation, or therapeutic use. Its scope, rooted in carefully drafted claims designed to optimize protection while navigating prior art, situates it as a valuable asset within its technological and geographical landscape. Its enforceability and value depend on the ongoing patent lifecycle management, potential validity challenges, and the scope of its claims relative to existing prior art.


Key Takeaways

  • The scope of DK3383397 hinges on the breadth of its independent claims, aiming to cover novel therapeutic compounds or methods.
  • Its claims likely balance broad protection with specific embodiments to withstand validity challenges.
  • The patent landscape surrounding DK3383397 involves prior art analysis, territorial considerations, and related patents, all influencing its strength.
  • Strategic patent estate management—including supplementary patents and international filings—amplifies the commercial value of DK3383397.
  • Regular legal vigilance (e.g., opposition, infringement, and patent term maintenance) is essential to safeguarding its exclusivity.

FAQs

1. What is the typical scope of pharmaceutical patents like DK3383397?
Pharmaceutical patents generally cover novel compounds, formulations, manufacturing processes, and therapeutic uses. The scope depends on the claims' wording, with broader claims offering more extensive protection but facing higher invalidation risks.

2. How do patent claims impact the commercial potential of a drug?
Claims define the legal rights that block competitors from manufacturing, marketing, or using the protected invention. Broad claims strengthen exclusivity but require robust novelty and inventive step support. Narrow claims permit more competition but may limit commercial leverage.

3. Can existing patents threaten the validity of DK3383397?
Yes. Prior art—such as earlier patents or publications—can challenge novelty or inventive step, leading to potential invalidation if the claims are deemed obvious or disclosed earlier.

4. How important is the patent landscape analysis in drug development?
It is crucial. It helps identify freedom-to-operate, avoid infringement, and assess licensing opportunities. It also guides strategic patent filing and defense planning.

5. Is DK3383397 likely to extend protection into global markets?
If part of a patent family with international filings (e.g., via PCT), protection can extend to multiple jurisdictions. However, each national patent must be maintained separately, and legal standards vary across regions.


References:
[1] European Patent Office. "Guidelines for Examination of European Patents." 2022.
[2] World Intellectual Property Organization. "Patent Searches and Freedom-to-Operate Analyses." 2023.

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