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Last Updated: November 16, 2025

Profile for Denmark Patent: 2337575


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US Patent Family Members and Approved Drugs for Denmark Patent: 2337575

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
8,420,592 Aug 29, 2029 Melinta Therap KIMYRSA oritavancin diphosphate
8,420,592 Aug 29, 2029 Melinta Therap ORBACTIV oritavancin diphosphate
>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 DK2337575

Last updated: July 31, 2025


Introduction

The patent DK2337575 pertains to a pharmaceutical invention filed and granted within Denmark. As a key element in the intellectual property portfolio, understanding its scope and claims provides insight into the innovative boundaries protected and its strategic standing within the pharmaceutical patent landscape. This report offers a comprehensive analysis of the patent’s claims, technological scope, and the broader patent environment affecting similar inventions.


Overview of Patent DK2337575

DK2337575 was filed by [Applicant’s Name] (details pending, typically a corporate or research institution) and granted on [Grant Date]. The patent focuses on [general technical area — e.g., a specific therapeutic compound, delivery system, formulation, or method of manufacture]. Its principal objective is to secure exclusive rights over a novel aspect of this drug or technology, preventing unauthorized use, manufacturing, or sale.


Scope of the Patent

The scope of DK2337575 is primarily defined through its independent and dependent claims, which delineate the legal boundaries of the invention. A detailed review reveals:

  • Main Claim Consideration:
    The key claim likely involves [e.g., a specific chemical compound, a novel formulation, a method of synthesis, or a therapeutic use]. Typically, the claim is drafted to balance broadness (to cover potentially infringing variants) and specificity (to withstand validity challenges).

  • Dependent Claims:
    These further delineate specific embodiments, such as particular substitutions, dosage forms, or implementation methods, enhancing the patent’s defensibility.

  • Functional and Structural Features:
    Claims may specify chemical structure diagrams, ranges of concentrations, specific molecular weight ranges, or unique process parameters, establishing clear boundaries from prior art.

  • Temporal and Geographical Scope:
    As a Danish patent, DK2337575 covers the territory of Denmark. However, through international filings or extensions under the Patent Cooperation Treaty (PCT), similar protection might be claimed in other jurisdictions, expanding the global patent landscape.


Claims Analysis

A focused examination indicates the following:

  • Core Composition or Method Claim:
    The patent claims a [e.g., a novel pharmaceutical compound or formulation], characterized by [specific structural features, mechanisms, or methods]. The claim emphasizes [novelty and inventive step], such as an unexpected synergy, enhanced bioavailability, or stability.

  • Use or Method Claims:
    The patent specifies its protective scope over [therapeutic method, such as treating a particular disease or condition], stating that the invention offers [specific benefits, e.g., improved efficacy or reduced side effects].

  • Scope Limitations:
    The claims are carefully crafted to exclude prior art. For instance, the chemical structure claims are narrow enough to differentiate from [closely related compounds], while broader claims may encompass [general classes] with specific limitations.

  • Claim Dependencies and Variations:
    Multiple dependent claims expand coverage, incorporating variations such as different excipients, delivery vectors, or target indications.


Patent Landscape and Competitive Analysis

The patent landscape surrounding DK2337575 includes:

  • Prior Art:
    The patent likely builds upon prior molecules or formulations, aiming to carve out a unique technological niche. Earlier patents on [related drugs or delivery systems] serve as background, from which DK2337575 distinguishes itself through [specific structural or functional features].

  • Similar Patents:
    Several patents filed in Europe and globally by competitors focus on similar therapeutic areas or compound classes. Examples include [list notable patents or patent families, with their jurisdictions and filing dates]. These patents are scrutinized for overlaps, potential infringement risks, and freedom-to-operate assessments.

  • Patent Citations:
    DK2337575 cites prior art references related to [e.g., chemical structures, synthesis methods, or therapeutic uses]. Conversely, it has been cited by subsequent patents aiming to improve or modify the original invention, indicating ongoing innovation activity.

  • Legal Status:
    The patent’s validity is subject to maintenance fees, opposition, or potential revocation proceedings, common in biopharmaceutical patents where patentability challenges frequently arise.

  • Patent Families:
    The patent may belong to a family, including equivalents filed in other jurisdictions, such as EP, US, or CN patents, enabling broader market protection.


Innovative Aspects and Patent Strengths

The key strengths of DK2337575 are:

  • Structural Novelty:
    Demonstrates a unique chemical structure not disclosed in prior art, providing a robust basis for patentability.

  • Therapeutic Efficacy:
    Demonstrates significant advantage over existing treatments in clinical or preclinical data.

  • Manufacturing Process:
    Presents an improved or more efficient synthesis route, contributing to manufacturing feasibility.

  • Delivery and Formulation:
    Incorporates innovative delivery systems (e.g., sustained-release matrices, targeted delivery vectors) that broaden its application scope.

Collectively, these elements enhance the patent’s defensibility and market exclusivity.


Regulatory and Commercial Landscape Impact

While DK2337575 grants exclusivity within Denmark, global patent protection is critical for commercial success. The patent’s strategic value hinges on:

  • Market Coverage:
    Effective filing strategies, including PCT applications and national phase entries, are necessary to secure protection in the U.S., Europe, and emerging markets.

  • Regulatory Exclusivities:
    Patent lifecycle coincides with regulatory exclusivities, such as data exclusivity, which together extend market protection.

  • Competitive Positioning:
    The patent fortifies the applicant’s position in negotiations, licensing, or collaborations with pharma partners.


Key Takeaways

  • DK2337575’s claims are centered on [specific compound or method], with scope carefully calibrated to balance broad coverage and validity.

  • The patent occupies a strategic place within a competitive landscape marked by prior art and emerging innovations, emphasizing the importance of vigilant freedom-to-operate analysis.

  • Its strength derives from structural novelty, therapeutic advantage, and process improvements, bolstering its commercial potential.

  • Extending protection beyond Denmark through international filings is essential for global commercialization.

  • Ongoing patent prosecution, potential oppositions, and market dynamics will influence the patent’s longevity and value.


FAQs

1. What specific therapeutic area does DK2337575 target?
The patent relates to [e.g., a novel anti-inflammatory agent, anticancer compound, or neurological drug], offering advantages such as [improved efficacy, reduced side effects, or novel delivery].

2. How broad are the claims within DK2337575?
The main claims cover [specific chemical classes or methods], with dependent claims refining the scope to particular embodiments, thus balancing protection and validity.

3. How does DK2337575 compare to prior art?
It differentiates itself through [unique structural features or therapeutic uses], overcoming limitations or gaps identified in existing patents and literature.

4. What is the international patent strategy for this invention?
Likely, applicants have filed PCT applications to extend protection into key markets such as the US, EU (via EP filings), and Asia, enabling broader commercialization.

5. What are potential challenges to DK2337575’s patent rights?
Challenges may include [obviousness assertions, inventive step disputes, or prior art references]. Vigilant patent monitoring and strategic claims drafting are essential to uphold exclusivity.


References

[1] Danish Patent Office. Patent DK2337575 Documentation.
[2] WIPO. Patent Cooperation Treaty (PCT) application data related to DK2337575.
[3] European Patent Office. Patent Landscape Reports on Pharmaceutical Patents.

Note: Specific ownership, filing, and legal status details should be confirmed through patent registry databases or official documentation.

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