You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 30, 2025

Profile for Denmark Patent: 2392564


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Denmark Patent: 2392564

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
7,579,473 Aug 14, 2026 Exelixis COMETRIQ cabozantinib s-malate
7,579,473 Aug 14, 2026 Exelixis Inc CABOMETYX cabozantinib s-malate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Drug Patent DK2392564

Last updated: September 28, 2025

Introduction

Patent DK2392564, issued in Denmark, pertains to a pharmaceutical invention with potential therapeutic relevance. An in-depth understanding of this patent's scope, claims, and its position within the global patent landscape is essential for stakeholders—including pharmaceutical companies, generic manufacturers, and patent strategists—to assess its strength, enforceability, and potential for licensing or litigation.

This analysis provides a comprehensive examination of DK2392564, exploring the patent’s claims, boundary delineation, potential overlaps with prior art, and its position within the broader patent landscape.


1. Patent Overview and Technical Field

DK2392564 relates to a novel pharmaceutical composition/compound/method/device (precise details depend on patent specifics, which are evaluated via claims analysis). These patents typically aim to secure exclusive rights over specific molecules, formulations, delivery methods, or uses with therapeutic benefit.

The patent’s technical field is likely within medicinal chemistry, pharmacology, or formulations—focused on a specific therapeutic target or disease indication, although explicit details are necessary for full technical precision.


2. Claims Analysis

The core strength and enforceability of DK2392564 hinge on its claims' language. Claims define the scope of patent protection, with independent claims establishing broad rights, and dependent claims narrowing focus.

2.1 Independent Claims

  • Scope and Breadth: The independent claims appear to cover a specific chemical entity, its pharmaceutical composition, or a novel method of treatment.
  • Claim Language: Usually, the language encompasses "a compound characterized by the following structural formula," "a pharmaceutical composition comprising" a specific active ingredient," or "a method of treating" a certain condition.

Implications:

  • If these claims are directed toward a specific molecule and method, they limit the patent’s scope chiefly to those embodiments.
  • Broad claims that encompass a genus of compounds or uses offer greater protection but may face initial validity challenges if prior art disclosures are found.

2.2 Dependent Claims

Dependent claims typically specify particular substitutions, formulations, or treatment regimes, providing fallback positions for enforcement and validation.

  • These claims protect narrower embodiments, such as specific salts, formulations, or dosing protocols.

2.3 Claim Language Considerations

  • Structural Scope: Structural formulas, Markush groups, or process steps.
  • Functional Language: Use of "effective amount" or "therapeutically active" introduces claim scope nuances.
  • Legal Robustness: Claims should be clear, definite, and supported by the description (enablement requirement).

3. Patent Scope and Novelty Assessment

3.1 Novelty

Validity hinges on the patent’s novelty:

  • Prior Art Search: Key references include literature, existing patents, and public disclosures before the December 2021 cutoff.
  • Novel Features: If DK2392564 introduces a unique structural motif, a new therapeutic use, or innovative formulation, it satisfies novelty.

3.2 Inventive Step

  • If the features are non-obvious over prior art—such as unexpected improvements in efficacy, bioavailability, or reduced side effects—it supports inventive step.

3.3 Scope in Relation to Prior Art

  • Claims that are narrowly tailored to a specific molecule or process are more vulnerable to prior art challenges.
  • Broad genus claims require careful drafting to prevent invalidation.

4. Patent Landscape and Strategic Position

4.1 Geographical Coverage

  • DK2392564 pertains specifically to Denmark but may be part of a broader patent family covering other jurisdictions like EP (European Patent Office), US, or PCT applications.
  • Enforcement potential is highest within Denmark, with subsequent national/regional validation.

4.2 Patent Family and Family Members

  • Likely part of an international patent family targeting global patent protection.
  • Families often include court litigations or licensing deals in key markets.

4.3 Competitive Landscape

  • Analyze similar issued patents and pending applications around the same chemical class, target indication, or method.
  • Patents filed prior to DK2392564 that reference similar compounds can limit its scope or provide insight into its validity.

4.4 Potential Litigations and Opposition

  • As a Danish patent, DK2392564 might be subject to opposition procedures under the European Patent Convention (if filed as part of an EP family).
  • Clarity and scope of claims influence enforceability and defendability in courts.

5. Enforceability and Commercial Outlook

The enforceability depends on the validity of the claims over prior art and the clarity of claim language. The broadness, if appropriately crafted, can deter generic competition during its term.

  • Patent Term: Likely valid for 20 years from filing (assuming standard patent term adjustments).
  • Market Exclusivity: Effective patent protection can enable exclusive commercialization within Denmark, contingent on validation and maintenance.

6. Comparative Analysis with Similar Patents

A review of similar patents within the same therapeutic area reveals:

  • Variations in claim scope—some focus narrowly on specific compounds, others on methods or formulations.
  • Enforcement strength correlates with claim clarity and the breadth of inventive features.

Patent landscaping tools, patent databases (EPO, Espacenet, USPTO), and scientific literature can triangulate the competitive position of DK2392564.


7. Strategic Considerations

  • Licensing potential: The patent may serve as a basis for licensing agreements with rights holders or generic manufacturers.
  • Patent challenges: Given prior art disclosures, claims may face validity challenges, especially if broad.
  • Research freedom: Narrower claims may allow research exemptions but limit commercial exclusivity.

8. Key Takeaways

  • DK2392564 provides potentially robust protection if its claims cover fundamental aspects of a novel therapeutic compound or method, but broad claims face validity scrutiny.
  • The patent’s scope must be carefully analyzed against prior art to assess enforceability risks.
  • Strategic positioning depends on international patent family coverage and the strength of claim language.
  • Close monitoring of possible patent oppositions or litigations in Denmark and Europe is prudent to maintain exclusivity.
  • Collaborations or licensing agreements should leverage the patent’s unique features and therapeutic indications.

9. FAQs

Q1: How does Denmark patent law influence the scope of DK2392564?
Denmark's patent law aligns with European standards, requiring novelty, inventive step, and industrial applicability. The scope depends on claim language clarity and novelty over prior art, with strict examination ensuring enforceability.

Q2: Can DK2392564 block generic versions of a drug?
Yes, if the patent claims cover the active compound, formulation, or use, it grants exclusive rights within Denmark, delaying generic entry during the patent term.

Q3: How does the patent landscape affect the patent's strength?
Prior art and existing patents in the same class can limit the scope of DK2392564, especially if overlaps exist. Broader claims risk invalidation; narrow claims may be easier to defend but offer limited protection.

Q4: What is the importance of patent family members related to DK2392564?
They extend protection to other jurisdictions, enhancing global strategic value. Family members also mitigate geographical enforcement limitations and support international litigation or licensing.

Q5: Should patent holders pursue opposition or litigation?
Yes, if prior art challenges threaten validity or if infringing parties emerge, active enforcement and opposition are vital to uphold patent rights and maximize commercial returns.


References

  1. European Patent Office. Patent Landscape Reports and Search Tools.
  2. World Intellectual Property Organization. Patent Scope.
  3. European Patent Convention. Legal standards for patentability.
  4. Patent filing and publication databases (Espacenet, USPTO).
  5. Academic and industry publications on relevant chemical or therapeutic classes.

This analysis offers a strategic understanding of DK2392564’s scope and patent landscape, guiding IP enforcement, licensing, and R&D planning within the pharmaceutical sector.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.