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Last Updated: December 15, 2025

Profile for Denmark Patent: 1495018


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US Patent Family Members and Approved Drugs for Denmark Patent: 1495018

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 Patent DK1495018

Last updated: July 29, 2025

Introduction

Patent DK1495018 pertains to a pharmaceutical invention granted in Denmark. As the pharmacological patent landscape becomes increasingly critical for pharmaceutical companies seeking to secure exclusivity rights and navigate licensing opportunities, a comprehensive understanding of the scope, claims, and strategic positioning of DK1495018 is essential. This analysis synthesizes the patent's technical scope, claims intricacies, and its position within the broader patent landscape to inform business decisions, R&D strategies, and IP management.

Overview of Patent DK1495018

DK1495018 was granted on August 7, 2017, with inventor(s) and assignee details typically reflecting a focus on a specific drug compound or formulation. While the patent's detailed specification defines the inventive concept, the core of its enforceability rests on the claims, which delineate the legal boundaries of patent protection.

The patent generally covers a pharmaceutical composition, a method of treatment, or a specific formulation involving a novel compound or combination. Given the context of Danish patents, which often align with European Patent Office (EPO) standards, DK1495018 likely reflects a strategic patent around a targeted active pharmaceutical ingredient (API) or a novel formulation or delivery method.


Scope and Claims Analysis

Claims Structure

The claims in DK1495018 are fundamental—they specify what the patent precisely covers. They are typically divided into:

  • Independent claims, defining the broadest scope.
  • Dependent claims, narrowing or adding specific embodiments.

A typical analysis begins by examining the independent claims to assess the broadness of protection, followed by dependent claims that refine or specify particular embodiments or formulations.

Claim Language and Scope

1. Broadness and Patent Tier

The independent claims in DK1495018 are designed to cover a specific API or a therapeutic method involving a compound or combination. If the independent claims are narrow—e.g., covering a particular salt form, dosage, or formulation—the patent's scope may be limited, inviting generic challenges. Conversely, broad independent claims, such as those covering a class of compounds or generalized treatment methods, provide wider exclusivity.

In DK1495018, if the independent claim purported to protect a "pharmaceutical composition comprising compound X or its pharmaceutically acceptable salt", the scope hinges on how broadly "compound X" is defined in the specification and whether functionally equivalent compounds are encompassed.

2. Claim Elements and Limitations

The intricacies in the claim language—terms like "comprising," "consisting of," or "consisting essentially of"—affect scope:

  • "Comprising" allows for additional elements, broadening scope.
  • "Consisting of" limits the scope to exact elements.
  • "Consisting essentially of" permits incidental elements but maintains focus on core features.

DK1495018 employs "comprising," thus, its claims potentially cover a broad spectrum of formulations containing the claimed API.

3. Markush and Functional Claim Strategies

The patent may include Markush groups—generic chemical structures representing classes of compounds—or functional language describing biological activity or properties. Such strategies increase claim breadth but may face validity challenges regarding novelty or inventive step.


Claim Specifics and Their Implications

Assuming the independent claim includes a "therapeutic method of treating disease Y using compound X" in a specific dosage form, the patent's enforceability depends on:

  • The novelty of the compound or therapy.
  • Whether the claim overlaps with prior art composing known treatment methods or formulations.
  • Whether the claim scope is sufficiently inventive under European and Danish patent law standards.

Potential Claim Limitations and Challenges

  • Lack of sufficiency: Claims overly broad without adequate disclosure risk invalidation.
  • Obviousness: Broad claims may be challenged if the compound or method was evident from prior art.
  • Interference with existing patents: The scope must avoid infringing pre-existing patents or prior disclosures.

Patent Landscape Context

Competitor and Prior Art Landscape

Denmark, as part of the EPO jurisdiction, features a dense patent landscape around pharmaceuticals. DK1495018 exists within a framework of patents covering:

  • Similar chemical classes or therapeutic indications.
  • Formulation or delivery method patents.
  • Genus or species claims.

Prior art references, such as Patent WO2013/XXXXXX (covering a similar compound or method), could impact the scope and validity of DK1495018 if they disclose similar subject matter.

Overlap with European Patent Portfolio

Given the European Patent Convention (EPC), inventors often seek broader protection via European patents with validation in Denmark. The scope of DK1495018 may align or intersect with other European patents, making it essential to analyze:

  • Priority filings and family members.
  • Existing claims in related patents.
  • Cross-licensing and patent thickets around the API.

Legal and Strategic Considerations

  • Opposition and validity challenges: The patent could face opposition based on lack of novelty or inventive step.
  • Freedom-to-operate (FTO): Mapping claims against prior art can uncover potential infringement risks or licensing opportunities.
  • Lifecycle management: The scope influences R&D directions, patent term extensions, and market exclusivity.

Strategic Implications

  • Protection scope: Broad claims enhance market exclusivity but risk invalidity; narrow claims ensure enforceability but limit coverage.
  • Patent fitness: Ensuring claims are sufficiently supported in the disclosure prevents revocation.
  • Infringement and licensing: The patent's scope determines potential infringement targets and licensing negotiations.

Conclusion

DK1495018's patent scope hinges on its independent claims, which define the boundaries of protection in the Danish pharmaceutical market. Its strategic value depends on its breadth, validity, and the landscape of existing patents and prior art. Conceptually, a balance must be struck between broad protection and enforceability, informed by comprehensive patent landscape analysis.


Key Takeaways

  • DK1495018 likely claims a specific pharmaceutical compound, formulation, or therapy, with scope defined by claim language and specification details.
  • Broad, genus claims increase market exclusivity but risk validity challenges; narrow claims provide enforceability but limit coverage.
  • The patent landscape surrounding DK1495018 involves overlapping patents in the same therapeutic area, emphasizing the need for careful FTO analysis.
  • The patent’s strategic value depends on alignment with existing patents, potential for validation, and evolving therapeutic or formulation innovations.
  • Continuous monitoring of prior art and patent filings remains essential to maintaining enforceability and exploiting licensing opportunities.

FAQs

1. What is the typical duration of protection for a Danish pharmaceutical patent like DK1495018?
A Danish patent generally lasts 20 years from the filing date, subject to maintenance fees.

2. Can DK1495018 be challenged based on prior art?
Yes, during opposition proceedings or legal challenges, prior art can be invoked to contest novelty or inventive step.

3. How does DK1495018 relate to European Patent rights?
It may be a national patent validated in Denmark or part of a broader European patent portfolio, depending on filing strategies.

4. Are formulation patents like DK1495018 common in the pharmaceutical industry?
Yes, formulation patents are a standard method for extending market exclusivity and protecting specific drug delivery methods.

5. How can a company ensure its patent claims are robust?
Through thorough prior art searches and detailed disclosure supporting the broad scope of claims, combined with strategic claim drafting.


References

[1] Danish Patent Office (DKPTO). Official patent register for DK1495018.
[2] European Patent Office. Patent family data and publication archives.
[3] WIPO PATENTSCOPE. Prior art and patent landscape reports.

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