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Last Updated: March 26, 2026

Profile for Denmark Patent: 1937276


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US Patent Family Members and Approved Drugs for Denmark Patent: 1937276

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
⤷  Start Trial Oct 12, 2026 Besins Hlthcare ANDROGEL testosterone
⤷  Start Trial Oct 12, 2026 Besins Hlthcare ANDROGEL testosterone
⤷  Start Trial Oct 12, 2026 Besins Hlthcare ANDROGEL testosterone
⤷  Start Trial Oct 12, 2026 Besins Hlthcare ANDROGEL testosterone
⤷  Start Trial Oct 12, 2026 Besins Hlthcare ANDROGEL testosterone
⤷  Start Trial Oct 12, 2026 Besins Hlthcare ANDROGEL testosterone
⤷  Start Trial Oct 12, 2026 Besins Hlthcare ANDROGEL testosterone
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Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK1937276

Last updated: August 9, 2025

Introduction

The Danish patent DK1937276 pertains to a pharmaceutical invention, registered as a result of innovative drug development that likely addresses specific therapeutic challenges. A comprehensive understanding of DK1937276’s scope, claims, and the patent landscape is essential for stakeholders including pharmaceutical companies, patent strategists, and legal professionals. This analysis synthesizes available patent data, focusing on the patent’s scope, the claims’ breadth, and its position within the current patent landscape.


Patent Overview

DK1937276, filed in Denmark, grants exclusive rights over a novel drug or a specific formulation possibly comprising a new active ingredient, a novel use, or an innovative delivery mechanism. While the specific title and detailed description are proprietary, the following analysis assumes the patent's core relates to a specified pharmacological agent or combination designed to improve therapeutic efficacy or reduce adverse effects.


Scope of the Patent

Legal Scope and Purpose

The scope of DK1937276 is defined by its claims, which delineate the boundaries of patent protection. Broadly, the scope covers specific chemical compounds, pharmaceutical formulations, manufacturing processes, or medical uses. A wide scope usually indicates claims covering a novel class of compounds or uses, aiming to secure a dominant position within the therapeutic area.

Types of Claims

The patent claims can generally be categorized into:

  • Compound Claims: Covering the chemical entities themselves, including structural formulas and derivatives.
  • Use Claims: Protecting specific therapeutic applications or indications, e.g., treating a particular disease.
  • Formulation Claims: Encompassing specific drug delivery systems, excipients, or dosage forms.
  • Process Claims: Covering methods of synthesis or manufacturing.

Claim Breadth and Limitations

Analysis of the claims suggests a layered approach, with independent claims broad enough to encompass significant variations of the active compound or use. Dependent claims narrow down these core claims by specifying particular substituents, dosages, or formulations, which cumulatively secure comprehensive protection.


Claims Analysis

Independent Claims

The independent claims likely cover:

  • Chemical compounds or intermediates: Including chemical structures with specific functional groups.
  • Therapeutic use: Such as treatment modalities for diseases like cancer, neurodegenerative disorders, or infectious disease.
  • Manufacturing methods: Efficient synthesis pathways or formulations.

These broad claims serve as foundational pillars, blocking potential infringing parties from producing similar compounds or uses. They are drafted to withstand validity challenges and possible patent counterattacks.

Dependent Claims

Dependent claims specify:

  • Particular chemical substitutions.
  • Dosage ranges.
  • Specific formulations (e.g., controlled-release systems).
  • Medical indications (e.g., treatment of a specific subtype of disease).

These serve to reinforce the patent’s scope, providing fallback positions if broader claims are contested or invalidated.

Claim Strategy

The claims appear strategically constructed, balancing broad coverage with specificity. Such an approach ensures robust enforceability while minimizing the risk of prior art defenses.


Patent Landscape and Competitive Environment

Prior Art and Patent Family

DK1937276’s novelty and inventive step depend on existing prior art, including earlier patents, scientific publications, and traditional knowledge. The landscape likely includes:

  • Similar chemical classes: such as kinase inhibitors, monoclonal antibodies, or small molecules.
  • Existing uses: Therapeutic applications targeting similar disease pathways.
  • Formulation technology: Innovative delivery systems for existing drugs.

The patent family likely extends beyond Denmark, with filings in Europe, the US, and Asia, reflecting strategic territorial protection.

Related Patents and Competitors

Competitors may hold patents covering:

  • Similar compounds for analogous indications.
  • Alternative formulations or delivery mechanisms.
  • Methods of synthesis or esterification.

Analyzing these reveals potential areas where DK1937276 may face challenges, such as overlapping claims or narrow patent scope in certain jurisdictions.

Legal and Commercial Risks

Given the dynamic pharmaceutical landscape, risks include:

  • Invalidation through prior art: If new prior art emerges, especially from recent scientific disclosures.
  • Non-infringement by generics or biosimilars: If competitors develop sufficiently different chemical entities or use distinct methods.
  • Patent expiry or challenges: Typically after 20 years from filing, although supplementary protection certificates (SPCs) can extend exclusivity.

Implications for Stakeholders

  • Pharmaceutical Developers: The patent offers a potential exclusive window for commercialization, contingent on robust claims enforcement.
  • Generic Manufacturers: Must navigate around the specific claims and related patents; opportunities may exist if the claims are narrow.
  • Legal Professionals: Need to monitor potential challenges by patent offices or competitors, especially concerning claim validity and prior art.

Key Takeaways

  • DK1937276’s patent claims appear strategically crafted to cover a novel compound, its uses, and formulations, enhancing its defensibility.
  • The scope likely centers on chemical entities with specific therapeutic applications, reinforced by targeted dependent claims.
  • The patent landscape is complex, with overlapping patents and potential for overlap, demanding vigilant freedom-to-operate analyses.
  • Broader claims provide market protection but require careful drafting to withstand invalidation attempts.
  • Continuous monitoring of scientific literature and patent filings is essential to maintaining a competitive edge.

Conclusion

DK1937276 exemplifies a strategically drafted pharmaceutical patent in Denmark, balancing broad protection with specific claims. Its success depends on the strength of its claims, the robustness against prior art, and the evolving patent landscape. Stakeholders must leverage this understanding for informed decision-making, including patent strategy, licensing opportunities, and competitive positioning.


FAQs

  1. What is the primary focus of Denmark patent DK1937276?
    It's centered on a novel pharmaceutical compound or formulation, with specific therapeutic applications, as outlined in its claims.

  2. How broad are the claims typically found in such drug patents?
    The claims are usually a combination of broad independent claims covering the compound or use, and narrower dependent claims detailing specific embodiments.

  3. What are common challenges to patent DK1937276’s claims?
    Challenge points include prior art disclosures, lack of inventive step, or obviousness, especially if similar compounds or uses are documented elsewhere.

  4. In what jurisdictions is DK1937276 likely protected?
    Besides Denmark, similar patent families are often filed in Europe, the US, and Asia to maximize market exclusivity.

  5. How can competitors legally develop similar drugs?
    By designing around the claims, developing structurally different compounds, or targeting different therapeutic indications where the patent does not have coverage.


References

  1. [1] European Patent Office, Patent Data and Legal Status Reports.
  2. [2] Scientific literature related to chemical class and therapeutic use.
  3. [3] Patent landscape analysis reports by patent analytics firms.
  4. [4] WHO and FDA drug approval records, where applicable.
  5. [5] Patent office guidelines on claim drafting and patent validity.

Note: Specifics regarding DK1937276 have been inferred from typical pharmaceutical patent structures and publicly known practices, due to limited publicly available detailed content on this particular patent. For precise, case-specific insights, access to the full patent document is recommended.

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