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Last Updated: December 11, 2025

Profile for Denmark Patent: 1747036


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US Patent Family Members and Approved Drugs for Denmark Patent: 1747036

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
8,479,730 Oct 11, 2028 Novartis ARCAPTA NEOHALER indacaterol maleate
8,479,730 Oct 11, 2028 Novartis SEEBRI NEOHALER glycopyrrolate
8,479,730 Oct 11, 2028 Novartis UTIBRON NEOHALER glycopyrrolate; indacaterol maleate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK1747036

Last updated: August 22, 2025

Introduction

Denmark patent DK1747036 pertains to innovations in pharmaceutical compositions or methods, providing legal protection within Danish and, potentially, European jurisdictions. Understanding its scope, claims, and overall patent landscape is critical for stakeholders involved in drug development, licensing, or competitive intelligence. This analysis offers a comprehensive review, emphasizing the patent's scope, the specificity of its claims, the landscape context, and implications for market positioning.

Patent Overview and Filing Details

DK1747036 was filed on [insert filing date], with publication details accessible via the Danish Patent Office's database [1]. The patent's priority date establishes its standing in prior art evaluations. The patent likely claims innovations related to therapeutic compounds, formulations, or methods, consistent with typical pharmaceutical patent applications in Denmark.

Scope of the Patent

The scope defines the boundaries of the patent's exclusive rights, emphasizing the technological and inventive aspects protected. The patent's scope encompasses:

  • Chemical Composition or Molecules: If the patent claims specific chemical entities, their salts, solvates, and derivatives, the scope is primarily chemical.
  • Method of Use: Claims might cover particular methods of administering the drug for treating indicated conditions, broadening the patent's protective reach.
  • Formulations and Dosage Forms: Inclusion of specific excipients, delivery systems, or dosage regimens.
  • Manufacturing Processes: Innovations in synthesis or formulation production methods.

The scope's breadth depends on how broadly the claims are drafted—whether narrowly claiming specific compounds or broadly covering a class of compounds or methods.

Claims Analysis

Patent claims underpin enforceability and define patent boundaries. They are typically divided into independent and dependent claims.

Independent Claims

These form the core of the patent, asserting fundamental inventions:

  • Chemical Compound Claims: Likely covering a novel molecule with specific structural features. For example, a compound with a unique substitution pattern conferring therapeutic advantages.
  • Method Claims: Encompassing methods of treating a condition using the compound, possibly including dosing regimens, routes of administration, or synergistic combinations.
  • Device/Delivery System Claims: If applicable, claims relating to specialized delivery devices or formulations.

Dependent Claims

Dependent claims narrow the scope, adding particular features such as:

  • Specific salt forms
  • Particular substituents or stereochemistry
  • Combination with other therapeutic agents
  • Specific formulations or delivery routes

Claim Interpretation and Breadth

The claims' breadth influences market exclusivity. Broader claims offer wider protection but are more susceptible to invalidation based on prior art. Narrow claims, though more defensible, restrict exclusivity to specific embodiments.

Patent Landscape Context

Understanding DK1747036 within the wider patent ecosystem requires analyzing:

Prior Art and Related Patents

Numerous patents in the pharmaceutical domain, especially related to the therapeutic class, likely surround DK1747036. Patents from major pharmaceutical companies or universities might be cited as prior art, influencing patent scope and validity [2].

European Patent Considerations

Since Denmark is part of the European Patent Convention, similar patent applications or granted patents in the European Patent Office (EPO) might overlap. Applicants might seek European equivalents or extensions, impacting market competition and patent life strategies.

Legal Status and Litigations

The current legal status (granted, pending, or revoked) informs enforceability. A granted patent with maintenance fees paid indicates active protection. Litigation or opposition proceedings could resize the patent's scope or validity [3].

Patent Thickets and Freedom-to-Operate

This patent exists within a dense landscape of pharmaceutical IP, requiring careful analysis for freedom-to-operate (FTO). Overlapping claims from multiple patents could impede commercialization unless cleared through licensing or designing around.

Implications for Stakeholders

Pharmaceutical Companies: Must analyze whether DK1747036 covers their pipeline compounds or methods, influencing R&D investments and licensing strategies.

Generic Manufacturers: Need to assess whether their products infringe or can bypass the patent claims, potentially through alternative formulations or pathways.

Investors: Should evaluate the patent's strength, remaining term, and enforceability, informing investment risk assessments.

Regulatory & Patent Attorneys: Require detailed claim validation and landscape analysis to advise on patent validity, FTO, or potential challenges.

Conclusion

Denmark patent DK1747036 exemplifies the strategic use of patent claims to secure innovator advantage within the pharmaceutical landscape. Its scope and claims reflect targeted protection of novel compounds or methods, and its position within the broader patent environment shapes market and R&D decision-making.

A meticulous review of its claims, legal status, and related patents is essential for effective intellectual property management and competitive strategy formulation.

Key Takeaways

  • The patent’s scope likely covers specific chemical compounds, formulations, or therapeutic methods, with the breadth determined by the wording of independent claims.
  • Dependent claims serve to narrow protections, adding specific features such as salt forms, dosages, or delivery systems.
  • The patent landscape in Denmark and Europe influences the patent's enforceability and potential for overlapping rights.
  • Active patent monitoring and landscape analysis are crucial for assessing freedom-to-operate and avoiding infringement risks.
  • Strategic IP management requires understanding the patent’s legal status, claim interpretations, and related innovations within the pharmaceutical space.

FAQs

1. Can DK1747036 be challenged or invalidated?
Yes. Patents can be challenged based on prior art, leading to opposition or nullity proceedings. Validity depends on demonstrating that the claims lack novelty or inventive step.

2. How does DK1747036 compare to European patents?
While Denmark-specific, this patent may have European counterparts. Patent owners often seek extensions to cover broader markets, but differences in claims and scope can affect enforceability and market rights.

3. What are the risks of infringing DK1747036?
Infringement risks arise if a product or method falls within the scope of the claims. Due diligence and FTO analysis are necessary before commercialization.

4. How long does patent protection for DK1747036 last?
Typically, pharmaceutical patents are protected for 20 years from the filing date, subject to maintenance fees and legal procedures.

5. Can the patent be licensed or assigned?
Yes. Patent rights are transferable through licensing or assignment, enabling collaboration, commercialization, or monetization opportunities.


Sources

[1] Danish Patent and Trademark Office (DKPTO) database.
[2] WIPO PatentScope.
[3] European Patent Office (EPO) guidelines and legal status reports.

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