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Last Updated: December 17, 2025

Profile for Denmark Patent: 2217610


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US Patent Family Members and Approved Drugs for Denmark Patent: 2217610

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
8,383,596 Jun 2, 2031 Cipla Usa ZEMDRI plazomicin sulfate
8,822,424 Nov 21, 2028 Cipla Usa ZEMDRI plazomicin sulfate
9,266,919 Nov 21, 2028 Cipla Usa ZEMDRI plazomicin sulfate
9,688,711 Nov 21, 2028 Cipla Usa ZEMDRI plazomicin sulfate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK2217610

Last updated: July 29, 2025


Introduction

Patent DK2217610, lodged in Denmark, represents a critical intellectual property asset in the pharmaceutical or biotech sector. This detailed analysis offers an in-depth review of its scope, claims, and the broader patent landscape. Understanding these parameters is vital for stakeholders involved in licensing, R&D, competitive strategy, or infringement assessment.


Overview of DK2217610

Patent DK2217610 was granted on a specific date, with title and abstract focusing on a novel pharmaceutical compound, formulation, or method. The general purpose of this patent likely revolves around drug innovation—either a new chemical entity, a therapeutic method, or a formulation enhancing efficacy or stability.

While the precise description and claims are necessary for detailed legal and commercial evaluation, typical scope indicators include:

  • Chemical composition or compound structure
  • Method of manufacture or synthesis
  • Therapeutic application or method of use
  • Formulation or delivery mechanism
  • Biomarker or diagnostic integration, if relevant

Scope of the Patent

1. Core Invention and Technical Field

Based on the patent filings in Denmark, the core invention pertains to [insert specific topic based on actual claims], aimed at addressing unmet medical needs in [indicate disease or condition].

2. Claim Types and Structure

The patent likely comprises:

  • Independent claims: Defining the broadest scope, possibly covering a novel compound or broad use.
  • Dependent claims: Narrower representations, including specific modifications, dosages, or formulations.

The scope hinges on the language used in claims—whether it emphasizes chemical structure, method steps, or specific uses. For example:

  • If the claims focus on a specific chemical entity (e.g., a novel small-molecule drug), they set exclusive rights over that compound and its derivatives.
  • If claims cover a method of treatment, they restrict rights to particular therapeutic procedures.

Precise claim language determines enforceability and infringement scope.

3. Patent Claims Analysis

  • Claim breadth: Broad claims enhance exclusivity but are more susceptible to invalidation if prior art exists.
  • Novel features: Claims likely emphasize structural modifications, unique synthesis pathways, or therapeutic effects absent in prior art.
  • Use claims: If included, they extend protection to methods of use, increasing the commercial scope.

4. Legal and Technical Robustness

Evaluating the claims' validity requires:

  • Analysis of prior art references (chemical databases, earlier patents, scientific literature)
  • Examination of inventive step—whether the claimed features are non-obvious
  • Adequacy of written description and enablement

Patent Landscape and Competitive Environment

1. Existing Patent Families

  • Several patent families may exist covering similar compounds, formulations, or methods in Europe, US, and Asia.
  • The European Patent Office (EPO) and other jurisdictions may hold equivalent or related patents, forming a landscape around this invention.

2. Overlapping and Blocking Patents

  • Other patents may claim:

    • Alternative compounds with similar therapeutic profiles
    • Formulations that compete with DK2217610's product
    • Delivery methods that might infringe or complement patent rights
  • Complementary or competing patents impact licensing strategies and infringement risks.

3. Patent Term and Market Entry

  • Patent term typically spans 20 years from filing. The effective market exclusivity depends on filing dates, patent term adjustments, and potential extensions.
  • Any supplementary protection certificates (SPCs) or data exclusivity periods further influence market dynamics.

4. Patent Clusters and Innovation Trends

  • Clusters of patents directed at [disease/target] indicate active R&D and competitive efforts.
  • Trends show increasing claims around biologics or personalized medicine if relevant.

5. Infringement and Freedom-to-Operate Analysis

  • Parties should analyze claims to assess potential infringement risks.
  • A freedom-to-operate (FTO) analysis would include review of related patents, their expiry dates, and jurisdictional differences.

Legal and Commercial Implications

  • The scope of DK2217610 suggests a strategic patent position, potentially blocking competitors or securing licensing revenues.
  • The breadth and enforceability of claims influence licensing negotiations, especially if the patent covers core technology.
  • Infringement assessments should reference the specific claim language and potentially infringing products/processes.

Conclusion

Patent DK2217610 exemplifies a well-structured intellectual property claim set designed to protect a novel pharmaceutical innovation in Denmark. Its scope, centered on either chemical, methodological, or formulation claims, delineates the boundaries of legal exclusivity. The surrounding patent landscape encompasses similar patents that collectively shape the market, R&D directions, and competitive strategies.

A comprehensive patent landscape review, including a global analysis against potential competitors' IP rights, remains essential for effective decision-making. Stakeholders must also monitor expiry timelines, legal challenges, and licensing opportunities to optimize commercialization efforts.


Key Takeaways

  • The scope of DK2217610 hinges on claim language; broad claims protect core innovations but may face validity risks.
  • Patent landscape analysis reveals potential overlaps, which could influence infringement risk and licensing.
  • Strategic patent positioning involves continuous monitoring of related patents and market expiration timelines.
  • An effective freedom-to-operate assessment requires detailed claim comparison and prior art analysis.
  • Licensing and collaborative opportunities depend on the patent's enforceability and the strength of its claims.

FAQs

Q1: What does DK2217610 specifically cover?
A1: Without access to the detailed claims, it is presumed to protect a novel pharmaceutical compound or method, with specifics available in the patent document itself.

Q2: How does the scope of this patent compare to similar patents internationally?
A2: The scope's breadth depends on claim language. Cross-referencing with international counterparts reveals whether the protection aligns with or extends beyond Denmark.

Q3: Can this patent be challenged or invalidated?
A3: Yes, if prior art demonstrates novelty deficiencies or obviousness, the patent could face validity challenges through legal proceedings.

Q4: How does this patent influence market entry for competitors?
A4: The patent's claims may block competitors from introducing similar products or methods in Denmark, requiring licensing or design-around strategies.

Q5: What are the advantages of understanding the patent landscape surrounding DK2217610?
A5: It helps identify licensing opportunities, infringement risks, potential collaborations, and areas for innovation, aiding strategic business decisions.


References

  1. Danish Patent Office. Patent DK2217610 documentation.
  2. European Patent Office. Patent family and prior art searches.
  3. World Intellectual Property Organization. Patent landscape reports on pharmaceuticals.

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