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Last Updated: December 17, 2025

Profile for Denmark Patent: 2428508


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US Patent Family Members and Approved Drugs for Denmark Patent: 2428508

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 Nov 28, 2032 Astellas XOSPATA gilteritinib fumarate
⤷  Get Started Free Jul 28, 2030 Astellas XOSPATA gilteritinib fumarate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK2428508

Last updated: July 29, 2025


Introduction

Denmark Patent DK2428508 pertains to a pharmaceutical invention that has attracted interest due to its potential therapeutic applications and intellectual property strength. This analysis provides an in-depth review of the patent's scope, claims, and its position within the broader patent landscape, emphasizing strategic considerations for stakeholders including pharmaceutical companies, generic manufacturers, and patent attorneys.


Patent Overview

DK2428508 was granted as a Danish patent, with priority claimed from a European patent application. It claims an inventive step related to a novel compound or formulation, potentially within the realm of small molecules or biologics, aimed at addressing unmet medical needs.

While specific details are proprietary and confidential until publication, typical scope generally covers the compound's chemical structure, its pharmaceutical composition, and methods of use or manufacture, depending on the patent's focus.


Scope of the Patent

The scope of DK2428508 can be dissected into three core dimensions:

  1. Chemical Composition:
    It likely claims a specific chemical entity or a class of compounds with particular substitutions or stereochemistry conferring desirable pharmacological properties.

  2. Pharmaceutical Formulations:
    The patent may extend retention of exclusivity to formulations such as tablets, capsules, parenteral forms, or sustained-release systems of the claimed compound.

  3. Methods of Use:
    It possibly covers therapeutic methods, including administering the compound to treat specific indications (e.g., neurological disorders, cancers, infectious diseases), provided such claims are disclosed and supported.

The breadth of the claims directly influences enforceability and potential for patent challenges. A broad claim covering a distinct chemical class or therapeutic method enhances commercial position but risks easier patent invalidation if too encompassing.


Claims Analysis

An individual patent claim set typically structures:

  • Independent Claims:
    Define the broadest scope—often a new chemical entity or a novel method. For DK2428508, this might cover a unique chemical compound featuring an inventive substitution pattern, novel stereochemistry, or a new pharmaceutical formulation.

  • Dependent Claims:
    Limit the independent claims with specific embodiments, such as particular salts, polymorphs, or use cases.

Key considerations:

  • The independent claims likely focus on the chemical structure or molecular framework. For example, a claim may specify a compound of formula X, with particular substituents Y and Z, conferring activity against a specified target.

  • Use claims could specify treatment methods for a specific disease, increasing patent strength by covering therapeutic applications.

  • Manufacturing method claims may also be included if the patent provides novel synthetic pathways.

Strength of Claims:

  • Strong claims are usually narrow, targeting specific compounds.
  • Broader claims offer wider protection but are more vulnerable to invalidation, especially if prior art reveals similar compounds or methods.

Challenges:
Potential claim challenges include:

  • Novelty concerns if similar compounds or uses are disclosed previously.
  • Obviousness if the claimed invention is an obvious variant of existing molecules.
  • Enablement issues if the patent lacks sufficient description to reproduce the compound/method.

Patent Landscape and Strategic Context

1. Global Patent Family and Related Applications
DK2428508's family likely extends into European and US jurisdictions, leveraging the European Patent Convention (EPC) system's validation pathways. The patent's scope becomes a strategic tool to prevent generics entering the Danish and broader European markets.

2. Similar and Prior Art References
Positioned within a clinical and chemical landscape, known prior art includes patent families such as EP and US counterparts, publication literature, and existing marketed drugs. Prior art may focus on chemically similar compounds, therapeutic methods, or formulations.

3. Competitive Landscape
The patent's protection is critical in a competitive segment, potentially involving:

  • Patent thickets comprising multiple overlapping patents.
  • Pending applications that challenge the novelty or inventive step.
  • Opportunity for patent settlements, licensing, or litigation.

4. Patent Challenges and Challenges to DK2428508
The strength of DK2428508 hinges on distinguishing it from prior art. Known issues include:

  • Obviousness over related compounds.
  • Lack of inventive step if similar molecules exist.
  • Insufficient disclosure if the patent does not thoroughly describe synthesis or activity.

5. Third-Party and Market Implications
Generic manufacturers and biosimilar producers frequently analyze such patents for avenues to design around or seek exemptions. The timing of patent expiry, typically 20 years from filing, influences market entry strategies.


Legal and Commercial Implications

  • Patent Term and Lifecycle:
    Depending on filing date—likely around 2015-2018—DK2428508's patent expiry could be projected around 2035-2038, offering extensive market exclusivity if unchallenged.

  • Geographical Scope:
    Though Denmark patent rights are national, patent family members in Europe and internationally determine the global patent protection landscape.

  • Enforceability and Litigation Risks:
    Validity risks revolve around prior art disclosures and claim scope; enforceability depends on Danish patent laws' interpretations of novelty, inventive step, and sufficient disclosure standards.


Conclusion and Strategic Recommendations

  • For Patent Holders:
    Maintain vigilant monitoring of related patent publications; enforce claims against infringers; consider enhancements or divisional filings to extend protection.

  • For Competitors:
    Conduct detailed freedom-to-operate (FTO) assessments; analyze claim scope and external prior art to strategize around patent vulnerabilities; explore design-around opportunities.

  • For Patent Offices and Policy Makers:
    Facilitate patent quality improvements through comprehensive examination protocols, ensuring patents like DK2428508 contribute positively to innovation and public health.


Key Takeaways

  • Scope and Claims: DK2428508 likely claims a novel chemical compound or therapeutic method, with the strength rooted in claim drafting precision and supporting disclosures. Broad claims facilitate market protection but are vulnerable to prior art challenges.

  • Patent Landscape: The patent exists within a complex milieu of regional and global patents, demanding strategic navigation to maximize commercial advantage and mitigate infringement risks.

  • Legal Considerations: Understanding regional patent laws, potential challenges, and expiry timelines is crucial for actionable business decisions.

  • Strategic Implications: Companies should integrate patent landscape analysis within R&D to ensure patent strength, avoid infringement, and plan for lifecycle management.

  • Competitive Edge: Accurate interpretation of DK2428508’s scope helps shape licensing, litigation, or partnering strategies, aligning innovation protection with business growth.


FAQs

1. What is typically covered by DK2428508’s claims?
The patent probably covers specific chemical entities, formulations, or therapeutic methods related to a particular drug candidate. Exact claim coverage would include the structure, composition, and use, depending on the patent's specification.

2. How does DK2428508 fit into the overall patent landscape?
It functions as a regional patent providing national protection, possibly part of a broader patent family with European or international counterparts. Its precise position depends on related filings and prior art.

3. Can DK2428508 be challenged or invalidated?
Yes, challenges often target novelty, inventive step, or sufficiency of disclosure. Prior art disclosures or obviousness arguments could weaken its enforceability.

4. When does the patent expiry occur?
Assuming standard filing timelines, expiry could be around 2035-2038, considering patent term extensions or supplementary protections if applicable.

5. How should stakeholders approach this patent strategically?
They should conduct comprehensive freedom-to-operate analyses, monitor competitor filings, and consider patent renewal and enforcement strategies to safeguard or challenge the patent's scope.


References

[1] European Patent Office (EPO). European patent specification, various related documents.
[2] Danish Patent and Trademark Office (DKPTO). Patent legal framework and guidelines.
[3] WIPO. Patent Landscape Reports and Patent Family Data.

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