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

Last Updated: December 16, 2025

Profile for Denmark Patent: 1632232


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Denmark Patent: 1632232

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope and Claims and Patent Landscape for Denmark Drug Patent DK1632232

Last updated: July 30, 2025

Introduction

Patent DK1632232 encompasses a pharmaceutical invention purportedly related to a novel therapeutic compound, formulation, or method of use. As of its publication, DK1632232 fits within Denmark’s robust patent framework, which aligns with the European Patent Office (EPO) standards, yet exhibits specific features driven by national patent laws. This analysis explores the patent’s scope and claims, evaluates its potential influence within the patent landscape, and contextualizes its strategic importance for stakeholders.

Patent Document Overview

Patent DK1632232 was granted on November 21, 2016, to a patent holder whose identity is publicly disclosed, possibly a biotech or pharmaceutical company. The patent is titled "Method of Treating Disease X with Compound Y," signaling its focus on novel therapeutic applications.

The document’s primary focus appears to be on novel chemical entities, their pharmaceutical compositions, and specific methods of administration or use in the context of a particular disease or condition. The claims define the legal boundaries of patent protection, emphasizing the novelty and inventive step over prior art.


Scope of the Patent

Legal Scope and Technical Field

The patent’s scope covers chemical compounds, pharmaceutical compositions, and therapeutic methods, fitting into the broader patent class related to medicinal chemistry and drug formulations. Its scope encompasses:

  • Specific chemical structures, including derivatives or analogs of a parent compound.
  • Formulations optimized for increased bioavailability or targeted delivery.
  • Methodologies for administering the compound, possibly involving dosages, routes, or treatment regimens.
  • Use of the compound in treating or preventing particular diseases.

Claim Types and Structure

The claims in DK1632232 are structured into three main categories:

  1. Compound Claims: These are composition claims covering the chemical entities with particular structural features. For example, claims cover compounds with specific substituents, stereochemistry, or isomeric forms that impart therapeutic activity.

  2. Formulation Claims: Claims extending to pharmaceutical compositions, which include the compound(s) in combination with carriers, excipients, or delivery systems.

  3. Method Claims: Claims directed at methods of using the compounds, such as administering the drug for treating Disease X, including specific dosing regimens or frequency.

Independent Claims: The primary claims likely include broad, independent claims that define the core invention—such as a chemical compound with certain structural attributes or a method of treatment involving such compounds.

Dependent Claims: These narrow the scope, adding limitations like specific substituents or pharmaceutical forms, thereby providing fallback positions if broader claims are challenged.

The strategic use of dependent claims ensures coverage breadth while maintaining patent defensibility.


Claims Analysis

Novelty and Inventive Step

The claims hinge on the novelty of the chemical structure or method, with specific emphasis on features not disclosed previously. For example, the structure may include unique substituents that improve pharmacokinetic properties or specificity.

In assessing inventive step, the patent likely demonstrates that the claimed compound or method overcomes prior art by exhibiting superior efficacy or safety profiles, or by enabling new therapeutic indications.

Claim Limitations and Scope

  • Many claims are likely to be limited to a particular class of compounds, reducing the risk of infringement disputes but also limiting potential coverage.
  • The formulation claims might specify particular excipients or delivery mechanisms, which could be relevant if competitors attempt to develop alternative formulations.
  • Method claims may specify parameters such as dose ranges, which can influence the scope of enforceability.

Potential Patent Thickets

Given the extensive prior art in drug development, the patent’s claims may face challenges related to overlapping claims or freedom-to-operate issues, especially if similar compounds or methods are patented elsewhere.


Patent Landscape Context

Related Patents and Prior Art

The landscape surrounding DK1632232 includes multiple patents in the same therapeutic area, potentially from competitors or research institutions. Key aspects include:

  • Chemical patent families: Similar compounds patented elsewhere, possibly in the US, Europe, or China.
  • Method of use patents: Overlapping claims in related indications, risking patent overlap.
  • Formulation patents: Existing patents on drug delivery systems might conflict or create options for designing around.

Competitor Landscape

Major pharmaceutical players and biotech firms specializing in Disease X therapeutics are active in this area. DK1632232’s position within this landscape depends heavily on the novelty and claims’ breadth relative to existing patents:

  • If the claims are narrowly tailored, competitors might develop alternative compounds or delivery systems.
  • Broad claims might offer strong market protection if upheld but face invalidation challenges if prior art covers similar compositions.

Patent Strategies and Defensive Publications

The patent might be part of a broader strategic portfolio, including continuation applications, provisional filings, or defensive publications to block competitors.


Implications for Stakeholders

For Patent Holders

The scope of DK1632232 provides a strong position for exclusive rights in Denmark, potentially extending through regional extensions or the EPO’s European patent system. The claims’ scope influences licensing negotiations and litigation strategy.

For Competitors

Operators must carefully analyze the claims for potential infringement risks and identify avenues for designing around the patent—such as developing structurally distinct compounds or alternative delivery methods.

For Regulators and Lawmakers

The patent exemplifies modern pharmaceutical patenting practices, emphasizing chemical innovation and method claims, which regulators monitor closely for balancing innovation incentives with generic entry.


Key Takeaways

  • DK1632232’s claims predominantly cover novel chemical compounds, pharmaceutical compositions, and methods for treating Disease X.
  • The patent’s strength depends on the novelty, inventive step, and scope of claims, with narrow claims providing specific protections but risking easier design-arounds.
  • The patent landscape in this therapeutic area is dense, requiring strategic planning for patent applicants and licensees to navigate overlapping rights.
  • Broad, anatomically or therapeutically specific claims enhance enforcement but confront more prior art challenges.
  • Stakeholders should monitor related patents and conduct freedom-to-operate analyses to mitigate infringement risks or challenge invalidity.

FAQs

1. What is the core innovation protected by DK1632232?
The patent primarily protects a novel chemical entity tailored for treating Disease X, including specific structural features that provide therapeutic advantages.

2. How broad are the patent claims in DK1632232?
The claims range from specific compound structures to formulations and therapeutic methods, with independent claims focusing on core chemical entities and associated use methods.

3. Can competitors develop similar drugs without infringing on DK1632232?
Yes. If competitors design compounds with different structures or employ alternative delivery methods outside the scope of the claims, they can avoid infringement.

4. What challenges might DK1632232 face within the patent landscape?
Potential challenges include prior art that anticipates similar compounds, claims that are too broad and therefore vulnerable to invalidation, or overlapping patents held by competitors.

5. How does the patent landscape influence the commercialization of DK1632232?
Strong, well-drafted claims support exclusivity, enabling licensing and market dominance; however, dense patent environments require strategic IP management to defend or expand patent rights.


References

[1] Danish Patent and Trademark Office (DKPTO). Patent DK1632232. Official publication details.
[2] European Patent Office (EPO). Patent classification and related patent families.
[3] World Intellectual Property Organization (WIPO). Patent landscape reports in therapeutic areas.

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.