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Last Updated: December 17, 2025

Profile for Denmark Patent: 2089361


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US Patent Family Members and Approved Drugs for Denmark Patent: 2089361

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
7,781,577 May 4, 2028 Lexicon Pharms Inc INPEFA sotagliflozin
8,476,413 May 29, 2028 Lexicon Pharms Inc INPEFA sotagliflozin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK2089361

Last updated: August 2, 2025

Introduction

Denmark Patent DK2089361 pertains to a specific innovation within the pharmaceutical domain, seeking protection for a novel drug, formulation, or method. As a professional drug patent analyst, an in-depth review of the patent's scope, claims, and its positioning within the broader patent landscape is crucial for stakeholders including pharmaceutical companies, legal entities, and R&D organizations. This analysis dissects the patent’s claims, defines its scope, and contextualizes its landscape analysis.

Patent Overview

DK2089361 was filed and granted in Denmark, endowing the patent owner exclusive rights within Denmark's jurisdiction. While specific filing or grant dates require further discovery, the patent's jurisdiction indicates its strategic relevance for the Scandinavian market, possibly serving as a basis for regional or international patent applications.

Given the typical structure, DK2089361 likely relates to a pharmaceutical compound, a formulation, a process, or a combination thereof. To delineate its scope, we analyze its claims, which delineate the scope of legal protection.


Claims Analysis

Types of Claims

The patent specification probably contains multiple claims categorized as:

  • Independent claims: Broadly define the core inventive aspect—such as a novel compound, therapeutic use, or method of manufacturing.
  • Dependent claims: Narrower, specify particular embodiments, variants, or embodiments of the independent claim.

Scope of Claims

Without access to the precise wording, a standard structure for pharmaceutical patents applies:

  • Compound claims: Covering a specific chemical entity or a class of entities with defined structural features.
  • Use claims: Covering a novel therapeutic application of the compound.
  • Formulation claims: Pertaining to specific pharmaceutical compositions.
  • Process claims: Describing manufacturing processes or methods.

Example Hypothetical Claim Structure (For illustration):

Independent Claim:
A compound of formula I, characterized by [structural features], or a pharmaceutically acceptable salt, solvate, or ester thereof.

Dependent Claims:
Further specify substituents, stereochemistry, or specific derivatives, e.g., "The compound of claim 1, wherein R1 is methyl."

Use Claim:
A method of treating [disease] comprising administering a therapeutically effective amount of the compound of claim 1.

Claim Breadth and Limitations

The scope’s breadth directly impacts enforceability and patent strategy:

  • Broad claims offer extensive protection but risk invalidation if prior art exists.
  • Narrow claims provide more specific protection but may be easier to design around.

For DK2089361, an optimal balance likely exists, protecting key innovations while remaining defensible against prior art challenges.


Patent Landscape Context

Prior Art and Related Patents

The landscape analysis involves reviewing previous patents, publications, and patent families within the same technological area:

  • Similar compounds or formulations: Patent literature often reveals prior art that may limit the scope.
  • Cited patents and literature: DK2089361 may cite or be cited by other patents, indicating research activity and potential patent thickets.
  • Patent families: The existence of family members in jurisdictions such as the EP, US, or China signifies geographic expansion strategies.

Competitive Landscape

Other patents within the same compound class or therapeutic area may influence the commercial viability and patent strength of DK2089361:

  • Overlap with existing patents: May lead to invalidity issues or licensing negotiations.
  • Novelty and inventive step: Determined by distinguishing the patent's claims over prior art.

Legal and Strategic Considerations

In Denmark, patent validity is scrutinized against prior art, emphasizing novelty and inventive step. Strategic patenting might include:

  • Filing of divisional or continuation applications to broaden or shield specific claims.
  • Prosecution history: Examination comments may provide insights into claim amendments and scope adjustments.

Patent Validity and Enforceability

Factors influencing validity include:

  • The novelty over prior art—assessed through patent searches and literature.
  • Inventive step—the non-obviousness of the claim over existing knowledge.
  • Adequate disclosure—fulfilling sufficiency requirements.

Enforceability hinges on clear claims, proper phrasing, and maintenance of annuities.


Legal Status and Lifecycle

The lifespan of DK2089361 depends on filing and grant dates, with a typical term of 20 years from the priority date (subject to payment of maintenance fees). Patent expiry status influences freedom-to-operate and potential generics entry.


Implications for Stakeholders

  • Pharmaceutical innovators can leverage this patent to secure regional exclusivity.
  • Legal entities should evaluate scope for potential infringement or challenges.
  • R&D firms can explore licensing or partnership opportunities.

Key Considerations for Patent Strategy

  • Maintain awareness of related patents in the region.
  • Focus on patent claim drafting that balances breadth and robustness.
  • Monitor patent family members across jurisdictions.
  • Prepare for potential opposition or litigation.

Key Takeaways

  • DK2089361 likely protects a novel pharmaceutical compound or formulation with targeted claims that define its scope.
  • The patent's strength depends on the breadth of independent claims and their differentiation from prior art.
  • Its patent landscape includes prior art in the same therapeutic class, necessitating continuous monitoring.
  • Strategic patent prosecution and lifecycle management are vital to sustain competitive advantage.
  • Enforcing rights in Denmark demands rigorous validation of claim validity against patentability criteria.

FAQs

Q1: How can I determine the scope of the claims in DK2089361?
A: Review the specific wording of the independent claims in the patent document, focusing on the structural features, applications, and embodiments disclosed.

Q2: What factors influence the validity of this patent?
A: Validity hinges on novelty, inventive step, and sufficient disclosure, assessed through prior art searches and examination.

Q3: How does DK2089361 fit into the broader pharmaceutical patent landscape?
A: It exists within a network of patents covering similar compounds, formulations, and methods, often building on or differentiating from prior arts.

Q4: Can this patent be challenged or licensed?
A: Yes; challenges can originate from prior art or competitors, while licensing can offer strategic commercial advantages.

Q5: What should be considered for enforcing rights under DK2089361?
A: Confirming claim enforceability, monitoring potential infringers, and preparing legal action if necessary.


References:

  1. [1] Danish Patent and Trademark Office (DKPTO) official patent database.
  2. [2] World Patent Index; World Intellectual Property Organization (WIPO) patent landscape reports.
  3. [3] European Patent Office (EPO) patent family documents related to DK2089361.
  4. [4] Patent documentation and prosecution history, if accessible via national or regional patent offices.

Note: Due to the specificity of DK2089361, some details may warrant further review of the patent document itself for precise claim language and legal status updates.

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