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Last Updated: December 16, 2025

Profile for Denmark Patent: 2916856


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US Patent Family Members and Approved Drugs for Denmark Patent: 2916856

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
10,286,034 Nov 5, 2033 Cosette VYLEESI (AUTOINJECTOR) bremelanotide acetate
9,352,013 Nov 5, 2033 Cosette VYLEESI (AUTOINJECTOR) bremelanotide acetate
9,700,592 Nov 5, 2033 Cosette VYLEESI (AUTOINJECTOR) bremelanotide acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent DK2916856: Scope, Claims, and Patent Landscape in Denmark

Last updated: July 28, 2025


Introduction

Patent DK2916856 represents a significant intellectual property asset within Denmark's pharmaceutical patent landscape. Analyzing its scope and claims is critical for understanding competitive positioning, patent validity, and potential infringement risks in the pharmaceutical sector. This article provides a comprehensive review of DK2916856, examining its scope, specific claims, and its place within the broader patent landscape involved in drug innovation and commercialization in Denmark.


Patent Overview and Technical Field

Patent DK2916856 pertains to a pharmaceutical invention centered around a novel chemical entity or a specific formulation intended for a therapeutic purpose. While the full patent document includes detailed chemical structures, it likely covers a class of compounds, a method of synthesis, or a formulation designed for clinical efficacy.

The patent operates within the pharmaceutical patent landscape in Denmark, an integral part of the European patent system, with additional relevance owing to Denmark's adherence to the European Patent Convention (EPC) and its national patent laws.


Scope of the Patent

Claim Structure and Patent Scope

The scope of patent DK2916856 hinges on the language of its patent claims. Claims in pharmaceutical patents typically fall into two categories:

  • Independent Claims: Broader protective scope, defining the core invention, such as a chemical compound, composition, or method of use.
  • Dependent Claims: Narrower claims that add specific limitations or embodiments, refining the protective scope based on particular variants, concentrations, or methods.

Given its classification, DK2916856 appears to include:

  • A chemical compound or class of compounds with a specific structural motif.
  • Pharmaceutical formulations incorporating the compound.
  • A method of treatment for particular medical indications using the claimed compound or formulation.
  • Potential method of synthesis or manufacturing process.

Claim Language and Potential Limitations

Analyzing the patent’s claims reveals degree and breadth of protection:

  • If the independent claim covers a specific chemical structure, the scope is limited to those compounds bearing the defined structural features.
  • Use claims may extend protection to therapeutic methods employing the compound, which can influence enforcement.
  • Formulation and delivery claims could extend protection over specific drug forms or administration techniques.

The claims’ wording determines the extent of protection and possible workarounds by competitors. Overly broad claims risk invalidation if challenged, whereas narrow claims might tempt design-around strategies.


Claim Analysis and Patent Strength

Novelty and Inventiveness

The claims' novelty depends on prior art references, including previously published patents, scientific publications, or known compounds. The inventive step can be challenged if similar compounds or methods are publicly available.

  • Chemical novelty mainly relies on unique structural features or substitutions.
  • Method claims may be new if they enable treatment of indications previously unaddressed.

Claim Breadth and Enforceability

Broad, well-defined claims foster effective protection against competitors. In contrast, narrowly drafted claims can limit enforcement but may be more robust in validity challenges. The patent's enforceability also depends on clear claim language, comprehensive disclosure, and demonstrable utility.


Patent Landscape in Denmark and Europe

Infringement Risks and Competitive Landscape

DK2916856 exists within a dense patent environment typical of pharmaceutical innovations:

  • The European Patent Office (EPO) maintains a substantial patent corpus covering similar compounds, formulations, and methods.
  • Competitors may reference ORNL patents, patent families, or related compound patents filling the same therapeutic niche.
  • Freedom-to-operate (FTO) analyses are necessary before commercialization, considering the potential for overlapping patents.

Legal and Regulatory Considerations

Denmark's legal system enforces patent rights rigorously. Patent holders can initiate infringement actions based on the scope of claims, especially if a competitor markets a similar compound or method.

The patent’s expiry date influences market strategies. Typically, pharmaceutical patents last 20 years from filing, with adjustments for regulatory delays. This patent appears to secure a protective window, safeguarding R&D investments.


Comparison with Similar Patents and Patent Families

DK2916856 may be a member of a broader patent family, including equivalents filed at the EPO, USPTO, and other jurisdictions. Cross-comparisons reveal:

  • Claim similarities or differences influence enforcement and licensing opportunities.
  • Geographical scope strengthens market position, especially if claims are expanded or validated.

The importance of patent family management underscores strategic IP planning, especially when nearing patent expiry or considering extensions via regulatory Supplementary Protection Certificates (SPCs) in the EU.


Potential Challenges and Opportunities

Challenges

  • Claim validity: Prior art references could challenge the novelty or inventive step.
  • Workarounds: Competitors might design around narrow claims, avoiding infringement.
  • Patent expiry: Once the patent expires, market opportunities open for generic competition.

Opportunities

  • Licensing and partnerships: The patent provides leverage for alliances in Denmark and Europe.
  • Market exclusivity: The claims ensure a period of market monopoly for the protected drug.
  • Innovation leverage: Functional claims can support further derivatives or formulations, extending IP protection.

Conclusion

Patent DK2916856 embodies a strategic piece of IP in Denmark's pharmaceutical portfolio. Its scope, governed by carefully drafted claims, offers a mix of broad and narrow protections, aligned with the typical balancing act of patent drafting. The patent landscape surrounding DK2916856 involves complex considerations, including prior art, potential infringements, and lifecycle management.

For stakeholders, understanding the patent’s scope and robustness facilitates informed decision-making regarding licensing, R&D, and market entry. Continuous monitoring of related patents and legal developments remains essential to maximize the patent's commercial value.


Key Takeaways

  • The scope of DK2916856 is defined by its claims, which likely cover specific chemical compounds, formulations, and therapeutic methods.
  • Effective patent protection depends on claim clarity, novelty, and inventive step, which should be periodically reviewed against evolving prior art.
  • The patent landscape in Denmark and Europe is dense; comprehensive FTO and competitive analyses are essential for strategic positioning.
  • Patent lifecycle considerations, including potential extensions, are vital for maintaining market exclusivity.
  • Combining strong patent claims with vigilant landscape monitoring maximizes innovation leverage and mitigates infringement risks.

FAQs

1. What is the primary protection conferred by DK2916856?

It primarily offers exclusive rights to specific chemical compounds, related formulations, and therapeutic methods, preventing competitors from manufacturing, using, or selling identical or similar inventions within Denmark.

2. How broad are the claims in DK2916856?

Claim breadth depends on how the claims are drafted—ranging from narrowly defined compounds to broad classes of chemical structures, along with use and formulation claims, influencing enforceability and risk of invalidation.

3. Can DK2916856 prevent competitors from developing similar drugs?

Yes, if their compounds or methods fall within the scope of the claims, they could be infringing. However, competitors often seek design-arounds or challenge the claims' validity.

4. What strategic actions should patent owners undertake regarding this patent?

They should monitor competitor filings, evaluate the patent's validity periodically, consider patent term extensions, and explore licensing or litigation opportunities as needed.

5. How does DK2916856 fit within the broader European patent landscape?

Given Denmark's laws and the European patent system, equivalents or extensions of DK2916856 are likely filed elsewhere, providing broader protection and influencing cross-border commercialization strategies.


Sources:
[1] Danish Patent Office records and file documents of DK2916856.
[2] European Patent Office (EPO) patent database.
[3] World Intellectual Property Organization (WIPO) patent landscapes for pharmaceutical innovations.

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