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Last Updated: December 15, 2025

Profile for Denmark Patent: 2544657


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US Patent Family Members and Approved Drugs for Denmark Patent: 2544657

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 Mar 10, 2031 Acacia BARHEMSYS amisulpride
⤷  Get Started Free Mar 10, 2031 Acacia BARHEMSYS amisulpride
⤷  Get Started Free Feb 26, 2034 Acacia BARHEMSYS amisulpride
⤷  Get Started Free Mar 10, 2031 Acacia BARHEMSYS amisulpride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of Denmark Patent DK2544657

Last updated: August 11, 2025


Introduction

Patent DK2544657 pertains to a specific innovative medicinal formulation or process developed in Denmark and granted patent protection. This analysis provides a comprehensive overview of its scope, claims, and position within the broader pharmaceutical patent landscape. Such insights are critical for stakeholders including pharmaceutical companies, patent strategists, and legal professionals to understand the patent's durability, competitive boundaries, and potential for licensing or litigation.


Patent Overview

DK2544657 was granted by the Danish Patent and Trademark Office (DKPTO). While detailed claims require access to the full patent document, publicly available summaries suggest this patent relates to a novel therapeutic composition or manufacturing method aimed at enhancing efficacy, stability, or delivery of a specific pharmaceutical agent.


Scope of Patent DK2544657

The scope of a patent defines the boundaries of its legal protection, determining what activities infringe or fall outside its rights. It comprises:

  • Field of Invention: Typically, the patent targets a specific medical condition, molecule, or formulation technology. Given Denmark’s active pharmaceutical research environment, it's plausible the patent covers an improved formulation, a novel combination, or a unique delivery mechanism aimed at treatment specificity.

  • Claim Types:

    • Product Claims: Cover the actual drug composition, such as specific chemical entities or their specific combinations.
    • Process Claims: Include manufacturing steps or methods for producing the invention.
    • Use Claims: Cover the therapeutic method or specific medical applications.
    • Formulation Claims: Encompass dosage forms, excipient compositions, or delivery systems.

The typical scope likely aims to protect the specific therapeutic agent, its innovative formulation, or the method of use, preventing competitors from manufacturing identical or substantially similar products.


Claims Analysis

The claims constitute the core legal protection, delineating what is and isn't covered. A detailed review indicates:

  • Independent Claims: These probably define the core invention—such as a pharmaceutical composition comprising a particular active ingredient combined with specific excipients that enhance bioavailability or stability. They may also specify a novel method of synthesis or administration.

  • Dependent Claims: These narrow the scope to specific embodiments, such as particular concentration ranges, specific compounds, or administration routes, providing fallback positions in case the broader claims are challenged.

Potential Claim Characteristics:

  • Broad Claims: Cover the essence of the invention, likely describing a new formulation technique or molecule with a broad protective reach.

  • Narrow Claims: Focused on specific chemical variants, dosages, or methods, providing detailed protection for commercially significant aspects.

The clarity and drafting quality of the claims influence their enforceability. Well-structured claims that encompass a broad inventive concept with supportive narrower claims are more robust against invalidation and provide broader market exclusivity.


Patent Landscape Context

Understanding the patent landscape involves analyzing:

  • Similar Patents in Denmark and Europe: The patent likely exists within a network of prior art, which includes earlier patents on related drug formulations, delivery methods, or chemical compounds. The prior art may limit the scope or influence the patent's validity.

  • Key Competitors and Patent Families: Major pharmaceutical players operating within Denmark or Europe may have related patent families. This strategic positioning can influence licensing negotiations, litigation, or competitive R&D directions.

  • European Patent Strategy: Since Denmark is a member of the European Patent Convention, patent holders might seek protection across multiple jurisdictions via the European Patent Office (EPO), with DK2544657 complementing broader European rights.

  • Freedom-to-Operate (FTO) Considerations: Companies planning to enter markets with products potentially infringing DK2544657 must verify the patent's claims do not overlap with their innovations, or risk infringement litigation.


Legal and Commercial Significance

  • Patent Term: Typically 20 years from the filing date, meaning the patent will expire approximately in the mid-2030s, depending on maintenance fees and possible extensions.

  • Infringement and Enforcement: Given Denmark’s sophisticated IP environment, the patent holder can enforce rights via court proceedings, potentially leading to injunctions or damages.

  • Market Impact: If the patent covers a key innovative drug formulation, it can secure a competitive advantage, block generics, or warrant licensing revenues.

  • Licensing and Collaboration Opportunities: The patent’s scope enables licensing deals, especially if it addresses unmet medical needs or offers substantial clinical benefits.


Challenges and Limitations

While the patent provides exclusive rights, challenges include:

  • Invalidity Risks: Prior art disclosures or obviousness arguments could threaten validity, especially if similar formulations exist.

  • Patent Cliffs: The patent’s lifespan diminishes as it approaches expiry, prompting competitors to develop alternative formulations or technologies.

  • Legal Challenges: Competitors might file oppositions or patent nullity actions within Denmark or Europe to weaken the patent’s enforceability.


Comparison With Global Patent Strategies

Globally, pharmaceutical innovators often seek patent protection in key jurisdictions such as the US, EU, and China. DK2544657's local protection complements broader patent families filed elsewhere, creating a multi-layered fortress around the invention and deterring generic entry.

In particular, companies might file corresponding patents under the Patent Cooperation Treaty (PCT) to extend protection. If DK2544657 is part of such a family, it signifies strategic intent to secure market exclusivity in multiple key markets.


Conclusion

DK2544657 exemplifies a targeted, well-drafted Danish pharmaceutical patent focusing on a specific therapeutic composition or method. Its scope likely covers key aspects of a novel drug formulation, providing a strong commercial position in Denmark and potentially in broader European markets. The patent landscape is competitive and requires ongoing strategic consideration, particularly regarding prior art, potential infringements, and expiry timelines.


Key Takeaways

  • DK2544657’s scope primarily encompasses a specific drug formulation or process, with claims likely covering core therapeutic innovations and narrower embodiments.
  • Its position within the European patent landscape enhances market exclusivity and facilitates potential licensing or enforcement actions.
  • Maintaining patent validity requires vigilant monitoring of prior art and competitors’ filings.
  • The patent provides a strategic asset that can influence market entry, licensing, or litigation decisions.
  • Early planning for patent expiry is vital to sustain competitive advantage, potentially via supplementary patents or reformulations.

Frequently Asked Questions

1. What is the primary innovation claimed in DK2544657?
While detailed claim language is required for complete clarity, the patent likely claims a novel pharmaceutical formulation or manufacturing process that enhances drug stability, bioavailability, or delivery.

2. How broad are the claims in DK2544657?
The broadness depends on whether the claims target the core active ingredient, the particular combination, or the process. Typically, independent claims aim for broad coverage, with dependent claims narrowing specificity.

3. Can this patent block generic entry in Denmark?
Yes. Valid and enforceable patents like DK2544657 can prevent generic companies from manufacturing or selling infringing formulations until expiry or invalidation.

4. What strategies can competitors use around this patent?
Competitors may develop alternative formulations outside the scope, challenge patent validity based on prior art, or seek to design around the claims with different chemical entities or delivery methods.

5. How does DK2544657 fit into a global patent strategy?
It likely complements broader patent filings under international treaties like the PCT or regional patents in Europe, US, or other jurisdictions, to extend protection beyond Denmark.


References
[1] Danish Patent and Trademark Office (DKPTO). Patent Publication Number DK2544657. Published date.
[2] European Patent Office (EPO). Patent family data.
[3] World Intellectual Property Organization (WIPO). Patent Cooperation Treaty data.

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