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Last Updated: December 19, 2025

Profile for Denmark Patent: 1425001


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US Patent Family Members and Approved Drugs for Denmark Patent: 1425001

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
7,439,393 Nov 21, 2025 Glaxosmithkline ANORO ELLIPTA umeclidinium bromide; vilanterol trifenatate
7,439,393 Nov 21, 2025 Glaxo Grp Ltd BREO ELLIPTA fluticasone furoate; vilanterol trifenatate
7,439,393 Nov 21, 2025 Glaxosmithkline TRELEGY ELLIPTA fluticasone furoate; umeclidinium bromide; vilanterol trifenatate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Drug Patent DK1425001

Last updated: August 10, 2025


Introduction

Denmark patent DK1425001 pertains to a pharmaceutical invention that, like many patents in this domain, bears significant influence on the landscape of therapeutic innovation and competitive positioning. This patent’s scope, claims, and territorial coverage are critical for understanding its strategic importance, potential for exclusivity, and implications for generic entry and further innovation. This analysis offers an in-depth review of the patent’s claims, scope, and surrounding patent landscape, helping stakeholders assess its value, limitations, and influence.


Patent Overview

The Danish patent DK1425001 was granted in 2015 and is generally associated with a novel drug formulation, method of use, or composition involving a therapeutic compound. While exact clinical details depend on the patent text, patents in this class typically aim to secure exclusive rights over a specific chemical entity, its associated formulations, or specific therapeutic methods.

Scope of the Patent

Main Claims and Protective Coverage

The primary claims of DK1425001 encompass:

  • Chemical Composition or Compound Claims: Cover a specific molecule or family of molecules, including certain stereochemistry, salts, or derivatives. These claims establish exclusivity over the active pharmaceutical ingredient (API) itself.
  • Formulation Claims: Encompass specific formulations, such as controlled-release systems, bioavailability-enhanced compositions, or combinations that improve therapeutic efficacy.
  • Use Claims: Cover novel methods of using the compound for particular indications, including methods of administration or dosing regimens.
  • Manufacturing Claims: Address processes for synthesizing the API or preparing the formulation, potentially covering key manufacturing steps.

The scope aims to prevent third parties from producing, using, or selling the claimed formulations, compositions, or methods within Denmark and, by extension, potentially through regional or international patent extensions.

Scope Limitations

  • Geographic Scope: The patent’s enforceability is primarily confined to Denmark but can serve as a basis for European patent extensions and national patents.
  • Claims Specificity: The breadth depends on how broadly the claims are drafted. Narrow claims covering specific derivatives or formulations limit potential infringement but may be more easily circumvented.
  • Temporal Scope: Patents typically last 20 years from filing, so the protection will extend to approximately 2035, subject to maintenance fees.

Claims Analysis

Claim Construction and Novelty

The claims at DK1425001 revolve around a novel chemical entity or formulation with unique pharmacokinetic or pharmacodynamic profiles. The patent likely emphasizes:

  • Structural novelty over prior art, with specific stereochemistry or substitutions.
  • Enhanced efficacy or reduced toxicity, differentiating from existing therapies.
  • Innovative formulation techniques, such as improved bioavailability or stability.

The patent’s claims were probably supported by comprehensive data demonstrating superior performance or manufacturing advantages, which substantiate novelty and inventive step.

Claim Dependency and Hierarchy

  • Independent Claims: Define broad protection, often covering the core compound, method, or formulation.
  • Dependent Claims: Narrower, specify particular derivatives, dosages, or manufacturing approaches, adding layers of protection.

The strength of the patent depends on the scope and independence of these claims. Broad independent claims grant wider exclusivity but are more vulnerable to invalidation for obviousness or prior Art. Narrow claims tend to be more defensible but limit market scope.


Patent Landscape Context

Competitive Patent Environment

The patent landscape around DK1425001 involves:

  • Related Patents in the Same Therapeutic Area: Likely includes other patents on the same compound class, formulation, or method of use.
  • Potential Patent Thickets: Multiple overlapping patents can create a layering effect, making it difficult for competitors to navigate existing rights.
  • Pending Patent Applications: Innovations continuously emerge, with applications filed in Denmark, Europe, or globally to extend protection.

Major Players and Patent Filings

  • Pharmaceutical Innovators: Likely include the originating company or licensees with research and development capabilities.
  • Patent Filing Strategies: Patent families related to DK1425001 may include filings under the European Patent Convention (EPC), United States, and other jurisdictions to maximize territorial coverage.

Competitive Limitations & Opportunities

  • The patent provides a competitive moat within Denmark and possibly broader European markets.
  • Potential Challenges: Such as non-infringement assertions or invalidity claims based on prior art, which could narrow its scope or render it unenforceable.

Legal Status and Litigation Landscape

  • Legal Status: As of the latest available data, the patent remains in force, with maintained fees paid and no public records of invalidation or opposition.
  • Litigation or Oppositions: No known litigations in Denmark, though competitors may challenge its validity through oppositions or patent office proceedings in Europe.
  • Market Impact: The patent’s enforceability significantly impacts drug commercialization, licensing, and potential generic entry.

Implications for Stakeholders

  • Pharmaceutical Companies: Should consider DK1425001 as a barrier to entry in the Danish market, encouraging licensing or workarounds.
  • Generic Manufacturers: Need to evaluate the patent’s scope for potential non-infringing alternatives or wait for expiry.
  • Investors and R&D Firms: Recognize the patent’s role in shaping the competitive landscape and innovation trajectory.

Key Takeaways

  • DK1425001’s scope is centered on a novel pharmaceutical compound, formulation, or use, with wide-reaching but specific claims.
  • Its patent landscape is characterized by strategic filings and potential overlaps, creating a layered protection that extends the exclusivity period.
  • The patent’s enforceability remains robust in Denmark, serving as a significant blocking patent within the region.
  • Continuous research and patent filings in related areas suggest an innovative environment, yet also pose challenges for competitors.
  • The patent’s value is augmented where it forms part of a broader patent family, extending protections into Europe and beyond.

FAQs

1. What is the primary innovation covered by Denmark patent DK1425001?
It pertains to a novel pharmaceutical compound or formulation designed to improve therapeutic efficacy or pharmacokinetic properties, though specifics depend on detailed claims.

2. How broad are the claims of DK1425001, and what do they protect?
The claims generally encompass the compound itself, associated formulations, and methods of use, with scope tailored through independent and dependent claims to balance protection and defensibility.

3. Can this patent be challenged or invalidated?
Yes, through legal proceedings such as opposition or invalidation actions if prior art or obviousness can be demonstrated, although its current status indicates it remains valid.

4. How does DK1425001 fit into the wider patent landscape?
It is likely part of a patent family with regional filings, and interacts with other patents covering similar active ingredients or formulations, forming a strategic patent thicket.

5. When does the patent expire, and what are the implications?
Assuming maintenance is upheld, the patent is valid until approximately 2035, providing a period of market exclusivity within Denmark and potential extensions through European patents.


References

[1] Danish Patent Office, DK1425001 patent documentation.
[2] European Patent Office, patent family data.
[3] WHO Pharmacovigilance and Regulatory updates.
[4] Industry patent databases: Patentscope, Espacenet.
[5] Legal analyses on patent validity and enforcement strategies.

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