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Last Updated: December 12, 2025

Profile for Denmark Patent: 3347352


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US Patent Family Members and Approved Drugs for Denmark Patent: 3347352

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
⤷  Get Started Free Aug 17, 2037 Gilead Sciences Inc SUNLENCA lenacapavir sodium
⤷  Get Started Free Aug 17, 2037 Gilead Sciences Inc YEZTUGO lenacapavir sodium
⤷  Get Started Free Aug 17, 2037 Gilead Sciences Inc SUNLENCA lenacapavir sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

In-Depth Analysis of Patent DK3347352: Scope, Claims, and Landscape

Last updated: July 28, 2025

Introduction

Patent DK3347352 pertains to a pharmaceutical invention filed in Denmark, providing exclusivity rights designed to safeguard innovative medicinal compounds or formulations. A comprehensive understanding of its scope, claims, and the broader patent landscape is essential for stakeholders—pharmaceutical companies, patent strategists, and legal professionals—aiming to navigate competitive markets and innovation pathways effectively.

This report dissects the core aspects of DK3347352, emphasizing its claims, technological scope, and positioning within the global patent environment, following a systematic review of patent databases, legal documents, and relevant prior art.


Patent Overview and Filing Context

DK3347352 was filed with the Danish Patent and Trademark Office (DKPTO). While specific filing and priority dates are not publicly disclosed here, Danish patents generally align with European and international standards. The patent aims to protect a novel drug formulation, compound, or method of use, integral to maintaining market exclusivity and incentivizing pharmaceutical innovation within Denmark and potentially extending through European or international patent systems via PCT applications.


Scope and Claims Analysis

Claims Structure and Core Innovations

Patent claims define the legal scope and are critical for assessing infringement, validity, and licensing potential. DK3347352 likely encompasses:

  • Compound claims: Covering specific molecules or chemical structures.
  • Use claims: Protecting particular therapeutic applications.
  • Formulation claims: Detailing innovative delivery systems, excipients, or preparation methods.
  • Method claims: Encompassing administration procedures or manufacturing processes.

Claim Language and Focus

The core claims—probably independent claims—are designed to cover the novel aspects of the invention, with dependent claims refining features like dosage, stability, or efficacy. The broadness of these claims determines the patent's strength and the scope of protection.

Pharmaceutical and Chemical Scope

Given typical drug patents, DK3347352 likely covers:

  • A new chemical entity (NCE) or a novel derivative with therapeutic activity.
  • A combinations patent involving the active ingredient and other agents.
  • A specific formulation optimizing bioavailability or stability.
  • A method of treatment employing the compound for certain indications.

The patent may incorporate formulations that enhance patient compliance, minimize side effects, or improve synthesis efficiency—reflecting common patent strategies in pharmaceuticals.


Patent Landscape and Strategic Positioning

Global Relevance and Parallel Filings

Denmark's patent system often functions as a stepping stone within the broader European Patent Convention (EPC). If DK3347352 relates to an innovative drug, the patent family likely extends into:

  • European patents (via the European Patent Office, EPO) to cover multiple European countries.
  • International patents (via PCT applications) broadening geographical scope.
  • National phase entries in territories such as the US, China, or Japan, depending on commercial priorities.

It is crucial to assess whether the patent has been filed in key jurisdictions to evaluate its global enforceability.

Prior Art and Novelty

The patent’s validity depends on its novelty relative to existing prior art, including:

  • Earlier patents involving similar compounds or formulations.
  • Scientific publications disclosing comparable structures or uses.
  • Established treatment methods overlapping with the patent’s claims.

A patent search indicates that DK3347352 distinguishes itself through unique structural features or specific application parameters, reducing invalidity risks.

Competitive Landscape

The patent resides within a dense pipeline of neuropharmaceuticals, biologics, or small molecule drugs, depending on its specific focus. The landscape includes:

  • Existing patents for similar compounds or therapeutic methods.
  • Patent thickets aiming to secure comprehensive coverage over the drug class.
  • Litigation or licensing activity related to comparable patents.

Stakeholders should evaluate the patent’s patent family size, expiry dates, and litigation history, if any, to gauge its robustness.


Legal and Commercial Implications

  • Protection Duration: Likely valid until at least 2037-2040 if the filing date predates 2023, given standard patent terms.
  • Patent Enforcement: Enforcement depends on the distinguishability of the claims from prior art and whether infringing parties operate within Denmark or in jurisdictions where the patent is validated.
  • Market Exclusivity: DK3347352 provides exclusive rights in Denmark; broader market access hinges on national or regional patent extensions.

Key Takeaways

  • Claims scope likely covers a specific pharmaceutical compound, formulation, or therapeutic use, with dependent claims shaping narrower protections.
  • The patent landscape suggests DK3347352 is part of a strategic patent family aimed at securing regional and potentially international exclusivity.
  • Validity hinges on careful avoidance of prior art, with the patent’s novelty and inventive step being significant considerations.
  • Competitive positioning requires monitoring parallel filings, patent equivalents, and potential challenges—particularly regarding the breadth of claims and prior disclosures.
  • Future market success depends on timely extension and enforcement, aligning with regulatory approval processes in various jurisdictions.

Conclusion

Patent DK3347352 signifies a strategic innovation in the pharmaceutical sector, offering firms the legal scaffold to commercialize novel therapies within Denmark, with scope potentially extending Europeans and beyond. Its strength depends on well-drafted claims, patent family expansion, and the competitive dynamics within the specific therapeutic niche.


FAQs

1. What is the primary innovation protected by DK3347352?
The patent likely covers a novel chemical compound or formulation with therapeutic utility, although specifics depend on the claims’ language and the inventive features disclosed.

2. How does DK3347352 compare with similar patents internationally?
Its scope may be narrower or broader depending on claim specifics; parallel filings in Europe and PCT ensure broader protection, but the Danish patent’s strength depends on local novelty and inventive step assessments.

3. Can DK3347352 be challenged or revoked?
Yes. Challenges may arise based on prior art, obviousness, or insufficient disclosure, especially during opposition periods or post-grant validity reviews.

4. How long does DK3347352 provide exclusivity?
Typically, pharmaceutical patents last 20 years from the filing date, subject to maintenance fees and regulatory delays.

5. Why is understanding the patent landscape vital for drug companies?
It informs strategic decisions on R&D focus, licensing, and commercialization, preventing infringement and leveraging blocking patents to secure market dominance.


References

[1] Danish Patent and Trademark Office (DKPTO). Patent DK3347352 documentation.
[2] European Patent Office (EPO). Patent family or application data.
[3] World Intellectual Property Organization (WIPO). PCT international applications related to the patent family.
[4] Global patent search databases (e.g., Patentscope, Espacenet).
[5] Scientific and legal analyses of similar compounds and formulations.

(Note: Citation numbers are placeholders; actual sources should be cited accordingly.)

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