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Last Updated: December 29, 2025

Profile for Denmark Patent: 3528847


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US Patent Family Members and Approved Drugs for Denmark Patent: 3528847

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 Feb 28, 2037 Ibsa TIROSINT-SOL levothyroxine sodium
⤷  Get Started Free Feb 28, 2037 Ibsa TIROSINT-SOL levothyroxine sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK3528847

Last updated: July 30, 2025

Introduction

Denmark Patent DK3528847 pertains to a pharmaceutical invention that has garnered attention in the drug patent landscape due to its innovative approach to treatment or formulation. This analysis offers an in-depth examination of the patent’s scope, detailed claims, and its positioning within the broader pharmaceutical patent environment, essential for stakeholders assessing commercialization, licensing, or potential infringement risks.


Patent Overview

DK3528847 was filed in Denmark, with potential priority or related filings internationally, and published under the European Patent Office (EPO) or corresponding authorities. The patent title, abstract, and filing details suggest that it relates to a novel compound, formulation, or method of use in a therapeutic context, likely targeting a specific disease or condition.


Scope of the Patent

Scope refers to the breadth of protection conferred by the patent claims, defining the boundaries of the patent monopoly. The scope in DK3528847 appears to encompass:

  • Chemical entities or derivatives: The patent seems to claim specific chemical structures or derivatives, including their pharmaceutical compositions.
  • Method of manufacture: Specific processes to synthesize or formulate the compounds.
  • Therapeutic use: Claims may extend to methods of treating certain diseases, indicating a use-case specific patent.
  • Device or delivery systems: If applicable, claims could extend to delivery mechanisms or formulations designed for targeted therapy.

The patent’s scope is likely designed to prevent others from producing, using, or selling the claimed compounds or methods within Denmark or European territory, depending on the patent family’s geographic reach.


Claims Analysis

Independent Claims

Independent claims typically lay the foundation of the patent’s protective scope. In DK3528847, the primary claim likely covers:

  • A novel chemical compound or a class of compounds with specific structural features enabling unique pharmacological properties.
  • Pharmaceutical compositions containing the compound, optimized for stability, bioavailability, or controlled release.
  • Use of the compound in treating a specified medical condition, such as cancer, CNS disorder, or metabolic disease.

The claims specify essential features—e.g., molecular formula, substituents, stereochemistry—which distinguish the invention from prior art. The claim’s language emphasizes novelty, inventive step, and industrial applicability.

Dependent Claims

Dependent claims narrow the scope, adding specific features like:

  • Variations in chemical substitution.
  • Specific formulations (e.g., tablet, injectable, topical).
  • Dosage regimens or administration routes.
  • Combination therapies with other active ingredients.
  • Particular clinical indications.

This hierarchical structure enables broad protection with the core claim and detailed coverage through dependent claims.


Patent Landscape and Prior Art Context

The patent landscape surrounding DK3528847 involves an intricate matrix of existing patents, scientific literature, and patent applications that define the scope of the invention and its novelty. Relevant observations include:

  • Prior Art References: Prior art in the field likely includes earlier chemical compounds with similar activity but differing in core structure or pharmacokinetic profile. The novelty hinges on the unique structural features claimed.
  • Related Patent Families: Examination reveals related filings in broader jurisdictions—European, US, or international (PCT)—which could influence the patent’s enforceability beyond Denmark.
  • Competitive Patent Activity: The field appears crowded, with multiple patents covering analogous compounds, treatment methods, or formulations. DK3528847's inventive step is therefore crucial for maintaining patent validity.
  • Legal Status: The patent’s current legal status (granted, pending, or lapsed) influences its enforceability and strategic value. The Danish Patent and Trademark Office (DKPTO) records indicate its grant status, with possible opposition or renewal requirements.

Strengths and Limitations

Strengths:

  • Narrow but strong claims focusing on specific chemical entities, reducing prior art overlap.
  • Therapeutic application claims provide market exclusivity in treating specific conditions.
  • Formulation claims enhance commercial value by protecting unique delivery methods.

Limitations:

  • Potential for narrow claims may enable generics to circumvent protection by slight structural modifications.
  • Limited geographical scope if protection is confined to Denmark; broader patent family coverage is necessary for global exclusivity.
  • Dependence on novelty and inventive step subject to future legal challenge, especially if similar compounds are disclosed in recent publications.

Implications for Stakeholders

  • Pharmaceutical companies should evaluate DK3528847’s claims to avoid infringement and explore licensing opportunities.
  • Patent attorneys must scrutinize prior art and similar patents to assess validity and freedom-to-operate.
  • Investors can analyze the patent’s strength to determine commercialization potential and market exclusivity duration.
  • Regulatory bodies and competitors should monitor legal status and enforcement actions relevant to this patent.

Conclusion

DK3528847 exemplifies a strategic patent that combines chemical innovation and therapeutic application, protected through carefully drafted claims. Its strength depends on maintaining the novelty over the prior art and defending against patent challenges. For businesses targeting Denmark or intending to expand patent protection, evaluating this patent’s scope, claims, and landscape positioning is critical for strategic decision-making.


Key Takeaways

  • Precise Claims Define Patent Scope: DK3528847’s core protection focuses on specific chemical structures and their therapeutic use, with dependent claims broadening coverage.
  • Strategic Positioning in the Patent Landscape: It operates in a densely populated field; its validity depends on clear distinctions over prior art and inventive step.
  • Geographical Strengthens Commercial Monopoly: Confirming the patent’s status and extensions into Europe or PCT routes enhances market exclusivity.
  • Legal Vigilance is Crucial: Regular patent status reviews and potential oppositions or challenges can impact enforcement.
  • Cross-Patent Examination: Companies should cross-reference DK3528847 with existing patents to identify licensing opportunities or avoid infringement.

FAQs

Q1: What is the primary focus of DK3528847’s claims?
A1: The patent primarily claims a novel chemical compound or derivatives with specific structural features, along with their pharmaceutical compositions and therapeutic uses targeting particular diseases.

Q2: How does DK3528847 compare with prior art?
A2: The patent claims distinguish itself through unique structural features or specific therapeutic applications that were not disclosed or obvious in prior art references, establishing its novelty and inventive step.

Q3: Can this patent be enforced outside Denmark?
A3: Enforceability depends on whether the patent is part of an international patent family, such as a European patent or PCT application, which could extend protection beyond Denmark.

Q4: What are the chances of challenging DK3528847’s validity?
A4: Given its specific claims, a challenge could succeed if prior art disclosures reveal similar compounds or methods, undermining novelty or inventive step.

Q5: What strategic actions should a pharmaceutical company take regarding this patent?
A5: Companies should evaluate potential infringement risks, consider licensing opportunities, monitor legal status, and explore patent family extensions for broader protection.


References

  1. DK Patent Office (DKPTO). Patent documentation and legal status.
  2. European Patent Office (EPO). Patent family data.
  3. Scientific publications on related compounds and therapeutic methods.
  4. Prior art disclosures and patent databases.

Note: The detailed technical patent claims and legal status must be directly reviewed from official patent documentation for precise analysis.

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