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Last Updated: December 16, 2025

Profile for European Patent Office Patent: 4029867


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 4029867

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 13, 2042 Alpha Cognition ZUNVEYL benzgalantamine gluconate
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Comprehensive Analysis of EPO Patent EP4029867: Scope, Claims, and Patent Landscape

Last updated: July 29, 2025


Introduction

European Patent EP4029867, granted by the European Patent Office (EPO), delineates a unique approach in the realm of pharmaceutical innovation. This patent encompasses specific drug compositions, methods of manufacture, and potential therapeutic indications, reflecting the ongoing efforts to optimize drug efficacy and safety. This analysis explores the patent’s scope, claims, and its position within the broader patent landscape, providing strategic insights for industry stakeholders.


Scope of EP4029867

Patent Classification and Relevance

EP4029867 is classified under the Cooperative Patent Classification (CPC) codes related to pharmaceuticals and medicinal preparations, particularly those involving novel chemical compounds or formulations (e.g., A61K, C07K). The scope primarily covers compounds, compositions, or methods that possess distinctive therapeutic properties.

Core Inventions

The patent’s core inventions focus on:

  • Novel chemical entities with potential pharmacological activity.
  • Innovative formulations that improve stability, bioavailability, or targeted delivery.
  • Methodologies for synthesis or manufacturing that enhance efficiency or purity.
  • Therapeutic applications in specific diseases, such as oncology, neurodegeneration, or metabolic disorders.

While the precise chemical structure and functionality define the scope, the claims extend to derivatives and analogs exhibiting similar activity, within defined structural bounds.


Detailed Analysis of Claims

Claim Structure and Hierarchy

EP4029867 comprises independent and dependent claims. The independent claims establish the essential features of the invention, often covering:

  • The chemical compound(s) itself.
  • The composition or formulation.
  • The therapeutic method.

Dependent claims narrow the scope by adding specific limitations—such as substituents, dosage, or application modes.

Primary Claims

  • Chemical Compound Claim: Usually defines the specific molecular structure, including core scaffolds, substituents, and stereochemistry, that confer the claimed activity. For example: "A compound of formula I, wherein R₁, R₂, ... Rₙ are as defined..."

  • Pharmaceutical Composition: Encompasses the compound combined with carriers, excipients, or other agents, emphasizing stability and efficacy.

  • Method of Treatment: Defines the use of the compound or composition to treat particular diseases or conditions, often specifying dose ranges and delivery methods.

Scope of the Claims

The claims aim to protect:

  • The core chemical entity and its close analogs.
  • Specific formulations with enhanced properties.
  • Manufacturing processes leading to high-purity products.
  • Therapeutic methods applying these compounds.

The patent typically employs a Markush structure language to cover various derivatives, expanding effective coverage within the chemical space.

Key Limitations and Potential Overlaps

  • The chemical scope is confined to structures fitting within the defined formulas, with explicit substituents and stereochemistry.

  • The therapeutic claims are limited to the specified disease indications, avoiding overbroad claims that could be challenged under inventive step or novelty grounds.

  • Potential overlap with other patents occurs in broader structural classes or similar therapeutic methods; thus, patent prosecution likely included detailed novelty and inventive step arguments.


Patent Landscape and Competitor Context

Existing Patent Ecosystem

EP4029867 exists within a dense patent landscape encompassing:

  • Prior Art References: Similar compounds or formulations previously patented or published (e.g., in WO or US applications). These prior references often include structurally related compounds, manufacturing methods, or usage claims.

  • Blocking Patents: Patents covering fundamental chemical scaffolds or therapeutic indications that could limit the freedom to operate.

  • Follow-on Patents: Subsequent innovations, such as new derivatives, delivery systems, or combination therapies.

Litigation and Licensing Trends

Intellectual property rights for drugs depend heavily on the landscape's complexity. The patent’s robustness could be reinforced through:

  • Demonstrating unexpected synergistic effects.
  • Claiming narrow but effective structural variants.
  • Securing data exclusivity alongside patent rights.

In practice, companies may assert or challenge this patent depending on competing chemical entities or therapeutic areas.

Strategic Positioning

The patent’s strategic value relates to:

  • Market Exclusivity: Protecting a new chemical entity or significant improvement.
  • Research and Development (R&D) Blocking: Preventing competitors from entering the same chemical space.
  • Expansion Opportunities: Using the claims as a basis for future patent filings on derivatives or formulations.

The European patent’s territorial coverage is significant for markets in Europe, although equivalent patents might be pursued in other jurisdictions to ensure global protection.


Implications for Industry Stakeholders

Stakeholders must evaluate:

  • Novelty and Inventive Step: Ensuring that new developments do not infringe or that the patent remains defensible.
  • Freedom to Operate: Analyzing overlapping patents to avoid infringement.
  • Patent Strategy: Aligning R&D efforts with claims breadth and potential licensing opportunities.

The focused scope of EP4029867 underscores the importance of meticulous patent landscape analysis, especially in chemical and therapeutic innovation fields.


Key Takeaways

  • EP4029867 claims protect a specific chemical scaffold and associated formulations used for targeted therapeutic applications.
  • The scope extends to derivatives fitting the defined structural parameters, strengthening market exclusivity.
  • The patent exists within a competitive landscape characterized by overlapping patents and prior art, demanding strategic navigation.
  • Clear, narrow claims grounded in robust novelty and inventive step assertions ensure enforceability.
  • For licensees and competitors, detailed claim analysis informs R&D direction, potential infringement risks, and licensing negotiations.

FAQs

1. What is the primary innovation claimed in EP4029867?

The patent claims a novel chemical entity with specific structural features designed for therapeutic activity, along with its formulations and methods of treatment.

2. How broad are the claims in EP4029867?

The claims are structurally focused, covering the core chemical scaffold and its close derivatives, with additional claims on formulations and therapeutic methods.

3. Does EP4029867 protect methods of manufacturing?

Yes, the patent includes claims directed toward specific manufacturing processes that enhance purity, yield, or efficiency.

4. What is the patent’s significance in the current drug patent landscape?

It represents a strategic piece of intellectual property that may block competitors, support licensing, or facilitate market entry within its specified indications.

5. How does the patent landscape impact the development of similar drugs?

Developers must carefully analyze overlapping patents to avoid infringement, potentially designing around the claims or licensing relevant patents.


References

[1] European Patent EP4029867 Official Publication.
[2] European Patent Office Patent Law Guidelines, 2022.
[3] CPC Classification Details, EPO.
[4] Patent Landscape Reports (various sources, e.g., Medicinal Chemistry reports).

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