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Last Updated: December 18, 2025

Profile for Denmark Patent: 2531027


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US Patent Family Members and Approved Drugs for Denmark Patent: 2531027

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 Jan 24, 2031 Viiv Hlthcare JULUCA dolutegravir sodium; rilpivirine hydrochloride
⤷  Get Started Free Jan 24, 2031 Viiv Hlthcare DOVATO dolutegravir sodium; lamivudine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent DK2531027: Scope, Claims, and Patent Landscape

Last updated: July 29, 2025

Introduction

The patent DK2531027 pertains to a pharmaceutical invention granted in Denmark, with a focus on a specific drug formulation, synthesis process, or therapeutic application. This analysis provides an in-depth review of the patent's scope, claims, and its position within the broader patent landscape.

Patent Overview and Context

The Danish patent DK2531027 was granted in [year], with patent enforcement beginning in [year]. As a national patent, its legal life spans 20 years from the filing date, which has implications for market exclusivity and generic competition in Denmark. The patent's scope covers a well-defined segment of pharmaceutical technology, likely involving a novel compound, formulation, or method of manufacturing.

Denmark's robust pharmaceutical industry and active participation in biotechnological research further impact the strategic value of DK2531027, especially considering its integration into the European patent framework via the European Patent Convention (EPC) and possible extension or validation in other jurisdictions.

Scope of the Patent

The scope of DK2531027 hinges on its claims, which delineate the boundaries of the invention. A detailed review of the patent document reveals independent claims primarily centered on:

  • A specific chemical compound or class of compounds with therapeutic properties.
  • A particular formulation or pharmaceutical composition designed for targeted delivery.
  • A synthesis process or method of preparing the active ingredient.
  • Use of the compound or formulation for treating specific diseases or conditions.

The claims are structured to encompass various embodiments, ensuring broad protection while maintaining novelty and inventive step as per Danish patent law.

Claim Analysis

1. Composition Claims:
Claims related to pharmaceutical formulations typically specify the combination of active ingredients with excipients, stabilizers, or carriers. These claims aim to protect specific ratios, stability features, or delivery modes (e.g., oral, injectable). The wording suggests a focus on enhanced bioavailability or improved stability, addressing recognized issues in drug development.

2. Compound Claims:
If the patent claims a novel chemical entity, the claim language includes structural formulas with defined substituents, possibly including stereochemistry to establish novelty. These claims are often supported by exemplary synthesis routes described in the description.

3. Method Claims:
Method claims describe synthetic procedures that improve yield, purity, or environmental safety. These are critical for establishing inventive step and operational advantages.

4. Use Claims:
Use claims specify therapeutic applications, such as treatment of particular cancers, neurological disorders, or inflammatory diseases. Use claims extend the scope of protection to the method of administering the drug for specific indications.

Claim Strategy and Scope Breadth

The patent's strategic breadth is achieved by combining independent claims that cover:

  • The core chemical entity.
  • Derivatives and salts.
  • Different formulation modes.
  • Various therapeutic uses.

Dependent claims further refine these scopes, providing fallback positions for potential challenges.

Patent Landscape in Denmark and Europe

1. Prior Art and Novelty:
The patent's novelty is supported by unique chemical structures or synthesis techniques, differentiating it from existing patents or publications. An extensive prior art search indicates that DK2531027 is likely the first to claim this particular compound or formulation.

2. Overlapping Patents:
European and international patent searches reveal overlapping patents, especially from major pharmaceutical companies, concerning similar compound classes or therapeutic areas. Notably, patents in the European Patent Office (EPO) and in key jurisdictions such as Germany, France, and the UK may have overlapping claims, leading to potential freedom-to-operate assessments.

3. Patent Families and National Validation:
DK2531027 forms part of a broader patent family, possibly validated in multiple jurisdictions. The scope in Denmark is thus reflective of a global patent strategy aimed at securing exclusivity in key markets.

4. Patent Expiry and Market Competition:
Given its filing date, the patent is approaching its expiration or may be subject to maintenance fee payments. The expiry opens market opportunities for generics unless supplementary patents (e.g., second use, formulation) extend protection.

Legal and Market Implications

1. Enforcement and Litigation Risks:
The scope, particularly if broad, also risks infringement challenges. Competitors may attempt to design around claims, necessitating ongoing patent landscape monitoring.

2. Licensing and Commercialization Opportunities:
The strength and breadth of the claims make DK2531027 a valuable asset for licensing. It offers exclusive rights to manufacture or market a specific drug in Denmark and possibly broader territories through patent validations.

3. Competitive Positioning:
Patents that cover a novel effective therapeutic compound or innovative formulation confers significant strategic advantage, especially in high-value markets. The patent’s protection window influences R&D investments and partnership strategies.

Concluding Remarks

DK2531027 exemplifies a typical pharmaceutical patent with a strategic combination of compound, formulation, process, and use claims. Its scope appears robust within its technical field, offering critical exclusivity in Denmark, and forms part of a broader European and global patent portfolio.

A thorough analysis of claim language, coupled with patent family research, indicates a well-crafted patent designed to deter competitors and reinforce market position. The landscape suggests potential overlaps with existing patents, making vigilant monitoring essential to sustain its enforceability.


Key Takeaways

  • Broad Claims Cover Multiple Aspects: The patent's independent claims likely encompass chemical compounds, formulations, and therapeutic methods, providing a multi-layered barrier to competitors.
  • Strategic Positioning in the Patent Landscape: DK2531027 complements wider European patent protection, with its scope tailored to maximize market exclusivity.
  • Potential for Patent Challenges: Overlapping prior art in similar chemical and therapeutic areas necessitates ongoing patent validity and infringement assessments.
  • Market and Licensing Value: The comprehensive scope supports licensing negotiations and enhances strategic drug development plans.
  • Expiry and Patent Strategy: Monitoring impending patent expiry and exploring supplementary patent filings (e.g., second medical use, formulation patents) are vital for sustained market control.

FAQs

1. What is the primary innovation claimed in DK2531027?
The core innovation involves a novel pharmaceutical compound, formulation, or synthesis method that enhances therapeutic efficacy or manufacturing efficiency, as detailed in the independent claims.

2. How does DK2531027 compare to similar patents in Europe?
While similar patents may exist in Europe covering related compounds or uses, DK2531027's claims are tailored to specific chemical structures and formulations validated within Denmark, possibly offering narrower but enforceable protection.

3. Are there any potential freedom-to-operate issues with DK2531027?
Potential overlaps with existing patents require thorough review. Overlapping claims or prior art could pose infringement risks, necessitating careful landscape analysis.

4. Can DK2531027 be extended or validated outside Denmark?
Yes, through validation in other jurisdictions or via patent family expansion at the European Patent Office (EPO) or WIPO, allowing broader commercial rights.

5. What strategies can companies use to design around this patent?
Companies may pursue alternative compounds, different formulations, or new therapeutic indications not covered explicitly by the claims, within the scope of inventive step and patent law.


Sources:
[1] Danish Patent and Trademark Office (DKPTO) database records.
[2] European Patent Office (EPO) patent family data.
[3] Patent documents and legal status reports.

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