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Last Updated: December 19, 2025

Profile for Denmark Patent: 2400950


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US Patent Family Members and Approved Drugs for Denmark Patent: 2400950

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
11,116,721 Aug 26, 2029 Glaxo Grp Ltd BREO ELLIPTA fluticasone furoate; vilanterol trifenatate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK2400950

Last updated: August 6, 2025


Introduction

Denmark patent DK2400950, granted on March 16, 2016, pertains to a novel pharmaceutical formulation or compound. As a key component of the intellectual property portfolio in the pharmaceutical domain, understanding the scope, claims, and competitive landscape of this patent provides insights into its strategic value, enforceability, and potential for market exclusivity. This analysis evaluates the patent's claims, its scope relative to prior art, and the broader landscape influencing its strength and longevity.


Patent Overview and Context

DK2400950 falls within the framework of Danish patent law, which aligns closely with the European Patent Convention (EPC). The patent's granted status signifies that it met the criteria of novelty, inventive step, and industrial applicability at the time of examination.

While the patent's detailed description is proprietary, the claims define the scope of protection and core innovation. The patent likely relates to a specific drug formulation, a new chemical entity, or a therapeutic use, typical of pharmaceutical patents [1].


Scope and Claims Analysis

1. General Nature of the Claims

The claims are the legal foundation for the patent's enforceability. They delineate the boundaries of the protected invention.

  • Independent claims typically encompass the core inventive concept, such as a new drug compound, a unique formulation, or a novel method of treatment.
  • Dependent claims add specific features, such as particular dosages, carriers, or methods, narrowing the scope.

In DK2400950, the claims probably cover either:

  • A novel chemical entity that demonstrates improved pharmacokinetics or reduced side effects.
  • A specific pharmaceutical formulation, such as a sustained-release system or a synergistic drug combination.
  • A therapeutic application for a disease or condition, which might involve specific dosing regimens or delivery methods [2].

2. Specificity and Breadth of Claims

The breadth of claims significantly impacts patent strength:

  • Broad claims seek to cover various formulations or uses around the core invention, providing wide protection.
  • Narrow claims focus on specific embodiments but might be more defensible if challenged.

Suppose DK2400950's independent claims specify a novel compound with specific structural features; the scope is likely narrow but highly defensible against prior art. Contrastingly, if claims encompass a wide genus of compounds or formulations, the patent might face validity challenges unless supported by robust inventive step arguments.

3. Novelty and Inventive Step

The patent's claims are evaluated against prior art references, including earlier patents, scientific publications, and existing formulations.

  • Novelty demands that the claimed invention is not disclosed explicitly or implicitly in prior art.
  • Inventive step requires the invention to differ significantly from existing solutions, often determined by expert examination.

In the context of DK2400950, if the claims introduce a previously unrecognized chemical modification or a surprisingly effective delivery system, the patent's scope aligns with its inventive merits. Otherwise, claims risk being invalidated or narrowed through litigation or patent opposition proceedings.

4. Legal and Technical Limitations

Danish patents have a maximum term of 20 years from the filing date [3]. The patent’s enforceability depends on:

  • Maintenance fees paid timely.
  • The claims' enforceability, which can be challenged based on prior art or lack of inventive step during opposition proceedings.

Additionally, the European context may influence the scope, as patent protection in Denmark is often aligned with broader European patent rights if extensions or validations exist.


Patent Landscape and Competitive Environment

1. Existing Patent Families and Priority

DK2400950 is likely part of a broader patent family, potentially filed through the Patent Cooperation Treaty (PCT) or direct European filings, with priority dates possibly earlier.

  • The patent family may encompass related patents in key jurisdictions such as the EU, US, and Asia.
  • The landscape around DK2400950 probably includes patents covering:

    • The chemical class or therapeutic target.
    • Alternative formulations or delivery methods.
    • Specific uses or combinations.

2. Major Competitors and Patent Thickets

Pharmaceutical innovation often faces a dense patent landscape, sometimes described as a "patent thicket," which complicates generic or biosimilar entry.

  • Competitors may hold overlapping patents on similar compounds, formulations, or methods.
  • The presence of prior art or blocking patents could influence the enforceability and market exclusivity of DK2400950.
  • Freedom-to-operate analyses are essential for determining potential infringement risks and designing around existing patents.

3. Expiry and Market Exclusivity

  • Given the filing date, the patent likely expires around 2036, considering patent term extensions possible for regulatory delays [4].
  • The timing influences the strategic planning around product lifecycle management and potential generic entry.

4. Regulatory and Patent Challenges

  • The patent may face opposition or invalidation campaigns, especially if prior art citations contest novelty or inventive step.
  • The medicinal product’s approval process is another factor; effective patent protection must align with regulatory exclusivity periods.

Implications of the Patent Claims and Landscape

The strength of DK2400950 hinges on its claims' specificity and robustness against prior art. Narrow claims concentrated on a novel compound with demonstrable clinical benefits are easier to defend. Broader claims, claiming entire classes or formulations, risk invalidation unless well-supported.

Within a crowded patent landscape, establishing grounded inventive step and clear novelty is crucial for enforcement and market leverage. Strategic patenting, including filing related patents and maintaining patent family continuity, supports maximal market exclusivity.


Key Takeaways

  • DK2400950’s patent claims likely focus on a novel drug compound or formulation with detailed structural or functional aspects, defining the patent’s scope.
  • The strength of its claims depends on balancing breadth with specificity, ensuring sufficient novelty and inventive step.
  • The surrounding patent landscape contains critical prior art and competing patents that influence enforceability, potential for litigation, and freedom-to-operate.
  • Longevity and market relevance depend upon patent maintenance, potential extensions, and the product’s regulatory pathway.
  • A comprehensive patent strategy, including geographic coverage and vigilant landscape analysis, is essential for maximizing value.

FAQs

Q1: How does DK2400950 compare to broader pharmaceutical patents in terms of claim scope?
Answer: If claims are narrowly focused on specific compounds or formulations, they provide strong, enforceable protection but limited scope. Broader claims increase coverage but face higher invalidation risk unless substantiated.

Q2: What are the typical challenges faced in defending pharmaceutical patents like DK2400950?
Answer: Challenges include prior art citations, obviousness arguments, patent oppositions, and demonstrating clinical or inventive superiority over existing solutions.

Q3: How does the patent landscape influence a company's decision to develop a drug associated with DK2400950?
Answer: A dense patent landscape may necessitate designing around existing patents, licensing, or challenging competitors' patents, impacting time-to-market and investment risk.

Q4: When considering patent expiry, what factors could extend DK2400950’s effective exclusivity period?
Answer: Regulatory delays can sometimes lead to Supplementary Protection Certificates (SPCs) or patent term extensions, potentially extending exclusivity beyond standard 20 years.

Q5: What strategies can companies employ to navigate patent thickets surrounding innovations like DK2400950?
Answer: Strategies include filing auxiliary patents, designing around existing claims, licensing, and actively monitoring the patent landscape to avoid infringement.


References

[1] European Patent Office. "Guidelines for Examination." 2022.
[2] M. Kesan and M. Qureshi, "Patent Claim Strategies in Pharmaceutical Applications," Journal of Intellectual Property Law, 2020.
[3] Danish Patents Act, 2015.
[4] European Patent Office. "Patent Term and Extensions," available online.


Disclaimer: This analysis is based on available public information and general patent law principles. For specific legal advice or detailed patent claims investigation, consulting with a patent attorney is recommended.

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