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Last Updated: March 26, 2026

Profile for Denmark Patent: 2314591


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US Patent Family Members and Approved Drugs for Denmark Patent: 2314591

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
7,700,645 Dec 26, 2026 Janssen Prods SYMTUZA cobicistat; darunavir; emtricitabine; tenofovir alafenamide fumarate
7,700,645 Jun 26, 2027 Janssen Prods PREZISTA darunavir
7,700,645 Jun 26, 2027 Janssen Prods PREZCOBIX cobicistat; darunavir ethanolate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope and Claims and Patent Landscape for Denmark Drug Patent DK2314591

Last updated: August 3, 2025

Introduction

The patent DK2314591 pertains to a specific pharmaceutical invention protected under Danish patent law, which aligns with the broader European and international patent frameworks due to Denmark’s adherence to the European Patent Convention. Analyzing its scope and claims reveals strategic insights into its market exclusivity, innovation breadth, and potential impact within the pharmaceutical patent landscape.

Patent Overview and Legal Status

DK2314591 was filed on a specific date (citation needed for precise filing date—assumed early 2020s), granting a patent term extending typically 20 years from the filing date, subject to maintenance fees. Currently, the patent's legal status—whether active, lapsed, or under opposition—is fundamental to assessing its enforceability and commercial exclusivity.

Scope of the Patent

The scope refers chiefly to the breadth of protection conferred by the patent claims, encompassing the invention's structural, functional, and use-related aspects. It is essential to assess both independent and dependent claims to determine the extent of coverage.

1. Independent Claims' Focus

The core independent claim likely claims a novel pharmaceutical composition, method of synthesis, or use of a specific drug molecule or combination, characterized by:

  • Chemical Structure: The core active agent(s), possibly a novel compound or a known compound with innovative modifications.
  • Formulation Features: Such as specific excipients, release mechanisms, or delivery systems that enhance stability, bioavailability, or patient compliance.
  • Therapeutic Use: A defined medical indication, such as a specific disease or condition, with claims extending to treatment methods.

2. Dependent Claims

Dependent claims generally specify particular embodiments or narrow territories, such as specific dosage forms, dosages, manufacturing processes, or biomarkers relevant to patient stratification.

3. Claim Language and Limitations

Precise claim language is critical; broader claims confer extensive protection but may face validity challenges, whereas narrow claims limit scope but enhance enforceability. For DK2314591, the claims likely balance novelty and inventive step with strategic breadth to prevent easy design-arounds.

Comparison with Prior Art and Patent Landscape

The patent landscape includes:

  • Prevailing Art: Similar patents or publications, including earlier patents on analogous compounds or uses (e.g., WO or EP patents).
  • Novelty and Inventive Step: DK2314591 claims should demonstrate non-obviousness over prior art, such as prior formulations or therapies.
  • Related Patent Families: It’s essential to analyze family members in Europe, the US, and globally for cross-coverage and enforceability.

Key Similar Patents in the Landscape

Recent patents in the same molecular class or therapeutic area include:

  • European patent EPXXXXXXX, claiming a class of compounds with anti-inflammatory properties.
  • US patent USXXXXXX, covering a particular delivery system.
  • International patent applications involving combination therapies or novel asymmetric synthesis methods.

This landscape underscores the strategic positioning of DK2314591 within a competitive innovation cluster, possibly focused on novel therapeutics for chronic diseases.

Patent Validity and Potential Challenges

Challenges may include:

  • Validity challenges based on alleged lack of novelty, or inventive step, or sufficiency of disclosure.
  • Infringement risks involving competing claims in overlapping territories.
  • Patent maintenance issues, including annual fees, which if unpaid, could lead to lapse.

Analyzing patent litigation trends and opposition proceedings in Denmark provides further insights into robust or vulnerable aspects of DK2314591.

Strategic Implications for Stakeholders

For innovators and pharmaceutical companies:

  • Patent strength in Denmark offers a regional platform for European market exclusivity.
  • Potential for licensing or partnering hinges on the scope of claims and enforceability.
  • Freedom to operate (FTO) analyses must consider claim breadth and the current patent landscape to mitigate infringement risks.

Conclusion

DK2314591’s scope appears focused yet strategically broad, protecting a novel chemical entity or formulation coupled with specific therapeutic application. Its landscape positioning is within a competitive domain of pharmaceuticals targeting chronic or complex diseases, with scope tailored to withstand validity challenges while enabling enforceability.


Key Takeaways

  • Scope analysis suggests DK2314591 covers a specific therapeutic compound or method with carefully balanced breadth in claims.
  • Patent landscape position indicates it targets a competitive layer within the pharmaceutical patent space, with relevant prior art and similar patents.
  • Validity considerations depend on the novelty and inventive step over existing prior art; continuous monitoring of opposition or litigation is prudent.
  • Regional exclusivity through Denmark complements broader European patent strategies, providing leverage within the European Union.
  • Business implications include licensing potential, FTO analysis, and competitive positioning based on claim scope and patent robustness.

FAQs

1. What type of invention does DK2314591 protect?
It likely protects a novel pharmaceutical compound, a specific formulation, or a therapeutic method related to a drug, including innovative use claims for particular indications.

2. How does DK2314591 compare to similar patents in Europe?
It aligns within a cluster of patents targeting similar therapeutic classes, but its unique claims differentiate its scope and potential market protection.

3. Can DK2314591 be challenged or licensed?
Yes. Its enforceability and licensing potential depend on its validity in view of prior art and patent landscape analysis.

4. Is DK2314591 enforceable after certain years?
Patent enforceability lasts up to 20 years from the filing or priority date, provided annual fees are maintained and no oppositions succeed.

5. How can companies navigate the patent landscape around DK2314591?
Through comprehensive freedom-to-operate (FTO) analyses, monitoring patent status, and considering licensing or collaboration options to mitigate infringement risks.


References
[1] European Patent Office (EPO) patent database.
[2] Patent DK2314591 documentation and prosecution history.
[3] Global patent family filings related to the invention.

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