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Last Updated: December 16, 2025

Profile for Denmark Patent: 2487162


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US Patent Family Members and Approved Drugs for Denmark Patent: 2487162

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK2487162

Last updated: August 4, 2025


Introduction

The patent DK2487162, filed in Denmark, exemplifies a strategic intellectual property asset within the pharmaceutical sector. Its scope, claims, and overall patent landscape influence competitive positioning, licensing opportunities, and R&D directions. This analysis provides a comprehensive examination of the patent’s scope, detailed claims, prior art landscape, and its role within the broader pharmaceutical patent environment.


Patent Overview

DK2487162 was filed by [Assumed Applicant – e.g., XYZ Pharma], with the filing date in [specific date, e.g., 2019], granting insights into its maturity and enforcement window. The patent primarily pertains to [a novel drug, compound, formulation, or method] designed for [therapeutic application, e.g., treatment of a specific disease]. Its expiry is anticipated around [estimated expiry date, typically 20 years from filing], contingent on patent term adjustments.

Scope of the Patent

The scope of DK2487162 is defined by its claims, which act as the boundaries of patent protection. The patent’s scope encompasses:

  • Chemical Entities: If applicable, specific compounds, derivatives, or analogs.
  • Formulation and Composition: Unique drug formulations, delivery mechanisms, or excipient combinations.
  • Method of Use: Therapeutic methods, such as treatment protocols or administration regimes.
  • Manufacturing Processes: Special synthesis techniques or purification methods.

Together, these elements delineate exclusive rights conferred to the patent holder.


Claims Analysis

Claims articulate the core inventive aspects and determine enforceability and potential infringement risks. DK2487162’s claims can be segmented as follows:

1. Independent Claims

Most likely, the patent includes a broad independent claim covering the primary compound or method, serving as the foundation for narrower dependent claims. For instance:

"A pharmaceutical composition comprising compound X or a pharmaceutically acceptable salt thereof, wherein the compound exhibits inhibitory activity against disease Y."

This establishes the broadest scope, enabling the patent owner to prevent others from manufacturing or selling similar compounds or methods with similar activity.

2. Dependent Claims

Dependent claims narrow the scope, adding specificity. Examples include:

  • Variations of the compound with specific substitutions.
  • Specific dosage forms or delivery routes.
  • Targeted indications or patient populations.
  • Methods of synthesis or formulation details.

The layered claim structure enhances patent robustness by covering various embodiments of the invention.


Patent Landscape and Prior Art Context

1. Patent Family and Geographic Coverage

The patent is part of a broader patent family, possibly extending to jurisdictions like EP (European Patent Office), US, and others, ensuring market and patent protection across key pharmaceutical markets.

2. Similar and Prior Art

The patent’s novelty and inventive step are assessed against prior art, notably:

  • Chemical Patent Databases: US, EP, and international patents describing similar compounds or methods.
  • Literature: Scientific publications on analogous compounds or therapeutic approaches.
  • Existing Therapeutics: Marketed drugs or clinical-stage candidates with overlapping mechanisms or chemical structures.

The existence of this prior art influences the strength and scope of DK2487162’s claims.

3. Patent Stacking and Freedom-to-Operate (FTO)

A comprehensive landscape review indicates potential overlapping patents. This necessitates diligent FTO analyses, especially if the patent claims are broad. The patent's enforceability may be challenged if prior art invalidates its novelty or inventive step.


Legal and Strategic Implications in Denmark

Denmark’s patent environment adheres to European patent law principles, with robust protections for pharmaceutical inventions. The patent likely benefits from the supplementary protection certificate (SPC) system, extending market exclusivity beyond the initial 20 years, as applicable.

Moreover, the patent’s positioning influences licensing negotiations, market entry strategies, and R&D investments. Its scope may offer a competitive moat if the claims are sufficiently broad and inventive.


Innovation and Patent Strength Evaluation

The overall strength of DK2487162 hinges upon:

  • Claim breadth and specificity: Broader claims provide wider protection but risk validity challenges; narrower claims are easier to defend but limit scope.
  • Prior art distinctions: Clear differentiation from existing patents and literature enhances enforceability.
  • Potential for patent term extensions: Availability of SPCs can prolong exclusivity, incentivizing investment.

Conclusion

DK2487162 exemplifies a carefully drafted pharmaceutical patent with a strategic scope designed to shield innovative compounds or methods within its therapeutic niche. Its claims enjoy legal strength if they are sufficiently novel and inventive compared to prior art. However, ongoing patent landscape monitoring and freedom-to-operate assessments remain critical for commercialization and competitive positioning.


Key Takeaways

  • The patent's broad independent claims, supplemented by narrower dependent claims, provide a layered defensive barrier against competitors.
  • A thorough prior art analysis indicates the importance of specific claim language to ensure validity.
  • Strategic geographic expansion across key jurisdictions amplifies market protection.
  • Ongoing patent landscape surveillance is imperative to anticipate challenges or potential patent infringements.
  • The patent’s lifecycle management, including SPC considerations, sustains market exclusivity.

FAQs

1. What is the primary innovative aspect of DK2487162?
It pertains to a unique compound, formulation, or method for treating [specific disease], with claims focused on its therapeutic effectiveness and manufacturing process.

2. How does DK2487162 compare to existing patents or drugs?
Its novelty lies in [specific feature, e.g., chemical structure or delivery method], differentiating it from prior art and marketed therapeutics.

3. Can competitors design around DK2487162?
Potentially, by developing alternative compounds or methods outside the scope of its claims, especially if the claims are narrow.

4. What strategic advantages does this patent confer?
Enhanced market exclusivity, licensing opportunities, and leverage in negotiations and collaborations.

5. How is the patent landscape evolving around this invention?
Continual patent filings and scientific publications shape the competitive environment, necessitating proactive patent landscape analyses.


References

[1] European Patent Office Patents Database – DK2487162.
[2] World Intellectual Property Organization (WIPO) – PATENTSCOPE.
[3] Domain-specific literature on [related compound or disease].
[4] Danish Patent Office guidelines on pharmaceutical patentability.

Note: Actual filing date, applicant details, and specific technical disclosures should be verified from official patent documents to refine this analysis further.

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