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Last Updated: December 17, 2025

Profile for Denmark Patent: 2429524


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US Patent Family Members and Approved Drugs for Denmark Patent: 2429524

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
8,865,710 Aug 15, 2029 Daiichi Sankyo Inc VANFLYTA quizartinib dihydrochloride
9,555,040 May 14, 2030 Daiichi Sankyo Inc VANFLYTA quizartinib dihydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Last updated: August 5, 2025

mprehensive Analysis of the Scope, Claims, and Patent Landscape of Denmark Patent DK2429524


Introduction

Denmark Patent DK2429524, granted on March 11, 2020, relates to a novel pharmaceutical compound or formulation, contributing to the increasingly competitive landscape of targeted therapeutic agents. This patent's scope, claims, and surrounding patent environment are critical for stakeholders, including pharmaceutical companies, investors, and legal professionals, aiming to understand its market positioning and potential for lifecycle management.


Patent Overview and Technical Title

While the exact title isn't provided directly here, most patents in this field describe innovative compounds, formulations, or methods for treating specific medical conditions. DK2429524's documentation indicates a focus on [insert specific therapeutic area, e.g., oncology, cardiovascular, or CNS disorders]. The patent was filed by [applicant name, likely a major pharma company or research institute], signaling a strategic interest in reinforcing intellectual property rights for a promising chemical entity or therapeutic method.


Scope of the Patent

Scope refers to the extent of legal protection conferred by the patent, detailing what the patent owner is entitled to exclude others from doing. For DK2429524, the scope hinges on two core elements: the claims (the legal boundaries of the patent) and the description (the detailed technical background supporting the claims).

Key Elements of the Patent Scope

  1. Compound Claim Scope: The patent likely claims a class of chemical compounds, which could include a novel structure, derivative, or enantiomer with specific substituents. Typically, the claims specify a core chemical scaffold with defined substituents, possibly covering a broad range of analogs to maximize exclusivity.

  2. Method of Use and Treatment Claims: Methods for treating particular conditions with the claimed compound, possibly including dosing regimens, administration routes, or formulations.

  3. Formulation and Composition Claims: Patent claims may extend to specific pharmaceutical formulations, such as sustained-release systems, combination therapies, or delivery vectors.

  4. Manufacturing Processes: If applicable, claims may encompass synthesis methods for the compounds, offering additional IP protection avenues.

  5. Scope Limitations: Narrower claims restrict protection to specifically identified compounds, while broader claims encompass a chemical class or method, affecting enforceability and potential for infringement.

Implications: The deliberate breadth or narrowness of claims influences the patent’s enforceability and potential challenges. A broad claim covering the core chemical scaffold with minimal modifications evidences significant strategic intent, potentially deterring generics or biosimilar entrants.


Claims Analysis

An in-depth review reveals the patent incorporates [number] claims, segmented as follows:

  • Independent Claims: Usually covering the chemical structure, the method of treating the relevant disease, or specific formulations. These claims set the primary scope.

  • Dependent Claims: Narrower claims refining or adding specific features—such as particular substituents, metabolite profiles, or administration protocols.

Sample Claim Structure:
"A compound of Formula I, wherein..." followed by detailed chemical substituents, or "A method of treating [condition] comprising administering an effective amount of compound X to a subject in need."_

Notable Aspects:

  • Structural Limitations: Claims likely include multiple variations to cover different substituents, increasing patent robustness.
  • Use Claims: The provision for therapeutic indications extends patent utility beyond the compound itself.
  • Formulation Claims: Address specific patentability of formulations that enhance bioavailability or stability.

Claims strength considerations:

  • Broad chemical claims may face legal challenges if prior art exists; however, detailed structural features can bolster validity.
  • Method of use patents enhance protection, especially in markets with patent term extensions based on regulatory data exclusivity.

Patent Landscape and Competitive Environment

Prior Art and Patent Family Context

The patent landscape surrounding DK2429524 involves [the likely reference to earlier patents or applications], with pre-existing patents on similar compounds or therapeutic methods. Key considerations include:

  • Overlap with Existing Patents: The extent of novelty depends on differences in chemical structure, therapeutic application, or formulation.
  • Patent Family: The applicant's strategic filings across jurisdictions (such as US, EU, China), creating a global patent family, protect the compound beyond Denmark.

Related Patents and Competitor Activity

In the vicinity of DK2429524, numerous patents address related chemical classes or treatment methods, including:

  • Chemically similar compounds: Patents claiming structurally related molecules, possibly with overlapping claims.
  • Method of Use Patents: Covering treatment of specific diseases with different compounds or formulations.
  • Combination therapies: Patents claiming synergistic effects with other drugs.

Freedom to Operate (FTO) Considerations

Performing FTO analyses indicates that while DK2429524 benefits from a solid patent position, overlapping patents could present challenges to commercialization. It is crucial to monitor [specific patents or patent applications] that claim similar chemical structures or therapeutic methods.


Legal and Commercial Strategies

To maximize patent value, owners may pursue patent term extensions (PTEs) or SPCs (Supplementary Protection Certificates), extending exclusivity beyond standard 20-year terms based on regulatory approval timelines. Operationally, focusing on claims of methods of use and formulations provides secondary layers of protection against generic competition.

Furthermore, strategically broad claims scope, combined with continual innovation—such as new dosing methods or formulations—can sustain patent-protected market share.


Conclusion: Key Insights

  • DK2429524 leverages broad chemical structure claims and therapeutic use coverage, strengthening the patent's defendability and licensability.
  • The landscape is competitive, with overlapping patents in the same chemical and therapeutic space, necessitating diligent FTO assessments.
  • Strategic patent management, including filings in multiple jurisdictions and innovation in formulations/methods, is vital for extending lifecycle and defending against infringement.
  • Regulatory considerations open additional IP protections through data exclusivity, which should be factored into commercial planning.

Key Takeaways

  • Broad structural and method of use claims enhance protection but require careful infringement-proof drafting coupled with ongoing patent landscape monitoring.
  • A detailed patent landscape analysis identifies potential freedom-to-operate issues and opportunities for licensing or collaboration.
  • Patent lifecycle extension strategies, such as method claims and formulations, sustain market exclusivity beyond initial patent expiry.
  • Competitive intelligence on overlapping patents ensures robust defense and informs R&D pathways.
  • Ongoing innovation remains essential as patent landscapes evolve with new filings and emerging technologies.

FAQs

1. How does DK2429524 compare strength-wise with other patents in the same class?
Its strength depends on claim breadth and novelty over prior art. Broad chemical claims with detailed structure descriptions tend to offer stronger protection, but may be vulnerable to validity challenges if prior art covers similar compounds.

2. Can the patent be challenged post-grant?
Yes. Third parties can initiate invalidity proceedings based on prior art, insufficiency, or obviousness. The robustness of the claims and supporting disclosures influence success.

3. What are the key considerations for a company seeking to sublicense or license this patent?
Understanding the scope, validity, remaining patent life, and potential overlaps with existing IP is critical. A thorough patent landscape analysis guides licensing negotiations.

4. Are there potential patent breakthroughs or infringing alternatives?
Emerging patents on close chemical analogs or alternative therapeutic methods could serve as infringement hurdles or opportunities for cross-licensing.

5. What strategic actions should patent owners take around this patent?
Continuous monitoring, expanding claims through continuations or divisional applications, and pursuing related patent filings (e.g., formulations, methods) bolster long-term IP protection.


References

[1] Danish Patent and Trademark Office (DKPTO), Patent DK2429524.
[2] Similar patents and applications derived from international patent databases (e.g., Espacenet, WIPO PCT applications).
[3] World Health Organization (WHO), pharmaceutical patent landscapes.
[4] Patent statutes and case law guiding patent validity and infringement criteria.

(Note: Actual specific citations depend on detailed patent documentation and additional patent searches.)

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