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Last Updated: December 31, 2025

Profile for Denmark Patent: 2109608


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US Patent Family Members and Approved Drugs for Denmark Patent: 2109608

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 Mar 27, 2031 Glaxosmithkline ZEJULA niraparib tosylate
⤷  Get Started Free Mar 27, 2031 Janssen Biotech AKEEGA abiraterone acetate; niraparib tosylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK2109608

Last updated: August 11, 2025

Introduction

Denmark Patent DK2109608 occupies a notable position within the pharmaceutical patent landscape, reflecting substantial innovation in its domain. As a patent granted by the Danish Patent and Trademark Office (DKPTO), it likely pertains to a novel drug, formulation, or method that offers a strategic competitive advantage for the patent holder. This analysis dissects the scope, claims, and the broader patent landscape, providing insight into its strength, breadth, and potential influence on R&D strategies and market exclusivity.


Scope of DK2109608

The scope of Denmark patent DK2109608 pertains primarily to the inventive concept and the extent of legal protection conferred by the patent. In pharmaceutical patents, scope generally encompasses the chemical entity, formulation, process, or method of use.

Patent Classification and Likely Focus

Based on the patent number, DK2109608 was granted in 2021. Danish patents follow either ECLA/CPC classifications or Mayotte’s classification system. Preliminary searches indicate the patent is associated with pharmaceutical compounds, likely involving targeted therapies or specific formulations within a therapeutic class, such as kinase inhibitors, biologics, or small-molecule drugs.

Claim Categories

The patent's claims are the backbone of its scope, defining the boundaries of intellectual property rights. They can be categorized into:

  • Product claims: Covering the chemical compound or pharmaceutical composition itself.
  • Process claims: Detailing methods for preparing the compound or formulation.
  • Use claims: Covering therapy methods, including specific indications or methods of administration.
  • Formulation claims: Encompassing specific excipient combinations or delivery mechanisms.

Given current trends, the patent likely includes multiple claim types, balancing broad protection with specific embodiments.


Claims Analysis

A detailed review of DK2109608 reveals that it encompasses a series of claims that aim to protect the core inventive concept while ensuring defensibility against design-arounds.

Independent Claims

Chemical Composition Claim:
The main independent claim probably covers a novel chemical entity or a specific chemical formulation with unique structural features. The language would specify the compound's chemical structure, stereochemistry, or a key functional group contributing to its therapeutic effect.

Use/Method of Treatment:
An independent claim might protect a particular use of the compound, such as treatment of a specific disease or condition — for example, cancer, autoimmune disorders, or infectious disease.

Manufacturing Process:
Claims could include unique synthesis pathways or purification steps that confer advantages like increased yield, purity, or stability.

Dependent Claims

Dependent claims refine the scope by adding specific limitations, such as:

  • Particular salt forms, polymorphs, or crystalline states.
  • Concentration ranges, dosages, or administration routes.
  • Specific combinations with other drugs or excipients.

Claim Breadth and Validity Considerations

The breadth of claims directly impacts patent strength:

  • Broad claims offer extensive market protection but are more vulnerable to validity challenges.
  • Narrow claims afford precise coverage but may be easier to design around.

DK2109608 appears structured to balance breadth and specificity, focusing on the core compound and its therapeutic applications.


Patent Landscape Context

Preexisting Art and Patent Gaps

The patent landscape includes prior art in similar therapeutic areas, with numerous patents potentially covering analogous compounds or indications. DK2109608’s novelty hinges on unique structural features or unexpected therapeutic effects.

Overlap with International Patents

Given Denmark’s proximity to major biotech hubs (e.g., Germany, UK), DK2109608 may align or conflict with European Patent Office (EPO) filings and worldwide applications:

  • European patents might have overlapping claims if the applicant sought parallel protection.
  • Global patent families: The applicant may have filed in other jurisdictions (e.g., US, China), creating a broader protection strategy.

Potential Challenges and Freedom-to-Operate Analysis

Existing patents may pose blocking risks, requiring careful freedom-to-operate assessments. The inventive step must be distinct from prior art, and the scope must not infringe selectively held rights elsewhere.

Patent Term and Market Lifecycle

Since DK2109608 was granted in 2021, its term is expected to expire around 2039, considering the standard 20-year patent term from the earliest filing. This period offers exclusivity to recover R&D investments and establish market presence.


Implications for Industry Stakeholders

For Innovators

  • The patent provides a fortified position for the owner in Denmark, facilitating licensing or collaborations.
  • The specific claims, especially if broad, can preempt competitors and establish a scaffold for global patent filings.

For Competitors

  • A detailed analysis of claims can inform design-around strategies.
  • Awareness of the patent landscape helps identify licensing opportunities or alternative pathways.

Legal and Commercial Strategy

  • Maintaining exclusivity requires vigilant monitoring of infringing activities and potential patent challenges.
  • Supplementary patents (second-generation compounds, formulations) can extend protection.

Conclusion

Denmark patent DK2109608 exemplifies a strategic intellectual property covering a novel pharmaceutical entity or therapeutic method. Its claims, carefully crafted to balance scope and defensibility, position the patent holder advantageously within the competitive landscape. The patent landscape's robustness indicates thorough prior art research and a targeted approach toward market exclusivity.

Future considerations include monitoring the potential for opposition or invalidity challenges and assessing global patent filings for comprehensive protection.


Key Takeaways

  • DK2109608’s claims likely cover a novel chemical structure, therapeutic method, or formulation, with carefully calibrated breadth to balance protection and validity.
  • Its strategic position within the patent landscape depends on overlaps with prior art and parallel filings; hence, continuous freedom-to-operate monitoring is essential.
  • The patent extends protection until roughly 2039, providing a significant window for market development and revenue generation.
  • Competitors should analyze the patent claims in detail to develop valid design-around strategies or consider licensing negotiations.
  • A comprehensive patent strategy involves extending protection through filings in other jurisdictions and securing complementary patents in related formulations or methods.

FAQs

Q1: What is the primary innovation protected by Denmark patent DK2109608?
The patent likely covers a novel pharmaceutical compound or specific method of use that addresses an unmet medical need, with structural or functional distinctions from prior art.

Q2: How broad are the claims of DK2109608?
While precise claim language requires analysis of the original application, the patent probably includes both broad compound claims and narrower use or formulation claims to ensure robust protection.

Q3: Can DK2109608 be challenged or invalidated?
Yes. Challenges can arise from prior art disclosures or obviousness arguments, especially if prior similar compounds or methods exist. The patent’s validity depends on the novelty and inventive step demonstrated during exam proceedings.

Q4: How does DK2109608 interact with international patent landscapes?
Applicants likely pursued parallel applications, such as through the EPO or PCT system, to extend rights globally. Patent family analysis helps determine overlaps and freedom-to-operate in different jurisdictions.

Q5: What strategies should patent holders adopt for maximum protection?
Continuous monitoring for potential infringements, filing supplementary patents for derivatives or improvements, and engaging in licensing or enforcement actions when necessary are key strategies.


References

  1. Danish Patent and Trademark Office (DKPTO). Patent DK2109608 Document.
  2. European Patent Office (EPO). Patent Classification and Related Applications.
  3. World Intellectual Property Organization (WIPO). Patent Family Information.
  4. Patent Scope. Analysis of Pharmaceutical Patent Trends.
  5. Industry reports on pharmaceutical patent strategies and landscape analysis.

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