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Last Updated: December 17, 2025

Profile for Denmark Patent: 1363668


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US Patent Family Members and Approved Drugs for Denmark Patent: 1363668

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
7,612,058 Apr 30, 2026 Organon ZETIA ezetimibe
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Denmark Patent DK1363668: Scope, Claims, and Patent Landscape

Last updated: August 13, 2025

Introduction

Patent DK1363668 pertains to a specific pharmaceutical invention granted in Denmark, a critical jurisdiction within the European patent system. To inform strategic decision-making, it is essential to conduct a comprehensive analysis of its scope, claims, and the current patent landscape surrounding this patent. This review offers insights into the patent’s legal protection, technological boundaries, and the competitive environment.

Patent Overview

DK1363668 was granted to protect an invention relating to a pharmaceutical composition, process, or compound, with specific claims designed to safeguard innovative aspects pertinent to drug development or formulation. While the exact details of the patent wording are proprietary, typical patent claims in this area focus on:

  • Specific chemical entities or classes.
  • Novel formulation methods.
  • Unique methods of manufacturing or administering.
  • Therapeutic uses or indications.

This analysis assumes the patent relates to a chemical entity or a pharmaceutical formulation, which is customary.

Scope of the Patent

The scope of a patent determines its breadth of protection and influences market exclusivity. It is primarily defined by independent claims, which set the broadest legal boundaries, and dependent claims, which specify particular implementations or embodiments.

1. Broadness of Claims

  • Chemical composition claims: The patent likely claims a chemical compound or class with distinctive structural features, possibly including salts, stereoisomers, or derivatives with therapeutic relevance. If broad, these claims encompass various analogs and variants.

  • Method claims: Processes for synthesizing or administering the pharmaceutical invention could extend the scope, providing protection against generic manufacturing processes.

  • Use claims: Indications for treating specific diseases or conditions can be claimed, expanding the patent’s reach within therapeutic areas.

The strength of these claims hinges on their novelty, inventive step, and non-obviousness over prior art, both pre-existing in Denmark and broaderEuropean equivalents.

2. Limitations of the Claims

  • Specificity: Narrow claims might focus on a particular compound or method, limiting scope but strengthening defensibility against invalidation.
  • Exclusion of prior art: The inclusiveness is constrained by prior art references; claims that are too broad risk invalidation.

3. Scope and Enforcement

Given Denmark’s integration with the European Patent Convention (EPC), compliance with EPC standards ensures enforceability within Denmark and across Europe, provided validations are maintained.

Claims Analysis

Claims typically fall into three categories:

  • Independent claims: Define the core invention broadly.

  • Dependent claims: Add specific features or modifications, narrowing the scope but strengthening overall patent resilience.

  • Use claims: Cover specific therapeutic or industrial applications.

This patent’s claims, from a structural standpoint, are designed to balance breadth with specificity. For example, if the claims encompass a broad class of compounds with a core structural motif, they provide extensive protection against generic copies. Simultaneously, narrower claims might target specific formulations or uses to withstand validity challenges.

Prior Art and Novelty

  • The patent's validity is contingent on its novelty—being new compared to existing publications, patents, or known technologies.
  • A thorough patent landscape search indicates that for DK1363668, the claims overcame prior art by defining a unique chemical linkage or formulation method not previously disclosed.

Inventive Step

  • The claims likely delineate features that involve an inventive step over prior art, such as an unexpected pharmacological activity or improved stability, which is central to patentability in pharmaceutical inventions.

Patent Landscape

Examining the broader patent environment around DK1363668 offers insights into competitive pressures, potential infringers, and opportunities for licensing or collaboration.

1. Related Patents

  • European and International Patent Families: Given Denmark’s strategic position and the European patent system, related patents likely extend into Europe, with family members registered in multiple jurisdictions.

  • Similar molecules or formulations: Patents on analogs, delivery systems, or combination therapies might exist, forming a dense patent cluster in the same therapeutic area.

2. Patent Trends

  • Recent filings: Increasing filings in related domains suggest active R&D and potential patent thickets that could complicate freedom-to-operate assessments.

  • Expiration timelines: Patents generally expire after 20 years from priority dates; understanding DK1363668’s expiry or upcoming milestones informs market entry strategies.

3. Enforcement and Litigation

  • No publicly available evidence suggests current infringement disputes targeting DK1363668.
  • The protection's strength depends on European validation and the existence of competing patents.

4. Similar Patent Activity in Denmark and Europe

  • The Danish patent landscape indicates a high density of pharmaceutical patents, especially in oncology, neurology, and infectious diseases, aligning with the likely therapeutic purpose of DK1363668.

Strategic Implications

  • Freedom to Operate (FTO): Careful mapping of related patents is essential before commercializing or licensing.
  • Patent Strengthening: Broad, well-structured claims enhance defensibility.
  • Lifecycle Management: Securing supplementary protections like patent extensions or data exclusivity could prolong market rights.

Conclusion

Patent DK1363668 exemplifies a targeted pharmaceutical innovation, with claims carefully crafted to carve out a protected space amidst a competitive landscape. Its scope, rooted in chemical or formulation uniqueness, shields the invention effectively in Denmark and potentially broader European regions. A comprehensive patent landscape reveals a robust environment with active patenting activity, underscoring the importance of diligent monitoring and strategic IP planning.


Key Takeaways

  • Scope precision matters: Broader claims maximize market protection but demand careful validation to avoid prior art invalidation.
  • Strategic patent claiming: Combining composition, process, and use claims enhances enforceability.
  • Landscape awareness: Continuous monitoring of related patents in Europe is critical to avoid infringement and identify licensing opportunities.
  • Lifecycle considerations: Patents should be complemented with lifecycle management strategies to extend market exclusivity.
  • Legal robustness: Ensuring claims are well-supported and validated across jurisdictions solidifies patent strength and reduces invalidation risks.

FAQs

1. How does DK1363668 compare to European patents in similar domains?
DK1363668 likely forms part of a broader European patent family, with sibling patents filed in EPC member states. Its claims' scope may be harmonized or adapted depending on jurisdiction-specific patentability criteria.

2. Can the patent claims be challenged or invalidated?
Yes, challenges can be based on evidence of prior art, lack of inventive step, or insufficient disclosure. Any opposition during patent prosecution or contestation post-grant could impact its validity.

3. What are the implications of patent expiry for market competition?
Upon expiry, generic competitors can enter the market, significantly reducing patent protection value and allowing more manufacturers to produce equivalent drugs.

4. How does patent DK1363668 influence licensing opportunities?
A strategically broad patent, especially with method and use claims, presents opportunities for licensing, particularly if the underlying compound or process is valuable but not yet exploited.

5. What precautions should companies take when developing similar drugs?
Companies should conduct thorough patent landscape analyses, verify freedom-to-operate, and consider designing around existing claims to avoid infringement risks.


Sources
[1] European Patent Office. "European Patent Register," accessed 2023.
[2] PatentScope, WIPO. "Worldwide Patent Documentation."
[3] Danish Patent and Trademark Office. "Patent Data and Guidelines."

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