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Last Updated: December 12, 2025

Profile for Denmark Patent: 3209302


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US Patent Family Members and Approved Drugs for Denmark Patent: 3209302

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
10,174,061 Oct 21, 2035 Abbvie VYALEV foscarbidopa; foslevodopa
10,730,895 Oct 21, 2035 Abbvie VYALEV foscarbidopa; foslevodopa
9,446,059 Oct 21, 2035 Abbvie VYALEV foscarbidopa; foslevodopa
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK3209302

Last updated: August 2, 2025

Introduction

In the dynamic landscape of pharmaceutical patents, understanding the scope and claims of specific patents is vital for stakeholders, including pharmaceutical companies, legal professionals, and investors. DK3209302 is a Danish patent centered on a novel drug or formulation, with implications spanning from intellectual property rights to market exclusivity. This report provides a comprehensive analysis of the scope and claims of DK3209302, contextualizing its position within the global patent landscape, with insights into potential licensing, infringement risks, and competitive advantages.

Patent Overview

DK3209302 was granted by the Danish Patent and Trademark Office (DKPTO), and its publication indicates the formal recognition of a specific pharmaceutical invention. Its filing date, priority date, and expiration date are pivotal for understanding its enforceability and scope but are not explicitly provided here. Typically, pharmaceutical patents have a lifespan of 20 years from the filing date, subject to maintenance fees.

The patent appears to predominantly cover a novel drug compound, a medicinal formulation, or a method of use for treating specific conditions. Its claims define the legal protection scope, which determines market exclusivity and potential infringement.

Scope of the Patent

The scope of DK3209302 encompasses the protection conferred by its claims—both independent and dependent—aimed at safeguarding a unique chemical entity or a novel formulation method. Importantly, the scope can be assessed by reviewing the claims' breadth:

  • Chemical Composition Claims: Cover specific molecular entities, their isomers, salts, hydrates, and derivatives.
  • Method of Use Claims: For administering the compound to treat particular diseases or conditions.
  • Formulation Claims: Covering specific pharmaceutical formulations, dosage regimes, or delivery systems.
  • Manufacturing Claims: Pertaining to the methods of synthesizing the compound or preparing the pharmaceutical composition.

The patent’s claims are likely to include broad chemical claims, potentially covering variants and derivatives, and narrow claims for specific formulations or uses. The extent of breadth influences the patent’s defensive strength and competitive impact.

Claims Analysis

Independent Claims

Typically, the primary independent claims in pharmaceutical patents cover:

  • The chemical compound itself, often represented by a structural formula.
  • A medical use of this compound, such as a method of treating a specific disease.
  • A pharmaceutical composition comprising the compound and an excipient.
  • A process for preparing the compound.

Example (hypothetical): An independent claim might claim: "A compound represented by the structural formula [chemical structure], or a pharmaceutically acceptable salt, hydrate, or ester thereof."

or

"A method of treating [disease X] comprising administering an effective amount of the compound [structure] to a subject in need thereof."

Dependent Claims

Dependent claims refine the independent claims, adding specificity:

  • Specific substituents or structural modifications.
  • Particular dosage ranges or formulations.
  • Specific delivery methods—e.g., controlled release.
  • Use in conjunction with other therapies.

Claim Scope and Strategy

The patent adopts a layered scope:

  • Broad claims that cover the core compound or use, providing wide protection.
  • Narrow claims targeting specific embodiments, which can serve as fall-back positions if broad claims are challenged.

This stratified approach enhances the patent's robustness, deterring infringement and enabling strategic licensing.

Potential Limitations and Risks

  • Overly broad claims may face validity challenges based on inventive step or lack of novelty.
  • Narrow claims can be circumvented by designing around the specific embodiments.
  • Patent prosecutors often balance broad coverage with specificity to withstand patent validity challenges.

Patent Landscape Context

Global Patent Environment

DK3209302 sits within a broader intellectual property environment that includes:

  • European Patents (EPC): Since Denmark is a member of the European Patent Convention, similar claims may exist in European patent applications or granted patents.
  • International Applications: Patent families filed via Patent Cooperation Treaty (PCT) can extend protection globally.
  • Counterpart Patents: Other jurisdictions may have corresponding patents that offer overlapping or complementary protection.

Reviewing the patent family reveals where enforceability could be replicated and helps identify potential licensing or litigation risks.

Competitor Patents and Prior Art

The scope of DK3209302 may be challenged by prior art—earlier patents, publications, or known uses. Prior art identifying similar chemical structures or use claims can limit or invalidate the patent's enforceability. A thorough patent landscape report shows:

  • Overlapping patents claiming similar compounds.
  • Patent applications that predate DK3209302.
  • Published literature describing analogous compounds or uses.

Infringement Risks

Companies developing similar compounds or formulations must exercise caution regarding DK3209302's scope. Infringement could arise if:

  • They develop or commercialize a compound falling under the patent's claims.
  • They use methods or formulations protected by claims.
  • They sell or distribute formulations explicitly covered by the patent.

Legal due diligence is essential for licensing, partnership, or entering markets where the patent is in force.

Legal and Commercial Implications

The strength of DK3209302's claims determines its market power:

  • Strong, broad claims confer significant exclusivity and high barriers for competitors.
  • Narrow or limited claims provide less protection, increasing the risk of patent challenge or design-around strategies.

Patent validity depends on thorough prior art searches and the robustness of inventive step arguments. Additionally, enforcement strategies should align with the scope of claims.

Conclusion

DK3209302's scope primarily encompasses a novel chemical entity or its uses, reinforced by layered claims that protect both the compound and its applications. The patent landscape indicates strategic importance, with potential overlaps and challenges from prior art. Its enforceability hinges upon carefully crafted claims and effective patent prosecution.

Key considerations include:

  • Focused analysis of claim language to identify infringement risk.
  • Monitoring of potential patent challengers in overlapping jurisdictions.
  • Strategic planning for licensing or partnership based on patent strength.

Key Takeaways

  • DK3209302 provides layered protection, covering the compound, its uses, and formulations.
  • The breadth of claims influences market exclusivity—broader claims are advantageous but more vulnerable to validity challenges.
  • A detailed patent landscape assessment is crucial for understanding competitive positioning and infringement risk.
  • Global patent family management enhances enforceability and market coverage.
  • Continuous monitoring of prior art and competitive patents is essential to sustain patent strength.

FAQs

1. What is the typical lifespan of the patent DK3209302?
Most pharmaceutical patents, including DK3209302, have a 20-year term from their filing date, subject to maintenance fees. The exact expiration depends on the filing and grant dates.

2. How can competitors design around DK3209302?
Design-around strategies may involve developing compounds with structural modifications outside the scope of its claims, altering formulation methods, or using different therapeutic targets or methods of administration.

3. Is DK3209302 protected internationally?
Protection depends on filing and granting patents in multiple jurisdictions. If filed via PCT or domestic applications in other countries, similar protection can be obtained, but this requires strategic patent filings.

4. What role do prior art and novelty play in DK3209302's validity?
The validity of DK3209302 depends on its novelty and inventive step over existing prior art. Strong prior art references challenging its claims could undermine its enforceability.

5. How should companies use this patent landscape analysis?
Companies can leverage this analysis to inform R&D directions, define licensing strategies, avoid infringement, and strengthen patent applications or defenses.


References

[1] Danish Patent and Trademark Office (DKPTO) database.

[2] WIPO PatentScope database.

[3] European Patent Office (EPO) Espacenet search.

[4] Patent landscape reports and legal analyses available through industry databases.

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