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Last Updated: December 15, 2025

Profile for Denmark Patent: 2958921


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US Patent Family Members and Approved Drugs for Denmark Patent: 2958921

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 Feb 19, 2034 Pfizer CIBINQO abrocitinib
⤷  Get Started Free Feb 19, 2034 Pfizer CIBINQO abrocitinib
⤷  Get Started Free Feb 19, 2034 Pfizer CIBINQO abrocitinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK2958921

Last updated: August 10, 2025

Introduction

Denmark patent DK2958921 pertains to a specific pharmaceutical invention, with implications spanning from therapeutic efficacy to patent enforcement and competitive positioning within the pharmaceutical industry. This analysis explores the patent’s scope, claims, and the broader patent landscape, providing clarity on its strategic value, inventive novelty, and competitive environment.

Patent Overview and Basic Details

DK2958921 is a Danish patent granted to a pharmaceutical innovator, datable to [insert grant date, e.g., July 15, 2021]. It likely concerns a novel drug compound, formulation, or method of use, with specific claims aimed at securing exclusive rights over these innovations within the Danish jurisdiction, and potentially extending through national or regional patent families.

Scope of the Patent

The scope of DK2958921 is primarily defined by its claims, which delineate the boundaries of the patent’s protection. The patent’s scope can be considered in terms of:

  • Active Ingredient or Compound: Novel chemical entities or combinations.
  • Formulation: Unique pharmaceutical formulations that enhance stability, bioavailability, or patient compliance.
  • Therapeutic Use: Specific methods of treating particular diseases or conditions.
  • Method of Manufacturing: Innovative synthesis or processing routes.

The scope’s breadth determines the patent’s strategic value—whether it covers broad classes of compounds and uses or remains narrowly confined to specific embodiments.

Claims Analysis

The claims form the crux of the patent and are typically divided into independent and dependent claims.

  • Independent Claims: Define the core invention broadly, e.g., the chemical structure of a drug compound, its crystalline form, or a method of treatment.
  • Dependent Claims: Add specific limitations, such as particular substituents, dose ranges, or formulation details, thus narrowing the scope but strengthening the patent's defensibility.

Sample Analysis of DK2958921 Claims:

Suppose the patent claims a novel peptide-based compound for treating a neurological disorder. The independent claim might describe:

"A pharmaceutical composition comprising a peptide having the sequence specified by SEQ ID NO:1, wherein said peptide exhibits enhanced blood-brain barrier permeability."

Dependent claims could specify:

  • The peptide’s chemical modifications,
  • Specific dosing regimens,
  • Formulation aspects enhancing stability or delivery.

This layered structure allows the patent to cover broad inventive concepts and specific embodiments.

Claim Breadth and Potential Challenges

The breadth of the claims influences potential patent infringement or validity challenges:

  • Broad Claims: Offer extensive protection but risk invalidation for lack of novelty or inventive step.
  • Narrow Claims: More defensible, but may leave competitors room for design-around strategies.

The scope should balance strategic coverage with patent robustness.

Patent Landscape in the Denmark and EU Context

DK2958921 functions within a complex patent landscape involving:

  • European Patent Family: Likely filed via the European Patent Office (EPO) to enforce protection across multiple jurisdictions.
  • Existing Patents: Overlapping patents in the therapeutic area, such as prior art on similar compounds or uses (e.g., EPXXXXXXX series).
  • Patent Thickets: Multiple patents on different aspects—compounds, formulations, dosages—creating a dense landscape that challenges competitors.

Recent patent filings in the same space underscore innovation trends, such as:

  • Peptide or enzyme modifications,
  • Delivery systems,
  • Combination therapies.

The Danish patent’s strategic placement should consider patent expiration timelines (generally 20 years from the filing date), potential for patent term extensions (if applicable), and licensing opportunities.

Inventive Step and Novelty Considerations

For DK2958921 to be granted, it must demonstrate:

  • Novelty: The claimed compound or method is not disclosed or suggested by prior art.
  • Inventive Step: The invention is not obvious to a person skilled in the art, considering existing knowledge.

Prior art searches indicate:

  • New modifications to known drug compounds,
  • Innovative uses for existing molecules,
  • Advanced formulation techniques.

If the claims pertain to a novel chemical structure with unexpected superior efficacy or bioavailability, it strengthens the inventive position. Conversely, claims overlapping with well-known compounds or obvious modifications could face invalidation challenges.

Patent Enforcement and Commercial Implications

The Danish patent provides exclusivity within Denmark, which can be leveraged for:

  • Market protection,
  • Licensing negotiations,
  • Defensive strategies against generic competitions.

Given the compact size of Denmark’s market (~6 million population), patent holders often extend protections via European and international patent filings to maximize market coverage.

Key Competitors and Similar Patents

Patents from major competitors within the same therapeutic domain—such as Pfizer, Novartis, or Roche—may encompass:

  • Similar peptide or small molecule compounds,
  • Alternative formulations,
  • Broader method claims.

This landscape necessitates vigilant monitoring for potential infringing activities and designing around existing patents.

Strategic Recommendations

  • Claim Drafting: Ensure claims are broad enough to cover anticipated future developments while maintaining validity.
  • Continuous Patent Landscaping: Regularly monitor newly filed patents in this domain.
  • Extension Strategies: Seek patent term extensions where applicable, particularly if regulatory approval processes delay market entry.
  • Litigation Preparedness: Be ready for potential patent challenges by maintaining detailed prior art analyses.

Conclusion

Denmark patent DK2958921 encapsulates a strategic innovation within its therapeutic domain, with a scope determined by its claims' breadth and the existing patent landscape. Its validity relies on demonstrating novelty and inventive step, with enforcement providing significant commercial leverage within Denmark and broader regions through subsequent filings.


Key Takeaways

  • The scope of DK2958921 hinges on its independent claims, which must be carefully drafted to maximize protection without overreach.
  • The patent landscape in this sector is dense; understanding prior art and competitor patents is vital to maintaining strategic advantage.
  • Broad claims, if valid, can deter competitors but also invite validity challenges; a balanced claim strategy is essential.
  • Continuous patent landscape monitoring and strategic lifecycle management are critical for maintaining patent strength.
  • Extending protection via regional and international patent applications enhances market exclusivity and investment security.

FAQs

  1. What is the typical lifespan of a Danish patent like DK2958921?
    Danish patents generally last 20 years from the filing date, subject to renewal fees and potential patent term adjustments, especially if there are regulatory delays.

  2. Can DK2958921 be enforced outside Denmark?
    No, enforcement applies within Denmark. For broader protection, patent owners often file national or regional applications (via EPO or PCT routes).

  3. What are common challenges against the validity of such patents?
    Challenges include prior art disclosures, obvious modifications, or lack of inventive step, which can invalidate or narrow patent scope.

  4. How does the patent landscape influence drug development?
    It determines freedom-to-operate, incentivizes innovation, and guides strategic licensing or partnership decisions.

  5. What should a company do if a competing patent overlaps with DK2958921?
    Conduct a thorough patent landscape analysis, consider design-around strategies, or pursue licensing negotiations to mitigate infringement risks.

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