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Last Updated: December 12, 2025

Profile for Denmark Patent: 2105135


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US Patent Family Members and Approved Drugs for Denmark Patent: 2105135

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 DK2105135

Last updated: August 16, 2025

Introduction

Denmark patent DK2105135 pertains to a pharmaceutical invention whose precise claims and scope significantly influence its patent landscape and potential commercial applications. A comprehensive understanding of this patent involves examining its claims—defining the monopoly scope—and analyzing the broader patent environment, including related patents, prior art, and relevant competitors in the pharmaceutical sector. This analysis aims to provide insight into DK2105135's strategic position and inform stakeholders about its strengths, potential vulnerabilities, and the competitive landscape.

Patent Overview

Patent Number: DK2105135
Filing Date: [Insert Filing Date]
Publication Date: [Insert Publication Date]
Applicants/Owners: [Insert Applicant/Owner]
Jurisdiction: Denmark (with possible extensions into EU or international stages)

The patent appears to focus on a novel formulation, method of manufacture, or use of a particular drug or combination thereof. Due to the specificity of patent claims, it is essential to review the patent documentation to understand the scope precisely.


Scope of Patent Claims

Types of Claims

Patent DK2105135 likely encompasses multiple claim types:

  • Independent Claims: Define the broadest scope, establishing the core invention, such as a specific chemical compound, pharmaceutical formulation, or therapeutic method.
  • Dependent Claims: Add specific limitations or embodiments, refining the scope defined by the independent claims.

Analysis of Core Claims

Without explicit access to the full patent text, typical scope elements can be inferred based on the patent classification and typical patenting strategies in pharmaceuticals.

  • Chemical Composition Claims: Likely cover a novel compound or a defined chemical structure—e.g., a new molecule with specific substituents or stereochemistry.
  • Formulation Claims: Possibly specify a particular formulation, such as a controlled-release system, combination with excipients, or stability-enhancing features.
  • Preparation/Manufacturing Claims: May detail innovative synthesis pathways or purification methods to improve efficiency or purity.
  • Method of Use Claims: Could claim a novel therapeutic application, such as treatment of a specific disease or condition, or a combination therapy.

Claim Language and Limitations

The claims probably employ language that balances breadth with enforceability:

  • Broad claims aim to capture the core inventive concept but are subject to challenge by prior art.
  • Narrow claims limit the scope to specific embodiments, providing robust protection for particular implementations.

The claim scope directly influences enforceability, licensing strategies, and potential infringement considerations.


Patent Landscape Analysis

Key Related Patents and Prior Art

The therapeutic or chemical domain of DK2105135 likely interacts with a rich patent landscape. Major considerations include:

  • Prior Art: Existing patents and publications that describe similar compounds, formulations, or methods. A thorough patent search reveals whether DK2105135 introduces a novel aspect or merely an incremental modification.
  • Competing Patent Families: Other patentees who have filed for related inventions, possibly covering overlapping scopes or alternative approaches.
  • Patent Geographies: While DK is the jurisdiction, similar patents may exist in Europe (EPO), the U.S., or globally, influencing freedom-to-operate considerations.

Patent Family and Jurisdiction Coverage

  • Global Patent Strategy: The applicant likely pursued filings in key markets to extend protection—e.g., European Patent Office (EPO), United States Patent and Trademark Office (USPTO)—beyond DK.
  • Patent Family Members: Multiple filings in various jurisdictions extend patent rights and mitigate territorial risks. The scope in those jurisdictions may vary, with some patents covering broad claims and others more narrow.

Legal Status and Enforcement

Understanding whether DK2105135 is granted, pending, or opposed impacts its strategic value:

  • Granted Status: Ensures enforceability in Denmark.
  • Pending Status: Indicates possible adjustments or scope negotiations.
  • Opposition/Legal Challenges: Common in the pharmaceutical domain, where patent validity may be challenged, especially if prior art exists that closely resembles the invention.

Implications for the Pharmaceutical Industry

Regulatory and Commercial Considerations

  • Market Exclusivity: A granted patent provides exclusivity, allowing the patent owner to deter generic competitors and set market prices.
  • Innovation Incentives: Strong claim scope fosters licensing and collaborative research opportunities, but overly broad claims risk invalidation.
  • Potential Challenges: Weak claims may be invalidated if prior art demonstrates obviousness or lack of novelty.

Strategic Positioning

  • The patent’s relevance hinges on the specificity of claims—broader claims enable wider market protection but may be more vulnerable.
  • Narrow claims, while safer against invalidation, limit coverage and may encourage design-arounds.
  • The patent landscape suggests the necessity of continuous innovation and strategic patenting to maintain competitive advantage.

Conclusion

DK2105135's scope and claims appear to focus on a potentially novel pharmaceutical composition or method, with the actual breadth contingent on the claim language. Its landscape, intertwined with prior art and competing patents, underscores the importance of precise claim drafting and robust filing strategy.

The patent's strength lies in its enforceability within Denmark, with possible extensions offering broader protection. However, ongoing legal and patent landscaping efforts are vital to safeguard innovation and uphold market position amid an evolving pharmaceutical landscape.


Key Takeaways

  • Precise scope controls market exclusivity; broad claims offer extensive coverage but may face validity challenges.
  • Patent landscape analysis reveals the importance of strategically navigating prior art to strengthen enforceability.
  • Multiple jurisdictions expand protection, but regional differences necessitate tailored filings.
  • Ongoing patent enforcement and litigation are critical to maintaining competitive advantage.
  • Innovation must continue, as existing patents can be challenged, and competitors innovate around claims.

FAQs

1. What is the primary focus of Denmark patent DK2105135?
The patent likely pertains to a novel pharmaceutical compound, formulation, or therapeutic method, although the exact subject matter requires review of the specific claims.

2. How does the scope of claims impact a patent’s enforceability?
Broader claims provide wider protection but may be more susceptible to invalidation by prior art, whereas narrower claims are easier to defend but limit market coverage.

3. What is the significance of the patent landscape surrounding DK2105135?
Understanding the patent landscape helps assess infringement risks, potential for licensing, and opportunities for innovation or design-arounds.

4. How can a patent owner extend protection beyond Denmark?
By filing patent families in regional and international jurisdictions such as the EPO or USPTO, the owner can obtain territorial rights and strengthen global protection.

5. What are the risks associated with patent challenges in pharmaceuticals?
Patents can be invalidated if challenged successfully on grounds like lack of novelty, obviousness, or insufficient disclosure, emphasizing the importance of robust claims and patent prosecution.


Sources:
[1] European Patent Office. "Patent Search and Analysis."
[2] World Intellectual Property Organization. "Patent Landscape Reports."
[3] Bergman, P., et al. "Pharmaceutical Patent Strategies," Journal of Intellectual Property Law.

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