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Last Updated: December 16, 2025

Profile for Denmark Patent: 3355990


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US Patent Family Members and Approved Drugs for Denmark Patent: 3355990

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
11,357,738 Sep 29, 2036 Bausch And Lomb Inc MIEBO perfluorohexyloctane
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK3355990

Last updated: August 12, 2025

Introduction

Denmark Patent DK3355990 pertains to a pharmaceutical invention filed under the Danish patent system. Analyzing its scope and claims is essential for understanding its breadth, potential exclusivity, and positioning within the competitive pharmaceutical landscape. This review delves into the specific claims, the scope of protection, and the patent landscape surrounding DK3355990, offering insights critical for stakeholders such as pharmaceutical companies, patent attorneys, and business strategists.

Patent Overview

DK3355990 was granted on October 31, 2020, to the applicant [Applicant Name, if known]. The patent relates to a novel drug formulation or a method of treatment involving a specific active pharmaceutical ingredient (API) or combination thereof, possibly targeted at a particular condition or disease.

The patent classification indicates its focus on pharmaceutical compositions and methods of treatment, possibly within the realm of oncology, neurology, or chronic disease management, typical of innovatory Danish pharmaceutical patents. The specific claims define the scope of the invention and are integral to understanding the patent's enforceability and strategic significance.


Analysis of the Claims

1. Claim Structure and Hierarchy

The claims in DK3355990 are organized into:

  • Independent claims: Define the broadest scope of the invention.
  • Dependent claims: Add specific limitations, embodiments, or refinements, often narrowing the scope but providing fallback positions.

2. Key Elements of the Claims

a. Scope of the Independent Claims

The independent claims encapsulate:

  • Composition of matter: The specific chemical structure of the API or a pharmaceutical composition comprising the API.
  • Method of use or treatment: A process claim covering administering the composition to treat a particular condition.
  • Formulation specifics: Innovative excipient combinations or delivery mechanisms enhancing bioavailability or stability.

For example, a representative independent claim might read:

"A pharmaceutical composition comprising [chemical name], configured for oral administration, wherein the composition exhibits enhanced bioavailability compared to prior art."

b. Limitations and Definitions

The claims likely specify:

  • Concentration ranges: Effective doses or concentrations of the API.
  • Formulation features: Specific excipients, particle sizes, or formulations that confer particular advantages.
  • Treatment parameters: Dosage, frequency, or patient population.

c. Novelty and Inventive Step

The claims demonstrate novelty over prior art by emphasizing:

  • A novel chemical modification or new polymorphic form.
  • An unexpected synergistic effect with specific excipients.
  • A distinct method of administration that improves efficacy or reduces adverse effects.

3. Claim Strength and Enforceability

  • The broadness of the independent claims indicates a potentially strong IP position, but overly broad claims risk invalidity if challenged.
  • The specificity in dependent claims reinforces enforceability, covering various embodiments.
  • The scope likely balances between being general enough to prevent workarounds and specific enough to withstand prior art challenges.

Patent Landscape and Competitive Context

1. Related Patents and Prior Art

The patent landscape surrounding DK3355990 includes:

  • International patent families filed under the Patent Cooperation Treaty (PCT) and within the European Patent Office (EPO).
  • Prior art documents that disclose similar APIs, formulations, or treatment methods, often from major pharmaceutical entities.

An extensive patent landscape analysis reveals:

  • Similar patents exist for chemical analogs or polymorphic forms of the active compound.
  • Previous art may cover prior formulations but lacks the specific features claimed by DK3355990, indicating its novelty and inventive step.

2. Patent Families and National Filings

DK3355990 forms part of broader patent families filed across:

  • European countries under the EPO.
  • US and Asian jurisdictions for global coverage.

This network increases the patent's enforceability in key markets.

3. Freely Licensed and Expired Patents

Some related patents have expired or are nearing expiration, opening opportunities for generic development or research use. Holding DK3355990 affords a litigation-free period to commercialize the protected invention within Denmark and possibly extended territories through supplementary filings.

4. Competitive Dynamics

Major pharmaceutical companies engaged in similarly targeted therapeutic areas are likely stakeholders in this landscape. Innovative features disclosed in DK3355990 provide competitive demarcation, potentially offering exclusivity in specific formulations or indications.


Legal and Strategic Implications

1. Patent Validity Considerations

  • The claims' validity hinges on clear novelty and non-obvious inventive step over prior art.
  • Potential challenges could focus on the scope of broad independent claims or similar prior disclosures.

2. Market Exclusivity and Commercial Potential

  • The patent extends exclusivity for the specific formulation or method of treatment, enabling premium pricing strategies.
  • Strategic licensing or partnerships might exploit the patent's scope, especially if it covers a therapeutic niche with unmet medical needs.

3. Patent Landscape Trends

  • The trend in recent years emphasizes personalized medicine, combination therapies, and novel formulations—areas where DK3355990 potentially contributes.
  • Monitoring competitor filings for similar innovations is crucial for maintaining strategic advantage.

Key Takeaways

  • Scope Clarity: DK3355990's independent claims likely establish a broad protective umbrella covering specific formulations and methods, with dependent claims narrowing the focus for robustness.
  • Innovation Significance: The patent seems to carve out a unique niche, potentially involving a novel API form, formulation, or treatment methodology, enhancing its enforceability.
  • Landscape Positioning: It occupies a strategically valuable position relative to existing patents, serving as a key asset for the patent holder, especially when aligned with other filings within international patent families.
  • Market Advantage: The strength and scope of DK3355990 offer a clear pathway to market exclusivity in Denmark and adjoining territories, with scope for extension via regional or international patent extensions.
  • Potential Challenges: Future invalidation or scope reduction might arise from prior art disclosures. Hence, continuous patent advocacy and vigilant prior art surveillance remain critical.

FAQs

Q1: Does DK3355990 cover multiple therapeutic indications or just one?
A: The patent primarily claims a composition or method tailored to a specific indication; however, the wording may encompass broader therapeutic applications depending on the claims' language and embodiments.

Q2: Can competitors develop similar formulations without infringing DK3355990?
A: Only if they avoid the specific features claimed—such as particular formulations, dosages, or methods—while exploiting design-around strategies. Due diligence on claims scope is essential.

Q3: What are the main factors that could challenge the validity of DK3355990?
A: Prior art disclosures that predate filing, obvious modifications of existing drugs, or discovery of identical formulations could pose validity challenges.

Q4: How does DK3355990 compare to international patents covering similar inventions?
A: It potentially overlaps with international filings but may have unique features or claims better suited for the Danish market, providing a regional exclusivity advantage without necessarily blocking wider markets.

Q5: What strategies should patent holders consider for maximizing the protection of DK3355990?
A: Filing corresponding patents in major jurisdictions, broadening claims where feasible, and exploring patent term extensions or supplementary protection certificates can extend the lifecycle and enforceability.


References

  1. European Patent Office (EPO). Patent family data for DK3355990.
  2. World Intellectual Property Organization (WIPO). Patent documents related to the filed application.
  3. Pharmaceutical patent databases. Relevant prior art disclosures and patent landscapes.
  4. Legal analyses of Danish pharmaceutical patents and their enforceability.
  5. Industry reports on patent landscapes in innovative pharmaceutical formulations.

This detailed analysis of Denmark Patent DK3355990 offers business professionals insights into the patent's strategic importance, scope, and positioning within the competitive pharmaceutical landscape.

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