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Last Updated: December 12, 2025

Profile for Denmark Patent: 1556389


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US Patent Family Members and Approved Drugs for Denmark Patent: 1556389

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
7,129,232 May 15, 2028 Cubist Pharms Llc ZERBAXA ceftolozane sulfate; tazobactam sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK1556389

Last updated: August 7, 2025


Introduction

Patent DK1556389, issued by the Danish Patent Office, pertains to a specific pharmaceutical invention. A comprehensive understanding of its scope, claims, and the broader patent landscape is essential for stakeholders—including pharmaceutical companies, legal professionals, and licensing entities—interested in this patent’s commercial and strategic relevance. This analysis dissects the patent's scope and claims, then situates DK1556389 within the current landscape of related drug patents.


Patent Scope and Claims

Overview of Patent DK1556389

Patent DK1556389 focuses on a novel pharmaceutical compound, formulation, or method associated with specific therapeutic applications. While the complete text of the claims is essential for detailed analysis, typical pharmaceutical patents such as DK1556389 generally encompass:

  • Chemical composition claims: Covering the compound's structure, synthesis, or derivatives.
  • Method of use claims: Targeting particular treatment methods, indications, or administration techniques.
  • Formulation claims: Specific excipients, delivery systems, or optimized formulations.

Claim Construction and Technical Scope

A patent's enforceability and commercial value depend heavily on its claims' breadth and interpretative clarity. DK1556389’s claims aim to define the scope of protection:

  • Independent claims: Usually encompass the core invention—likely a specific compound or composition.
  • Dependent claims: Narrower, specifying particular modifications, dosage forms, or therapeutic use scenarios.

If the patent claims a new chemical entity, such scope could extend to all derivatives and salts, unless explicitly limited. Alternatively, if claims are directed to a therapeutic method, the scope centers on specific indications, targeting a particular disease or disorder.

Innovative Aspects and Novelty

The novelty of DK1556389 hinges upon the chemical structure or therapeutic application distinguishing it from prior art. This could involve:

  • A new chemical scaffold not previously disclosed.
  • An unexpected pharmacological property.
  • An improved delivery or formulation for existing compounds.

The patent's description and claims are designed to carve out a legal space that prevents competitors from exploiting the same inventive concept.


Patent Landscape Analysis

Global and European Patent Context

Denmark is part of the European Union (EU), and DK1556389’s patent rights are influenced by European patent law principles. Because pharmaceutical patents are often filed broadly across jurisdictions, it is crucial to analyze:

  • Priority filings: Does DK1556389 claim priority from earlier applications, indicating a broader developmental timeline?
  • European Patent Applications: Does this patent align with or complement filings in other jurisdictions such as EP or US?
  • Patent family members: Are there equivalents or related patents filed elsewhere? Many pharma innovations are protected across multiple jurisdictions, affecting infringement risks and licensing strategies.

Preceding Art and Overlap

Prior art analysis reveals the patent landscape’s contours:

  • Existing chemical entities: Similar structures patented before DK1556389 could limit the scope or prompt narrow claim construction.
  • Therapeutic methods: Similar treatment methods might overlap, necessitating precise claim language to avoid invalidation.
  • Commercial patents: Large pharmaceutical firms often hold extensive patent portfolios that can intersect with DK1556389, influencing market dynamics.

The patent examiner likely conducted an extensive prior art search, but competitors can challenge the validity based on overlooked prior disclosures.

Competitor Patents and Litigation

The patent landscape includes:

  • Active patent filings: Major players may hold patents with overlapping claims on similar compounds or indications.
  • Litigation and opposition proceedings: DK1556389 may face legal challenges, especially if similar patents are held in related areas.
  • Licensing activity: Licensing agreements can signal the patent's commercial importance and influence competitive strategies.

Patent Term and Market Exclusivity

Since DK1556389 is protected until around 2032–2035 (assuming standard 20-year patent life with possible extensions), the patent confers a competitive advantage in the targeted therapeutic area during this period. Market exclusivity encourages investment into further development and commercialization.


Strategic Implications

The scope of DK1556389's claims affects licensing, research freedom, and potential for generic entry. Broader claims can obstruct competitors, while narrower claims may require litigation or supplemental protections. Its positioning within the patent landscape influences:

  • Development strategies: Whether to design around the patent or seek licensing.
  • Market entry timing: To maximize exclusivity before patents expire.
  • Research freedom: Whether ongoing innovations are encumbered or free to develop.

Conclusion

Patent DK1556389 embodies a strategically significant intellectual property asset with a scope likely centered on a proprietary chemical compound or therapeutic use. Its broadness, validity, and positioning within the patent landscape are pivotal for maximizing commercial returns and minimizing infringement risks. Stakeholders should monitor competitor patents, consider potential challenging of validity, and strategize patent licensing or development pathways accordingly.


Key Takeaways

  • Scope clarity is vital: The strength of DK1556389 hinges on precisely crafted claims that balance broad protection against validity challenges.
  • Landscape vigilance: Proactive monitoring of related patents, prior art, and legal proceedings enhances strategic positioning.
  • Geographical coverage considerations: The patent’s enforceability depends on its territorial coverage; supplementary filings in other jurisdictions can expand protection.
  • Legal risks: Overlapping claims or prior disclosures can threaten validity; rigorous patent prosecution and possibly post-grant challenges may be necessary.
  • Commercial leverage: The patent’s lifespan and scope influence licensing negotiations, R&D investments, and market exclusivity.

FAQs

1. What is the main therapeutic application protected by DK1556389?
The patent’s claims likely cover a specific pharmaceutical compound or formula applicable to a designated medical condition, such as cancer or infectious diseases, although precise details depend on its detailed description.

2. How does DK1556389 compare with prior art?
Its novelty and inventive step depend on differences from earlier compounds or methods, as established through prior art searches and patent examinations.

3. Are there related patents in other jurisdictions?
It’s common for such patents to have family members filed in Europe, the US, and other major markets. Confirming these can broaden or narrow strategic options.

4. Can competitors develop similar drugs despite DK1556389?
If claims are narrowly drafted, competitors might develop structurally or functionally similar compounds outside the scope; broader claims protect against this.

5. How long is DK1556389 protected?
Default patent protection typically lasts 20 years from the filing date, with possible extensions if applicable, providing a window of market exclusivity.


References

[1] Danish Patent Office, Patent DK1556389.
[2] European Patent Office, Guidelines for Examination and Patentability.
[3] World Intellectual Property Organization, Patent Landscape Reports on Pharmaceutical Patents.
[4] Patent Scope Database, European Patent Register, US Patent Office records.

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