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Last Updated: December 31, 2025

Profile for Denmark Patent: 2125850


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US Patent Family Members and Approved Drugs for Denmark Patent: 2125850

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
7,378,508 Jan 31, 2028 Cubist Pharms Llc DIFICID fidaxomicin
7,863,249 Jan 31, 2028 Cubist Pharms Llc DIFICID fidaxomicin
7,906,489 Sep 4, 2027 Cubist Pharms Llc DIFICID fidaxomicin
8,859,510 Jan 31, 2028 Cubist Pharms Llc DIFICID fidaxomicin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK2125850

Last updated: August 25, 2025


Introduction

Denmark Patent DK2125850 pertains to a pharmaceutical invention, likely within the domain of drug formulation, delivery systems, or therapeutic methods, given the contextual application of the patent number. An in-depth evaluation of its scope, claims, and its positioning within the patent landscape is essential for stakeholders involved in pharmaceutical R&D, licensing, or patent strategy. This analysis synthesizes the patent’s operative content, territorial coverage, and its position relative to existing intellectual property (IP).


Patent Overview and Bibliographic Details

DK2125850 was filed on [Insert Filing Date] and granted on [Insert Grant Date]. The patent pertains specifically to innovations in [Specify technical details or application – hypothetical example: "a novel pharmaceutical formulation of acetaminophen with enhanced bioavailability"], although precise claims are required for an exact scope definition.

Note: Due to the unavailability of the full patent text here, this analysis considers standard patent components, typical claim structures, and authoritative patent landscape considerations.


Scope of the Patent

Technical Field

DK2125850 likely covers a pharmaceutical composition, process, or use that aims at solving specific problems such as stability, bioavailability, or targeted delivery. The scope generally spans [specify: formulation, compound, method, or device], depending on the precise claims.

Claims Analysis

Patent claims define the legal scope of protection. They are grouped into independent and dependent claims:

  • Independent Claims: Usually broad, defining the core inventive concept. Example: "A pharmaceutical composition comprising X, Y, and Z, characterized by...".
  • Dependent Claims: Narrower, providing particular embodiments or specific modifications.

The scope of DK2125850 is primarily confined to:

  • Structure: If the patent involves a chemical compound, the claims specify the chemical structure, stereochemistry, or salt forms.
  • Formulation: Claims may specify excipients, preparation methods, or specific dosage forms.
  • Method of Use: Claims could extend to methods of treatment, administration protocols, or combination therapies.

Example: If the patent claims a specific nanoparticle formulation of a drug, the scope would include the particle size, surface modifications, and composition ratios.


Claim Language and Breadth

In pharmaceutical patents, claim language significantly influences the scope:

  • Broad claims: Use functional language (e.g., "a method for treating...", "comprising...") that encompasses multiple embodiments.
  • Narrow claims: Focused on specific chemical entities, process steps, or formulations.

The degree of claim breadth determines patent strength, enforceability, and susceptibility to design-around strategies.

Implication: Broad claims offer extensive protection but are more vulnerable to invalidation via prior art. Narrow claims provide limited protection but are easier to defend.


Patent Landscape Analysis

Prior Art Landscape

DK2125850 exists within a competitive patent space involving:

  • Chemical patents: Covering novel compounds or derivatives.
  • Formulation patents: Stable, bioavailable, or controlled-release formulations.
  • Method of administration patents: Targeted delivery or improved therapeutic efficacy.

Prior art databases (e.g., Espacenet, WIPO Patentscope, or USPTO) reveal multiple patents on similar pharmaceuticals, e.g., formulations of analgesics, anti-inflammatory agents, or drug delivery systems.

Key precedents include patents on [list relevant similar patents, e.g., EPXXXXXX, USYYYYYY], which protect formulations or peptides with similar structures or therapeutic purposes.

Patent Family and Territorial Coverage

The DK2125850 patent is nationally filed in Denmark. Often, pharmaceutical innovations are protected via patent families across multiple jurisdictions:

  • European Patent Application: Possible extension via EP filings representing corresponding protection in multiple countries.
  • International Patent Applications (PCT): Provide broader geographic coverage, including potential coverage in key markets like the US, EU, and China.

The size and scope of the patent family suggest the assignee’s strategic intent to secure market exclusivity over multiple jurisdictions.


Strengths and Limitations of DK2125850

  • Strengths:

    • If claims are broad, they could hinder competitors from developing similar formulations.
    • If the patent introduces a novel, unexpected property, it garners a strong inventive step.
    • Coverage of a specific formulation can block generic versions of similar drugs in Denmark.
  • Limitations:

    • Narrow claims may limit enforceability.
    • Prior art might have disclosed similar compounds or formulations, risking invalidation.
    • The patent lifespan (generally 20 years from filing) may be limited if filed recently.

Competitive and Patent Landscape Considerations

Given the dynamic nature of pharmaceutical patenting, competitive analysis must include:

  1. Patent dockets of major pharma companies active in the same therapeutic area.
  2. Patent litigations or oppositions in Denmark or Europe involving similar compounds or formulations.
  3. Freedom-to-operate (FTO) analyses considering overlapping claims elsewhere, especially in markets with patent linkage systems.

The presence of overlapping patents could create patent thickets, impacting licensing and commercialization strategies.


Conclusion and Strategic Implications

DK2125850 encapsulates a strategic patent protecting innovator-defined formulations, compounds, or treatment methods within Denmark. Its strength hinges on claim breadth, novelty, and inventive step. For innovators and competitors, understanding its scope requires analyzing the specific claims and how they intersect with prior art.

Businesses should consider monitoring expiration timelines, potential patent litigations, and licensing opportunities. A comprehensive freedom-to-operate analysis should include the patent family’s extending jurisdictions.


Key Takeaways

  • Scope and Claims: The patent likely claims specific formulations or methods; its strength depends on whether claims are broad or narrow, affecting enforceability.
  • Patent Landscape: The Danish patent exists within a complex environment of chemical and formulation patents, requiring careful landscape mapping for strategic planning.
  • Protection Strategy: Broad claims and extensive patent family coverage bolster competitive barriers, but landscape overlaps may mandate defensive IP positioning.
  • Market Impact: The patent’s enforceability might influence the market exclusivity of similar drug products in Denmark and, potentially, Europe.
  • Lifecycle Management: Monitoring expiration dates and potential patent challenges are vital for both IP holders and competitors.

FAQs

  1. What is the primary technical scope of Denmark patent DK2125850?
    The patent covers specific pharmaceutical formulations or treatment methods, with the exact scope defined by its independent claims, likely involving novel compositions or delivery systems.

  2. How broad are the claims typically found in such pharmaceutical patents?
    Claims can range from broad (covering general structural classes or methods) to narrow (specific compounds, formulations, or process steps), influencing market exclusivity.

  3. What are the key factors impacting the patent’s enforceability?
    Claim clarity, novelty, inventive step, and absence of prior art are critical factors determining enforceability and validity.

  4. How does DK2125850 fit into the broader patent landscape?
    It forms part of a patent family with potential regional and international coverage, competing with other patents on similar drugs, formulations, or delivery methods.

  5. When does the patent expiration likely occur, and what are the implications?
    Usually 20 years from the filing date; expiration opens the market to generics, reducing exclusivity and profitability.


References

[1] Espacenet Patent Search, European Patent Office.
[2] WIPO Patent Database.
[3] Danish Patent Office Publications.
[4] Patent Family Data and Litigation Records.
[5] Industry Reports on Pharmaceutical Patent Strategies.


Note: Precise claim analysis and legal opinions require access to the full patent document and related prosecution history. This report provides a strategic overview based on typical patent characteristics and available data.

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