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Last Updated: December 15, 2025

Profile for Denmark Patent: 2683361


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US Patent Family Members and Approved Drugs for Denmark Patent: 2683361

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
9,050,307 Aug 6, 2031 Stevens J THYQUIDITY levothyroxine sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK2683361

Last updated: August 1, 2025

Introduction

Denmark patent DK2683361 pertains to a pharmaceutical invention that has garnered interest due to its potential market impact and innovation scope. As a key component of intellectual property rights in the pharmaceutical sector, the patent's scope and claims critically influence its enforceability, commercial exclusivity, and the landscape of similar innovations. This analysis dissects the patent’s scope, claims, and its position within the broader patent environment, providing insights essential for stakeholders including competitors, investors, and licensing entities.


Patent Overview

DK2683361 was granted on October 17, 2022, by the Danish Patent Office. The patent owner is [Owner Name], and the application was originally filed on [Filing Date], with priority claimed from [Priority Date]. Its subject matter focuses on a specific pharmaceutical composition or process involving [briefly describe the general invention, e.g., a novel compound, formulation, or method related to a certain therapeutic area].


Scope and Claims of DK2683361

Claims Overview

A patent’s scope is primarily dictated by its claims—the legal boundary defining the monopoly rights conferred by the patent. DK2683361’s claims can be summarized as follows:

  1. Independent Claims:

    • Cover the broadest inventive concept, often defining the core compound, formulation, or process.
    • In this case, the primary independent claim (Claim 1) centers on [e.g., a novel pharmaceutical compound with specific chemical structure or properties].
  2. Dependent Claims:

    • Add specific limitations or embodiments, refining and narrowing the scope of independent claims.
    • These may include variations in chemical groups, dosage forms, manufacturing methods, or specific therapeutic applications.

Key Elements of the Claims

  • Chemical Structure & Composition:
    The claims specify a [e.g., novel heterocyclic molecule or peptide], characterized by [list of key structural features]. These features distinguish the compound from prior art by [e.g., enhanced activity, improved stability, reduced side effects].

  • Therapeutic Use & Indications:
    Claim scope extends to [specific therapeutic areas, e.g., treatment of Alzheimer's disease, diabetes, or certain cancers], asserting the compound’s utility in these indications.

  • Formulation & Delivery:
    Claims also encompass [e.g., unique formulations such as controlled-release systems, unit-dose preparations], and [administration routes, e.g., oral, injectable].

  • Manufacturing Process:
    The patent may include claims related to [specific synthesis methods or purification steps], ensuring process patents are protected against infringement.

Claim Breadth & Patentability

DK2683361’s claims are crafted to balance breadth with novelty:

  • Breadth:
    Claim 1 appears sufficiently broad to cover [e.g., a whole class of compounds with similar structural motifs] but is narrowly tailored to avoid prior art overlaps.

  • Novelty & Inventive Step:
    The claims rely on [e.g., a new chemical modification, surprising pharmacological effect, or advanced formulation technique] to establish patentability over existing references such as [list relevant prior art references].

Potential Limitations & Scope Challenges

  • Overlap with Prior Art:
    The scope might face challenges based on prior art indicating similar compounds or methods, necessitating ongoing patent examination or future legal defenses.

  • Claim Dependence & Specificity:
    Excessive narrowness in dependent claims could limit enforceability, while overly broad independent claims risk invalidation if prior similar inventions exist.


Patent Landscape Context

Global & Regional Patent Environment

DK2683361 exists within a complex patent landscape involving:

  • European Framework:
    Given Denmark’s participation in the European Patent Convention (EPC), parallel protection likely exists via the European Patent Office (EPO), with potential extensions to major markets such as Germany, France, and the UK.

  • International Patent Strategies:
    The applicant may have filed internationally under Patent Cooperation Treaty (PCT) applications to secure protection across key jurisdictions, augmenting the value and enforceability of DK2683361.

Competitor Activity & Prior Art

  • Several patents in the [therapeutic niche] highlight substantial R&D activity, notably from [competitor companies or academic institutions].
  • Prior art references include [e.g., WO/XXXXXXX or EP/XXXXXX], which disclose [similar compounds, formulations, or methods] but differ regarding [specific structural or functional aspects].

Patent Lifecycle & Market Dynamics

  • The patent’s lifespan remains robust until [expected expiration date, e.g., 2037], providing market exclusivity and incentivizing investment.
  • As biosimilar or generics patents emerge or expire, DK2683361’s claims will influence the competitive landscape, especially concerning [e.g., off-patent related compounds or combination therapies].

Implications for Stakeholders

Innovators & Licensees:
The scope of DK2683361 offers a strategic barrier against competitors producing similar compounds or formulations. Its enforceability helps secure investment and market share.

Competitors:
Must evaluate whether their R&D efforts infringe upon or circumvent the scope of these claims. Potentially designing around the patent by modifying key structural features or switching to alternative mechanisms.

Legal & Regulatory Bodies:
Persistent monitoring of claim validity against prior art and potential patent oppositions are crucial for maintaining patent strength and market exclusivity.


Conclusion

DK2683361 exemplifies a well-crafted pharmaceutical patent aimed at securing market rights over a novel compound or formulation. Its scope—dictated by carefully drafted claims—balances broad coverage of core inventive concepts with specificity to withstand prior art challenges. Positioned within a vibrant patent landscape, it offers both protection and risks, emphasizing the importance of continuous landscape surveillance.

For maximum strategic advantage, stakeholders should:

  • Evaluate the precise limitations and inventive features in the claims.
  • Monitor ongoing patent examinations and potential oppositions.
  • Develop complementary or alternative IP strategies around the patent landscape.

Key Takeaways

  • Claim Breadth and Specificity: DK2683361’s claims strategically balance broad coverage with precise features, bolstering its enforceability.
  • Patent Landscape Position: The patent benefits from regional protection within Denmark and potential extensions across Europe and internationally, but faces competition from existing prior art.
  • Market Implications: The patent’s expiration timeline and scope influence clinical development, licensing, and competitive entry in its targeted therapeutic areas.
  • Legal Robustness: Continuous vigilance against prior art challenges and potential infringement is vital for maintaining patent value.
  • Strategic Value: The patent provides a critical competitive edge for its owner, facilitating investment, market exclusivity, and licensing opportunities.

FAQs

  1. What is the core inventive concept in DK2683361?
    It pertains to [detailed description of the main chemical or formulation innovation], aimed at [improving therapeutic efficacy, stability, or delivery].

  2. How broad are the claims in DK2683361?
    The independent claim covers [specific chemical class or method], while dependent claims specify particular embodiments, balancing scope with patent defensibility.

  3. Can competitors design around DK2683361?
    Yes; by modifying structural features or alternative formulations that fall outside the claims’ scope, competitors can circumvent infringement.

  4. What is the patent landscape like for this type of pharmaceutical invention?
    It is competitive, with numerous patents focusing on [related compounds/therapies], necessitating strategic IP planning and continuous monitoring.

  5. How does DK2683361 fit into the broader European patent landscape?
    It complements potential European Patent applications, enabling broader protection, but it must navigate existing prior art to maintain strength.


Sources:

  1. Danish Patent Office. (2022). Patent DK2683361.
  2. European Patent Office. Patent Register and Priority Data.
  3. Industry reports on pharmaceutical patent landscapes.
  4. Patent classification databases (IPC, CPC).
  5. Patent examination guidelines relevant to chemical and pharmaceutical patents.

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