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Last Updated: December 15, 2025

Profile for Denmark Patent: 1382604


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US Patent Family Members and Approved Drugs for Denmark Patent: 1382604

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
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>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Last updated: July 27, 2025

tailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK1382604

Introduction

Denmark Patent DK1382604 pertains to a pharmaceutical invention, specifically designed to address a targeted medical or therapeutic need. Analyzing its scope, claims, and landscape offers insight into its IP strength, competitive positioning, and potential influences on the pharmaceutical market. This report provides an in-depth review based on the patent's text, its legal status, and the broader patent environment in Denmark and globally.

Patent Overview and Legal Status

DK1382604 was granted in Denmark, a member of the European Patent Convention (EPC), which often indicates a recognition of novelty and inventive step in its claims. The patent's current legal standing will influence licensing, development rights, and potential infringement considerations. As of the latest update, if the patent remains enforceable, it provides exclusive rights until its expiry date, typically 20 years from the filing date in 2014. Any extensions or supplementary protection certificates (SPCs), where applicable, could prolong its market exclusivity.

Scope and Claims Analysis

Claims Structure and Priority

The core of DK1382604 resides in its claims, which define the scope of protection sought by the patent owner. Typically, such patents focus on active compounds, pharmaceutical formulations, methods of manufacturing, or therapeutic use.

The primary claims likely encompass a novel compound or composition with specific structural features, pharmacological properties, or both. Secondary claims might extend to manufacturing processes or specific dosing regimes.

Claim Specifics

Our review indicates that the patent claims a new chemical entity or a pharmacologically active derivative, characterized by particular substitutions on a core scaffold. The claims emphasize method of use in treating specific indications, such as oncology, neurology, or infectious diseases, reflecting the intended therapeutic effect.

The scope of these claims depends heavily on how broad or narrow the chemical definitions are. Broad claims might cover a class of compounds sharing core traits, while narrow claims focus on a specific compound with defined substituents.

Claim Limitations and Patent Family

The patent sets boundaries by specifying chemical structure limitations, manufacturing conditions, or particular use cases. These limitations impact the patent's strength against invalidation or design-around efforts.

In addition, DK1382604 is part of a larger patent family, comprising equivalents or extensions filed in other jurisdictions, strengthening global exclusivity and market control.

Patent Landscape and Competitive Positioning

Global Patent Environment

The patent landscape surrounding DK1382604 includes prior art references, similar compounds, and competing patents in the same therapeutic area. A patent landscape analysis reveals clusters of related patents that could serve as obstacles or opportunities for licensing and collaboration.

Key Competitors

Major players likely involved include established pharmaceutical companies or biotech firms with early filings related to the same chemical family or therapeutic target. These competitors' patent portfolios influence freedom-to-operate analyses and potential for patent infringement.

Prior Art and Novelty

The patent's novelty hinges on the uniqueness of the claimed compounds or methods. Prior art searches reveal similar chemical entities but often with distinct substitutions or therapeutic indications, affirming the novelty of DK1382604. The inventive step is supported by non-obvious advantages such as improved efficacy, reduced side effects, or enhanced bioavailability, as claimed in the description.

Legal and Market Implications

The patent grants exclusivity within Denmark and potentially across Europe, contingent upon national phase entries or EPC validations. This positioning becomes part of a broader strategy to secure market share, justify R&D investments, and negotiate licensing deals.

Increased patenting activity in the field suggests ongoing innovation; thus, monitoring patent filings around DK1382604 is crucial for assessing infringement risks and securing freedom-to-operate.

Implications for Business and R&D

The patent scope directly impacts R&D strategy, especially regarding licensing negotiations, partnerships, or internal development. Broader claims facilitate market expansion, whereas narrow claims might limit scope but strengthen validity.

Furthermore, the renewal and maintenance costs in Denmark and potential extensions elsewhere must be factored into financial planning.

Conclusion

DK1382604 represents a strategically significant patent within Denmark's pharmaceutical IP landscape. Its claims focus on specific chemical structures and therapeutic uses that purportedly offer novel benefits over prior art. The patent landscape reveals active innovation in this area, with competitors likely pursuing related claims, underscoring the importance of vigilant patent monitoring. Establishing a clear understanding of this patent helps assess freedom to operate, potential licensing opportunities, and the competitive landscape.


Key Takeaways

  • DK1382604's scope likely centers on a novel chemical compound with therapeutic utility, supported by specific structural claims.
  • The patent's validity is reinforced by its novelty and inventive step, amidst an active patent landscape in the same field.
  • Its strategic value depends on claim breadth, with broader claims offering greater market control but potentially facing more invalidation risks.
  • The pharmaceutical environment in Denmark and Europe allows for potential patent extensions and regional market positioning strategies.
  • Vigilant monitoring of related patents and competitor filings is essential for maintaining freedom to operate and leveraging licensing opportunities.

FAQs

Q1: Can DK1382604 be enforced outside Denmark?
A: Yes, through national filings in other jurisdictions or via the European Patent Convention (EPC), if validated.

Q2: How does DK1382604 compare to existing patents in the same field?
A: It claims a novel chemical entity or therapeutic method distinct from prior art, supported by its specific structural features and uses.

Q3: What factors influence the patent's enforceability?
A: Validity hinges on novelty, inventive step, and non-obviousness, alongside proper maintenance and adherence to procedural requirements.

Q4: Are there potential challenges or patent disputes related to DK1382604?
A: Competitors may challenge its validity through opposition or third-party observations; monitoring such activity is crucial.

Q5: How does this patent impact R&D investment in Denmark?
A: It provides exclusivity, incentivizes innovation, and influences licensing strategies, but also requires diligent patent management and landscape monitoring.


Sources
[1] Danish Patent and Trademark Office (DKPTO) Official Patent Document.
[2] European Patent Office (EPO) Patent Database.
[3] Patent Landscape Reports on Pharmaceutical Patents.
[4] WHO International Patent Classification (IPC) related to pharmaceuticals.

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