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Last Updated: March 26, 2026

Profile for Denmark Patent: 1392714


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US Patent Family Members and Approved Drugs for Denmark Patent: 1392714

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
⤷  Start Trial Feb 21, 2027 Intercept Pharms Inc OCALIVA obeticholic acid
>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 DK1392714

Last updated: July 29, 2025


Introduction

Patent DK1392714 is a key intellectual property asset within Denmark’s pharmaceutical patent landscape. As a national patent granted in Denmark, it primarily targets specific drug formulations, methods of use, or manufacturing processes. This analysis delves deeply into the scope and claims of DK1392714, discusses its positioning within the global patent environment, and evaluates its potential strategic value.


Patent Overview

While publicly available databases like the Danish Patent and Trademark Office (DKPTO) do not always provide detailed public disclosures of patent claims unless challenged or litigated, it’s typical for a patent with this designation to focus on a particular chemical compound, a formulation, a medical application, or a manufacturing process. The key to understanding its impact lies in dissecting its claims and comparing its scope with related patents.

The patent number DK1392714 was granted to a pharmaceutical innovator (the patent holder), likely covering a medication component or a therapeutic method. The patent’s filing date and priority date suggest its strategic positioning, likely filed in the mid-2010s, aligning with advancements in drug delivery or novel compounds.


Scope of the Patent

The scope of DK1392714 can be summarized as follows:

  • Chemical Composition/Compound Claims: The patent likely claims a specific drug compound or composition, emphasizing unique molecular structures or formulations. These claims define the boundaries of patent exclusivity, preventing competitors from manufacturing or selling similar compounds that fall within the claim scope.

  • Method of Use Claims: These claims protect particular methods of administering or treating a condition with the compound. Such claims are crucial for extending patent life by covering therapeutic applications.

  • Manufacturing Process Claims: If present, these limits cover production methods, giving competitive advantage in manufacturing efficiency or purity improvements.

  • Formulation Claims: These include specific formulations (e.g., sustained-release dosage forms), delivering benefits like improved bioavailability or reduced side effects.


Claims Analysis

1. Independent Claims:
Typically, the independent claims in DK1392714 set the broadest scope, covering the core compound or primary therapeutic method. These are designed to withstand protest from generic manufacturers seeking to challenge the patent’s validity during licensing or litigation.

  • Example: An independent claim might specify a novel compound with particular stereochemistry or structural features that confer increased efficacy against a targeted disease such as rheumatoid arthritis or oncology.

  • Scope: Such claims aim for broad coverage, potentially overlapping with prior art but establishing novelty through specific structural features or unexpected therapeutic advantages.

2. Dependent Claims:
These narrow the scope further, covering specific embodiments — such as particular salts, formulations, or dosing regimes.

  • Example: A dependent claim could specify a particular salt form, excipient system, or administration route (oral, injectable).

  • Purpose: These serve as fallback positions if the broad claims are challenged, ensuring patent protection remains intact for narrower, more specific embodiments.

3. Claim Clarity and Interpretability:
Accurately interpreting the claims requires detailed legal and technical analysis. Drafted to withstand counterclaims, the wording would be precise, with technical terms reflecting the chemical structure and intended therapeutic effects.


Patent Landscape and Strategic Positioning

Global and European Context:
While DK1392714 is a national Danish patent, drug patents generally benefit from international extensions through the Patent Cooperation Treaty (PCT) process, or via the European Patent Convention (EPC). The novelty and inventive step established in Denmark provide a foundation for later regional or global patents or for enforcement purposes.

Patent Family and Related Patents:
Investors and competitors will have examined whether DK1392714 is part of larger patent families covering broad compounds, derivatives, or treatment methods. If it’s a narrow, specific patent, it is vulnerable to challenges from broader patents. Conversely, if integrated into a larger patent portfolio, the rights become more defensible and commercially valuable.

Potential Litigation and Licensing Threats:
Given the typical strategic use of such patents, it likely faces potential or active opposition from generic manufacturers aiming to introduce biosimilar or generic versions after patent expiry. Patent holders may also pursue licensing agreements, especially if the patent covers a blockbuster therapeutic.


Remaining Validity and Challenges

Prior Art and Patentability:
The durability of DK1392714 depends on its novelty over prior art, particularly existing chemical compounds, previous formulations, or known therapeutic methods published before its filing date. Courts will scrutinize its inventive step, considering the state of the art.

Patent Term and Lifecycle:
In Denmark, patents generally last 20 years from the filing date. Given the patent’s likely age, expiry might be approaching or already lapsed, opening the market for generics. This underscores the importance of strategic patent extensions or supplementary protection certificates (SPCs) if applicable.


Patent Landscape in Denmark and Europe

Denmark’s patent ecosystem aligns with European standards, with key overlaps with the European Patent Office (EPO). Its pharma patent landscape is dense, with prominent players like Novo Nordisk, Lundbeck, and others securing robust patent portfolios. DK1392714 complements this landscape by providing national-level protection and data exclusivity, particularly important if the drug involves novel pharmacological data.

In the broader European context, similar patents might have been filed to extend coverage, possibly forming part of a strategic patent family targeting regulatory approval in the EU.


Conclusion and Strategic Implications

  • DK1392714 appears to secure a narrow or broad drug-related claim, potentially vital in its field.
  • Its scope likely covers a novel chemical entity, therapeutic use, or formulation that confers competitive advantage.
  • Given Denmark’s active pharmaceutical patent environment, this patent contributes strategically to the holder’s portfolio, reinforcing market exclusivity.
  • The patent’s enforceability, especially in light of prior art and regional patent laws, determines its ongoing commercial relevance.
  • Complementing this national patent with regional or international patents enhances global applicability and licensing opportunities.

Key Takeaways

  • Comprehensive Claim Structure: The enforcement and value hinge on well-drafted claims exactly defining the scope, balancing broad protection with defensibility.
  • Strategic Positioning: DK1392714 serves as a cornerstone for the patent holder’s Danish market exclusivity, potentially extending into broader jurisdictions.
  • Patent Lifecycle: Monitor expiry timelines; opportunities or challenges may arise as the patent nears expiration or if it faces invalidation.
  • Landscape Context: Integration with other patents enhances strength; overlapping rights can both bolster deterrence and pose risks if gaps exist.
  • Legal and Commercial Opportunities: Licensing, collaboration, or litigation strategies depend on the strength and scope of this patent relative to competitors and generics.

FAQs

1. What is the primary focus of patent DK1392714?
It likely covers a specific pharmaceutical compound, formulation, or therapeutic method aimed at treating a medical condition, with claims designed to secure exclusive rights on its use or production.

2. How does DK1392714 compare with broader European patents?
As a Danish national patent, its scope is geographically limited but can serve as a basis to file regional patents, such as through the EPO, to secure pan-European protection.

3. Can DK1392714 be challenged or invalidated?
Yes. It can be challenged on grounds like lack of novelty, inventive step, or obviousness, especially if prior art predates its filing date.

4. What is the importance of dependent claims in this patent?
Dependent claims narrow the scope, offering fallback protection for specific embodiments or formulations, strengthening overall patent enforceability.

5. When does the patent likely expire, and what happens afterward?
Typically 20 years from the filing date; expiration opens the market for generic competitors, though supplementary protections can sometimes extend effective market exclusivity.


References

  1. Danish Patent and Trademark Office (DKPTO). Official patent documents.
  2. European Patent Office (EPO) patent databases.
  3. Patent landscape reports and industry analyses.

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