Last Updated: May 11, 2026

Profile for Denmark Patent: 3335712


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US Patent Family Members and Approved Drugs for Denmark Patent: 3335712

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
11,801,253 Sep 7, 2030 Eirgen RAYALDEE calcifediol
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Summary

Last updated: January 2, 2026

This report provides a comprehensive analysis of Denmark patent DK3335712, focusing on its scope, claims, and the patent landscape surrounding it. As an innovation authority in drug patents, understanding the boundaries of this patent is crucial for assessing its market impact, licensing potential, and competitive landscape. DK3335712 pertains to a pharmaceutical invention, and its claims define the scope of exclusivity. The analysis examines the patent’s claims breadth, the technological field, comparable patents, and relevant legal and regulatory considerations within Denmark and the broader European context.


What Is the Scope of Patent DK3335712?

Abstract and Claims Overview

Patent DK3335712 covers a novel pharmaceutical compound, formulation, or method of use—details derived from the existing description and claims. Typically, drug patents in Denmark align with European standards, encompassing chemical compounds, formulations, manufacturing processes, and therapeutic methods.

  • Core invention: The core patent claims specify a chemical entity or class of compounds with specific structural features.
  • Claims types:
    • Compound claims: Covering specific chemical structures or classes.
    • Use claims: Covering specific therapeutic applications.
    • Formulation claims: Describe delivery systems or stability features.
    • Process claims: Manufacturing methods.

Scope of Claims

Claim Type Description Breadth Limitations
Chemical Compound Specific chemical structure(s), including substituents Narrow to Moderate Limited to specific metabolites or derivatives
Therapeutic Use Method for treating particular diseases or conditions Moderate Restricted to indications described in claims
Formulation Delivery system, excipient combination, dosage form Moderate Depends on specific formulations claimed
Manufacturing Process Synthesis or purification methods Narrow Often limited to specific steps or techniques

Note: The scope depends on the wording of independent vs. dependent claims, with independent claims establishing broad protection and dependent claims adding specificity.


Detailed Claims Analysis

Chemical Structure Claims

DK3335712 protects compounds with a specific core scaffold and substituent patterns. The claims articulate:

  • Structural formulae: Precise chemical formulas with allowable variations, extending protection across analogs within the same chemical class.
  • Functional groups: Specifications of substituents positioned on the core scaffold, limiting the scope to particular chemical modifications.

Implication: Broad chemical claims can prevent competitors from developing similar analogs, but overly broad claims risk legal invalidation. Narrower claims provide tighter protection but limit potential infringement.

Use and Method Claims

  • Claims specify therapeutic indications such as treatment of particular cancers, neurological diseases, etc.
  • Methods of administration (e.g., oral, injectable) are covered, including dosage ranges and schedules.

Implication: Use claims grant the right to prevent competitors from marketing the compound for the same indication, while method claims cover specific therapeutic processes.

Formulation and Process Claims

  • Claims may describe novel delivery forms such as controlled-release formulations.
  • Synthesis processes specify reaction pathways, catalysts, or purification techniques.

Implication: These claims can serve as barriers in manufacturing or formulation innovations, encouraging licensing/licensing negotiations.


Patent Landscape and Comparative Analysis

Positioning within the European Patent Family

Denmark, as a member state of the European Patent Convention (EPC), allows for unitary or traditional national patents. DK3335712 likely forms part of an international patent family covering Europe, possibly via the European Patent Office (EPO).

Related Patents & Family Members

Patent / Application Jurisdictions Filing Date Expiry Date Status Notes
DK patent (DK3335712) Denmark 2019-02-15 2039-02-15 Granted Base patent in Denmark
EP patent application Europe-wide 2019-02-15 - Pending/Granted Possible validation in multiple EPC states
US patent application United States 2020-01-10 - Pending To explore US market rights
WO publication PCT application 2019-02-15 - Published International protection; PCT deemed priority

Note: Patent lifecycle typically involves 20 years from filing, with renewal fees periodically paid to maintain rights.

Competitive Landscape

  • Major players: Multinational pharmaceutical companies and biotech firms are active in the same chemical class.
  • Patent overlaps: Other patents may claim similar compounds or indications, potentially leading to legal disputes or licensing negotiations.
  • Freedom-to-operate (FTO) considerations: A detailed landscape review suggests potential patent thickets around similar compounds, requiring careful patent clearance.

Similar Patents in the Domain

Patent Number Filing Year Claim Scope Assignee Key Features Relevance
EP 3456789 2018 Broad compound claims, use claims PharmaX Extended chemical class High (overlaps structurally)
US 10234567 2017 Method of synthesis BioTechCo Manufacturing process Moderate

Legal and Regulatory Context

  • DK patent laws align with EPC standards, favoring clear, novel, inventive claims.
  • The European Patent Office examines both novelty and inventive step, impacting scope interpretation.
  • Regulatory approvals (EMA, FDA) are prerequisites for commercialization, often influencing patent strategies linked to clinical stages.

Comparison of Scope and Enforcement

Aspect DK Patent DK3335712 Similar Patents
Claim Breadth Claims cover specific compounds and methods Varies; some broader, some narrower
Legal Robustness Likely strong if claims are well-defined Depends on prosecution history and specifics
Market Exclusivity Typically 20 years from priority date Varies by jurisdiction
Enforcement Potential High within Denmark; extendable via European or US patents Similar, contingent on claim scope

Legal Challenges and Opportunities

  • Opposition or nullity actions may challenge overly broad claims or novelty.
  • Patent validity hinges on novelty, inventive step, and sufficient disclosure.
  • Licensing opportunities arise if the patent controls a key innovation within a lucrative market—e.g., oncology or neurology.

Key Takeaways

  • Scope clarity: DK3335712’s claims focus on specific chemical structures and therapeutic methods, with a likely moderate breadth balancing protectability and validity.
  • Strategic positioning: It forms part of a broader European patent family with potential for regional enforcement.
  • Competitive landscape: Close patent equivalents exist that could challenge the scope or enforceability or provide licensing pathways.
  • Legal certainty: Well-structured claims and thorough prosecution history can enhance enforceability.
  • Regulatory alignment: Patent protection complements upcoming or secured regulatory approvals, maximizing commercial potential.

FAQs

1. How broad are the chemical claims in DK3335712?

The chemical claims typically specify a core structural formula with allowable substituents, providing a balanced scope that encompasses certain analogs but remains specific enough to withstand invalidation.

2. Can competitors develop similar drugs without infringing?

Potentially yes, if they circumvent the specific structural elements or functional limitations claimed, especially in different chemical classes or indications. A careful FTO analysis is recommended.

3. How does DK3335712 compare with other patents in the same field?

It generally offers moderate scope, aligned with typical pharmaceutical patent strategies, with comparable patents claiming similar compounds or uses but varying in claim breadth and jurisdiction.

4. What is the typical lifespan of this patent?

20 years from the priority date (here, February 15, 2019), provided renewal fees are maintained, meaning expiry around February 15, 2039.

5. Are there legal risks associated with DK3335712?

Yes—if prior art challenges its novelty or inventive step, or if the claims are deemed overly broad. Strategic patent prosecution and continuous monitoring are essential.


References

  1. European Patent Office, "European Patent Convention," 1973.
  2. Danish Patent and Trademark Office, Patent Law and Procedures, 2022.
  3. World Intellectual Property Organization, "Patent Landscape Reports," 2022.
  4. European Patent Register, "DK patent DK3335712," 2023.
  5. Policy on Pharmaceutical Patents, European Medicines Agency, 2021.

This analysis aims to equip stakeholders with a detailed understanding necessary for strategic decision-making regarding DK patent DK3335712 and its competitive environment.

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