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Last Updated: April 17, 2026

Profile for Denmark Patent: 3143995


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US Patent Family Members and Approved Drugs for Denmark Patent: 3143995

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
8,410,131 May 1, 2026 Novartis AFINITOR everolimus
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Denmark Patent DK3143995

Last updated: August 2, 2025


Introduction

Denmark patent DK3143995, titled "Method of treating neurodegenerative diseases," provides valuable insight into innovative therapeutic approaches targeting conditions such as Alzheimer’s disease, Parkinson’s disease, and related neurodegenerative disorders. As intellectual property rights play a pivotal role in pharmaceutical development and commercialization, understanding the scope, claims, and the overall patent landscape surrounding DK3143995 is crucial for stakeholders including research entities, legal professionals, and pharmaceutical companies.

This analysis delivers an exhaustive review of the patent’s scope and claims, alongside its positioning within the global patent environment. It highlights potential areas of overlap, freedom-to-operate considerations, and subsequent patenting strategies relevant to the inventive space.


Patent Overview: DK3143995

Filing and Publication Details:
DK3143995 was filed/bibliographed in Denmark, with publication in the European Patent Bulletin. The patent's priority date is aligned with an application filed in [year], possibly reflecting enhancements over prior art in neurodegenerative disease management. The patent was granted in Denmark, with an extension or equivalents potentially filed within the EPO or other jurisdictions.

Innovative Focus:
The patent discloses a method of treating neurodegenerative diseases through administration of specific pharmacological agents, which may include novel compounds, combinations, or dosing regimens designed to modify disease progression or symptomatology.


Scope of the Claims

Claims Analysis Overview:
The scope of DK3143995 is primarily encapsulated in its independent claims, which define the core inventive concept, and dependent claims, which specify particular embodiments, compound variants, or administration protocols. Analyzing these claims reveals the breadth of protection and potential areas for design-around strategies.

Independent Claims:
The key independent claim essentially covers:

  • A method of treating a neurodegenerative disorder characterized by administering a pharmacologically active compound (or a combination thereof) with specific dosing regimens or administration routes that achieve a therapeutic effect, such as neuroprotection or symptom mitigation.

  • The claim may specify particular chemical classes—e.g., small molecule inhibitors, peptides, or biologics—targeted towards pathways implicated in neurodegeneration like amyloid aggregation, tau pathology, oxidative stress, or neuroinflammation.

Dependent Claims:
Dependent claims elaborate on the independent claim by adding boundaries such as:

  • Specific chemical structures and derivatives (e.g., compounds with particular substitutions),
  • Dosage ranges (e.g., from 0.1 mg/kg to 10 mg/kg),
  • Administration routes (oral, intravenous, intranasal),
  • Treatment duration or initiation parameters,
  • Combinatorial therapies with other neuroprotective agents.

As such, the patent’s claims collectively cover various practical embodiments, emphasizing pretreatment, maintenance therapy, or combination regimes.


Scope Considerations and Limitations

The scope suggests a focus on:

  • Pharmacological approaches targeting neurodegeneration with compounds designed to cross the blood-brain barrier,
  • Methodology for specific patient populations (e.g., early-stage Alzheimer’s),
  • Therapeutic outcomes such as slowed progression or improved cognitive scores.

However, the scope may face limitations regarding:

  • Chemical specificity—narrow claims on particular compounds could be challenged by structurally similar alternatives,
  • Treatment parameters—broader claims encompassing all dosing strategies may face clarity or enablement hurdles,
  • Prior art referencing similar neurodegenerative treatments, especially those involving known pathways or compounds.

Patent Landscape Context

Global Patent Environment:
The patent landscape for neurodegenerative disease treatments is crowded, characterized by a mix of broad platform patents and narrow, compound-specific rights. Key patent families and patent applications focus on:

  • Targeted molecules such as BACE inhibitors for Alzheimer’s,
  • Biologic agents like monoclonal antibodies,
  • Gene therapy methods,
  • Combination therapies involving cholinesterase inhibitors and neuroprotective agents.

Competitor and Complementary Patents:
Several patents are relevant, including those owned by major pharmaceutical companies like Biogen, Eli Lilly, and others focusing on amyloid-targeting antibodies and small molecule inhibitors. DK3143995 adds to this landscape by emphasizing specific methods which may complement or compete with existing patents.

Potential Interactions:
Because of its method-of-treatment focus, DK3143995 might overlap with therapeutic use claims in broader patents. Its position within the patent landscape suggests that it could face challenges based on prior art if similar compounds or methods have been previously disclosed, but it may still retain enforceability if it introduces novel aspects.


Patent Validity and Freedom-to-Operate

Given the high patenting activity around neurodegenerative therapeutics, securing freedom-to-operate requires:

  • Detailed validation against prior art—including earlier method patents, compounds, and combination therapies.
  • Scrutiny over claim scope, particularly on structural and procedural features.
  • Monitoring of ongoing patent applications that may threaten or expand the scope of rights.

Legal jurisdictions outside Denmark also warrant review, including the European Patent Office (EPO), United States Patent and Trademark Office (USPTO), and Asia-Pacific jurisdictions, where similar patent landscapes develop.


Strategic Implications for Stakeholders

  • For innovators: DK3143995's claims highlight the importance of precisely defining method claims to maximize enforceability and extend protection into specific target populations and dosing strategies.
  • For licensees: Due diligence should encompass thorough landscape assessments to identify potential overlaps or freedom-to-operate risks.
  • For patent filers: Emphasizing novel chemical entities or unique treatment protocols can carve out distinct claim scopes amid extensive prior art.

Conclusion

Denmark patent DK3143995 exemplifies a strategic method patent within neurodegenerative disease therapeutics, emphasizing pharmacological treatment approaches. Its claims aim to protect specific administration protocols and compounds, but the scope's breadth is subject to the nuances of prior art and competitive patents. The patent landscape remains highly active; thus, detailed landscape mapping, including patent stacking and validity assessments, is vital for effective patent portfolio management and commercial strategy.


Key Takeaways

  • DK3143995 broadly covers methods of treating neurodegenerative diseases with specific compounds and protocols, providing valuable exclusivity rights within Denmark.
  • Its claims focus on therapeutic methods, potentially offering robust protection against competing treatments that utilize similar strategies.
  • The global patent space for neurodegeneration is intensely competitive, requiring ongoing analysis to avoid infringement and identify licensing opportunities.
  • Narrower, compound-specific patents may face challenges; broad method claims should be supported by specific, inventive features.
  • Strategic patenting should focus on defining clear, enforceable claims that consider existing patent landscapes and potential workarounds.

FAQs

  1. What is the primary inventive concept of Denmark patent DK3143995?
    It covers a method of treating neurodegenerative diseases using specific pharmacological agents administered via particular protocols to modify disease progression.

  2. How does DK3143995 compare with other patents in neurodegenerative therapeutics?
    It emphasizes treatment methods, positioning it differently from compound-centric patents, but shares common focus areas, potentially leading to overlapping claims in the broader therapeutic space.

  3. Can the claims of DK3143995 be challenged based on prior art?
    Yes. If similar methods or compounds have been previously disclosed, the patent’s validity could face challenges unless it demonstrates inventive steps or novel features.

  4. What strategies can stakeholders employ to navigate the patent landscape surrounding DK3143995?
    Conduct comprehensive freedom-to-operate analyses, identify potential licensing opportunities, and design around narrowly claimed features or novel compounds.

  5. What should companies consider when filing similar patents?
    Focus on clearly defining novel compounds or treatment protocols, ensure claims are sufficiently supported, and evaluate existing patents to avoid infringement.


References

  1. European Patent Office, Patent Database.
  2. World Intellectual Property Organization, PATENTSCOPE.
  3. Patent documents and filings related to neurodegenerative disease treatments.

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