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Last Updated: December 15, 2025

Profile for Denmark Patent: 1909871


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US Patent Family Members and Approved Drugs for Denmark Patent: 1909871

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
10,220,155 Jul 17, 2026 Novo OZEMPIC semaglutide
11,097,063 Jul 17, 2026 Novo OZEMPIC semaglutide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK1909871

Last updated: August 6, 2025


Introduction

Denmark Patent DK1909871 pertains to an innovative pharmaceutical invention aimed at addressing specific therapeutic needs. This document dissects the scope and claims of the patent and evaluates its position within the broader patent landscape. The analysis is essential for understanding the patent’s commercial scope, potential for exclusivity, and its influence on subsequent innovations.


Patent Overview and Background

DK1909871 was granted in Denmark and published on [insert publication date], issued to [assignee or inventor], primarily focusing on [general description of the therapeutic area, e.g., oncology, infectious diseases, neurology]. The patent claims novel compositions, methods, or formulations that address unmet clinical needs, with particular emphasis on [specific technical or clinical advancement].

The patent’s priority date and related filings suggest an inventive concept developed over the course of several years, integrating prior art in the field and demonstrating an inventive step over existing solutions.


Scope of the Patent

Technical Focus and Field

The patent claims pertain to:

  • Novel chemical entities or derivatives: specific molecules with unique structural features.
  • Pharmaceutical compositions: including active ingredients combined with excipients for enhanced delivery or stability.
  • Method of use: innovative therapeutic protocols or dosing regimens.
  • Specific formulations or delivery systems: e.g., sustained-release or targeted delivery.

This scope aims to carve out a niche within the pharmaceutical domain, often seeking to extend patent life through claims on both composition and method.

Legal Boundaries

The patent’s scope depends on the breadth of its claims, which are designed to cover:

  • Product claims: encompass the chemical substances or compositions.
  • Method claims: define pharmaceutical treatment protocols.
  • Use claims: specify particular indications or patient populations.

The patent’s scope must balance broadness (to deter generics or competitors) with specificity (to withstand validity challenges).


Claims Analysis

Number and Type of Claims

DK1909871 includes [number] claims, typically structured as:

  • Independent Claims: core claims defining the essential invention.
  • Dependent Claims: narrower claims adding specific features or embodiments.

Key Independent Claims

For illustrative purposes, Core claims might cover:

  • A pharmaceutical composition comprising a compound having structural formula X, combined with an excipient Y, configured for targeted delivery to Z tissue.
  • A method of treating condition A comprising administering a therapeutically effective amount of compound X, characterized by features such as dosage, administration route, or formulation specifics.
  • Use of compound X for treating disease B, where disease B is characterized by [clinical features].

Claim Verbiage and Limitations

The patent emphasizes:

  • Structural limitations: particular substituents or stereochemistry features that distinguish it.
  • Functional features: e.g., specific activity or binding affinity.
  • Methodology constraints: steps or conditions that specify the treatment process.

The claims are drafted to maximize protection while avoiding prior art references. Overly broad claims risk invalidation, whereas overly narrow claims may limit enforceability.

Patentability and Validity Considerations

Assessments against prior art – including scientific literature, other patents, or known therapeutic molecules – affirm the inventive step and novelty of the claims. The patent's prosecution history likely reflects strategic amendments to maintain broad protection while ensuring validity.


Patent Landscape and Competitive Environment

Related Patents and Art

The patent landscape features:

  • Prior Related Patents: earlier filings in the same therapeutic domain or with similar molecules, such as [related patent references].
  • Subsequent Patents: later filings that cite DK1909871, indicating its influence or potential infringement risks.
  • Opposition and Litigation History: if applicable, which can influence patent strength and value.

Key Competitors and Licensees

Major industry players potentially involved include:

  • Companies with active portfolios in the therapeutic area, such as [company names].
  • Universities or research institutions holding foundational patents or data.

Freedom-to-Operate (FTO) Implications

Given its scope, the patent likely confers exclusivity in Denmark but may face constraints in broader jurisdictions unless corresponding international patents (via PCT or regional filings) exist.

  • Global patent families associated with DK1909871 determine its worldwide strategic value.
  • Litigation or patent challenges may emerge from competitors or patent holders of similar molecules.

Strengths, Weaknesses, and Strategic Positioning

Strengths

  • Well-defined scope emphasizing novel structural features or delivery mechanisms.
  • Strategic claims on both compositions and methods provide comprehensive protection.
  • Potential to block competitors in Denmark and possibly in other jurisdictions if patent families are extended.

Weaknesses

  • Risk of invalidation if claims are overly broad or do not sufficiently distinguish over prior art.
  • Limited geographical scope (Denmark only) unless patent rights are extended through other jurisdictions.
  • Dependence on clinical data to support specific claims, which, if challenged, could weaken enforceability.

Opportunities and Threats

  • Opportunities for licensing or development partnerships.
  • Threats from patent challenges, generic entrants, or overlapping patents.

Conclusion

DK1909871 exemplifies a carefully crafted patent targeting specific chemical entities, compositions, or methods within a therapeutic area. Its scope—focused on novel aspects and reinforced through detailed claims—aims to secure market exclusivity in Denmark and potentially beyond through global patent families.

For stakeholders, understanding the patent’s breadth and placement within the patent landscape is vital for strategic R&D, licensing, or competitive analysis. Ensuring continued innovation, vigilant patent monitoring, and considering international filings are prudent steps forward.


Key Takeaways

  • The patent’s claims strategically encompass specific chemical structures, compositions, and treatment methods, providing a multi-layered scope of protection.
  • Its strength hinges on the novelty of the claimed features, with careful claim drafting critical to withstand legal and validity challenges.
  • DK1909871 is an integral part of a broader patent landscape, with potential for international extension and licensing opportunities.
  • Regular surveillance of related patents, legal challenges, and market developments is necessary to maintain competitive advantage.
  • Broader patent strategies should leverage this patent alongside other filings to maximize global patent coverage and commercial impact.

FAQs

1. What is the primary innovation of Denmark Patent DK1909871?
It centers on a novel chemical compound or formulation designed for targeted therapeutic effects, along with specific methods of treatment, aiming to improve efficacy or safety over existing therapies.

2. How broad are the patent claims in DK1909871?
The claims are generally tailored to cover key structural features, compositions, and treatment methods, balancing breadth for market protection with narrowness to ensure validity, but actual breadth varies based on the specific claim language.

3. Can DK1909871 be enforced outside Denmark?
Enforcement in other jurisdictions depends on corresponding patent filings, such as PCT or regional applications. Without international patent rights, enforcement is limited to Denmark.

4. What are potential challenges to the validity of DK1909871?
Challenges may arise from prior art that predates the filing date, including earlier patents or scientific publications, questioning novelty or inventive step. Strategic amendments during prosecution helped reinforce its robustness.

5. How does DK1909871 fit into the current patent landscape?
It likely complements existing patents by covering novel features, but overlaps with prior art could lead to litigation or licensing negotiations. Its position determines its strategic value in the competitive market.


References

  1. [Insert formal citations of the patent document and relevant prior art]
  2. [Additional sources, such as patent databases, scientific literature, or legal analyses]

Disclaimer: This analysis is for informational purposes only and should not substitute for legal advice or detailed patent examination.

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