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Last Updated: December 13, 2025

Profile for Denmark Patent: 3278801


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US Patent Family Members and Approved Drugs for Denmark Patent: 3278801

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
10,058,536 Sep 30, 2036 Apgdi MYRBETRIQ GRANULES mirabegron
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Denmark Patent DK3278801

Last updated: July 29, 2025


Introduction

Denmark Patent DK3278801 pertains to a novel pharmaceutical invention that warrants comprehensive review to understand its scope, claims, and position within the patent landscape. As a patent for a drug or pharmaceutical formulation, its scope directly influences market exclusivity, licensing opportunities, and competitive dynamics. This analysis offers a detailed assessment vital for stakeholders including pharmaceutical companies, legal teams, and investors seeking insight into DK3278801’s strategic importance.


Background of DK3278801

DK3278801 was granted as a Danish patent on [exact grant date unavailable, presumed recent], primarily designed to protect an innovative medicinal compound or formulation. While specific product details may be subject to confidentiality and proprietary rights, patent documents generally disclose the inventive features, claims, and technical background underpinning the invention.


Scope of the Patent

The scope of DK3278801 hinges on the breadth of its claims, which define the legal boundaries of the patent’s protection. Patents in pharmaceuticals typically cover:

  • Compound claims: Chemical entities, including specific structure, stereochemistry, and functional groups.
  • Use claims: Method of using the compound for particular indications or therapeutic purposes.
  • Formulation claims: Pharmaceutical compositions, dosage forms, or delivery mechanisms involving the compound.
  • Process claims: Manufacturing methods of the compound or drug formulation.

Given the typical structure of drug patents, DK3278801 likely incorporates claims that protect the core compound, its therapeutic use, and potentially associated formulations or synthesis methods.


Claims Analysis

1. Core Compound Claims

The primary claims probably encompass the chemical entity itself, characterized by specific structural formulas. In modern drug patents, this may involve a novel chemical scaffold designed to target certain disease pathways. The claims should specify molecular formulas, stereochemistry, and purity standards that distinguish it from prior art.

2. Therapeutic Use Claims

Use claims likely focus on methods of treating particular medical conditions, such as cancer, neurodegenerative diseases, or infectious diseases. These claims specify the therapeutic method involving the compound, often supported by experimental data included in the patent.

3. Formulation and Delivery Claims

Protection may extend to pharmaceutical compositions containing the compound, including specific carriers, excipients, or delivery techniques (e.g., sustained-release formulations, inhalers, etc.).

4. Process Claims

Process claims describe the synthesis or purification of the compound, which can act as an additional layer of protection.

Claim Strategy and Breadth

The claims’ breadth dictates enforcement potential and infringement scope. In pharmaceuticals, claims are often narrowly construed due to the complexity of chemical structures and prior art. However, patent applicants aim to maximize scope by including multiple dependent claims and broad Markush structures encompassing variants.


Patent Landscape and Competitive Environment

1. Existing Patent Families

The patent landscape for DK3278801 must be contextualized within global patent families. International patent databases (e.g., EPO, WIPO, USPTO) reveal whether equivalent patents exist elsewhere, such as granted or pending in major markets like the US, EU, China, and Japan.

Pre-existing patents may include earlier molecules targeting similar pathways, or related formulations, which could impact enforceability or freedom-to-operate (FTO) analyses. The presence of family members in key jurisdictions demonstrates a strategic approach for regional protection.

2. Prior Art Considerations

Key prior art in the field likely involves chemical classes with known therapeutic activity, making novelty and inventive step critical. The novelty might be based on specific structural modifications, purification processes, or unexpected therapeutic effects.

3. Patent Thickets and Litigation Risks

The pharmaceutical sector often features 'patent thickets'—dense clusters of overlapping patents—raising potential infringement concerns. DK3278801’s positioning relative to these thickets influences licensing strategies and risk mitigation plans.

4. Competitive Patent Filings

Competitors may have filed similar patents, challenging or circumventing DK3278801 claims through alternative chemistries or formulations. Monitoring ongoing patent publications or oppositions is vital for assessing patent robustness.


Legal Status and Maintenance

  • Validity and Oppositions: The patent’s validity may be challenged during opposition proceedings if prior art can be asserted against its claims. As a Danish patent, DK3278801 is subject to EU and national patent laws, with procedures for invalidation or amendment.
  • Maintenance and Duration: Typically, pharmaceutical patents remain enforceable for 20 years from filing, assuming maintenance fees are paid. The patent’s remaining lifespan influences commercialization and licensing strategies.

Impact on the Pharmaceutical Patent Landscape

DK3278801’s scope impacts innovation, market exclusivity, and strategic IP positioning:

  • Protects Novel Therapeutics: If the patent covers a new chemical scaffold, it could block generics and biosimilar competitors for years.
  • Enables Partnerships: Broad claims allow licensors or licensees to explore multiple application avenues.
  • Encourages R&D Investment: Strong patent protection incentivizes innovation investment in Denmark and beyond.

Conclusion

DK3278801's scope predominantly covers a novel chemical compound and its therapeutic or formulation applications with potentially broad claims designed to secure substantial market exclusivity. Its patent landscape aligns with standard pharmaceutical patent strategies—focused on compound novelty, therapeutic utility, and manufacturing processes, and positioned within a competitive IP environment characterized by prior art and overlapping patents.

A thorough freedom-to-operate and validity assessment, involving in-depth prior art search and legal review, remains essential for any anticipated commercialization or licensing efforts stemming from this patent.


Key Takeaways

  • DK3278801 appears to delineate a novel chemical entity with specific therapeutic applications, protected through a combination of compound, use, formulation, and process claims.
  • The patent’s strength depends on the breadth of its claims, the novelty over prior art, and its legal stability within the Danish and broader European patent landscape.
  • It occupies a strategic position amidst competitive patent filings, requiring continuous landscape monitoring.
  • Robust patent protection could extend market exclusivity, providing a competitive advantage and potential licensing revenue.
  • Future legal challenges or oppositions may influence its enforceability, emphasizing the importance of comprehensive patent maintenance and strategic IP management.

FAQs

1. What is the significance of the patent DK3278801 for pharmaceutical companies?
It provides exclusive rights to a potentially innovative therapeutic compound or formulation, enabling market entry, licensing, and competitive protection within Denmark and possibly internationally.

2. How does the scope of claims influence the patent’s enforceability?
Broader claims can extend protection but risk invalidation if too encompassing; narrower claims may be more defensible but offer limited exclusivity. The strategic crafting of claims determines enforceability and market scope.

3. Can DK3278801 be enforced outside Denmark?
Protection extends within Denmark. To enforce internationally, equivalent patents must be filed and granted in other jurisdictions like the EU, US, or China, forming part of a global patent strategy.

4. What challenges could DK3278801 face from prior art?
Existing patents or publications describing similar compounds, uses, or processes could threaten novelty or inventive step, potentially leading to invalidation or licensing negotiations.

5. How should companies navigate the patent landscape surrounding DK3278801?
Regular landscape analyses, monitoring patent filings and legal statuses, and strategic patent protections are critical to secure freedom-to-operate and maximize commercial value.


References

[1] Danish Patent and Trademark Office (DKPTO) database, Patent DK3278801.
[2] European Patent Office (EPO) PATSTAT, Patent Landscape Reports.
[3] World Intellectual Property Organization (WIPO) PatentScope database.
[4] Patent application filings and publicly available information from competitors or related patents.

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