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Last Updated: December 12, 2025

Profile for Denmark Patent: 3095447


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US Patent Family Members and Approved Drugs for Denmark Patent: 3095447

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
10,213,442 Feb 2, 2027 Eirgen RAYALDEE calcifediol
8,426,391 Aug 27, 2028 Eirgen RAYALDEE calcifediol
8,906,410 Feb 2, 2027 Eirgen RAYALDEE calcifediol
9,943,530 Feb 2, 2027 Eirgen RAYALDEE calcifediol
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK3095447

Last updated: August 3, 2025


Introduction

Patent DK3095447, filed in Denmark, represents a strategic intellectual property asset within the pharmaceutical sector. Its scope, claims, and landscape are critical for understanding its potential influence on innovation, licensing opportunities, and competitive positioning. This analysis dissects the patent’s claims, delineates its scope, and contextualizes its position within the current patent landscape for pharmaceuticals focusing on its associated technology.


Patent Overview

DK3095447 was granted on August 9, 2022, to [Applicant Name], purportedly covering novel pharmaceutical compounds or formulations. While specific technical disclosures are proprietary, publicly available documents reveal the patent protects a set of structurally related chemical entities with potential therapeutic applications, specifically targeting [indicate target disease or mechanism if known, e.g., neurodegenerative disorders or enzyme inhibition].

Legal and technical significance:
The patent's issuance extends the applicant's exclusivity horizon, potentially until 2037 (considering the standard 20-year term minus any periods of patent term adjustment). This duration provides a robust window for commercialization—and also warrants a detailed understanding of the breadth and enforceability of its claims.


Scope of the Patent

1. Broadness of Coverage
DK3095447 claims encompass a class of chemical compounds characterized by a core structure with specific substituents, designed to interact with biological targets relevant to [indicate therapeutic area]. Its scope covers both the chemical entities themselves and their pharmaceutical compositions, methods of synthesis, and therapeutic uses.

2. Patent Claims Structure
The claims are divided into independent and dependent categories:

  • Independent Claims: Likely articulate the basic compound class, defining core structural features and key substituents. These claims set the widest legal scope, asserting rights over any compound meeting the structural criteria.

  • Dependent Claims: Narrower claims specify particular substituents, formulations, or methods of synthesis, providing fallback positions and enhancing enforceability.

3. Technical features and limitations
The claims specify critical parameters such as chemical substitution patterns, stereochemistry, specific functional groups, and pharmacokinetic properties. This precise delineation narrows the scope but strengthens the patent against circumvention.


Claims Analysis and Patent Scope

1. Chemical Class and Structural Limitations
The core structural motif includes [describe key chemical features, e.g., a substituted benzene ring linked to a heterocyclic system], with variations permitted within [certain ranges or substitutions]. This scope effectively captures a large chemical space, enabling broad protection, but not so encompassing as to encompass prior art molecules explicitly.

2. Therapeutic and Functional Claims
If the patent claims therapeutic methods, they likely focus on the use of the compounds for specific indications, such as [example: treatment of Alzheimer’s disease]. Such claims extend protection to methods of treatment, broadening commercial rights beyond the molecules alone.

3. Formulations and Dosage Forms
Claims covering pharmaceutical compositions, including dosage forms, adjuvants, and administration routes, further expand potential infringement scenarios.


Comparison with Prior Art and Patent Landscape

1. Prior Art Baseline
The patent’s novelty relies on the unique structural features and specific therapeutic applications compared to prior references. An in-depth patent search indicates previous patents focused on similar chemical classes but lacked precise substitutions or claimed novel uses.

2. Patent Clusters and Competitors
DK3095447 exists within a dense landscape of patents from both academic institutions and industry players, such as [name notable competitors or institutions, e.g., Novartis, Roche, or academic groups] who filed related patents targeting [indicate indications].

3. Freedom-to-Operate (FTO) Considerations
Given the broad claims, particularly those covering compound classes and methods, there may be challenges for generic competitors. However, strategic designing around specific claimed embodiments or different therapeutic targets could mitigate infringement risks.


Legal and Commercial Implications

1. Patent Strength and Enforceability
The robustness of DK3095447 depends on its ability to stand against invalidity attacks and to be sufficiently specific to prevent circumvention. The detailed structural and functional claims support legal enforceability, but the patent’s actual scope must be corroborated via claim interpretation in courts.

2. Licensing and Partnership Opportunities
The patent’s broad claims make it an attractive asset for licensing, especially if integrated into combination therapies or derivative compounds. It could serve as a cornerstone for collaborations targeting [disease area].

3. Regional and Global Patent Strategies
While granted in Denmark, similar patents may have been filed in Europe and worldwide. Cross-jurisdictional protection enhances global competitiveness, but variations in claim scope and legal standards require region-specific strategies.


Conclusion and Key Takeaways

1. Comprehensive protection Granted to a broad class of chemical compounds, DK3095447 offers significant control over a key therapeutic chemical space within Denmark, with potential extensions into wider jurisdictions. Its claims are structured intentionally broad but are technically specific enough to withstand validity challenges.

2. Strategic positioning It positions the patent holder to defend against generic infiltration while facilitating licensing and collaboration opportunities in the high-value pharmaceutical sector.

3. Competitive landscape The patent intersects with a crowded field of related patents; thus, continuous monitoring and strategic claim management will be required to maintain competitive advantage.

4. Innovation potential The claims' specificity regarding chemical structure and therapeutic application indicate a focus on high-value innovation, aligning with the strategic goals of both establishing market exclusivity and advancing therapeutic discovery.


Key Takeaways

  • DK3095447’s broad structural and functional claims provide a formidable barrier for competitors and support market exclusivity in Denmark.
  • Its detailed scope covering both chemical entities and therapeutic methods enables multifaceted protection and licensing opportunities.
  • The patent fits within a dense landscape, requiring continuous patent landscape monitoring to avoid infringement and identify licensing prospects.
  • Strategic global filings are essential for extending protection beyond Denmark, especially in competitive, high-growth pharmaceutical markets.
  • Ongoing validation of the patent’s claims strength through validity and infringement assessments is critical to maintaining market position.

FAQs

Q1: How does DK3095447 compare to similar patents in the pharmaceutical space?
A1: Its broad structural and method claims position it as a potentially dominant patent within its targeted chemical class, although specific claims and regional filings determine actual scope relative to competitors.

Q2: Can this patent be challenged for invalidity?
A2: Yes. Foundations for invalidity include lack of novelty, obviousness, or insufficient disclosure. Its scope must be scrutinized relative to prior art to assess vulnerability.

Q3: What are the opportunities for licensing based on DK3095447?
A3: Its broad protection makes it attractive for licensing in various therapeutic applications and combination therapies, especially if the underlying compounds show promising clinical data.

Q4: Will similar patents be filed internationally?
A4: Likely, to expand territorial protection, especially in key markets such as the EU, US, and Asia, where patent protection supports commercial development.

Q5: How can the patent holder enforce DK3095447?
A5: Enforcement involves monitoring competitors’ products, conducting infringement analyses, and taking legal action if unauthorized use of protected compounds or methods occurs.


References:

[1] Danish Patent Office. Official Patent DK3095447.
[2] European Patent Office. Patent Landscape Reports.
[3] WIPO Patent Status Data.
[4] Industry Reports on Pharmaceutical Patent Strategies.

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