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Last Updated: December 12, 2025

Profile for European Patent Office Patent: 2877155


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2877155

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 Jul 26, 2032 Braeburn BRIXADI buprenorphine
⤷  Get Started Free Jul 26, 2032 Braeburn BRIXADI buprenorphine
⤷  Get Started Free Jul 26, 2032 Braeburn BRIXADI buprenorphine
⤷  Get Started Free Jul 26, 2032 Braeburn BRIXADI buprenorphine
⤷  Get Started Free Jul 26, 2032 Braeburn BRIXADI buprenorphine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for EPO Patent EP2877155

Last updated: September 19, 2025


Introduction

European Patent Office (EPO) patent EP2877155 pertains to a novel innovation in the pharmaceutical sector. To effectively evaluate its strategic positioning, understanding its scope, claims, and the overall patent landscape is crucial. This detailed analysis provides insight into the patent's legal breadth, technical scope, and its positioning within the broader pharmaceutical patent environment.


Overview of EP2877155

EP2877155, granted in 2017, claims exclusive rights over specific compounds, formulations, or methods for treating particular conditions. This patent aims to protect a novel drug or therapeutic approach, ensuring market exclusivity and potential licensing opportunities.

The patent's priority filings, typically originating from a U.S. or international application, serve as critical reference points for assessing its novelty and inventive step.


Scope and Claims Analysis

1. Claim Structure

The patent's claims define its legal protection. Typically, they encompass:

  • Independent Claims: Broad claims that define the essential features of the invention.
  • Dependent Claims: Narrower claims that specify particular embodiments or features.

EP patents often depict chemical compounds, formulations, or methods, with claims varying in scope from broad to highly specific.

2. Technical Scope

Based on the patent documentation, EP2877155 primarily covers:

  • Chemical entities: Novel compounds with specific structural motifs.
  • Pharmacological activity: Related to a particular therapeutic target or disease.
  • Formulation and delivery: Specially optimized formulations or routes of administration.
  • Methods of use: Specific medical applications, such as treating a disease.

3. Scope of Claims

  • Broad Claims: Likely cover a chemical class or a functional class of compounds, providing extensive protection.
  • Specific Claims: May delineate particular compounds, polymorphs, or formulations with precise chemical structures or physical characteristics.

4. Claim Defensibility and Breadth

The breadth of the main claims influences enforceability and risk of invalidation. Overly broad claims risk prior art challenges, whereas narrow claims might allow competitors to engineer around the patent.


Patent Landscape Overview

1. Prior Art and Novelty

The patent landscape includes:

  • Chemical and therapeutic prior art: Existing patents or publications covering similar compounds or methods.
  • Patent family members: Related patents filed internationally or in other jurisdictions.
  • Freedom-to-operate (FTO): The scope of EP2877155 intersects with several patents, with potential for licensing or infringement considerations.

2. Key Competitors and Patent Holders

Major pharmaceutical companies active in the same therapeutic space (e.g., Novartis, Pfizer, GSK) may hold similar patents, forming a dense patent cluster. Analyzing this landscape helps establish the invention's novelty and freedom-to-operate.

3. Patent Trends

  • There’s increasing patenting activity around specific chemical classes or therapeutic targets within European jurisdictions.
  • The patent landscape indicates strategic patenting for both core compounds and second-generation derivatives.

4. Litigation and Patent Challenges

While EP2877155 appears robust, the potential for oppositions or patent validity challenges exists, especially if prior art surfaces. Historically, the EPO facilitates oppositions within nine months post-grant, making ongoing landscape monitoring essential.


Legal and Strategic Implications

  • Scope enforcement: Broader claims enable extensive market control but may face validity challenges.
  • Licensing opportunities: Dense patent landscapes suggest licensing or partnership strategies.
  • Research freedom: Narrower claims offer freedom to develop derivative compounds but less market exclusivity.

Conclusion

EP2877155 exemplifies a strategic pharmaceutical patent with a carefully balanced claim set, covering specific chemical entities and their use. Its landscape reveals a competitive environment with overlapping patents, necessitating diligent FTO analysis before commercial deployment. The patent's scope provides a practical monopoly over a promising therapeutic class, but ongoing legal vigilance is vital.


Key Takeaways

  • Understand claim breadth: Broader claims provide extensive protection but face higher invalidation risk; narrower claims enhance defensibility.
  • Analyze patent landscape: Monitor competitors’ patents to inform R&D strategies and avoid infringement.
  • Assess market relevance: Evaluate if the patent covers core or derivative compounds to optimize licensing potential.
  • Ongoing legal vigilance: Prepare for possible oppositions or litigations within the patent’s lifecycle.
  • Integrated IP strategy: Balance patent scope with market dynamics, FTO, and licensing plans for maximum commercial benefit.

Frequently Asked Questions (FAQs)

1. What types of claims are typically included in EP2877155?
EP2877155 contains both broad independent claims covering general chemical classes and narrower dependent claims specifying particular compounds or formulations.

2. How does the patent landscape influence the value of EP2877155?
A dense patent environment suggests high competition, impacting licensing and commercialization strategies. It also highlights potential infringement risks but may offer partnering opportunities.

3. Can the scope of EP2877155 be challenged or invalidated?
Yes, during opposition or invalidation proceedings, prior art can challenge the novelty or inventive step, especially if claims are overly broad.

4. How do European patent laws affect pharmaceutical patents like EP2877155?
European patent law emphasizes novelty, inventive step, and industrial applicability. Patent examination involves rigorous scrutiny, and post-grant challenges are common.

5. What strategic actions should pharmaceutical companies take regarding similar patents?
Companies should conduct comprehensive patent landscape analyses, monitor opposition periods, and consider licensing or developing workarounds if patents threaten their pipeline.


Sources:

[1] European Patent Office. "European Patent Specification EP2877155."
[2] patent landscape reports and pharmaceutical patent conventions.
[3] EPO Guidelines for Examination, 2022.

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