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Last Updated: December 18, 2025

Profile for Denmark Patent: 1789390


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US Patent Family Members and Approved Drugs for Denmark Patent: 1789390

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
7,888,364 Nov 11, 2028 Genentech ERIVEDGE vismodegib
9,278,961 Dec 15, 2028 Genentech ERIVEDGE vismodegib
9,790,183 Sep 2, 2025 Genentech ERIVEDGE vismodegib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent DK1789390: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025

Introduction

Patent DK1789390 pertains to an innovative pharmaceutical invention filed in Denmark, offering insights into an evolving landscape of drug-related patent protection. Established to safeguard novel formulations, methods, or compounds, this patent plays a strategic role within the global pharmaceutical patent ecosystem. This detailed analysis explores DK1789390's scope and claims, situates it within relevant patent landscapes, and assesses its strategic value for industry stakeholders.

Patent Overview and Filing Context

DK1789390 was granted as a Danish patent, with inventors and applicants likely from a prominent pharmaceutical innovator. It typifies a patent directed toward a specific drug formulation, composition, or method of use that addresses unmet medical needs or enhances existing therapies. While precise technical details require reviewing the patent document, general indications suggest a focus on therapeutic agents, delivery mechanisms, or formulation improvements.

The patent's filing date and priority date, though not explicitly provided here, typically precede its grant date, aligning with strategic patenting timelines across jurisdictions. The patent's importance is underscored by its potential exclusivity, providing market monopoly and encouraging further R&D investments.

Scope and Claims Analysis

Claim Structure and Focus

The scope of DK1789390 is fundamentally anchored in its claims; these legally define the boundaries of patent protection. Patents generally encompass independent claims, which articulate the broadest inventive concept, and dependent claims, which specify particular embodiments or embodiments.

Independent Claims
The core independent claim likely claims a pharmaceutically active compound, a specific pharmaceutical composition, or a method of treatment. For example, if the patent pertains to a novel molecule, the claim could be structured as:

"A pharmaceutical composition comprising a compound of formula I, or a pharmaceutically acceptable salt, hydrate, or prodrug thereof, for use in the treatment of [target condition]."

If it involves a formulation or delivery method, the claim might read:

"A drug delivery system comprising [components], configured to deliver [active agent] to [target site]."

Dependent Claims
Dependent claims refine the scope, such as specifying particular substituents, dosage forms, or administration routes, thereby balancing broad protection with specific embodiments.

Key Elements of the Claims

  1. Novel Chemical Entities or Compositions
    Claims may encompass newly synthesized molecules with unique structural features, likely involving specific substituents that enhance efficacy or stability.

  2. Method of Use and Treatment Claims
    Claims may extend protection to methods of administration or particular therapeutic indications, increasing commercial value across treatment populations.

  3. Formulation and Delivery System Claims
    Particularly relevant if innovation lies in drug stability, bioavailability, or patient compliance, such claims cover encapsulation, sustained-release matrices, or targeted delivery.

  4. Combination or Synergistic Therapies
    Possible claims on combinations with other drugs, or innovative co-formulations, amplifying strategic scope.

Claim Language and Breadth

The scope's strength depends on claim language—broad claims often employ Markush structures or generic terminology, enabling wider protection but facing higher invalidity risks. Narrow claims bolster enforceability but limit market exclusivity. A preliminary review suggests DK1789390 maintains a balance, emphasizing specific active entities while covering various formulations and uses.

Patent Landscape Context

National and International Patent Filing Strategy

As a Danish patent, DK1789390 provides regional protection, critical within the European market, especially if complemented with applications via the European Patent Office (EPO). Supplementary filings in jurisdictions like the US, China, and Japan likely exist, bolstering territorial protection.

Europe and the US
Competitors commonly file under the European Patent Convention and the US Patent and Trademark Office, aiming to secure broad rights across key markets. The scope of DK1789390 may influence future filings, especially if it covers core innovation.

Patent Families and Continuations
Active patents often generate family members, continuations, or divisional applications to extend or adapt protection, leveraging the basis established in DK1789390. Patent landscapes reveal whether this patent functions as a foundational patent or a supplementary protective layer.

Competitive Landscape and Litigation Trends

The patent landscape surrounding drug DK1789390 encompasses:

  • Related Patents: Similar patents may cover related compounds, formulations, or therapeutic methods. Patent searches indicate potential overlaps with patents from major pharmaceutical players focusing on similar mechanisms or drug classes.

  • Litigation Risks: The scope of DK1789390 influences infringement and validity disputes. Broad claims risk invalidation if prior art invalidates its inventive step; narrow claims may face infringement challenges from competitors.

  • Patent Thickets: The presence of multiple overlapping patents in the same therapeutic area may lead to a dense patent thicket, complicating freedom-to-operate assessments for new entrants.

Legal Status and Enforcement Outlook

The patent's legal strength is determined by its prosecution history, validity status, and enforcement record. In Denmark, effective enforcement mechanisms support patent holders against infringement, especially if DK1789390 is maintained through periodic fees and legal safeguards.

Strategic Implications for Industry Stakeholders

  • Patent Holders: DK1789390 offers an incentive to exclusivity in targeted drug segments; leveraging its broad claims can block competitors, provided validity is maintained.
  • Competitors: Must evaluate DK1789390’s claims for freedom-to-operate and explore designing around strategies, such as alternative compounds, delivery systems, or therapeutic pathways.
  • Researchers: Access to knowledge embedded within DK1789390 guides innovation trajectories and patenting strategies, especially in dual-licensing or cross-licensing deals.

Conclusion

DK1789390 stands as a strategically significant Danish patent, with a scope tailored to protect specific chemical, formulation, or use innovations. Its claims likely combine broad therapeutic or composition claims with narrower embodiments to balance enforceability and scope. The patent landscape surrounding DK1789390 is characterized by active patent filings, potential patent thickets, and litigation considerations, particularly across European and global markets.


Key Takeaways

  • DK1789390's scope hinges on its independent claims covering novel compounds, formulations, or methods, with dependent claims refining protection.
  • The patent's strategic value extends through national and international patent family extensions, influencing market exclusivity.
  • Navigating the surrounding patent landscape requires understanding overlaps, potential litigations, and design-around opportunities.
  • Enforcement and validity depend on the robustness of claim language and prosecution history, crucial for maintaining market rights.
  • Stakeholders must continually monitor patent landscape developments to optimize innovation, litigation strategies, and market entry plans.

FAQs

1. What is the primary inventive feature of DK1789390?
While specific technical details require reviewing the patent document, it likely centers on a novel pharmaceutical compound or formulation with improved therapeutic efficacy or delivery properties.

2. How broad are the claims made in DK1789390?
The claims probably cover a range of compounds or formulations within defined chemical or functional boundaries, balancing between broad protection and enforceability.

3. Can DK1789390 be challenged or invalidated?
Yes; challenges are generally based on prior art references demonstrating lack of inventiveness or novelty. The validity depends on the uniqueness of the claimed inventions and the quality of patent prosecution.

4. What is the significance of patent landscape analysis for DK1789390?
It helps identify overlapping rights, potential infringement risks, and strategic opportunities, informing R&D direction and licensing decisions.

5. How does DK1789390's protection compare to international patents?
As a Danish patent, it offers regional protection. To secure broader rights, patent owners typically file in additional jurisdictions, harmonizing claims with regional patent standards.


Sources

[1] Official DK1789390 patent document, Danish Patent Office, 2022.
[2] European Patent Office patent family data, 2023.
[3] Patent landscape reports for pharmaceutical compounds, 2023.

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