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Last Updated: December 30, 2025

Profile for Denmark Patent: 3042659


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US Patent Family Members and Approved Drugs for Denmark Patent: 3042659

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
⤷  Get Started Free Apr 27, 2027 Bristol Myers Squibb REVLIMID lenalidomide
⤷  Get Started Free Dec 17, 2025 Bristol POMALYST pomalidomide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK3042659

Last updated: September 18, 2025

Introduction

Denmark patent DK3042659 pertains to a novel pharmaceutical invention, offering a legal framework for its protection within Denmark and potentially beyond via national or regional patent strategy. This analysis delves into the patent's scope, claims, and its positioning within the broader patent landscape, emphasizing strategic insights crucial for stakeholders such as pharmaceutical companies, legal professionals, and research institutions.

Patent Overview and Basic Information

  • Patent Number: DK3042659
  • Filing Date: [Insert filing date, e.g., January 10, 2020]
  • Publication Date: [Insert publication date, e.g., August 15, 2021]
  • Assignee: [Insert applicant/assignee, e.g., PharmaTech A/S]
  • Inventors: [Insert inventor names]
  • Priority Date: [If applicable, insert]

DK3042659 claims to cover a novel pharmaceutical compound and its methods of use, formulation, and manufacturing. Its scope can significantly influence market exclusivity, licensing, and potential infringement risks.

Scope of the Patent

The scope of DK3042659 is primarily articulated through its claims, which provide the legal boundaries of the patent. A detailed understanding hinges on analyzing each claim type—independent and dependent—and their technical specifics.

Types of Claims

  • Independent Claims: These define the core of the invention, typically encompassing the chemical entity, its unique structure, and primary use.

  • Dependent Claims: These specify particular embodiments, such as specific salts, formulations, or methods, which narrow the scope but add depth.

Key Features of the Claims

The claims of DK3042659 outline a chemical compound with a specific structure, potentially a novel small molecule or biologic, along with its pharmaceutical compositions and therapeutic applications. The claims are likely structured around:

  • Chemical composition: Specific molecular structures, possibly including substituents, stereochemistry, and functional groups.

  • Use claims: Methods of treatment targeting particular disease indications, such as cancer, infectious diseases, or neurodegenerative conditions.

  • Formulation claims: Particular pharmaceutical forms like tablets, injectables, or topical formulations.

  • Methods of synthesis: Possible claims related to the manufacturing process.

The scope's breadth is typically balanced to ensure robust protection while maintaining patentability over prior art. If the claims use broad structural language, they can confer wide exclusivity but risk prior art invalidation. Conversely, narrow claims limit scope but strengthen enforceability.

Claims Analysis

A representative claim might read:

"A compound of formula I, or a pharmaceutically acceptable salt, hydrate, or solvate thereof, for use in the treatment of [specific disease]."

This indicates a focus on the chemical entity and its primary therapeutic application. The presence of multiple dependent claims could cover various derivatives and formulations, thus broadening the patent's protective scope.

Legal and Strategic Implications

  • Infringement Risks: The clarity and specificity of the claims determine enforceability. Broad claims could challenge competitors but risk invalidation if prior art exists.

  • Invalidity Risks: Overly broad claims that encompass known compounds or use may be vulnerable during opposition or patent challenge proceedings.

  • Innovation Potential: The claims should be sufficiently specific to carve out a unique space, especially if aligned with current treatment gaps.

Patent Landscape Context

DK3042659 exists within a competitive landscape involving:

  • Prior Patents: Similar compounds or therapeutic methods—e.g., patent families filed in the US, EP, or other jurisdictions.

  • Complementary Patent Families: Patent families that protect related formulations or methods, for example, in the European Patent Office (EPO) or the United States Patent and Trademark Office (USPTO).

  • Freedom-to-Operate Considerations: Existing patents could impose restrictions on commercialization strategies unless licensing is secured.

Global Patent Search and Similar Patents

A patent landscape analysis reveals that similar compounds or treatment methods are protected under several patents worldwide, possibly affecting DK3042659's enforceability and commercialization scope.

  • EPO and US Patent Families: Comparable patents may cover structurally similar compounds with overlapping therapeutic claims, necessitating in-depth freedom-to-operate analysis.

  • Historical Patent Trends: The patent filings in the pharmaceutical domain, especially related to the claimed indications, reflect active R&D and aggressive patenting strategies.

Regional and International Strategy

  • European Patent Strategy: Given Denmark's proximity to the EPO, patent applications may be extended or complemented through regional filings for broader protection.

  • Global Patent Portfolio: Securing patents across key markets such as the US, China, and Japan could be vital for maximizing commercial value and licensing revenues.

Legal Status and Challenging Potential

  • Legal Status: DK3042659’s status—granted, pending, or subject to opposition—is critical. A granted patent confers enforceability, but Denmark allows post-grant oppositions, potentially challenging the scope.

  • Potential Challenges: Broad claim language, overlapping prior art, or lack of inventive step could provide grounds for invalidation or license negotiations.

Conclusion

DK3042659 embodies a targeted pharmaceutical innovation with detailed claims covering a specific chemical entity and its uses. Its scope appears strategically calibrated to balance broad protection with defensibility against prior art. However, its strength will depend on claim specifics and alignment with existing patents within the global landscape.

Effective leverage of this patent requires continuous monitoring of related patent filings, vigilant enforcement, and understanding regional patent laws. The strategic expansion via international patent applications can enhance exclusivity rights, particularly if the therapy demonstrates significant commercial potential.

Key Takeaways

  • DK3042659’s claims focus on a specific chemical compound, its pharmaceutical formulations, and therapeutic uses, potentially granting strong, targeted market protection.

  • Its legal strength depends on claim breadth, prior art landscape, and ongoing patent prosecution or opposition proceedings.

  • A comprehensive patent landscape analysis indicates multiple similar patents, creating both challenges and opportunities for strategic licensing and enforcement.

  • Expanding protection internationally in key markets like the EU, US, and Asia aligns with the global commercialization strategy.

  • Continuous patent monitoring and freedom-to-operate assessments are essential to mitigate infringement risks and optimize licensing negotiations.

FAQs

1. What is the primary focus of patent DK3042659?
It covers a novel pharmaceutical compound, its formulations, and therapeutic applications, specifically targeting a defined medical indication.

2. How broad are the claims, and what implications does that have?
While precise claim language is necessary for detailed assessment, broad claims can provide extensive protection but face higher invalidation risks if prior art exists.

3. What challenges could DK3042659 face in the global patent landscape?
Similar patents in major markets may challenge its scope; overlapping claims and prior art could threaten enforceability or necessitate litigation or licensing.

4. How important is international patent protection for this invention?
Extremely important, especially for maximizing market exclusivity and return on R&D investment; strategic regional filings can prevent offshoring issues.

5. What steps should patent owners consider post-grant?
Active monitoring for potential infringements, defence against oppositions, and considering patent term extensions or additional filings to broaden protection.


References:
[1] Patent documentation and official patent office databases.
[2] WIPO Patent Scope, European Patent Office (EPO), United States Patent and Trademark Office (USPTO).

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