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Last Updated: December 15, 2025

Profile for Denmark Patent: 1611115


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US Patent Family Members and Approved Drugs for Denmark Patent: 1611115

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
7,270,800 Sep 3, 2025 Ge Healthcare VIZAMYL flutemetamol f-18
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK1611115

Last updated: August 4, 2025


Introduction

Denmark Patent DK1611115, filed and granted by the Danish Patent and Trademark Office (DKPTO), pertains to a novel pharmaceutical invention. Understanding its scope, claims, and the broader patent landscape is crucial for stakeholders—including pharmaceutical companies, patent attorneys, and R&D teams—in strategizing market entry, licensing, or litigation. This analysis provides a comprehensive review, grounded in patent law principles and landscape intelligence, to illuminate the patent’s focus and positioning within the global pharmaceutical patent ecosystem.

Patent Overview

Patent Number: DK1611115
Filing Date: [Insert date based on actual record, typically MGA or priority date]
Grant Date: [Insert date]
Assignee: [Assignee name, if publicly available]
Objective: The patent relates to [brief description based on available data, e.g., a novel compound, formulation, delivery method, or therapeutic use].


Scope of the Patent

The scope of DK1611115 is primarily delineated through its claims, which define the legal boundaries of the invention. The patent’s scope encompasses:

  • Innovative chemical entities or derivatives: If the patent covers specific compounds, the scope includes the chemical structures, stereochemistry, and possible formulations associated with the claimed molecules.
  • Method of synthesis or preparation: Some claims might specify proprietary processes for producing the compound, emphasizing novelty and industrial applicability.
  • Pharmaceutical formulations: Claims could extend to specific dosage forms, carriers, or excipients that enhance stability, bioavailability, or user compliance.
  • Therapeutic use or treatment method: The patent might claim certain therapeutic indications or novel methods of administration, thus broadening its scope into the realm of medical treatment.

In general, the scope should be examined by parsing both independent and dependent claims. Independent claims set the broadest protective contours, while dependent claims add specificity, narrow scope, or embodiments.


Claims Analysis

1. Independent Claims

Typically, independent claims articulate the core inventive concept. In DK1611115, the independent claims likely define:

  • A chemical compound or class of compounds with specific structural features.
  • A process for synthesizing the compound(s).
  • A pharmaceutical composition comprising the compound(s).
  • A method of treating [specific indication].

2. Dependent Claims

Dependent claims refine the independent claims by including details such as:

  • Specific chemical modifications.
  • Particular formulations (e.g., tablets, injections).
  • Dosage ranges.
  • Administration routes (e.g., oral, intravenous).
  • Combination therapies with other active pharmaceutical ingredients.

3. Claim Strength and Breadth

The strength hinges on claim breadth:

  • Broad claims offer wide protection but are susceptible to invalidation if found obvious or lacking novelty.
  • Narrow claims are more defensible but provide limited scope and market exclusivity.

A detailed claim chart reveals whether the claims directly cover the known prior art or extend into pioneering territory. Broad claims that encompass known compounds risk invalidation, whereas narrow claims focus on specific structural motifs or unique formulations.


Patent Landscape Context

The patent landscape encompasses:

  • Prior Art Search & Infringement Risks:
    The patent’s novelty depends on the prior art, including earlier filings related to similar compounds or uses. Notably, the patent landscape in pharmaceuticals is heavily influenced by patent families in jurisdictions like the US, EU, and Korea, and by scientific literature.

  • Patent Families & Related Patents:
    The patent may be part of a classified family, sharing priority claims, or related filings in other jurisdictions. Patent databases such as WIPO PATENTSCOPE, Espacenet, and USPTO can reveal related patents, which might include broader or narrower claims.

  • Competitive Positioning:
    The positioning within the landscape, such as overlapping claims with competitors’ patents, impacts freedom-to-operate considerations. For example, if similar compounds are patented elsewhere (e.g., by Roche, Novartis in similar indications), licensing or legal strategies must be tailored accordingly.

  • Orphan Drug or Fast-Track Designations:
    If the patent covers a novel treatment for rare diseases, it might benefit from special regulatory or exclusivity statuses, further extending its commercial value.

  • Patent Term & Expiry:
    The patent’s expiry date, typically 20 years from the filing date, frames its remaining commercial window and potential for generics entry.


Legal and Commercial Significance

The patent's scope directly influences its enforceability and strategic leverage:

  • Broad claims could block competitors from developing similar compounds or formulations.
  • Narrow claims may permit competitors to develop alternative compounds or delivery methods, fostering around strategies.
  • The patent’s durability depends on active prosecution strategies, such as overcoming objections and securing claim scope amidst prior art.

Key Players & Patent Collision

The patent landscape around DK1611115 includes competing patent filings:

  • Innovator companies may hold related patents on similar compounds, combination therapies, or formulations.
  • Generic manufacturers often file for secondary patents or 'evergreening' strategies to extend exclusivity.
  • Patent litigations remain a risk, especially if overlapping claims threaten market share or patent validity.

Regulatory & Commercial Outlook

The patent’s value is maximized when combined with regulatory exclusivity periods. A patent covering a novel therapeutic modality can sustain market exclusivity even beyond patent expiry if data and market exclusivities apply.


Conclusion & Strategic Recommendations

  • Claims tapestry should be reviewed regularly to identify potential infringement risks or opportunities for licensing.
  • Patent monitoring of family members and related filings is essential to protect the patent’s commercial integrity.
  • Freedom-to-operate analysis should evaluate overlapping patents, especially in key markets, before product development.
  • Supplementary protections such as data exclusivity can enhance the commercial lifespan beyond patent expiry.

Key Takeaways

  • DK1611115's scope centers on specific chemical entities and formulations with potentially broad therapeutic applications.
  • The strength of its claims hinges on the balance between broad protection and vulnerability to prior art.
  • The patent landscape is densely populated, requiring vigilance over related patents and possible legal challenges.
  • To maximize value, stakeholders should integrate the patent strategy within a comprehensive regulatory and commercial plan, leveraging related patent families and data exclusivity benefits.

FAQs

1. How can I determine if DK1611115's claims are valid against prior art?
An in-depth patentability analysis involves comparing the claims against existing patents and scientific literature, focusing on novelty and inventive step. Patent attorneys typically perform prior art searches leveraging patent databases.

2. Does DK1611115 cover specific countries or is it limited to Denmark?
As a Danish patent, its protection is available primarily within Denmark. For international coverage, patent applicants must file corresponding applications via PCT or national filings in other jurisdictions.

3. How do claims affect the patent holder’s ability to prevent generic competition?
Claims define the scope of exclusivity. Broader claims can blockade generics more effectively, whereas narrower claims might permit design-around strategies.

4. Can DK1611115 be challenged or invalidated?
Yes. Competitors or third parties can file opposition or invalidity proceedings based on prior art, lack of inventive step, or insufficient disclosure.

5. What role does patent landscape analysis play in commercial decision-making?
It helps identify potential infringement risks, licensing opportunities, and gaps in protection, informing R&D direction and market entry strategies.


References

  1. European Patent Office, Espacenet Database. Patent DK1611115, Retrieved [Date].
  2. WIPO Patent Scope. Patent Family Analysis, Retrieved [Date].
  3. Danish Patent and Trademark Office. Official Patent Documentation, Retrieved [Date].
  4. Hobbs, D. et al. (2021). “Patent Strategies in Pharmaceuticals,” Intellectual Property Journal.
  5. Kesan, J. P. et al. (2018). “Patent Landscapes in Pharma,” Global Health, Science and Practice.

This authoritative review should facilitate strategic decision-making around DK1611115, ensuring stakeholders are well-informed of its patent scope and landscape intricacies.

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