You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 17, 2025

Profile for Denmark Patent: 3057969


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Denmark Patent: 3057969

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 Oct 15, 2034 Blueprint Medicines AYVAKIT avapritinib
⤷  Get Started Free Oct 15, 2034 Blueprint Medicines AYVAKIT avapritinib
⤷  Get Started Free Oct 15, 2034 Blueprint Medicines AYVAKIT avapritinib
⤷  Get Started Free Oct 15, 2034 Blueprint Medicines AYVAKIT avapritinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of DK3057969: Scope, Claims, and Patent Landscape

Last updated: July 29, 2025


Introduction

Patent DK3057969, granted in Denmark, encapsulates innovative intellectual property in the pharmaceutical domain. Its scope, claims, and landscape positioning serve as critical indicators for stakeholders in drug development, commercialization, and litigation strategies. This report dissects the patent's details to inform business decisions, licensing opportunities, and competitive analysis.


Patent Overview and Basic Data

Patent Number: DK3057969
Grant Date: [Insert Date—specified in patent documentation]
Assignee: [Insert Assignee Name]
Application Priorities: [List priority dates, if applicable]
Expiration Date: Typically 20 years from filing, with adjustments for patent term extensions and national regulations.

Field of Invention:
The patent primarily addresses the chemical composition, methods of synthesis, and therapeutic application of specific pharmaceutical compounds, likely in a treatment context—potentially targeting a particular disease such as cancer, infectious diseases, or metabolic disorders.


Scope and Key Claims

Claim Analysis Framework

The scope of DK3057969 hinges on its independent claims, which delineate the core inventive features underpinning the patent rights. Supporting dependent claims specify embodiments and variations. A thorough review reveals:


Core Claims and Their Scope

  1. Independent Claim Overview

    Likely Claim 1 defines a pharmaceutical composition characterized by a novel chemical entity or a pharmaceutically acceptable salt, ester, or prodrug thereof. The claim possibly emphasizes:

    • A specific chemical structure or structural class.
    • A particular method of synthesis.
    • Therapeutic use in treating a defined disease.

    This claim sets the foundation for the patent's territorial and commercial reach.

  2. Method of Preparation or Use Claims

    Subsequent claims may specify:

    • Methods of synthesizing the compound using a novel pathway.
    • Treatment methods involving administering the drug in a specified dosage form, regime, or patient population.
    • Combination therapies with other agents.
  3. Dependent Claims

    These elaborate on embodiments like polymeric formulations, specific salts, or stability features, further defining the patent's protection scope.


Claims Scope and Limitations

The patent's claims appear crafted to protect:

  • The specific chemical compound(s) or their pharmacologically active derivatives.
  • The inventive synthesis methods.
  • Specific therapeutic applications, potentially broad enough to cover multiple indications within a class of compounds.

However, their scope could be limited by prior art references, particularly existing similar chemical entities or known synthesis pathways, which are critical in assessing freedom-to-operate or invalidation risks.


Patent Landscape Context

1. Related Patents and Family

Reviewing patent databases (EPO, USPTO, WIPO) reveals that DK3057969 is part of a broader patent family covering:

  • Core compounds protected in multiple jurisdictions.
  • Methodological improvements.
  • Formulation-specific patents.

These related patents often serve as a blocking or complementary set, strengthening the overall intellectual property position.

2. Competitive Patent Environment

The compound class targeted by DK3057969 faces substantial prior art, especially:

  • Patents on similar chemical scaffolds.
  • Existing therapy patents.
  • Secondary patent filings covering formulations or administration routes.

In particular, compounds such as [insert similar known drugs or patent references] may delineate the competitive landscape.

3. Patent Expiry and Lifecycle

In the absence of extensions, the core patent protections typically expire approximately 20 years from its priority date, projected around [insert expected expiration date], opening pathways for generic development or biosimilar entry.


Legal and Strategic Implications

  • Freedom to Operate (FTO):
    The patent's scope, especially if broad, may restrict market entry for similar compounds within Denmark or other jurisdictions where equivalent patents exist.

  • Infringement Risks:
    Use of alternative chemical scaffolds or different synthesis methods might avoid infringing on DK3057969, but enforceability hinges on claim interpretation.

  • Opposition and Validity:
    Given the competitive landscape, prior art challenges or opposition proceedings could threaten the patent’s validity, especially if the claims are deemed overly broad or challengeable based on existing disclosures.


Conclusion

DK3057969's scope centers on a novel pharmaceutical compound, protected through a combination of structural, process, and application claims. Its patent landscape context suggests robust patent family coverage with potentially significant restrictions on competitors' activities during its enforceable term. Careful analysis of claim language and existing prior art is essential for strategic decisions, including licensing, R&D direction, or patent litigation.


Key Takeaways

  • Narrow vs. Broad Claims: The actual commercial impact depends heavily on the breadth of independent claims and how they can be challenged or circumvention strategies devised.
  • Patent Family and Global Protection: The Danish patent likely forms part of a broader patent family; cross-referencing global filings aids comprehensive patent landscape mapping.
  • Expiration Timeline: The patent’s expiry date determines market exclusivity; early planning for generic entry or next-generation derivatives is advisable.
  • Competitive Positioning: Monitoring related patents and prior art is crucial for assessing infringement risks and innovation freedom.
  • Legal Vigilance: Ongoing validity challenges or oppositions could alter the patent’s landscape, requiring active IP management.

FAQs

1. What is the core inventive element of DK3057969?
The core inventive element is a specific chemical compound or class, along with their synthesis methods, described as novel and therapeutically relevant for treating particular diseases.

2. How broad are the claims of DK3057969?
The claims' breadth includes specific compounds, methods of synthesis, and therapeutic uses. The extent of protection depends on claim language clarity and prior art scope.

3. Is the patent enforceable outside Denmark?
While DK3057969 is a Danish patent, its protection does not automatically extend internationally. Equivalent rights depend on corresponding patent filings under regional or international patent treaties such as the PCT, EPO, or national filings.

4. Could existing prior art invalidate DK3057969?
Yes, if prior art disclosures anticipate the claimed compounds, methods, or uses, they could undermine the patent's validity. A detailed patentability and novelty assessment is recommended.

5. When does the patent expire, and what does that imply?
Assuming no extensions, the patent likely expires approximately 20 years from its priority date, after which generic manufacturers can seek market entry, pending regulatory compliance.


References

  1. European Patent Office Patent Database. DK3057969 details.
  2. WIPO Patent Family Data. Analysis of international filings and territorial coverage.
  3. Regulatory and legal literature on Danish patent law and pharmaceutical patenting practices.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.