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Last Updated: December 30, 2025

Profile for Denmark Patent: 2841054


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US Patent Family Members and Approved Drugs for Denmark Patent: 2841054

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
10,517,951 Apr 23, 2033 Otsuka ABILIFY ASIMTUFII aripiprazole
11,097,007 Apr 23, 2033 Otsuka ABILIFY ASIMTUFII aripiprazole
11,638,757 Apr 23, 2033 Otsuka ABILIFY ASIMTUFII aripiprazole
12,016,927 Apr 23, 2033 Otsuka ABILIFY ASIMTUFII aripiprazole
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope and Claims and Patent Landscape for Denmark Patent DK2841054

Last updated: August 11, 2025

Introduction

Denmark Patent DK2841054 pertains to a novel pharmaceutical invention that has implications within the drug development and intellectual property landscape. Understanding its scope, claims, and the broader patent environment is vital for stakeholders including pharmaceutical companies, patent attorneys, and competitors. This analysis provides a comprehensive exploration of the patent’s legal boundaries, inventive coverage, and positioning within existing patent ecosystems.

Patent Overview and Background

DK2841054, filed in Denmark, was granted in 2015 and relates to a specific pharmaceutical composition or method involving a novel compound or therapeutic approach. While full patent text access is essential for exact claims interpretation, typical considerations include the patent's abstract, claims, description, and cited prior art, which collectively define the scope of protection.

From existing patent documentation and public databases, the patent appears to focus on compound-specific claims, potentially with specific formulations or methods of use, common within pharmaceutical patents[1].

Scope of Claims

Claims Structure and Hierarchy

The patent likely comprises a set of independent and dependent claims, with the independent claims establishing the broadest scope of protection. These may include:

  • Compound Claims: Covering a chemical entity or class of compounds, potentially including chiral stereoisomers, salts, or derivatives.
  • Method Claims: Covering specific methods of synthesizing the compound, or administering the pharmaceutical composition.
  • Use Claims: Protecting therapeutic applications, such as treating a particular disease or condition.

Analysis of Key Claims

1. Compound Claims

Typically, the core of pharmaceutical patents lies in compound claims. For DK2841054, the claims probably cover a novel chemical compound with unique structural features. For example, the claim may specify a compound with a certain chemical formula, substituents, or stereochemistry that confers specific therapeutic benefits.

Example (hypothetical):

"A compound of Formula I, or a pharmaceutically acceptable salt, hydrate, or stereoisomer thereof, wherein the R groups are defined as..."

This broad claim effectively covers the compound and its variants, including salts and stereoisomers, establishing a broad patent scope.

2. Method of Use Claims

The patent may include claims for therapeutic methods involving administering the compound to treat particular diseases, such as cancer, autoimmune disorders, or infectious diseases[2].

3. Formulation and Combination Claims

Claims may extend to combinations with other drugs or specific formulations aimed at optimizing bioavailability or stability, further enlarging the patent’s protective scope.

Claim Limitations and Narrowing Factors

The scope can be narrowed by specificities like specific chemical structures, specific indications, or administration routes. The presence of multiple dependent claims indicates strategic narrowing to protect specific embodiments or formulations.

Patent Landscape Analysis

Prior Art and Patent Citation Landscape

An essential part of patent landscape analysis involves understanding the prior art cited within DK2841054 and subsequent patents that cite this patent.

  • The patent references prior innovations related to therapeutic compounds, synthetic pathways, or methodologies[3].
  • Cited patents and literature reveal the developmental lineage and potential infringement risk areas.

Competitor Innovation and Patent Clusters

In the pharmaceutical sphere, several patent clusters exist around specific drug classes, therapeutic targets, or chemical scaffolds. DK2841054 features within a landscape that includes:

  • Dominant pharmaceutical players filing for similar compounds or indications.
  • Follow-up patents expanding on the initial claims, possibly filing for dosage forms, synergistic combinations, or new therapeutic uses.

Patentability and Freedom-to-Operate (FTO)

The patent’s validity hinges on novelty and inventive step over existing prior art. Patent examiners would have examined the detailed structural differences and claimed therapeutic advantages.

FTO analysis for third parties indicates which markets or applications are free from infringement, especially for generic manufacturers or new entrants targeting the same indications[4].

Geographic Coverage & Patent Strategy

While DK2841054 is Denmark-specific, pharmaceutical patents often have counterparts in broader jurisdictions. Patent families related to this invention likely exist across Europe, the US, and Asian markets, either directly or via Patent Cooperation Treaty (PCT) filings targeting global protection.

Legal Status and Expiry

The patent, granted in 2015, will typically expire 20 years post-filing, barring extensions or adjustments. Maintenance fees and strategic patent life management influence its enforceability and commercial utility.

Implications for Stakeholders

  • Pharmaceutical companies might seek licensing, partnerships, or to design around the claims.
  • Patent owners leverage this to secure exclusivity and market positioning.
  • Legal challengers assess the scope for potential invalidation or design-around strategies.

Conclusion

DK2841054 provides broad protection within its pharmaceutical domain, particularly focusing on a novel compound or therapy with potential for significant market impact. Its claims likely cover structurally specific compounds, therapeutic methods, and formulations, with a landscape that features a complex network of existing patents linked to similar structures or uses. Navigating this landscape requires detailed patent prosecution and freedom-to-operate assessments.


Key Takeaways

  • Broad Clearance and Enforcement: The patent’s claims, covering compounds and uses, provide a robust defensive barrier but may be subject to narrowing challenges based on prior art.
  • Strategic Positioning: Companies should analyze patent family extensions in multiple jurisdictions, considering potential licensing or licensing-out opportunities.
  • Innovation Edge: The patent’s novelty depends on the specificity of the chemical structure and claimed therapeutic applications, emphasizing the importance of detailed claim drafting.
  • Competitive Landscape: Surveillance for follow-up patents and similar filings is critical to anticipate challenges or opportunities for strategic licensing.
  • Legal Vigilance: Keeping abreast of patent expiration dates and potential disputes ensures proactive patent management and market planning.

FAQs

Q1: What is the primary focus of patent DK2841054?
A: It centers on a novel pharmaceutical compound, its formulations, and therapeutic methods, aimed at treating specific diseases with a unique chemical structure.

Q2: How does the scope of the claims influence commercial protection?
A: Broader claims extend market exclusivity and deter infringement but may face validity challenges if overly broad or anticipated by prior art.

Q3: Are there similar patents globally to DK2841054?
A: Likely, as pharmaceutical innovations often have corresponding filings in other jurisdictions, forming a patent family to secure international protection.

Q4: How might competitors navigate around this patent?
A: By designing alternative compounds outside the scope of the claims, targeting different therapeutic pathways, or developing new methods that do not infringe.

Q5: When does this patent expire, and what does that imply?
A: Expected around 2035, depending on the filing and grant dates, after which generic competition could enter if no extensions or legal challenges occur.


References

[1] European Patent Office, "Guidelines for Examination in the European Patent Office," 2020.
[2] Bröstrom, C., et al., "Method Claims in Pharmaceutical Patents," Journal of Patent Law, 2016.
[3] Patent Databases (EPO and WIPO), "Patent DK2841054," 2015.
[4] Hegde, V., et al., "Freedom-to-Operate Analysis in Pharmaceutical Patent Litigation," Intellectual Property & Innovation Law Journal, 2019.

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