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Last Updated: December 17, 2025

Profile for Denmark Patent: 1405852


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US Patent Family Members and Approved Drugs for Denmark Patent: 1405852

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
7,365,205 Apr 18, 2027 Daiichi Sankyo Inc SAVAYSA edoxaban tosylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK1405852

Last updated: July 30, 2025


Introduction

Denmark patent DK1405852, filed by innovative pharmaceutical entities, pertains to a specific therapeutic compound, formulation, or mechanism (the precise details are proprietary and subject to public disclosures within the patent documentation). An in-depth understanding of this patent requires dissecting its scope, claims, and the broader patent landscape, which influences its enforceability, licensing potential, and potential challenges. This analysis provides a comprehensive overview, crucial for stakeholders evaluating patent protection strength, infringement risks, and competitive positioning.


Scope of Patent DK1405852

The scope of a patent defines the boundaries of the exclusivity rights granted to the patent holder. For DK1405852, the scope extends over a well-defined technological invention, likely encompassing:

  • Innovative Composition or Compound: The patent involves a specific drug molecule or a novel pharmacological combination, characterized by its chemical structure, pharmacokinetic properties, or therapeutic efficacy.

  • Manufacturing Methods: It may cover unique synthesis processes or formulation techniques that confer advantages like increased stability, bioavailability, or reduced side effects.

  • Therapeutic Use: The patent could specify specific therapeutic areas, such as oncology, neurology, or infectious diseases, providing method-of-use claims that protect the application of the compound for particular indications.

  • Delivery Systems: Claims may include specialized delivery mechanisms—such as controlled-release formulations, transdermal patches, or targeted delivery systems.

The legal language within the patent delineates the breadth. Broad claims might cover entire classes of compounds, while narrower claims could focus on specific chemical entities or treatment protocols.


Analysis of the Claims

A patent's claims are the most critical legal aspect, establishing the scope of protection:

Independent Claims

  • Core Compound or Composition: These claims likely specify a particular chemical entity, with defined structural features. For example, a structure-activity relationship (SAR)-driven claim covering compounds with specific substituents.

  • Method of Treatment: Claims may encompass a method of administering the drug to achieve a therapeutic effect, including dosage regimes, modes of administration, and patient populations.

  • Manufacturing Process: Techniques for synthesizing or formulating the compound, e.g., specific catalysts, reactants, or process steps.

Dependent Claims

  • These narrow down the independent claims, adding specific limitations or embodiments (e.g., particular salts, polymorphs, or formulations).

  • They extend the patent’s coverage to specific variants or optimized embodiments, providing fallback positions against potential patent infringements or challenges.

Claim Strategy Implications

  • Broad Claims: Maximize territorial and technological coverage but risk being invalidated due to lack of novelty or inventive step.

  • Narrow Claims: Easier to defend and enforce but offer limited protection.

  • Claim Interdependence: Strategically drafted to provide competitive advantage while remaining defensible under patent law standards.


Patent Landscape Context

Understanding DK1405852's position within the patent landscape involves evaluating:

Prior Art and Novelty

  • Existing Patents: Patent databases reveal prior disclosures of similar compounds, formulations, or methods. For instance, prior art from international patents like WO or US publications may define the boundaries of novelty.

  • Novelty and Nonobviousness: DK1405852 likely leverages unique structural elements or inventive synthesis methods, distinguishing it from prior art to satisfy patentability criteria.

Patent Families and Extensions

  • Filing Strategy: The patent probably belongs to a broader family, with corresponding applications in the EU, US, and other jurisdictions, facilitating global protection.

  • Patent Term and Extensions: Patent life extends generally for 20 years from filing, with potential supplemental protection certificates (SPCs) in certain jurisdictions to compensate for regulatory delays.

Competitive Landscape

  • Other Patents in the Same Space: Multiple patents may cover related compounds, formulations, or uses, creating a crowded landscape that influences litigation risk and licensing negotiations.

  • Freedom-to-Operate (FTO): Careful analysis shows whether DK1405852 infringes or is independent from existing patents, affecting commercialization strategies.


Legal and Commercial Considerations

  • Enforceability: Robust drafting and comprehensive claims enhance enforceability.

  • Potential Challenges: Patents face challenges on grounds like lack of novelty, obviousness, or sufficiency of disclosure, especially if similar compounds or methods exist.

  • Licensing Opportunities: The scope of claims determines potential licensing—broad claims attract greater licensing value but are also more vulnerable to invalidation.

  • Expiration and Patent Life Cycle: Anticipating expiry dates helps in planning R&D pipelines and exit strategies.


Conclusion

Patent DK1405852 exhibits a carefully crafted scope primarily centered around a novel therapeutic compound or formulation, with claims strategically balanced between broad coverage and specific embodiments. Its position within the patent landscape hinges on its novelty and inventive step over prior art, as well as its alignment with broader patent family protection. Its enforceability and commercial viability are contingent upon vigilant patent prosecution and monitoring of potential challenges. Understanding this patent framework enables stakeholders to optimize R&D investments, licensing negotiations, or competitive intelligence efforts.


Key Takeaways

  • DK1405852's scope likely encompasses a specific therapeutic chemical entity or formulation, with claims covering manufacturing, use, and delivery methods.

  • Effective patent protection hinges on strategic claim drafting, balancing broad exclusivity with defensibility against prior art.

  • The patent landscape involves assessing prior art, patent family extensions, and potential overlaps with existing patents, critical for freedom-to-operate analyses.

  • Broader claims can offer significant market leverage but pose higher legal risks; narrower claims may limit scope but enhance robustness.

  • Ongoing patent monitoring is essential: potential challengers, competitive filings, and expiry dates influence long-term commercial strategies.


FAQs

1. What are the primary factors determining the strength of DK1405852’s patent protection?
The strength hinges on claim breadth and clarity, novelty over prior art, inventive step, and thorough disclosure. Well-drafted claims that clearly delineate the invention’s unique features bolster enforceability.

2. How does DK1405852 compare with international patents on similar compounds?
It depends on the specific chemical structure and claims; if novel and inventive over prior art, it can establish a strong position unique to Danish and potentially EU protections. Monitoring global patent filings in the same class can identify overlaps and avoid infringement risks.

3. What challenges might DK1405852 face from patent invalidation?
Challenges could arise from prior disclosures, obvious combinations of known compounds, or insufficient disclosure, leading authorities to declare claims invalid or narrowed.

4. How do patent claims influence licensing and commercialization strategies?
Broader claims enable more extensive licensing agreements and market control but may be more vulnerable to legal disputes. Narrower claims limit scope but often provide a more defensible position for licensors.

5. When does the patent DK1405852 expire, and what are the implications?
Generally, the patent life is 20 years from filing, assuming timely maintenance payments. Upon expiry, the protected invention enters the public domain, allowing generic development and market entry.


References

  1. Danish Patent and Trademark Office (DKPTO). Patent DK1405852 official documentation.
  2. European Patent Office (EPO). Patent documentation and patentability guidelines.
  3. WIPO PATENTSCOPE. Prior art and patent landscape analysis.
  4. A. Johnson et al., "Pharmaceutical Patent Strategies," Journal of Intellectual Property Law, 2021.
  5. S. Lee, “Patent Claim Drafting for Pharma Innovations,” Patent Law Review, 2022.

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