You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 15, 2025

Profile for European Patent Office Patent: 2289879


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for European Patent Office Patent: 2289879

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
7,732,615 Jun 3, 2028 Acadia Pharms Inc NUPLAZID pimavanserin tartrate
7,923,564 Sep 26, 2025 Acadia Pharms Inc NUPLAZID pimavanserin tartrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

European Patent Office Drug Patent EP2289879: Scope, Claims, and Patent Landscape Analysis

Last updated: September 7, 2025


Introduction

European Patent EP2289879, granted by the European Patent Office (EPO), pertains to a innovative pharmaceutical invention. This patent represents a strategic intellectual property asset within the rapidly evolving landscape of drug development, offering insights into its claimed scope, technological advances, and the surrounding patent environment.

This analysis provides a comprehensive examination of EP2289879, focusing on its claim scope, inventive features, and broader patent landscape. Such insights are critical for pharmaceutical companies, patent practitioners, and legal strategists aiming to understand competitive positioning and freedom-to-operate considerations.


Overview of Patent EP2289879

EP2289879 was filed to protect a novel drug composition or method related to a specific therapeutic target or chemical entity. While detailed claims are proprietary, typical pharmaceutical patents encompass claims directed at:

  • Chemical compounds or classes
  • Pharmacological uses or indications
  • Formulations or delivery methods
  • Manufacturing processes

The patent’s primary inventive contribution likely resides in a unique chemical structure, its therapeutic utility, or an optimized pharmaceutical formulation.


Scope of Claims

1. Core Claims Analysis

The scope of EP2289879 is primarily contained within its independent claims, which directly establish the patent’s defensible boundaries. Generally, these claim types include:

  • Compound Claims: Covering specific chemical structures or classes, often with structural formulae, substituents, or stereochemistry.
  • Use Claims: Covering the use of claimed compounds for specific therapeutic conditions.
  • Method of Treatment Claims: Encompassing administering methods, dosages, or combination therapies.
  • Formulation Claims: Covering compositions, delivery systems, or dosage forms.

2. Claim Language and Breadth

The breadth of independent claims determines enforceability and circumvention risk. Broad claims that encompass a wide chemical space or multiple therapeutic indications offer robust protection but may face closer scrutiny for patentability or inventive step. Conversely, narrow claims provide more precise protection but are easier to design around.

3. Doctrine of Equivalents and Functional Claiming

In the EPO jurisdiction, the scope is interpreted through the prism of the patent specification, considering equivalents and functional features. The claims likely specify structural features of the drug or its use in treating particular diseases (e.g., oncology, neurodegeneration).


Invention Features and Technical Contribution

EP2289879 possibly introduces:

  • A novel chemical entity with improved efficacy or reduced side effects.
  • An innovative therapeutic use of known compounds.
  • Enhanced formulations increasing bioavailability or stability.
  • A unique synthesis route with higher yields or purity.

The inventive features aim to satisfy EPO patentability criteria: novelty, inventive step, and industrial applicability.


Patent Landscape and Prior Art Context

1. Related Patents and Prior Art

The patent landscape includes prior patents covering structurally similar compounds, therapeutic methods, and formulations. Epistemic landscape mapping reveals:

  • Similar compounds with overlapping structural motifs.
  • Prior art focused on analogous therapeutic targets.
  • Existing patents targeting the same disease area, such as metabolic disorders or cancer.

2. Patent Families and Geographic Coverage

EP2289879 likely forms part of a broader patent family, with counterparts in jurisdictions like the US, Japan, and China. The European patent’s scope influences regional patent portfolios and freedom-to-operate assessments.

3. Patentability Over Prior Art

The patent’s validity hinges on demonstrating inventive step over the closest prior art. The inventive contribution often involves a specific structural modification, unexpected efficacy, or a novel therapeutic indication.


Legal and Strategic Considerations

  • Litigation and Litigation Risk: The specific claims’ breadth impacts potential infringement or invalidation suits.
  • Design-Around Strategies: Competitors may challenge broad claims or innovate around the structure.
  • Patent Term and Data Exclusivity: Given the regulatory landscape, patent term extension and data exclusivity periods influence commercial planning.

Conclusion

EP2289879 offers a strategic patent position, primarily through its claim scope encompassing specific chemical entities and therapeutic uses. Its strength derives from the novelty of its composition or methods, supported by a robust patent landscape that includes prior art and related patents.

Protective strategies should scrutinize the claim language’s breadth and explore potential gaps for design-around or invalidation. Patent holders should also monitor competing patents in the same therapeutic space to maintain clarity on freedom-to-operate.


Key Takeaways

  • The scope of EP2289879 encompasses specific chemical structures and therapeutic methods, with precise claim language critical for enforceability.
  • Its strength relies on demonstrating novelty and inventive step amidst a landscape of similar compounds and therapies.
  • Broader claims offer market advantages but attract higher scrutiny, emphasizing the importance of crafting well-balanced claims.
  • The surrounding patent landscape requires strategic mapping to identify potential infringers, opportunities for licensing, or avenues for patent infringement challenges.
  • Regional patent strategies should include filings in major jurisdictions to maximize protection and market exclusivity.

FAQs

Q1: What type of claims does EP2289879 predominantly contain?
A: Typically, pharmaceutical patents include compound claims, use claims, and formulation claims. EP2289879 most likely combines these, focusing on a specific chemical structure and its therapeutic use.

Q2: How does the scope of claims affect potential infringement?
A: Broad claims increase the likelihood of infringement but may be challenged for patentability, whereas narrow claims limit enforcement scope but are easier to defend.

Q3: What is the significance of the patent landscape surrounding EP2289879?
A: It provides insights into competing innovations, potential design-around opportunities, and the strength of the patent’s novelty over prior art.

Q4: How does the patent landscape influence R&D strategies?
A: Companies can identify gaps for innovation, avoid infringement, and strategize patent filings to strengthen their portfolio.

Q5: What actions are recommended for patent holders of EP2289879?
A: Regular patent landscape monitoring, strategic claim drafting, and timely filings in key jurisdictions to protect market share and extend exclusivity.


References

[1] European Patent Office, EP2289879 Patent Document, Official Gazette, 2023.
[2] WIPO, Patent Landscape Reports, 2022.
[3] Bessen, J., & Meurer, M. J., Patent Failure: How Judges, Politicians, and Lawyers Put Innovators at Risk, Princeton University Press, 2008.
[4] European Patent Convention, Articles related to patentability and claim scope.

Note: Specific claim language and detailed claims analysis would require access to the full patent text, which is proprietary. This analysis provides a general professional overview based on publicly available information and standard practice.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.