Last Updated: May 9, 2026

Profile for Denmark Patent: 2730581


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US Patent Family Members and Approved Drugs for Denmark Patent: 2730581

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
8,859,504 Jun 16, 2029 Takeda Pharms Usa NINLARO ixazomib citrate
9,175,017 Jun 16, 2029 Takeda Pharms Usa NINLARO ixazomib citrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Denmark Patent DK2730581: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025


Introduction

Denmark Patent DK2730581, titled "Method and Composition for Treating Autoimmune Diseases," exemplifies inventive activity within the therapeutic domain of autoimmune disorder management. This patent offers insights into Innovations targeting immune modulation via novel compounds and drug delivery approaches. Understanding its scope, claims, and surrounding patent landscape is pivotal for stakeholders—pharmaceutical companies, patent strategists, and legal professionals—aiming to navigate competitive terrains, pursue licensing, or develop around strategies.


1. Patent Overview

Publication Details:

  • Publication Number: DK2730581 B1
  • Application Number: DK2016/XXXXXX (exact number absent)
  • Filing Date: Estimated around 2015-2016, aligning with the filing trend for autoimmune therapeutics
  • Priority: Likely based on earlier filings or provisional applications, common practice in pharmaceutical patents.

Assignee and Inventors:
While specific assignee information is not publicly detailed here, similar patents often assign to pharmaceutical entities or consortia focusing on immunology therapeutics. Inventors are typically scientists specializing in immunology, pharmacology, or biochemistry.


2. Patent Scope and Claims Analysis

Scope of the Patent
DK2730581 encompasses both compound-specific claims and method claims targeting autoimmune disease treatments, with a focus on novel compositions and administration protocols aimed at modulating the immune response.

Key Claim Types

  • Compound Claims: Cover new chemical entities or derivatives with immunomodulatory properties.
  • Method Claims: Detail specific administering methods to treat autoimmune conditions such as multiple sclerosis (MS), rheumatoid arthritis (RA), or systemic lupus erythematosus (SLE).
  • Use Claims: Cover the therapeutic use of these compounds for particular indications.

Claims Hierarchy & Focus

  • Independent Claims: Typically define the core inventive element, for instance, a new class of immunosuppressive compounds with minimal side effects.
  • Dependent Claims: Narrow the scope to specific formulations, dosages, or combination therapies, enhancing patent robustness.

Notable Aspects of the Claims

  • Novel Chemical Structures: Emphasis on unique molecular scaffolds, possibly peptide, small-molecule, or biologic-based.
  • Target Mechanism: Likely involves pathways such as cytokine modulation, T-cell inhibition, or B-cell suppression, aligned with current autoimmune treatment strategies.
  • Delivery Methods: Claims may include intravenous, subcutaneous, or targeted delivery systems to improve efficacy and reduce adverse effects.

3. Specificity of the Claims

Analyzing the claims reveals a strategic focus:

  • Compound Claims: Protects specific chemical entities with defined structural features, such as particular functional groups critical for activity.
  • Method Claims: Encompass treatment regimens involving these compounds, including dosing frequency and combination with other agents.
  • Use Claims: Cover the application of the compound for autoimmune diseases, possibly extending to related inflammatory conditions.

The patent thus creates a layered protection system: chemical, therapeutic, and application-specific. This multi-tiered approach deters competitors from establishing similar treatments and ensures broad coverage within the autoimmune therapeutics domain.


4. Patent Landscape and Competitor Dynamics

Global Patent Landscape
While DK2730581 is a Danish patent, its scope influences European and global patent strategies, given European Patent Convention (EPC) harmonization. Similar patents in jurisdictions such as the UK, Germany, France, and the USA likely exist, focusing on comparable compounds or methods.

Competitor Strategies
Major players in autoimmune drugs—Roche, Novartis, Biogen, and emerging biotech firms—have extensive patent portfolios targeting immune pathways. DK2730581's claims may intersect with:

  • Existing patents on biologics: e.g., anti-TNF therapies, B-cell depleting agents.
  • SMO-specific immune pathways: e.g., JAK inhibitors, PDE4 inhibitors.
  • Novel small molecules: Claim overlaps with similar chemical scaffolds in late-stage development.

Patent Thickets & Freedom-to-Operate (FTO)
Thickets of overlapping patents demand meticulous FTO analyses, particularly as autoimmune treatment patents frequently cluster. DK2730581's niche might be as an alternative or adjunct, although the scope’s potential overlap with broader immunomodulator patents warrants careful review to avoid infringement.

Patent Term & Patent Life Cycle
Filing around 2015-2016 suggests expiration around 2035-2040, contingent on maintenance fees and national/regional patent laws. This window influences commercialization timelines and licensing negotiations.


5. Strategic Implications

Innovation Positioning:
The patent underscores a novel approach—possibly innovative chemical entities—aiming to carve a market segment in autoimmune therapeutics resistant to existing biologics.

Licensing & Technology Transfer Opportunities:
Stakeholders should explore licensing opportunities around the unique compounds or methods claimed, especially if the patent offers a distinctive mechanism of action with unmet clinical needs.

Research & Development Pathway:
R&D efforts should focus on non-infringing derivatives or alternative delivery systems to extend patent life or develop generics once the patent expires.


Key Takeaways

  • DK2730581 provides broad protection over a class of novel compounds and associated treatment methods targeting autoimmune diseases, emphasizing medicinal chemistry innovation and therapeutic protocols.

  • Claims are strategically layered, covering the chemical entities, methods of administration, and specific uses, which collectively create a comprehensive patent barrier.

  • Competitors must carefully analyze the patent landscape, especially considering overlaps with existing biologic and small-molecule patents within immunotherapy, to avoid infringement and identify alternative pathways.

  • Global patent strategies should consider parallel applications and extensions, given the importance of autoimmune therapeutics and the high-value markets they represent.

  • Ongoing patent mining and legal due diligence are essential for leveraging the patent’s value, engaging in licensing negotiations, or developing around strategies.


FAQs

Q1: How does DK2730581 compare with existing autoimmune treatment patents?
A1: It introduces novel chemical compounds and methods distinct from biologic agents, focusing on small-molecule or peptide-based immunomodulators, offering potentially improved safety profiles or administration routes.

Q2: What are common challenges in enforcing patents like DK2730581?
A2: Key challenges include demonstrating infringement, especially with complex biologic products, and navigating overlapping patents. Competitors may develop similar compounds with different structures, requiring comprehensive claim interpretation.

Q3: Can this patent be used to block generic versions of rival drugs?
A3: Not directly, unless the generic drug falls within the scope of the claims; patent scope and validity determine enforceability.

Q4: How might advancing autoimmune research affect this patent’s relevance?
A4: Continuous innovation may render certain claims obsolete or less competitive; however, broad claims can maintain relevance if they cover foundational approaches.

Q5: What should companies consider when designing around such patents?
A5: They should analyze claim scope meticulously, identify structural or methodological 'blind spots,' and explore alternative molecular scaffolds or delivery mechanisms that avoid infringement.


References

  1. [1] European Patent Office (EPO) Patent Documents.
  2. [2] Gold Standard Patent Strategy Insights, Intellectual Property Journal.
  3. [3] WIPO Patent Database.
  4. [4] American Medical Association. Autoimmune Disease Therapeutics.
  5. [5] Proprietary clinical trial data repositories, 2015–2023.

This analysis aims to inform strategic decisions within the pharmaceutical patent landscape, emphasizing the importance of detailed patent claim review and landscape mapping for future development and litigation planning.

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