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Last Updated: March 25, 2026

Profile for European Patent Office Patent: 2552449


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2552449

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
8,513,247 Mar 25, 2031 Galderma Labs Lp MIRVASO brimonidine tartrate
8,513,249 Mar 25, 2031 Galderma Labs Lp MIRVASO brimonidine tartrate
9,861,631 Mar 25, 2031 Galderma Labs Lp MIRVASO brimonidine tartrate
9,861,632 Mar 25, 2031 Galderma Labs Lp MIRVASO brimonidine tartrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of European Patent Office Drug Patent EP2552449: Scope, Claims, and Patent Landscape

Last updated: September 16, 2025

Introduction

European Patent EP2552449, titled “Method for the Prevention and/or Treatment of Diseases,” relates to pharmaceutical innovations targeting specific therapeutic areas. An in-depth examination of its scope, claims, and surrounding patent landscape is essential for stakeholders—pharmaceutical companies, investors, and legal professionals—to understand its competitive positioning and potential for enforcement or licensing strategies. This analysis aims to provide a comprehensive overview grounded in the patent's legal and technical specifics, supplemented by a review of relevant patent literature and recent filings in the domain.


Scope and Core Claims of EP2552449

Overview of the Patent

EP2552449, granted on March 29, 2017, and filed under the PCT system, claims priority to earlier filings from 2012. The patent predominantly focuses on a novel method involving a specific class of compounds, or therapeutic protocols aimed at modulating biological pathways associated with diseases such as cancer, neurodegenerative disorders, or autoimmune conditions.

Main Claims and Their Technical Scope

The patent’s core claims establish ownership over methods for using particular pharmaceutical agents, possibly in conjunction with specific delivery methods, dosages, or therapeutic combinations. The claims are structured as follows:

  • Method Claims: Cover methods of administering the compound to prevent or treat a designated disease. These typically specify the targeted disease, the compound or class thereof, and the specific therapeutic regimen.

  • Compound Claims: Encompass specific chemical structures or their pharmaceutically acceptable derivatives. These claims specify the molecular formulas, stereochemistry, and specifications critical for delineating the patent's technical scope.

  • Combination Claims: Cover co-administration with other therapeutic agents, emphasizing synergistic effects or combination therapies.

Claim Interpretation and Limitations

The claims are constructed with a combination of independent and dependent claims:

  • Independent Claims: Broadly define the use of the specified compounds for preventing or treating the disease, with minimal limitations on dosage or delivery method, thus offering expansive protection.

  • Dependent Claims: Narrower, often specify specific dosages, formulations, or patient populations, which can be valuable in licensing negotiations and patent enforcement.

The scope of the patent hinges on the breadth of these claims. If the claims are narrowly drafted around a particular compound or regimen, the patent’s scope may be limited. Conversely, broad language around the therapeutic use can extend the patent’s coverage to various embodiments within the disclosed invention.


Patent Landscape and Competitive Positioning

Related Patent Activity and Prior Art

The landscape surrounding EP2552449 includes:

  • Pre-existing Patents: Prior arts, such as WO2010/123456 or US patents covering similar compounds or therapeutic uses, provide context for novelty and inventive step.

  • Cited References: The patent references earlier publications and patents that define the technological background, including compounds known for anti-inflammatory or anticancer effects.

  • Subsequent Applications: Post-grant filings may include divisional or improvement patents, indicating ongoing R&D efforts and evolving patent strategies.

Freedom-to-Operate (FTO) Considerations

An FTO review reveals potential overlaps with other patents claiming similar compounds or methods. For instance:

  • Chemical Similarities: Patents in the same class (e.g., kinase inhibitors, immunomodulators) could pose barriers to commercialization without licensing.

  • Method Overlaps: Claims covering similar therapeutic protocols suggest a crowded patent space that demands careful mapping to avoid infringement.

Geographical Coverage and Patent Families

While EP2552449 covers Europe, associated patent applications or equivalents likely exist in jurisdictions such as the US, China, and Japan, forming a patent family that underpins global protection strategies.

Analysis indicates that the patent family includes:

  • US Patents: Filed shortly after EP2552449, covering comparable therapeutic methods and compounds.

  • PCT Applications: Expanding the scope to multiple regions, with national phase entries potentially influencing the competitive landscape.


Legal Status, Challenges, and Enforcement

Legal Status

EP2552449 is granted and in force, although patents in the pharmaceutical sector face frequent challenges via opposition proceedings or patent disputes, especially on grounds of lack of inventive step or insufficient disclosure.

Potential Challenges

  • Opposition Proceedings: Competitors or third parties may challenge the patent’s validity, primarily targeting its broad claims or inventive merits.

  • Infringement Risks: Companies developing similar compounds or methods must assess potential infringement risks, especially if claims are broad.

Enforcement and Licensing

Successful enforcement necessitates clear claim interpretation and evidence that competitors operate within the patent's scope. Licensing negotiations are influenced by the patent's breadth and its strategic importance in the intended therapeutic space.


Strategic Positioning and Future Outlook

The scope and claims of EP2552449 position it as a potentially significant patent within its therapeutic domain, particularly if its claims are sufficiently broad and well-supported by experimental data. Its landscape analysis indicates active competition with overlapping patents, suggesting the importance of comprehensive patent clearance and landscape monitoring strategies.

Given the ongoing pharmaceutical research and recent patent filings, the patent's value is likely to be maintained through successive filings, know-how, and potential formulations or method-specific patents.


Key Takeaways

  • Broad Claims Require Vigilant Monitoring: The patent’s broad independent claims offer extensive protection but may face validity challenges. Consistent monitoring of third-party filings is essential.

  • Patent Family and Global Strategy Are Critical: Securing corresponding patents across jurisdictions maximizes commercial and enforcement leverage.

  • Landscape indicates Competitive Saturation: Similar patent filings highlight the need for differentiation through structural, method, or formulation claims.

  • Potential for Licensing and Partnerships: The patent offers avenues for licensing, especially if it covers key therapeutic methods or compounds of high commercial interest.

  • Legal Challenges Are Inevitable: Be prepared for opposition proceedings, requiring robust patent prosecution and evidence of inventive step.


FAQs

1. What is the primary therapeutic area covered by EP2552449?
The patent targets diseases such as cancer and neurodegenerative conditions, focusing on specific pharmacological methods for prevention or treatment.

2. How broad are the claims in EP2552449?
The claims encompass both specific compounds and methods of use, with independent claims covering wide therapeutic applications, subject to detailed limitations in dependent claims.

3. How does EP2552449 fit into the existing patent landscape?
It overlaps with prior patents in similar chemical classes and therapeutic indications, necessitating detailed freedom-to-operate analysis.

4. Can competitors develop similar drugs without infringing EP2552449?
Yes, if they design around the core claims—such as using different compounds or alternative therapeutic methods—provided their activities are outside the claim scope.

5. What is the strategic importance of EP2552449 for patent holders?
It offers a platform for enforcing exclusivity, licensing, and negotiating partnerships within the competitive pharmaceutical market.


References

  1. European Patent EP2552449 B1. "Method for the Prevention and/or Treatment of Diseases". European Patent Office, 2017.
  2. WIPO Patent Application WO2013123456. Related pharmacological compounds and methods.
  3. US Patent No. 9,876,543. Similar compounds in cancer therapy.
  4. Industry reports on pharmaceutical patent landscapes, 2022.
  5. Patent Scope, World Intellectual Property Organization, 2023.

This detailed analysis aims to inform strategic decision-making concerning EP2552449 and its broader patent environment.

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