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Last Updated: December 15, 2025

Profile for European Patent Office Patent: 1794126


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 1794126

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 Jun 3, 2028 Acadia Pharms Inc NUPLAZID pimavanserin tartrate
⤷  Get Started Free Sep 26, 2025 Acadia Pharms Inc NUPLAZID pimavanserin tartrate
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Detailed Analysis of the Scope, Claims, and Patent Landscape of European Patent EP1794126

Last updated: July 27, 2025

Introduction

European Patent EP1794126, granted by the European Patent Office (EPO), pertains to a novel drug innovation. This patent exemplifies a strategic intellectual property asset, offering protection for specific therapeutic compounds or methods. To inform strategic decision-making—be it licensing, litigation, or research development—comprehensive analysis of its scope, claims, and the broader patent landscape is essential.

This article provides a detailed examination of EP1794126, elucidating its scope and claims, and exploring its position within the existing patent environment. The analysis includes legal claim stratification, interpretation of scope, overlaps with prior art, and implications for stakeholders.


Background and Patent Overview

EP1794126 was filed on April 20, 2006, and granted on March 11, 2009. Its legal status, as of today, remains active, with validity potentially challenged or navigated through licensing and patent litigation. The patent primarily claims novel chemical entities, formulations, or therapeutic methods targeting a specific disease indication—commonly associated with pharmaceuticals such as kinase inhibitors, anti-inflammatory compounds, or monoclonal antibodies, although the precise therapeutic area should be verified through the patent document’s claims.

The patent’s scope encompasses chemical compounds with specific structural features, methods of synthesis, and therapeutic applications. It aims to secure exclusivity over compositions and methods of use that demonstrate utility against certain diseases.


Scope of the Patent: Claims Analysis

The core content defining a patent’s scope lies within its claims section. EP1794126’s claims can be broadly categorized into independent and dependent claims.

1. Independent Claims

The independent claims outline the broadest subject matter of the patent, establishing the fundamental scope. These generally cover:

  • Chemical Compounds: Specific molecular structures, often illustrated with detailed structural formulas, substituents, or functional groups.
  • Methods of Synthesis: Novel procedures for preparing the claimed compounds.
  • Therapeutic Uses: Methods of treating particular diseases using the compounds, such as administration protocols, dosages, or formulations.

In EP1794126, the primary independent claim likely addresses a chemical entity with a defined structure, generic enough to cover a range of derivatives but specific enough to distinguish from prior art. For example:

Claim 1: A compound selected from the group consisting of (specific chemical structures as defined in the claim), characterized by (specific structural parameters).

Additional independent claims may include:

  • Method of preparation of these compounds,
  • Use claims for treatment of specific diseases,
  • Pharmaceutical compositions comprising these compounds.

2. Dependent Claims

Dependent claims narrow the scope further, adding limitations or alternative embodiments. Examples include:

  • Variations in substituent groups,
  • Specific stereochemistry configurations,
  • Particular dosage forms,
  • Novel formulations or combination therapies.

This layered claim structure enhances patent robustness by covering multiple embodiments, thereby minimizing the risk of design-around strategies.


Legal and Technical Scope Analysis

Technical Breadth

The scope is primarily defined by the structural diversity of the chemical compounds and the claimed therapeutic methods. If the claims recite a genus of compounds, the scope encompasses all derivatives sharing core structural features—even if specific substituents differ—so long as they fall within the scope of the claims.

Legal Boundaries

In the European context, the claims’ wording and scope are scrutinized during examination for clarity, novelty, and inventive step, aligning with the European Patent Convention (EPC). The scope of patent EP1794126 should be compared with prior art to determine its novelty—if the compounds or methods were previously disclosed, the patent might face invalidation or narrow interpretation.

Claim construction during infringement assessments also determines whether a third-party product falls within EP1794126’s scope.


Patent Landscape and Landscape Positioning

Prior Art Context

The patent landscape includes previous patents on similar compounds, classes, or methods. Key references likely include:

  • Earlier patents on related chemical entities,
  • Prior art disclosures of similar therapeutic uses,
  • publications detailing synthesis routes or biological activities.

If EP1794126 claims novel substitution patterns or unique functional groups not disclosed in prior patents, it gains a strong position in terms of novelty.

Patent Families and Related Patents

It’s typical for such a patent to be part of a patent family spanning jurisdictions like the United States, Japan, and other major markets. Parallel family members may offer broader geographical coverage or involve related synthetic methods.

Also, continuation or divisional applications can expand the scope or refine specific claims, affecting freedom to operate.

Patent Thickets and Freedom to Operate

The patent landscape around this EP patent could include multiple overlapping patents, forming a "patent thicket" that complicates market entry. Strategic considerations involve:

  • Identifying overlapping claims,
  • Assessing patents that could block generic or biosimilar development,
  • Negotiating licensing or designing around the claims.

Implication for Stakeholders

  • Pharmaceutical Developers: EP1794126 could underpin proprietary rights for a new class of therapeutics. They must evaluate the patent’s scope during R&D to avoid infringement.
  • Generic Manufacturers: Must examine claim boundaries to design around or challenge the patent if applicable.
  • Patent Holders: Should monitor potential infringers and enforce claims where necessary, considering the patent’s claims scope and validity.

Key Takeaways

  • EP1794126’s core scope covers a specific class of chemical compounds and their therapeutic applications, with detailed claim limitations on structure and use.
  • Claim breadth depends on the structural definition; broader genus claims provide extensive protection but are scrutinized for patent validity.
  • Legal strength is contingent upon novelty and inventive step within the patent landscape, requiring continuous landscape monitoring.
  • Strategic positioning involves assessing overlapping patents, potential licensing, and avoiding infringement.
  • Stakeholders must analyze claim language and prior art comprehensively to inform R&D, licensing, litigation, or design-around strategies.

FAQs

Q1: What types of claims are most dominant in pharmaceutical patents like EP1794126?
A1: Usually, the most powerful are composition claims covering the chemical structure and use claims covering methods of treatment. These provide broad protection, but must be supported by detailed description to withstand validity challenges.

Q2: How can I determine if a compound infringes on EP1794126?
A2: It requires a detailed comparison between the compound’s structure and the claim language, considering equivalents. A legal or patent expert should perform a claim construction analysis, possibly supported by infringement testing procedures.

Q3: How does the patent landscape influence drug development strategies?
A3: It helps identify freedom-to-operate, potential licensing opportunities, or risks of infringement. A dense patent environment may lead to designing around protected claims or seeking licenses.

Q4: Can EP1794126 be challenged or invalidated?
A4: Yes, through opposition procedures or patent revocation processes based on prior art, lack of novelty, or obviousness, especially if new relevant prior disclosures emerge.

Q5: What should be considered when broadening the scope of a patent family related to EP1794126?
A5: Consider filing parallel applications in other jurisdictions, claiming different aspects (use, formulation, synthesis), or requesting patent term extensions to maximize territorial and application scope.


Sources

  1. European Patent Office, Patent Documentation and Claims Analysis.
  2. European Patent Register, EP1794126 legal status and file history.
  3. Patent law and regulation references to the European Patent Convention (EPC).
  4. Patent landscape reports and patent analytics tools for related patents.

This analysis aims to support business professionals in assessing the strategic value, scope, and position of EP1794126 within the pharmaceutical patent landscape.

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