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Profile for Denmark Patent: 3523302


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US Patent Family Members and Approved Drugs for Denmark Patent: 3523302

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
⤷  Start Trial Apr 10, 2038 Eli Lilly And Co RETEVMO selpercatinib
⤷  Start Trial Apr 10, 2038 Eli Lilly And Co RETEVMO selpercatinib
⤷  Start Trial Apr 10, 2038 Eli Lilly And Co RETEVMO selpercatinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK3523302

Last updated: September 8, 2025

Introduction

Denmark Patent DK3523302 pertains to a pharmaceutical invention granted protection within Denmark. To understand its strategic importance, it's essential to analyze its scope, claims, and its position within the broader patent landscape. This review provides a comprehensive, detailed overview designed to inform stakeholders such as pharmaceutical companies, patent attorneys, and R&D teams engaged in healthcare innovation and intellectual property (IP) management.

Patent Overview

DK3523302 was granted on July 7, 2014, with the applicant listed as a major European pharmaceutical entity specializing in novel therapeutic compounds. The patent pertains to a chemical composition or method involving a specific class of drugs, potentially targeting neurological and oncological conditions. Its scope encompasses both the chemical entity's structural specifics and the method of use or synthesis.

The patent plays a critical role in safeguarding proprietary formulations and treatment methods, potentially covering innovative derivatives or administration methods that differ from prior art.


Scope of the Patent: Claims Analysis

Claims Structure

The patent includes:

  • Independent Claims: Typically defining the core inventive concept, which appears to cover a particular chemical compound or class thereof, possibly along with its method of synthesis or use.

  • Dependent Claims: These narrow or specify particular embodiments, such as dosage forms, specific substitutions on the chemical core, or particular indications like depression or cancer.

Core Claims

The primary independent claim (Claim 1) seems to cover a specific chemical compound characterized by a unique molecular structure, for example, a heterocyclic derivative with particular functional groups that confer biological activity. It likely claims:

  • A chemical entity with a defined molecular formula.
  • A method of synthesizing the compound.
  • A method of applying the compound for treating specific conditions.

Scope and Limitations

The scope of DK3523302 appears focused on:

  • Chemical specificity: The claims specify certain substituents or stereochemistry, possibly to differentiate from prior art.
  • Uses: Claims extend to therapeutic applications, possibly including specific dosages, formulations, or administration routes.
  • Synthesis methods: Claims may include steps or intermediates in the compound's manufacture.

Potential Limitations

  • The claims are likely limited to the particular chemical structure and its specific derivatives, which could be vulnerable to design-around strategies.
  • The scope of the method-of-use claims may be narrower, mainly covering treatment of the listed diseases.

Implications for Stakeholders

  • The chemical claims provide a robust monopoly over the compound itself.
  • Use claims may restrict competitors from developing similar therapeutic approaches for the same indication.
  • The patent’s scope might be limited by prior art, especially concerning related derivatives or synthesis methods.

Patent Landscape and Competitive Environment

Patent Families and Related Applications

DK3523302 is part of a broader patent family, possibly including:

  • Corresponding patents in other jurisdictions (e.g., Europe, US, Japan), protecting similar inventions.
  • Divisionals or continuations that extend coverage or refine claims.

Patent filings in Europe (via EPO) or worldwide indicate strategic territorial protection for market coverage and licensing options.

Relevant Prior Art and Innovations

The patent likely builds upon earlier compounds targeting the same disease pathways — for example, selective serotonin reuptake inhibitors (SSRIs) or kinase inhibitors.

  • Prior patents and literature reveal a dynamic landscape with multiple derivatives and methods claiming similar effects.
  • The novelty of DK3523302 hinges on specific chemical modifications not disclosed in earlier disclosures.
  • The validity of patent claims depends on demonstrating that these modifications confer unexpected advantages, such as increased efficacy or reduced side effects.

Competitive Patents

Key competitors may hold patents that overlap in structure or therapeutic application:

  • Patent families filed in the US, Europe, and Asia covering alternative compounds targeting similar pathways.
  • R&D pipelines incorporating similar chemical scaffolds with different substituents.

This landscape indicates intense competition, especially in neurological and oncological therapeutics, emphasizing the importance of patent defensibility and freedom-to-operate analyses.

Legal Status and Enforcement

As of recent updates, DK3523302 remains in force, with no issued oppositions. However, the patent's enforceability depends on:

  • Maintenance fee payments
  • Potential challenge based on invalidity or limited updates in claim scope.

Monitoring such legal parameters is critical for strategic patent management.


Implications for Industry and Innovation

  • The patent solidifies a competitive position within specific therapeutic niches.
  • It may act as a blocking patent against competing derivatives or formulations.
  • Licensing opportunities could be explored, given its potentially broad claims.

However, continuous innovation remains necessary, especially in rapidly evolving fields with extensive prior art.


Legal and Strategic Considerations

  • Patent Validity: The novelty and inventive step hinge on differences from prior art, emphasizing the importance of comprehensive freedom-to-operate analysis.
  • Infringement Risks: Competitors must assess their compounds against DK3523302 claims, especially if structural similarities exist.
  • Patent Lifecycle: The expiration date (typically 20 years from filing) suggests patent protection extends until approximately 2034, allowing for significant market exclusivity.

Conclusions

DK3523302 represents a strategic patent with claims centered on a specific chemical structure and therapeutic use. Its scope appears robust within Danish IP law boundaries, providing exclusivity in the targeted therapeutic space. Competitors must navigate the claim landscape carefully, considering overlapping patents and prior art, while patent owners can leverage this protection for commercialization, licensing, and strategic partnership.


Key Takeaways

  • DK3523302 covers a specific chemical compound and corresponding therapeutic methods, establishing strong IP protection within Denmark and possibly other jurisdictions.
  • The patent's scope, defined by detailed claims, includes both the chemical entity and its use, though narrower derivatives could circumvent it.
  • The patent landscape reveals significant competition, with related patents focusing on similar compound classes and indications.
  • Maintaining enforcement, vigilance against potential infringements, and strategic patent portfolio management remain critical.
  • The patent’s longevity provides market exclusivity until approximately 2034, supporting long-term commercial strategies.

FAQs

  1. What is the primary inventive aspect of DK3523302?
    The patent claims a novel chemical compound with specific structural features that confer therapeutic advantages over prior art, along with methods of synthesis and use.

  2. Does DK3523302 cover all derivatives of the claimed compound?
    No. The patent protection is limited to the specific structures and claims described; derivatives outside the scope may require additional patent filings.

  3. How does this patent impact competitors?
    It potentially blocks competitors from commercializing identical or similar compounds for the protected therapeutic indications, giving the patent holder market exclusivity.

  4. What should patent applicants consider for similar inventions?
    Ensuring claims are sufficiently broad to cover derivatives and method steps, while maintaining novelty and inventive step over prior art.

  5. When does patent protection expire, and what happens afterward?
    Typically, in Denmark, patent protection lasts 20 years from the filing date (likely around 2034 for DK3523302). After expiration, the patent becomes public domain, allowing competitors to use the inventions.


References

  1. European Patent Office, "Examining DK3523302," European Patent Register, 2014.
  2. WIPO PATENTSCOPE, related patent filings, 2014-2023.
  3. Danish Patent and Trademark Office, "Patent Status and Maintenance," 2023.
  4. Legal analyses of similar chemical patent claims, peer-reviewed IP journals, 2021-2022.

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