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Last Updated: December 15, 2025

Profile for Denmark Patent: 2167046


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US Patent Family Members and Approved Drugs for Denmark Patent: 2167046

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
10,905,694 Apr 7, 2030 Otsuka JYNARQUE tolvaptan
10,905,694 Apr 7, 2030 Otsuka SAMSCA tolvaptan
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK2167046

Last updated: August 13, 2025

Introduction

Denmark Patent DK2167046 pertains to a proprietary pharmaceutical invention, encompassing specific formulations, methods of use, or manufacturing processes. As an integral asset within the pharmaceutical patent landscape, understanding the scope and claims of DK2167046 is essential for stakeholders—including generic manufacturers, research organizations, and competitors— aiming to navigate potential infringement risks, licensing opportunities, or innovation pathways. This analysis dissects the patent's scope, claims, and its positioning within the broader patent landscape.

Patent Overview and Background

DK2167046 was granted by the Danish Patent Office, reflecting a focus on an innovative approach or formulation pertaining to a therapeutic agent. While precise details depend on the patent document's text, typical content comprises a detailed description, claims defining the legal scope, and classifications indicating the technological domain.

Generally, pharmaceutical patents in Denmark align with European patent conventions, often classified under the International Patent Classification (IPC) codes relevant to chemistry and pharmaceuticals[1]. DK2167046’s technical scope likely involves a novel compound, formulation, or method designed to improve efficacy, stability, delivery, or manufacturing.

Scope of the Patent

Legal Scope and Limitations

The scope of DK2167046 is primarily dictated by its claims, which define the boundaries of the patent’s enforceability. Its scope covers the patented invention's specific embodiments, materials, methods, or uses described in the claims.

In Danish and European patent law, the claims are interpreted with a focus on the literal meaning, considering the description and drawings[2]. The scope can be bounded by:

  • Product claims: Covering a specific drug compound, formulation, or derivative.
  • Method claims: Covering a particular process of manufacturing or administering the drug.
  • Use claims: Covering a particular therapeutic application or indication.

Potential Types of Claims

Based on typical pharmaceutical patents, DK2167046 may include:

  • Compound claims: Covering a particular chemical entity with defined structural features.
  • Formulation claims: Covering a specific combination of excipients, carriers, or delivery systems.
  • Method claims: Covering methods for synthesizing the compound or administering the drug.
  • Use claims: Covering therapeutic applications, such as treatment of specific diseases.
  • Stability or bioavailability claims: Covering formulations with enhanced pharmacokinetics.

The scope's breadth determines the patent's ability to prevent competitors from developing similar but slightly modified versions.


Analysis of the Claims

Independent Claims

The core of the patent, independent claims, define the broadest legal rights and typically encapsulate the invention's inventive essence. For DK2167046, these likely include:

  • A chemical compound with particular structural features.
  • A pharmaceutical composition comprising the compound.
  • A method of preparing the compound or delivering therapy.

The language in independent claims is intentionally broad to maximize protection. The scope depends on how narrowly or broadly these claims are drafted.

Dependent Claims

Dependent claims specify particular embodiments, such as:

  • Specific substituents or functional groups.
  • Concentrations or dosage forms.
  • Methods of manufacturing with particular steps.

These serve to fortify the patent's defensibility and provide fallback positions if independent claims are challenged.

Claim Scope Analysis

  • Breadth: If the claims use broad language, such as covering all derivatives of a core structure, the patent might block a wide array of potential competitors.
  • Narrower Claims: Focused claims improve validity but may offer limited protection.
  • Potential for Revocation: Overly broad claims risk invalidation based on prior art; thus, the actual scope is often carefully calibrated during prosecution.

Patent Landscape and Strategic Positioning

Comparative Patents and Priority

DK2167046's patent family may include filings in other jurisdictions such as the European Patent Office (EPO), United States Patent and Trademark Office (USPTO), and other key markets, reflecting strategic territorial coverage. The priority date and filing sequence influence its validity and enforcement strategies.

Similar patents in the landscape generally focus on:

  • Innovative chemical structures,
  • Delivery systems for enhanced efficacy,
  • Combinations with existing therapies,
  • Manufacturing processes.

Competitive Landscape

The landscape features patents from major pharmaceutical companies and biotech firms, especially if the invention pertains to blockbuster or niche therapies. The presence of overlapping claims indicates a competitive environment, where patent thickets may influence freedom-to-operate analyses.

For instance, if DK2167046 claims a novel chemical entity, it might be adjacent to patents covering related compounds or treatment methods, requiring careful freedom-to-operate evaluations.

Legal Status and Enforceability

The patent's legal status (granted, maintained, or challenged) affects its strategic utility. Allowances, oppositions, or invalidations could reshape the competitive scenario. As a Danish patent, enforcement is potentially straightforward within Denmark, but broad protection may depend on foreign counterpart patents.


Innovative Aspects and Limitations

  • Novelty & Inventive Step: The patent's validity hinges on demonstrating novelty over prior art and an inventive step. The detailed description must establish unexpected advantages over previous compounds or formulations.
  • Potential Limitations: If claims are too broad without sufficient inventive step, they risk invalidation under challenge. Similarly, if dependent claims are narrowly tailored, they provide limited protection.

Implications for Stakeholders

  • Pharmaceutical Developers: DK2167046 provides a defensible position for the claimed compound or method, potentially blocking generic entrants.
  • Generic Manufacturers: Without designing around the specific claims, they may need licensing agreements or work on alternative compounds.
  • Research Institutions: The scope limits may guide innovation efforts or licensing negotiations.
  • Legal and Patent Strategists: Understanding the detailed claims aids in designing licensing, litigation, or licensing strategies.

Conclusion

DK2167046 exemplifies a carefully drafted pharmaceutical patent with potential broad or narrow scope depending on its claims. Its landscape reflects competitive technologies and innovative priorities in the drug development space. Stakeholders must perform detailed claim chart analyses and freedom-to-operate investigations grounded in the specific language and jurisdictional enforceability of the patent.


Key Takeaways

  • The patent scope is primarily dictated by its claims, which likely encompass a chemical compound, formulation, and method of use or manufacture.
  • A broad independent claim provides extensive protection but risks validity challenges; narrower dependent claims protect specific embodiments.
  • DK2167046’s patent landscape overlaps with other filings, necessitating a landscape review to assess infringement and freedom to operate.
  • Effective patent management involves monitoring legal status, evaluating potential validity issues, and considering international counterparts.
  • Strategic utilization of the patent includes licensing, enforcement, and guiding R&D efforts, emphasizing the importance of nuanced claim interpretation.

FAQs

Q1: How does the scope of DK2167046 influence potential patent infringement cases?
A1: The scope determines the extent of protection. Broad claims can prevent a wide array of similar compounds or methods, while narrow claims restrict enforcement rights to specific embodiments. Accurate interpretation of claim language is crucial in infringement analysis.

Q2: Can DK2167046 be challenged or invalidated?
A2: Yes, if prior art demonstrates prior existence or obviousness, or if claims are overly broad, the patent can face validity challenges in opposition or litigation proceedings.

Q3: How does the patent landscape affect competitors’ freedom to operate?
A3: Overlapping patents may limit commercialization options without licensing or designing around protected claims. A comprehensive landscape analysis helps identify gaps and avoid infringement.

Q4: What strategic actions can patent holders take based on DK2167046?
A4: They can pursue licensing deals, enforce patent rights, or develop complementary innovations that expand or reinforce their portfolio, while monitoring potential infringers.

Q5: How does DK2167046 relate to international patent protections?
A5: The patent's value and enforceability increase with corresponding filings in other jurisdictions. Coordination of patent families across regions is essential for global protection and market strategy.


References

[1] European Patent Office. (2022). Patent Classification & Search.
[2] European Patent Convention, Article 69.

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