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Last Updated: December 16, 2025

Profile for Denmark Patent: 3909966


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US Patent Family Members and Approved Drugs for Denmark Patent: 3909966

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
10,172,871 Apr 17, 2034 Biogen Inc ZURZUVAE zuranolone
9,512,165 Apr 17, 2034 Biogen Inc ZURZUVAE zuranolone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK3909966

Last updated: October 20, 2025


Introduction

Denmark Patent DK3909966 pertains to a specific pharmaceutical invention, offering a comprehensive framework for understanding its scope, claims, and position within the patent landscape. Analyzing such patents is crucial for pharmaceutical companies, generic manufacturers, and legal entities to determine patent enforceability, possible points of entry, and the competitive environment.


Patent Overview and Bibliographic Data

  • Patent Number: DK3909966
  • Filing Date: [Specific date not provided; typically available in patent documents]
  • Issue Date: [Specific date not provided]
  • Applicant/Assignee: [Information typically available from the patent document]
  • Patent Type: Utility patent (assumed)
  • Jurisdiction: Denmark (European Patent Office or national level)

Scope of the Patent:

The scope of DK3909966 hinges upon its claims, which define the legal boundaries of the patent rights. The patent likely relates to a drug entity, formulation, method of use, or a manufacturing process, typical of pharmaceutical patents.

Core Focus:

  • The patent appears to cover a novel pharmaceutical composition, potentially involving a specific active pharmaceutical ingredient (API), joint formulations, or delivery systems.
  • It may also encompass methods of manufacturing or methods of treatment involving the API.

The precise scope involves the specific claims, which, in pharmaceutical patents, often include both independent and dependent claims.


Claims Analysis

Independent Claims

These are the broadest and define the core invention:

  • Typically, the primary claim delineates the composition, such as a drug formulation comprising specific active ingredients at defined concentrations.
  • Alternatively, it could specify a treatment method with particular steps or therapeutic effects.

For DK3909966, the independent claims likely describe:

  • A pharmaceutical composition containing a specific compound or combination (e.g., a novel molecule, a known API with an innovative excipient, or a new delivery mechanism).
  • The method of administering the drug, perhaps targeting a specific medical condition or patient population.

Dependent Claims

  • Narrower claims that specify particular embodiments, such as dosage forms (tablets, injections, patches), concentration ranges, pharmacokinetic properties, or administration regimens.
  • These provide fallback positions and define specific, enforceable subsets of the invention.

Claim Interpretation and Validity

  • The broadness of initial claims determines the scope and potential for infringement.
  • Narrower claims mitigate invalidity risks but limit exclusivity.
  • The claims likely balance innovative features with patentability requirements (novelty, inventive step, industrial applicability).

Patent Landscape Context

Prior Art and Related Patents

  • The patent probably cites prior art comprising existing drugs, formulations, or methods.
  • It may intersect with patents in the therapeutic area—e.g., oncology, neurology, or metabolic disorders.
  • Related patents in Denmark or broader European jurisdictions may cover similar compositions or methods.

Competitor Landscape

  • Similar patents are typically filed by big pharma or biotech companies, especially if targeting lucrative markets.
  • The invention's novelty could hinge on a unique compound, novel formulation, or improved delivery system.

Legal Status and Enforcement

  • The patent's enforceability depends on national patent laws, deadlines, and any oppositions or litigations.
  • In Denmark, national patents are granted after examination for novelty and inventive step.
  • Potential oppositions or challenges can occur if prior art or validity issues arise.

Implications for the Pharmaceutical Industry

Patent Positioning

  • DK3909966 potentially offers a competitive edge if it covers a first-in-class compound or a superior formulation.
  • The scoped claims can prevent generic entry or compel licensing negotiations.

Licensing and Commercialization

  • Broad claims allow for licensing deals or partnerships.
  • Narrower claims may limit scope but reduce infringement risks.

Market Strategies

  • Patent protection in Denmark complements broader European and global patents.
  • Parties must evaluate patent family coverage and regional validity.

Legal and Commercial Considerations

  • Patent infringement is assessed based on whether a competing product falls within the scope of claims.
  • Patent validity could be challenged if prior art undermines novelty or inventive step.
  • Patent lifecycle management involves monitoring expiration dates, potential extensions, and competitor filings.

Conclusion

DK3909966 exemplifies a strategic pharmaceutical patent, with a scope built around its claims, which likely cover a specific drug formulation or treatment method. Its position within the patent landscape hinges on its breadth relative to prior art and related patents, influencing its enforceability and commercial value. The patent’s strength ultimately depends on the precision of its claims, the validity of its inventive concept, and its regional and international patent family coverage.


Key Takeaways

  • Scope is defined by carefully crafted claims, balancing broad protection against the risk of invalidity.
  • Understanding claim structure (independent vs. dependent) is crucial for assessing enforceability.
  • Patent landscape analysis reveals the level of innovation relative to prior art and competitors.
  • Strategic patent positioning enables effective market exclusivity and licensing opportunities.
  • Monitoring patent validity and legal status is essential for long-term commercial planning.

FAQs

  1. What is the primary focus of patent DK3909966?
    It likely covers a specific pharmaceutical composition, formulation, or treatment method involving a novel API or delivery system designed for therapeutic efficacy.

  2. How broad are the claims typically in such pharmaceutical patents?
    Independent claims are generally broad, covering the core invention, while dependent claims narrow down to specific embodiments, versions, or formulations.

  3. Can DK3909966 be challenged or invalidated?
    Yes. Patent validity can be challenged based on prior art, lack of inventive step, or insufficient disclosure. Oppositions can be filed in Denmark within six months after patent grant.

  4. How does the patent landscape influence the commercial strategy?
    It shapes decisions around market entry, licensing, and R&D investment by delineating the competitive scope and potential infringement risk.

  5. What is the significance of regional patents like DK3909966 in the global drug market?
    Regional patents provide national or local exclusivity, but companies often file for international patents (via PCT or EPO) to secure broader protection and to defend or challenge market positions globally.


References

[1] Danish Patent and Trademark Office (DKPTO). Patent DK3909966 - Details and legal status.
[2] European Patent Office (EPO). Patent family and related filings.
[3] WIPO. Patent landscape reports for the relevant therapeutic areas.
[4] Patent laws of Denmark. Regulatory guidelines for pharmaceutical patents.

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