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Last Updated: December 29, 2025

Profile for Denmark Patent: 3372281


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US Patent Family Members and Approved Drugs for Denmark Patent: 3372281

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 Apr 28, 2026 Viiv Hlthcare APRETUDE cabotegravir
⤷  Get Started Free Apr 28, 2026 Viiv Hlthcare CABENUVA KIT cabotegravir; rilpivirine
⤷  Get Started Free Apr 28, 2026 Viiv Hlthcare VOCABRIA cabotegravir sodium
⤷  Get Started Free Feb 4, 2031 Viiv Hlthcare APRETUDE cabotegravir
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Denmark Drug Patent DK3372281: Scope, Claims, and Patent Landscape

Last updated: August 8, 2025

Introduction

Patent DK3372281 pertains to a specific pharmaceutical invention granted in Denmark, representing the country’s intellectual property regime’s stance on innovative medicinal formulations. Analyzing its scope, claims, and position within the patent landscape offers strategic insights into its potential market exclusivity, competitive advantages, and landscape overlap with existing patents.

Overview of Patent DK3372281

DK3372281, filed in Denmark, has granted protection for a novel drug formulation or application. While the specific patent document details are not provided here, typical patent analysis involves examining the claims' language, scope, and the technological field.

The patent’s effective scope hinges on the inventive features claimed, the breadth of claims, and their legal enforceability within Denmark and potentially in European or global markets through extensions or filings in other jurisdictions.

Scope of the Patent: Definition and Implications

The scope of patent DK3372281 is primarily defined by its claims, outlining the boundaries of exclusivity. A patent’s scope determines the breadth of innovations protected—whether broad or narrow.

Claims Analysis

Claims serve as the legal definition of the invention; their language reveals whether the patent covers:

  • Compound-specific claims: Protecting a specific chemical entity or biological molecule.
  • Formulation claims: Covering specific combinations of excipients, delivery systems, or formulations.
  • Method claims: Encompassing particular methods of manufacturing or administering the drug.
  • Use claims: Covering specific medical indications or therapeutic applications.

Claim Structure and Breadth:
In the current landscape, patents often comprise core independent claims with multiple dependent claims further narrowing the scope. For DK3372281:

  • Independent claims likely focus on a specific formulation or use—e.g., a novel lipid-based delivery system, a new crystalline form, or a unique method of synthesis.
  • Dependent claims potentially specify particular excipients, dosages, or process parameters, providing fallback positions and incremental rights.

The broader the claims (e.g., encompassing all formulations containing a particular active ingredient), the more comprehensive the patent's protective scope, but potentially more susceptible to invalidation if broader prior art exists. Conversely, narrow claims protect specific embodiments but limit enforceability.

Main Inventive Features

For pharmaceutical patents, key inventive features often include:

  • Novel chemical modifications of known compounds.
  • Unique formulation strategies enhancing bioavailability or stability.
  • Innovative delivery mechanisms (e.g., nanoparticle systems, slow-release matrices).
  • Specific manufacturing processes reducing impurities or costs.

The claims must clearly delineate these features, differentiating from prior art to withstand invalidation challenges.

Patent Landscape Context

Understanding DK3372281’s position within the broader patent landscape involves examining:

Prior Art and Patent Citations

  • Pre-existing patents in the same chemical class or therapeutic area can limit scope or trigger patent invalidation.
  • Forward citations indicate influence or infringement risks. A high citation count suggests the patent is influential but also potentially subject to challenges.

Related Patent Families

Given Denmark's integration with the European Patent Office (EPO), patent applicants often file family members across jurisdictions:

  • European Patent Applications: Possible counterparts providing broader or narrower protection.
  • International PCT Applications: Offering extended territorial rights and strategic positioning.

By analyzing these related filings, stakeholders can assess the global scope and freedom-to-operate.

Overlap with Existing Patents

Potential overlaps may involve:

  • Active pharmaceutical ingredients (APIs): Known compounds with similar formulations.
  • Delivery systems: Comparable nanocarrier or sustained-release technologies.
  • Use claims: Existing patents claiming the same indication or therapeutic method.

Differentiation strategies include emphasizing unique chemical forms, manufacturing processes, or delivery routes.

Legal and Commercial Significance

The scope of DK3372281 impacts:

  • Market Exclusivity: Broader claims afford longer and more comprehensive protection.
  • Freedom to Operate: Narrow claims or overlapping patents require diligent clearance to commercialize.
  • Patent Strength: Robust claims that withstand invalidation bolster licensing, partnership negotiations, and litigation defenses.

Strategic Recommendations

  • Conduct Freedom-to-Operate (FTO) Analyses: Identify patent overlaps.
  • Evaluate Patent Strengths and Weaknesses: Through expert infringement and validity reviews.
  • Consider Filing Continuation or Divisionals: To extend protection or refine claim scope based on emerging art.
  • Monitor Patent Citations: To identify potential licensing or infringement opportunities.

Conclusion

DK3372281 exemplifies a targeted approach to pharmaceutical patenting in Denmark, with its scope dictated by claim language and inventive features. Its position within the patent landscape influences its strategic value. By understanding the specific claims and their technological breadth, stakeholders can optimize patent assets, mitigate infringement risks, and capitalize on exclusivity rights.


Key Takeaways

  • Claim language is crucial: Broader claims offer extensive protection but risk validity challenges; narrow claims provide specificity but limited scope.
  • Patent landscape awareness: Overlapping patents impact freedom-to-operate and must be carefully analyzed to avoid infringement.
  • Strategic patent management: Supplementing DK3372281 with international filings and continuations can enhance global patent coverage.
  • Innovation differentiation: Emphasize unique formulation or process features to strengthen patent standing.
  • Legal vigilance: Regular monitoring of citations and potential challenges safeguards patent value.

FAQs

1. What is the significance of the claims in DK3372281?
Claims define the legal boundaries of the patent's protection, determining what aspects of the invention are protected and how enforceable they are against infringers.

2. How does DK3372281 compare to other pharmaceutical patents in Denmark?
Its significance depends on claim breadth, inventive novelty, and overlap with existing patents. Analyzing its claims and citations helps establish its relative strength.

3. Can DK3372281 be enforced outside Denmark?
Not directly. For broader protection, filing corresponding patents in other jurisdictions, such as through the European Patent Office or PCT system, is necessary.

4. What factors influence the patent landscape surrounding DK3372281?
Active factors include prior art patents, patent citations, related family filings, and potential overlapping claims in the same therapeutic or technological area.

5. How can stakeholders optimize the value of DK3372281?
By conducting comprehensive patent landscape analyses, expanding jurisdictional coverage, and continuously monitoring for potential infringements or invalidations.


Sources:

  1. European Patent Office (EPO) patent database.
  2. Danish Patent and Trademark Office (DKPTO).
  3. Patent publications and legal status reports.
  4. Prior art and patent citation analyses from patent databases.

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