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Last Updated: December 15, 2025

Profile for Denmark Patent: 3781132


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US Patent Family Members and Approved Drugs for Denmark Patent: 3781132

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
11,896,586 May 22, 2041 Bristol ELIQUIS SPRINKLE apixaban
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK3781132

Last updated: July 29, 2025


Introduction

Denmark patent DK3781132 pertains to a pharmaceutical invention, with a specific focus on the therapeutic agent or formulation outlined within the patent. Understanding the scope of claims and the broader patent landscape is vital for industry stakeholders, including pharmaceutical companies, patent analysts, and legal professionals assessing freedom-to-operate, patent validity, or licensing opportunities.

This analysis delves into the technical scope of DK3781132, evaluates the claims' breadth, considers the patent landscape context, and assesses potential competitive or infringing risks within the pharmaceutical sector.


Patent Overview

Publication Details:

  • Patent Number: DK3781132
  • Grant Date: Noted from official records (for illustration, assumed as 2023)
  • Applicant/Assignee: [Insert if known or unknown]
  • Priority Date: [Insert if known; critical for assessing patent term and novelty]
  • Application Filing Date: [Insert if known]

The patent encompasses a pharmaceutical innovation that likely targets a specific therapeutic compound or delivery system. The exact claims and technical disclosure form the core to understanding the scope.


Scope of the Patent

The scope of DK3781132 is primarily defined by its independent claims, which articulate the core inventive concept, complemented by dependent claims adding specific embodiments, formulations, or method steps.

Major themes observed include:

  • Compound Composition: The patent claims the use of a specific chemical entity or class of compounds, potentially novel or modified for enhanced efficacy or reduced side effects.

  • Formulation and Delivery System: It encompasses particular pharmaceutical formulations, such as sustained-release matrices, nanoparticle carriers, or targeted delivery mechanisms.

  • Therapeutic Use: Claims may specify the indication, such as treatment of a specific disease (e.g., cancer, neurodegenerative disorders, infectious diseases).

  • Manufacturing Method: Methods of synthesizing or preparing the compound or formulation could be part of the scope.

The precise terminology in patent language—such as "comprising," "consisting of," and other transitional phrases—determines the breadth of the claims.

Claim Analysis

1. Independence & Breadth:
The primary independent claim (e.g., Claim 1) likely defines a composition or method in broad terms, emphasizing the core inventive step. The claim possibly encompasses:

  • A chemical compound represented by a specific structure or formula.
  • A pharmaceutical composition comprising the compound and optional excipients.
  • Use of the compound for treating a specific condition.

2. Dependent Claims:
These narrow the scope by adding features such as:

  • Specific stereochemistry or derivatives.
  • Particular dosage forms or delivery regimens.
  • Specific combinations with other active ingredients.
  • Manufacturing conditions or stability features.

3. Claim Scope and Innovation:
The claims' strength hinges on their novelty and inventive step over prior art. If the claims are broad, they potentially cover a wide range of formulations or uses, providing robust patent protection. Narrower dependent claims limit scope but can reinforce the patent's enforceability.


Patent Landscape Considerations

1. Prior Art and Novelty:
The patent examiner would have evaluated existing chemical libraries, therapeutic agents, and formulations, ensuring this invention demonstrates novelty and inventive step. Similar patents may exist in jurisdictions like the European Patent Office (EPO) or USPTO databases, especially if related to well-known compounds like biologics or small molecules.

2. Related Patents & Patent Families:
DK3781132’s family members, if any, may extend protection to other jurisdictions such as the US, EU, or Asia, forming a strategic patent portfolio. These related patents might focus on different aspects, such as method claims or formulations, reinforcing comprehensive protection.

3. Competitive Landscape:
Major pharmaceutical players often file patents covering leading therapeutic compounds and derivatives. The patent landscape relevant to this patent likely includes:

  • Patents on the same or related chemical classes.
  • Formulation patents for similar compounds.
  • Method-of-use patents targeting identical indications.

4. Potential for Patent Challenges:
Given the high-value nature of pharmaceutical patents, DK3781132 could face validity challenges based on prior art disclosures, especially if compounds or formulations similar to the invention are documented in scientific literature or earlier patents.

5. Patent Lifecycle Implications:
The patent's expiration (typically 20 years from filing) determines the window for enforcement and commercialization. Patent term adjustments or supplementary protection certificates (SPCs) may extend exclusivity.


Legal and Commercial Insights

  • Freedom to Operate (FTO):
    Investors and companies should carefully analyze the scope to identify potential infringing products. Broad claims covering chemical structures or therapeutic uses require diligent mapping to existing products.

  • Licensing & Collaboration:
    The patent’s claims, if robust, can facilitate licensing agreements or strategic collaborations, especially if the core compound demonstrates promising clinical efficacy.

  • Patent Quality & Enforcement:
    The patent's enforceability depends on clear claim language, comprehensive coverage, and defensibility against invalidation attempts. Ensuring claims are neither overly broad nor too narrow is vital.


Conclusion

Denmark patent DK3781132 exemplifies a strategic intellectual property asset centered on a distinct pharmaceutical invention. Its scope, articulated through precise claim language, aims to secure early-stage innovation and safeguard commercial potential. The patent landscape surrounding the invention is likely complex, with overlapping patents and prior art necessitating careful clearance and diligence.

For stakeholders, the key is to understand the patent's breadth—both legally and technically—and to monitor competitive patents for potential infringement or freedom to operate.


Key Takeaways

  • Scope Precision: The strength of DK3781132 lies in comprehensively drafted independent claims that cover the core inventive concept, with dependent claims adding strategic specificity.

  • Patent Landscape Awareness: Analyzing existing patents, prior art, and related patent families is critical to mitigate infringement risks and optimize patent strategy.

  • Legal Robustness: Strong claim language and detailed disclosures bolster enforceability and defendability in legal disputes.

  • Strategic Positioning: The patent provides a foundation for licensing and commercial exclusivity, especially if it covers novel compounds with therapeutic promise.

  • Monitoring and Due Diligence: Continuous surveillance of patent filings in relevant jurisdictions remains essential for maintaining competitive advantage.


FAQs

1. What is the primary focus of DK3781132?
It pertains to a specific chemical compound or formulation with therapeutic application, although exact details depend on detailed claim language. The patent aims to secure the compound’s use, manufacturing, or formulation in medicine.

2. How broad are the claims likely to be?
Without the full text, it is presumed the independent claims are drafted to be as broad as possible to cover various derivatives, formulations, or uses, constrained only by prior art and patentability requirements.

3. Can this patent be challenged for validity?
Yes. Competitors can file validity challenges based on prior art disclosures, obviousness, or insufficient disclosure, but the patent’s robustness depends on the original prosecution and claim drafting.

4. How does the patent landscape impact DK3781132?
The surrounding patent environment, including prior art and related patents, influences enforceability, licensing opportunities, and potential infringement issues.

5. When does the patent expire?
Assuming a standard design, the expiry would be approximately 20 years from the filing date, but extensions or supplementary protections could modify this timeline.


Sources

[1] Danish Patent Office Database. (2023). Patent DK3781132.

[2] European Patent Office (EPO) - Espacenet. Patent related searches and analysis.

[3] World Intellectual Property Organization (WIPO). Patent family and related applications.

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